Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Recent progress in biodiversity research on the Xylariales and their secondary metabolism


The families Xylariaceae and Hypoxylaceae (Xylariales, Ascomycota) represent one of the most prolific lineages of secondary metabolite producers. Like many other fungal taxa, they exhibit their highest diversity in the tropics. The stromata as well as the mycelial cultures of these fungi (the latter of which are frequently being isolated as endophytes of seed plants) have given rise to the discovery of many unprecedented secondary metabolites. Some of those served as lead compounds for development of pharmaceuticals and agrochemicals. Recently, the endophytic Xylariales have also come in the focus of biological control, since some of their species show strong antagonistic effects against fungal and other pathogens. New compounds, including volatiles as well as nonvolatiles, are steadily being discovered from these ascomycetes, and polythetic taxonomy now allows for elucidation of the life cycle of the endophytes for the first time. Moreover, recently high-quality genome sequences of some strains have become available, which facilitates phylogenomic studies as well as the elucidation of the biosynthetic gene clusters (BGC) as a starting point for synthetic biotechnology approaches. In this review, we summarize recent findings, focusing on the publications of the past 3 years.


Recent studies relying on bioinformatics, molecular ecology, and phylogenetics have revealed a very high species diversity in the fungal kingdom, and according to some estimates, there are several million undescribed species [1]. Recent studies using high-throughput and third generation sequencing techniques are now able to depict the diversity very accurately and often hitherto unknown phylogenetic lineages of fungi are detected [2, 3]. It often has been postulated that these unknown fungal organisms may constitute a great resource for new enzymes, drugs, agrochemicals, and other useful natural molecules, but by far not all groups of fungi have a diverse secondary metabolism. This has only been proven for certain taxonomic entities like the order Xylariales, from which a large number of unique carbon skeletons have already been discovered during the course of classical natural product screening programmes.

The current paper follows up on the review by Helaly et al. [4], where the state-of-the-art on secondary metabolite discovery and various correlations to biodiversity research had been described for this fungal order, taking the most important papers that were published until 2017 into account. Only 3 years later, a lot of new information has accumulated and it is already time for an update. The present paper is roughly divided in three parts, the first two of which are dealing with interesting new compounds from the two large families within Xylariales, Xylariaceae, and Hypoxylaceae (for illustrations of representative species see Fig. 1), and the third part covers recent taxonomic, chemoecological, and phylogenomic studies of these fungi.

Fig. 1

Stromata of some tropical and subtropical species of Xylariales. a Xylaria melanura. b X. telfairii. c X. grammica. d Hypoxylon haematostroma. e Pyrenopolyporus hunteri. f H. griseobrunneum. Images were kindly provided by Esteban B. Sir

Novel secondary metabolites from the Xylariaceae sensu stricto (Fig. 2)

After recent taxonomic revisions, in which other families like the Hypoxylaceae have been excluded, and only counting the genera that have been studied by molecular phylogenetic methods or examination of the asexual stages, the Xylariaceae sensu strictu presently comprise 33 genera and over 1000 (and up to 1230) species, of which more than 50% belong to the genus Xylaria [5, 6]. The number of accepted Xylaria taxa vary from 570 to 670 in these recent overviews, depending on whether synonyms and variations are counted. The genus Xylaria has never been subjected to a world monograph using modern, polythetic methodology. From the outcome of such work in other genera of the Xylariales, it is possible that Xylaria actually comprises several thousands of species of which the majority remains to be recognized and formally described [7].

Fig. 2

Secondary metabolites recently described from the genera Amphirosellinia, Ascotricha, Dematophora, Nemania, and Stromatoneurospora

For this reason, it is not surprising that most of the new metabolites reported from the family were derived from Xylaria species, as highlighted in a comprehensive review some years ago [4], for which we provide an update from the past years. It is important to note that most of the metabolites of Xylaria reported over the past decade have actually been isolated from endophytic strains.

Besides Xylaria, only for some genera of the Xylariaceae novel secondary metabolites have been described in the past 3 years. Those included Nemania, Rosellinia, and Dematophora, the latter of which has recently been resurrected and emended [8]. Most other genera, even larger ones like Hypocopra and Kretzschmaria, are nearly untapped concerning their secondary metabolites. This may be the case because they have rarely been collected or because they are not easy to cultivate.

Most of the compounds described today are still discovered by the classical method of axenic cultivation, either in submerged culture or on solid media, and successive extraction. However, other approaches like biotransformation, co-cultivation, epigenetic modification, and heterologous expression are encountered occasionally and will be discussed herein as well.

Subsequently, the genera for which novel secondary metabolites have been described in the past 3 years will be dealt with, and secondary metabolites by their affiliation to different compound classes. Some papers published prior to 2018 will be included herein for the sake of integrity in concurrence with the latest review [4], which covers most of the literature on secondary metabolites from Xylariales up to the end of 2017. We preferentially treat compounds that were not already reported previously [4, 9, 10].

The genus Amphirosellinia was not studied for secondary metabolites until recently, when the first natural product, coriloxin (1), was discovered from cultures of Amphirosellinia nigrospora [11]. Coriloxin represents a known cyclohexenone derivative [12] and was found to have weak antimicrobial activities. However, the crude extract of the fungus showed stronger bioactivities than the purified compound against phytopathogenic bacteria like Ralstonia solanacearum and plant-pathogenic fungi like Magnaporthe oryzae, suggesting either the presence of additional bioactive compounds in the extract and/or synergistic effects of 1 with other components. Those results render the producing organism A. nigrospora an interesting target for further research on its biocontrol capabilities against crop diseases.

Ascotricha was already described to produce orsellinic acid-glucosides in 2017, where short-time cultivation of a sea mud-derived Ascotricha sp. in submerged media led to isolation of two glucosides comprised of orsellinic acid and d-threitol, e.g. (2R,3R)-1,2,3,4-butanetetraol-1,4-diorsellinate (2) [13]. For 2, even a synthesis was described shortly after [14]. No biological activities were reported for those compounds from Ascotricha; however, they represent the first natural products from a genus that is otherwise still untapped.

Species of Dematophora were up to recently included in the genus Rosellinia, but were segregated due to differing asexual morphs and a well-defined clade in phylogenetic analyses [8]. The same paper also described two novel bioactive isopimarene diterpenoids from D. bunodes, (previously known as R. bunodes) named dematophoranes A (3) and B. The compounds showed weak antibacterial activity against Bacillus subtilis and Staphylococcus aureus and weak cytotoxic activities against mouse fibroblasts (cell line L929) and cervix carcinoma cells (KB 3.1). Other purified but known isopimarenes like myrocin B and the glucoside hymatoxin K were already reported from other species of Xylariales and Hypocreales. In addition, the presence of additional compounds with MS data that could not be matched to the entries in the available natural product databases was observed, making Dematophora spp. a worthwhile genus to examine more thoroughly.

Nemania is one of the largest genera in the Xylariaceae and some of its species are relatively well-studied. Recently, an endopyhtic isolate named Nemania bipapillata isolated from a red alga was described to produce botryane-type sesquiterpenoids [15]. This class of compounds had so far not been described from this genus, but from species of Hypoxylon and Daldinia, both belonging to the Hypoxylaceae [16, 17]. Among the compounds isolated from N. bipapillata, a nor-sesquiterpene named nemenonediol A (4) showed the most potent inhibition of human acetylcholinesterase (27.7% inhibition at 100 µM) in comparison to the reference galanthamine (90% at 100 µM) [15]. Furthermore, the sesquiterpene (2R,4R,5R,8S)-4-deacetyl-5-hydroxy-botryenalol (5) showed the strongest effect among the isolated botryanes against human butyrylcholinesterase (7.3% inhibition at 100 µM vs. 82% in the galanthamine control).

Cytochalasans are a class of hybrid polyketide-non-ribosomal peptide (PKS-NRPS) natural products of fungal origin, of which many representatives are known for their activity against the eukaryotic actin skeleton [18]. Cytochalasans are distributed over many genera within Xylariales, including the large families Xylariaceae and Hypoxylaceae. In 2019, the known 19,20-epoxycytochalasin C (6) and D, as well as 18-deoxy-19,20-epoxycytochalasin C were described from an endophytic Nemania sp. [19]. These three cytochalasans were found to have antiplasmodial and phytotoxic activities, but also high toxicity against mammalian cells. However, it was also shown elsewhere that the cytotoxicity against the actin skeleton is not irreversible for several cytochalasans like (6) [18]. In addition, recently discovered biological effects like the inhibition of biofilm formation in the human pathogenic bacterium Staphylococcus aureus must be due to other mechanisms of action because bacteria do not possess an actin cytoskeleton [20]. This also concerned the recently isolated sacchalasins from stromata of Daldinia sacchari, an endemic species of South Asia [21].

A species of Rosellinia, which is the second largest genus in the Xylariaceae, was recently described to produce a novel cytochalasin, jammosporin A (7) [22], along with other known cytochalasans. The producer strain is an endoypte that was tentatively identified as “R. sanctae-cruciana” by sequencing of the ITS nrDNA (see Future Outlook Section for the validity of this approach). Jammosporin A (7) was found to be mildly cytotoxic against MOLT-4 cells with an IC50 value of 20 µg/mL. Cytochalasin C was concurrently isolated and assessed for its bioactivity showed stronger effects against MOLT-4 (IC50 6 µg/mL). These activities are rather low as compared to the nanomolar inhibitory concentrations that are known from other members of the cytochalasan class.

The genus Stromatoneurospora, erected in 1973, was alternatively assigned to the families Hypocreales, Xylariales, and Sordariales due to inconclusive morphological characteristics. A recent finding of the type species of the genus, S. phoenix, finally enabled a molecular characterization using multigene phylogeny [23]. Thereby, S. phoenix was placed close to the coprophilous genera like Poronia and Podosordaria within the Xylariaceae. Complementarily, a screening of its secondary metabolites revealed two novel eremophilane sesquiterpenoids named phoenixilanes A (8) and B, which were found devoid of promising bioactivities in antimicrobial and cytotoxicity assays. Besides, several chemotaxonomically meaningful metabolites were isolated, e.g., punctaporonin B, known from Poronia spp., and 8,9-dehydroxylarone, reported from a Xylaria sp., thereby confirming the phylogenetic classification to the Xylariaceae [23]. These results highlight the significance of a combination of different techniques, like molecular phylogeny and chemotaxonomy, for taxonomic assignment within the order Xylariales.

Cytochalasans from Xylariaceae (Fig. 3)

Several hundred representatives of the cytochalasans, fungal PKS-NRPS natural products, have been described to date [24], but still new derivatives are being continuously reported. Species of the genus Xylaria continue to be among the most prolific producers of these molecules [25].

Fig. 3

Recently reported cytochalasans from Xylaria spp.

A recent example is Xylaria cf. curta, which was isolated as an endophyte from potato stem tissue. Cultures of this fungus yielded numerous interesting metabolites after extensive preparative work. Among those, the curtachalasins (e.g. 910) as well as xylarichalasin A (11) have to be highlighted due to their unprecedented core structures: the former harbor a tetracyclic backbone [26, 27], while in the latter, a highly complex hexacyclic structure was found [28]. Curtachalasins A (9) and B were found devoid of promising bioactivities in initial screenings for cytotoxicity and antimicrobial activities [27], indicating that they do not act on the actin system like other members of the class. In a subsequent publication [26], the authors assessed the ability of curtachalasins C (10) and E to revert fluconazole-resistance in Candida albicans. When 10 was given in combination with the antimycotic fluconazole, strong reversal of antifungal activity was observed. These results emphasize the vast range of bioactivity that can be exhibited by cytochalasans, once they are being subjected to a broad biological characterization. Xylarichalasin A (11), however, showed the strongest activity against human cancer cell lines MCF-7 (IC50 6.3 µM) and SMMC-7721 (8.6 µM), besides weaker cytotoxicity against others. Notably, these activities are much weaker than those of the first reported cytochalasins, which have IC50 in the nanomolar range. Lately, a new derivative, curtachalasin Q, was reported from an endophytic Xylaria sp. isolated from roots of Damnacanthus officinarum, but was found devoid of cytotoxic activity [29].

A novel cytochalasin was isolated from a marine-derived Xylaria sp. and named cytochalasin P1 (12) [30], which is the 19,20-epoxide of the known cytochalasin P. Curiously, its cytotoxicity against human tumor cell lines was strong against SF-268 and MCF-7 (IC50 1.37 and 0.71 µM, respectively), but absent against NCl-H460 or HepG2 cells (IC50 > 100 µM), suggesting selective cytotoxic effects.

A report of novel cytochalasans with phytotoxic activities has been published recently [31]. Besides some known cytochalasans, the novel epoxycytochalasins Z17 and -Z8, as well as epoxyrosellichalasin (13) have been described. Epoxyrosellichalasin (13) as well as the known cytochalasin K showed very strong shoot elongation inhibition against wheat (IC50 of 18.9 µM), which were stronger than that of the reference glyphosate (42.3 µM). The known 10-phenyl-[12]-cytochalasin Z16, cytochalasin K and E exhibited strong root elongation inhibition (IC50 of 17.4, 22.6, and 19.7 µM, respectively). Glyphosate, again used as a reference, showed weaker inhibition (38.1 µM). Curiously, cytochalasin K was a highly potent inhibitor of root elongation against turnip, which was ~50 times more active than glyphosate (IC50 1.6 vs. 83.1 µM). Despite these interesting findings, the authors also state that the high cytotoxicity and nonavailability in ton-scales precludes cytochalasins from biotechnological applications [31]. Still, these findings highlight the potential of cytochalasans as potent agents against diverse biological targets and suggest further investigations into their mode of action.

Furthermore, the known cytotoxic compounds cytochalasin C and D were isolated from Xylaria cubensis and evaluated for their phytotoxic potential [32]. An assay was conducted measuring the length of wheat coleoptiles (sheath protecting the emerging shoot in monocotyledons, e.g. grasses) to assess the phytotoxicity. Both, cytochalasins C and D exhibited a stronger growth inhibition than a commercially available herbicide containing oxyfluorfen [32]. These results might be used as a starting point for further studies investigating the use of cytochalasans as crop-control agents. However, their potent cytotoxicity must also be taken into account.

Five new cytochalasans were isolated from a solid-state rice fermentation of X. longipes of an unreported host, along with seven known congeners. The novel compounds were found to be derivatives of known cytochalasans and showed weak cytotoxicity of IC50 > 40 µg/mL against human cell lines like HL-60 or A-549 [33].

From cultures of a Xylaria sp. isolated from the mangrove Xylocarpus granatum, a novel cytochalasan named xylarisin B (14) was isolated [34]. In assays evaluating the inhibitory effect on acetylcholinesterase (AChE)- and α-glucosidase, 14 was found devoid of activity.

Cultivation of a wood-decaying Xylaria sp. also afforded an unprecedented cytochalasin named xylochalasin (15) [35]. It was found to be weakly active against HeLa cells (IC50 57 µg/mL), and even less active against other human cancer cell lines like HT29, HCT116, Vero, or MCF-7 (IC50 90 to >100 µg/mL).

Terpenoids and hybrid-terpenoids from Xylariaceae (Fig. 4)

A group of eremophilane sesquiterpenoids named nigriterpenes A–F was isolated from a termite-nest-derived X. nigripes [36]. Those compounds were assessed for their inhibitory effects on lipopolysaccharide (LPS)-induced inducible nitric oxide synthase and cyclooxygenase-2 expression in microglial BV-2 brain cells. Especially nigriterpene C (16) showed a strong inhibition (IC50 1.8 µM) compared to the LPS vehicle control (5.7 µM), and was furthermore shown to attenuate microglial NO production in a concentration-dependant matter. Hence, the authors conclude that 16 (besides formannoxin alcohol, a known compound that was concurrently isolated) might be an interesting candidate as an anti-neuroinflammatory agent [36].

Fig. 4

Recently reported terpenoids and terpenoid-hybrids from Xylaria spp.

Moreover, several nor-isopimarene terpenoids named xylarinoditerpenes A–R [37] and two isopimarenes designated xylarilongipins A (17) and B [38] were recently reported. These terpenoids were isolated from a fungicolous strain of X. longipes, growing on fruiting bodies of the basidiomycete Fomitopsis betulina. Both groups of compounds showed immunosuppressive activities against cell proliferation of concanavalin A-induced T-lymphocytes and LPS-induced B-lymphocytes. The strongest suppression was exhibited by xylarinoditerpene I (18) with an IC50 of 1 µM against induced T-lymphocytes, which indicates a strong immunosuppressive activity in comparison with the reference dexamethasone (IC50 1.6 µM).

Two new isopimarene glycosides named xylapapusides A (19) and B were reported from cultures of an endophyte tentatively identified as X. papulis that had been isolated from the plant Lepidagathis stenophylla [39]. Compound 19 showed inhibition of NO production in LPS-induced RAW264.7 macrophages of ca. 34%, indicating a moderate effect as compared to the positive control, aminoguanidine (ca. 79% inhibition). In addition, a group of drimane sesquiterpenoids named xylariaines A–C was found in culture extracts of the same fungus [40]. These were assessed for their inhibitory effect on AChE and found to be weakly active with an enzyme inhibition of 18% exhibited by xylariaine B (20), as compared to the positive control tactrine (56.7%).

A number of antibacterial compounds, including a new eremophilane sesquiterpenoid named xylareremophil (21), were reported from a Xylaria sp. [41]. Xylareremophil (21) exhibited weak antibacterial activity (MIC: 25 µg/mL) against Micrococcus luteus and Proteus vulgaris.

A novel abietane diterpenoid named hydroxydecandrin G (22) from an endophytic Xylaria sp. [31] exhibited very strong shoot elongation inhibition against wheat (IC50 of 23.6 µM), which was stronger than that of the reference glyphosate (42.3 µM), suggesting potential as a natural herbicide.

In addition, a triterpene glycoside named mannosylxylarinolide (23) was reported from another endophytic Xylaria sp., but no data on biological activities were included in this publication [42].

From cultures of X. allantoidea, the known terpenoids demethylincisterol A3 and chaxine C were isolated [43]. Chaxine C (24) was moderately active against human HeLa and primate Vero cells lines with IC50 values of around 3 µg/mL. Chaxins, which were first reported from fruiting bodies of the edible mushroom Agrocybe chanxingu as active ingredients responsible for suppression of osteoclast formation [44], did not show activities against murine UAMS-32 cells. The occurrence of the rare chaxin skeleton in both, the Ascomycota and Basidiomycota is puzzling because normally these two subphyla do not share many common secondary metabolites.

Non-ribosomal peptides from Xylariaceae (Fig. 5)

Xylaria ellisii was recently described as a novel species that colonizes conifers as an endophyte but forms stromata on hardwood in North America [45]. Concurrently, the fungus was studied for biologically active secondary metabolites, which revealed eight new cyclic pentapeptides designated ellisiiamides A (25)−H. Only ellisiiamides A–C were actually purified, while the structures of the remaining congeners were derived from LC–MS analyses. Assessment of the antimicrobial activities of ellisiiamides revealed no promising effects. Besides these pentapeptides, several known compounds like griseofulvin, cytochalasans, hirsutatin A, and piliformic acid were detected, underlining the chemical potential of this new species. The antifungal effects observed can probably be attributed to griseofulvin and the cytochalasans. In any case this study is exemplary because it provides sound taxonomic data on the endophytic X. ellisii and allows for manifold follow-up work on its ecology and the biological functions of its secondary metabolites. Needless to say, the molecular identification of X. ellisii included a multigene genealogy and detailed morphological studies, rather than just generation of rather inconclusive ITS sequences, and the fungal cultures as well as the sequence data are deposited in the public domain.

Fig. 5

Recently reported non-ribosomal peptides from Xylaria spp.

Another description of cyclic pentapeptides was reported from a Xylaria sp. isolated from the Chinese medical plant Sophora tinkinensis [46]. The compounds, which were given the trivial names xylapeptide A–B (2627), showed moderate but selective antibacterial activities. Minimum inhibitory concentrations (MIC) of 26 against Bacillus sp. were 12.5 µg/mL, while 27 additionally exhibited moderate antibacterial activity against various bacteria including the pathogenic Staphylococcus aureus (MIC 6.25–12.5 µg/mL). Furthermore, xylapeptide B (27) showed moderate antifungal effects against Candida albicans with a MIC of 12.5 µg/mL. Notably, 26 had the uncommon l-pipecolinic acid incorporated in its peptide structure, while 27 had an l-proline at this position. With this being the only difference between both compounds, contribution of this amino acid residue to antimicrobial activity is indicated. Moreover, antiviral or cytotoxic activities were evaluated but not observed.

Cultivation of a wood-decaying Xylaria sp. also afforded a novel cyclic pentapeptide as well as an unprecedented cytochalasin [35]. The cyclic pentapeptide pentaminolarin (28) showed weak inhibition against HT29 and HCT116 cell lines (IC50 32 and 38 µM).

Macrolide polyketides from Xylariaceae (Fig. 6)

Recently, a patent was published dealing with a macrolide from X. curta designated E1011 (29), which showed cytotoxic effects against several human cancer cell lines [47]. This macrolide 29 is a bisacetylated, diastereomeric derivative of the anthelmintic 14-membered macrolide clonostachydiol (30), which was originally isolated from the fungus Clonostachys cylindrospora [48], but found in a Xylaria sp. [49] recently. E1011 (29) exhibited moderate cytotoxicity against diverse human cell lines like HL-60 or A-549 with IC50 values of 4.9 and 25.6 µM, respectively [47]. Clonostachydiol (30), was also found to be weakly cytotoxic (KB: IC50 39 µg/mL, NCI-H187: 17 µg/mL) [49].

Fig. 6

Recently reported macrolides from Xylaria spp.

A 10-membered macrolide was isolated from X. feejeensis. No name was assigned, but its systematical name is (5E)-10-heptyl-3,4,5,8,9,10-hexahydro-5,8,9-trihydroxy-2H-oxecin-2-one (31) [50]. It was assessed for its potential to inhibit osteoclastogenesis, as an excessive osteoclastogenesis is clinically associated with diseases like osteoporosis or rheumatoid arthritis. A strong inhibition in terms of reduced numbers as well as areas of osteoclasts was observed, which renders 31 an interesting target to study further.

Benzenoids and lactones from Xylariaceae (Fig. 7)

A number of natural products was recently described from a termite nest-derived X. fimbriata. In total, seven benzoid ethers named fimbriethers A–G were isolated and characterized [51]. Assessment of their anti-inflammatory activity via a nitric oxide inhibition assay in RAW264.7 cells resulted in fimbriethers B (32), E, and G to exhibit moderate anti-inflammatory activity. Hence, fimbriethers may serve as agents against inflammation in mammals, given that none of them are cytotoxic against RAW264.7.

Fig. 7

Recently reported benzenoids and lactones from Xylaria spp.

An investigation into the secondary metabolism of an endophytic Xylaria sp. from leaves of Hevea brasiliensis resulted in isolation of 18 compounds in total with description of the new natural products xylarianins A–D [52]. The xylarianins comprise compounds of three different classes: while xylarianin A (33) is an oxydibenzenoid, B (38) represents a chromone backbone, and C (43) and D are succinic acid derivatives. Along with the xylarianins, three known oxydibenzenes were isolated. All 18 compounds were evaluated for their inhibitory effect on human carboxylesterase 2 (hCE2). The oxydibenzenoids like 33 (IC50 10.43 µM) were found to be moderately active in comparison to the positive control loperamide (1.31 µM), which is a selective inhibitor of hCE2 and clinically used as medication against diarrhea. Highest activity among the isolated compounds was exhibited by the known oxydibenzenoid 2-(2,4-dimethoxy-6-methylphenoxy)-4,6-dimethoxy-benzoic acid methyl ester (IC50 6.69 µM).

A co-cultivation approach with Penicillium crustosum and a Xylaria sp. derived from roots of Sonneratia caseolaris was used to isolate four new, alkylated benzenoid natural products designated penixylarins A–D, along with two known benzenoids [53]. While the two known compounds as well as penixylarins C (34) and D were produced by the Xylaria sp. under axenic conditions, penixylarins A–B were only found in the co-cultures. Bioactivity evaluation showed that 34 in particular exhibited activity against Mycolicibacterium phlei with an MIC of 6.25 µg/mL. Against Vibrio parahemolyticus, an MIC of 12.5 µg/mL was measured. The positive control ciprofloxacin showed MIC of 1.56 and 12.5 µg/mL, respectively.

Furthermore, new dibenzoxepin derivatives named arugosins O (35) to Q were reported from an unidentified Xylariaceae sp. [54]. No effects were observed in assays evaluating antibacterial or cytotoxic activities. Generally, arugosins are rather widespread among fungi, given that they were reported from coprophilous, marine-derived, and endophytic genera, among others [55,56,57].

Xylaria feejeensis is biologically associated with the mangosteen fruit and was thus examined for its capability to biotransform plant metabolites to novel derivatives [58]. One of the secondary metabolites produced by said plant is the xanthone β-mangostin, which is associated with anti-inflammatory, antibacterial, antimalarial, and antimycobacterial activities. Cultivation of X. feejeensis with β-mangostin resulted in two novel natural products, mangostafeejin A (36) and B, both of which occurred as (+) and (−)-isomers. No bioassays were reported, but the results make an interesting case for investigation of the plant-fungus ecology on the secondary metabolite level.

The novel hexaketides xylarodons A (37) and B were isolated from an endophytic Xylaria sp. [59], and tested for cytotoxic effects and inhibition of tyrosine kinase but were found devoid of activity.

A number of small polyketides were characterized from an ascospore-derived strain of a Xylaria sp., whose stromata were collected from rotten wood [60]. Submerged cultivation of the fungus yielded two chromones, 6-ethyl-8-hydroxy-4H-chromen-4-one and 6-ethyl-7,8-dihydroxy-4H-chromen-4-one (39), as well as two isocoumarins, 3,4-dihydro-8-hydroxy-7-methoxy-3-methylisocoumarin and 3,4-dihydro-5,7,8-trihydroxy-3-methyl-isocoumarin (45). Compound 39 had weak activity against HT29 and HCT116 cells (IC50 16.5 and 23.1 µg/mL), and 39 and 45 exhibited anti-inflammatory effects against LPS-stimulated RAW264.7 macrophages with IC50 values of 1.6 and 3.0 µg/mL, respectively. The results indicated a comparable or even slightly stronger activity than the positive control, diclofenac [60].

A number of (dimeric) chromones were reported from a Xylaria sp. [61] isolated from the leaves of the rubber tree Hevea brasiliensis. Besides known monomeric chromones, three new dimeric compounds named xylaromanones A (40) to C were described, which constitutes the first occurrence of such dimers from the genus Xylaria [61].

Two new pyranone derivatives named xylaropyranones B to C (41) [62] were isolated from an endophytic Xylaria sp. along with xylaropyranone, which is known from X. feejeensis [63], and annularins A and C. All except for annularin C were tested for cytotoxic and tyrosinase-inhibitory activity, but found devoid of noticeable effects. Another occurrence of pyranones was reported from an endophytic Xylaria sp. and named Xylariahgins A (42)–F [64]. An assessment of their cytotoxicity against human tumor cell lines such as HL-60, A-549, and MCF-7 was unsuccessful.

Occurrence of antibacterial metabolites was reported from Xylaria sp. within two publications: in the first work [65], a new pyranone, 6-heptanoyl-4-methoxy-2H-pyran-2-one (44), was reported, while the second publication gave account on a novel phthalide named xylarphthalide A (46) [66]. Both compounds showed weak activities against Escherichia coli and Staphylococcus aureus (44, MIC 50 µg/mL) or E. coli and Bacillus subtilis (46, MIC 12.5 µg/mL), respectively.

The antifungal agent griseofulvin (47), originally found in Penicillium griseofulvum, is well-studied and even clinically applied against dermatophytosis. However, research for more potent derivatives is ongoing using X. cubensis as an alternative producer. In a recent study, 47 was semisynthetically derivatized to form fluorinated analogs, as fluorine was expected to strongly alter the chemical properties when incorporated [67]. Of the eleven compounds generated, only 7-fluoro-7-dechlorogriseofulvin (48) showed an activity similar to 47 against the skin-infection causing Microsporum gypseum. While no analog was shown to be more potent than the natural product, structure–activity relationships could be deduced and a simple way of incorporating fluorine into natural products was demonstrated.

Miscellaneous secondary metabolites from Xylariaceae (Fig. 8)

Co-cultivation is a regularly applied approach to induce activation of so-far silent gene clusters. One recent positive example of a novel backbone discovered is the meroterpenoid wheldone (49), which was produced (presumably) by X. flabelliformis when co-cultured with two different Aspergillus spp., respectively [68]. A moderate cytotoxicity was measured for 49 with lowest IC50 values of 2.4 µM against MDA-MB-435 (human melanoma cancer cell line). As the authors state that both, X. flabelliformis and one of the Aspergillus sp. were genome-sequenced, a correlation to the biosynthetic gene clusters (BGC) can be made and the actual producer of 49 proven.

Fig. 8

Recently reported miscellaneous secondary metabolites from Xylaria spp.

Another approach to attain novel natural products is heterologous gene expression. Recently, this concept has been utilized by mixing genes responsible for production of the potent statins (of which lovastatin is the most famous representative) from two producing organisms, Aspergillus terreus and X. grammica, in Saccharomyces cerevisiae [69]. This ultimately resulted in MS/MS predictions of two novel structures, O-acetylmonacolin J and “methylbutyryl DA_FR901512”. Even though neither of the new compounds were purified, application of this approach highlights the vast amount of novel chemistry that can be created using combinatorial approaches.

X. longipes is a fungus known for production of the antifungals xylarin and xylaramide [70, 71], as well as the succinic acid derivative piliformic acid [72]. In the past years, further progress was reported, starting with biotransformation studies of the fluoroquinolone antibiotic ciprofloxacin in 2018 [73]. The authors showed that cultures of X. longipes are able to derivatise ciprofloxacin, reducing its antibacterial activity by 75–88%. Before, the authors already showed similar effects when giving other fluoroquinolones to the fungus [74, 75]. These studies are very interesting examples of how fungi may be utilized for bioremediation purposes.

Furthermore, a multitude of new (thio)-alkaloids has been isolated from X. longipes. These compounds, named xylaridines A (50) to B [76], as well as thio derivatives thereof named xylaridines C–D (51) [77], were assigned as NRPS-PKS hybrids, which seems unlikely given the chemical structures of the compounds. Even though none of them were found to exhibit promising activities in antimicrobial or cytotoxicity assays, the biosynthesis seems to be very interesting to decipher due to the chemical complexity of the nitrogen and/or sulfur-containing structures.

In addition, derivatives of the known stromatal metabolites from Xylaria, xylaral and xylactam, were reported in 2017 [78]. The benzofuranon xylaral B was described along with two new isoindolinones, xylactams C–D, from fruiting bodies of X. polymorpha. No bioactivities were reported, but this report matches well with former examinations of stromatal secondary metabolites from X. polymorpha and other Xylaria species [79]. The xylarals are actually chemotaxonomic markers that were previously used to separate morphologically similar species like X. mesenterica from the hypoxyloid genus Entonaema.

The X. allantoidea culture that yielded the chaxins produced also a novel cerebroside named allantoside (52) [43]. However, no cytotoxicity was measured for 52.

From stroma-derived cultures of Xylaria cf. cubensis, an amino-amindine, 2,5-diamino-N-(1-amino-1-imino-3-methylbutan-2-yl)-pentamide (53), was discovered along with several diketopiperazines and furanones [80]. No antimicrobial or cytotoxic activities were found for this new compound.

Novel secondary metabolites from species of the Hypoxylaceae sensu stricto

The Hypoxylaceae were resurrected by Wendt et al. [81] to accommodate the genera that were formerly placed in Xylariaceae (sensu lato) that have a nodulisporium-like anamorph, in agreement with a multi-locus genealogy. In contrast to the Xylariaceae sensu strictu, many of their species accumulate large amounts of pigments and other secondary metabolites in their stromata, which are also of importance for chemotaxonomic purposes.

Cytochalasans from Hypoxylaceae (Fig. 9)

Aside from Xylaria spp., species of the Hypoxylaceae like Hypoxylon or Daldinia are known for production of a multitude of cytochalasan PKS-NRPS secondary metabolites. A recent publication assessing the effects of 25 selected cytochalasans on the actin skeleton by immunofluorescence shed some light on the mode of action of these molecules [18]. Preliminary structure-activity relationships of cytochalasans were derived and it was shown that actin-disrupting effects are reversible in some cytochalasans, while being permanent in others. However, the work also described two unprecedented cytochalasans from Hypoxylon fragiforme, named fragiformins C and D (54). While fragiformin C attained incomplete actin disruption at 5 µg/mL and was partially reversible, fragiformin D (54) was highly active, yielding complete disruption at 1 µg/mL without reversibility [18].

Fig. 9

Recently reported cytochalasans from species of the Hypoxylaceae

A recent biosynthetic study investigated the function of cryptic P450 monooxygenases involved in cytochalasan biosynthesis from H. fragiforme as well as Pyricularia oryzae [82], both natural cytochalasan producers. Using combinatorial biosynthesis, six P450 genes were individually expressed in two ΔP450 mutants of Magnaporthe grisea, respectively. This led to induction of a number of unprecedented cytochalasans and indicated the functions of the tailoring P450 monooxygenases involved in cytochalasans biosynthesis in both producer organisms. Concurrently, while examining negative controls of H. fragiforme for the heterologous expression, a new cytochalasan was discovered and named fragiformin E, but not characterized concerning its bioactivities.

In 2019, a novel cytochalasan from fruiting bodies of Daldinia concentrica was isolated and named daldinin (55), along with two known ones [83]. Assessment of the cytotoxic activities showed that 55 exhibited weak cytotoxic activity against several cell lines like SK-LU-1 or MCF-7 with IC50 values of 11.4 and 13.5 µM, respectively. It has to be noted that 55 carries the same trivial name as the azaphilone pigments daldinins described from the very same fungus [84].

Azaphilones from Hypoxylaceae (Fig. 10)

Lately, a number of fossil samples from the medieval age resembling fruiting bodies of Hypoxylon spp. were analyzed morphologically, microscopically, and chemotaxonomically to allow for species determination as no intact DNA was available for sequencing [85]. Combination of these three methods allowed for some of the specimens to be determined as H. fragiforme. Especially LC–MS analysis of the samples was noteworthy, as even after ca. 1000 years intact azaphilone pigments were observed, which is remarkable given the fact that these pigments are known (and even named) for spontaneous reactions with diverse nitrogen species [86].

Fig. 10

Recently reported azaphilones from species of the Hypoxylaceae

By comparing fossilized and fresh material, a number of unidentifiable peaks was found in both samples. Hence, fresh material of H. fragiforme was used to isolate a number of azaphilones. Besides the known mitorubrin-type pigments, two further congeners of the dimeric rutilin-type azaphilones like rutilin C (56), as well as the fatty acid-carrying fragirubrins A (57) to E were discovered [85]. Follow-up work on those compounds yielded fragirubrins F–G as well as novel heterodimers composed of mitorubrin- and fragirubrin-type azaphilones named hybridorubrins A (58) to D [87]. Assessment of the biofilm formation capabilities of 5658 and some congeners against Staphylococcus aureus showed that the dimeric rutilins and hybridorubrins exhibit particularly strong effects, which lie in a range with the biofilm-inhibiting microporenic acid A [88]. Electronic Circular Dichroism measurements allowed for assignment of H. fragiforme azaphilones into three stereochemical groups. The first one contains the C-8(R)-configured, acyl-carrying lenormandins and fragirubrins; the second one comprises the (S)-configured, orsellinic acid-carrying mito-rubrins and dimeric rutilins, while the third one includes the dimeric hybridorubrins, which are composed of one (R)- as well as one (S)-configured azaphilone subunit.

Concurrently, genome analysis of H. fragiforme revealed two distant, cross-acting BGC to be responsible for production of different azaphilone classes and subsequent tailoring. The findings underline the potential of combining natural product chemistry and state-of-the-art genome sequencing techniques as a powerful tool.

Terpenoids and terpenoid-hybrids from Hypoxylaceae (Fig. 11)

In 2017, a number of drimane sesquiterpenoid-isoindolinone hybrids named fendlerinines A–D (59) as well as drimane-phthalide compounds designated fendlerinines E–F were described from a saprotrophic fungus identified as “Hypoxylon fendleri” collected from Thailand [89]. It remains unclear whether the taxonomy of the strain is correct according to the current concept because this species has only been safely recorded from America (the type is from Venezuela) and there are many similar taxa in tropical Asia. However, this strain has an extraordinarily diverse secondary metabolism. Subsequent work on the fungus yielded 13 additional drimane-phthalides, namely fendlerals A (60)−C, fendleric acids A–C, fendlerins A–D (61), fendlerols A–B, and fendlerinine G [90]. Curiously, 61 even carries two drimane units. The fendlerals A (60) and B showed weak activities against the malaria parasite Plasmodium falciparum with IC50 of ca. 4 µM, as compared to the reference dihydroartemisin with and IC50 of ca. 2 nM. Furthermore, strong antibacterial effects against Bacillus cereus (MIC 1.56 µg/mL vs. vancomycin 1–2 µg/mL) and antifungal activity against the plant-pathogen Colletotrichum capsici (MIC of 6.25 µg/mL vs. amphotericin 3.13 µg/mL) were observed. However, the compounds also showed cytotoxicity in the rage of 5–10 µM and are obviously not selective enough to envisage any further development as antiinfective drugs.

Fig. 11

Recently reported terpenoids/hybrid-terpenoids from species of the Hypoxylaceae

A study on secondary metabolites of the related endolichenic fungus H. fuscum isolated from Usnea sp. yielded two drimane diterpenoid-glucosides 16-α-d-glucopyranosyl-(62) and 16-α-d-mannopyranosyl-oxyisopimar-7-en-19-oic acid [91]. Along with these compounds, a brasilane-type sesquiterpenoid-glucoside named hypoxyside (63) was discovered, which represents the first brasilane from the genus Hypoxylon. Hypoxyside (63) was shown to exhibit cytotoxicity against K562 cells with an IC50 value of 18.7 µM, which is weak compared to the reference cisplatin (3.8 µM), while for the glucoside compounds like 62 no activities were observed. Furthermore, antimicrobial assays did not show an effect of any of the isolated compounds.

A recent study of Annulohypoxylon truncatum revealed the presence of the known terpenoid-glucoside brasilane A, along with two unprecedented congeners named brasilanes D–E (64), all carrying N-acetylglucosamine as their glycone units [92]. Concurrent analysis of the recently published genome sequence of the fungus [93] allowed for identification of the BGC bra responsible for brasilane assembly. Using heterologous expression in Aspergillus oryzae, the functions of the respective genes in the bra BGC were assessed. Curiously, BraB constitutes the first example of a fungal N-acetylglucosamine transferase, suggesting biotechnological and/or chemical applications due to its broad substrate tolerance.

Macrolide polyketides from Hypoxylaceae (Fig. 12)

One macrolide recently reported from a member of the Hypoxylaceae is hypoxylide (63), which was discovered from an endophytic Annulohypoxylon sp. derived from the mangrove Rhizophora racemosa [94]. The compound 65 features a naphthalenone moiety fused to a 10-membered lactone ring, which represents a novel backbone structure. However, no effects in assays measuring cytotoxic or antibacterial activity of 65 were observed.

Fig. 12

Recently reported macrolides from species of the Hypoxylaceae

Furthermore, screening of the endolichenic H. fuscum that also yielded hypoxyside (63), gave rise to another 10-membered macrolide named 5,6-epoxyphomol (66), besides the known phomol [91]. Both exhibited weak cytotoxicities with IC50 values of 15.9–32.7 µM against K562, SW480, and HepG2 cell lines, as compared to cisplatin, which showed IC50 values of 3.8–6.8 µM.

Benzenoids, lactones, and other small cyclic molecules from Hypoxylaceae (Fig. 13)

Investigations of the stromata of the recently described Annulohypoxylon viridistratum [95] yielded three unprecedented, fully conjugated benzo[j]fluoranthenes named viridistratins A–C, along with the known truncatones A and C [96]. A broad-spectrum antimicrobial activity against bacteria and fungi was measured for viridistratins A and B (67), with the strongest activity exhibited by 67 against Mucor hiemalis with an MIC of 4.2 µg/mL, as compared to nystatin (66.7 µg/mL). Furthermore, 67 showed a strong cytotoxicity against the human cell lines A-431 and A-549 with IC50 values of 1.1 and 1.4 µM, respectively. Due to their distinctiveness, the viridistratins can serve as chemotaxonomic marker compounds for A. viridistratum.

Fig. 13

Recently reported benzenoids, lactones, and other small cyclic molecules from species of the Hypoxylaceae

Extraction of secondary metabolites from fruiting bodies of Daldinia concentrica led to the isolation of the novel isoindolinones daldinans B–C, the phthalides daldinolides A and B, and the binaphthalene daldiquinone [97]. Only daldiquinone (68) exhibited anti-angiogenesis activity measured via inhibition of human umbilical vein endothelial cells (HUVEC) growth with an IC50 of 7.5 µM, with cytochalasin B as positive control (IC50 0.2 µM). The identification of this fungus is dubious because D. concentrica sensu strictu has never been safely recorded from Japan and Asia.

Within the same work reporting on a multitude of new terpenoids from a species potentially representing H. fendleri (see Terpenoids section), several terphenyls were reported [89]. Apart from rickenyls C–E known from H. rickii [98], four new terphenyls named fendleryls A (69) to D were isolated [89]. Fendleryls A−D exhibited no antimicrobial activity, but weak cytotoxicity against NCI-H187 and Vero cells with IC50 values of 48 and 49 µM, respectively. Follow-up work also afforded fendleryl E, which showed no promising bioactivities in antimicrobial or cytotoxic activity assays [90].

An approach exploiting upregulation of enzymes to obtain novel chemistry was presented in 2017 [99]. The authors cultured a Daldinia eschscholtzii from mantis-gut, a producer of dalesconols, and supplemented the epigenetic modifier procaine. This led to incorporation of guest intermediates into the dalesconol bioassembly lines, which resulted in isolation of the novel dalesconol derivatives (+)- and (−)-dalescones A–G. Assessment of the IL-1β production inhibition, whose secretion represents NLRP3 inflammasome activation, showed that especially (−)-dalescone D (70) exhibited a strong inhibitory effect. IC50 values of 70 were 3.9 µM, which is ca. five times more active as compared to the positive control andrographolide, which had an IC50 of 21.5 µM.

In a follow-up work, axenic cultivation of D. eschscholtzii without supplements revealed two dalesconol-related stereoisomers, (+)- and (−)-galewone (71), which harbor a spiro-connection [100]. Both isomers and the racemate were assessed for their anti-fibrotic activites; (−)-galewone (71) showed low IC50 values of 3.7 µM against fibrosis-involved CFSC-8B cells, but a comparably low activity against Lx-2 cells (IC50 26.7 µM), suggested a selective effect.

Screening of cultures of D. eschscholtzii isolated from the mangrove Bruguiera sexangula yielded a number of tetralones and chromones, of which daldiniones A–E and helicasolides D–E represent unprecedented structures [101]. Curiously, daldinione E (72) contains an unusual 7-membered lactone ring. Bioactivity testing of those tetralones and chromones in an α-glucosidase inhibition assay remained fruitless.

The fungicolous H. invadens, which was only described in 2014, exhibits a unique lifestyle by growing on a member of its own genus, H. fragiforme [102]. So far, only volatile organic compounds have been described from H. invadens [103], but a recent investigation into its secondary metabolites revealed the known naphthoquinones flaviolin (73) and 3,3′-biflaviolin (74) to be produced in submerged cultures [104]. Only known as products of the melanin biosynthesis when the underlying pathway was actively influenced (e.g. by adding melanin biosynthesis-inhibiting fungicides [105]), 7374 were found to be produced in large amounts without any intervention, but the reason for that remains dubious. Assessment of the bioactivities of 7374 against microbes and mammalian cell lines did not yield interesting results.

A large number of known as well as novel benzenoids, benzopyranes, and benzopyrane-glucosides has been isolated from an endophytic D. eschscholtzii from Dendrobium chrystotoxum [106], along with one cyclohexene named daldinium A (75). No significant bioactivities were found in antimicrobial assays, but one glucoside, 7-O-α-d-ribosyl-5-hydroxy-2-methyl-4H-chromen-4-one (76), induced a glucose consumption rate of 17.3%, as compared to the positive controls insulin and berberine (24.8 and 24.6%, respectively). For the very same strain, cultivation in red ginseng medium led to isolation of daldinisin (77) [107], an unprecedented benzopyran naphthalene glucoside, and a lactone, 8-hydroxylhelicasolide. Weak anti-AChE activity was observed with inhibition of 38.8% at 50 µM for 77, while the positive control tactrine showed 64.9% inhibition at 0.333 µM.

A screening of cultures of an endolichenic isolate of H. fuscum furthermore yielded several known benzopyrones and -furanones, with the new hypoxyolides A (78) and B belonging to the latter class [91]. Weak cytotoxicity with IC50 values of ca. 20 µM were observed against K562, SW480, and HepG2 cell lines for these compounds. Even though in this case only ITS sequence barcoding was used to assign the species, the identification seems to be reliable because H. fuscum is one of the species in the genus that has a specific ITS nrDNA sequence.

Several furanoids were described from a raspberry leaf-derived H. submonticulosum [108] (a species that was recently transferred to Hypomontagnella [109]). Cultivation of the fungus led to the isolation of trienylfuranol A (79) as well as trienylfuranones A and B. Due to instability of the three compounds, a semisynthetically obtained derivative of 79, (1S,4R)-1-hexyl-dihydro-4-methylfuran-2(1H)-one, was evaluated for its fungicidal properties due to similarities of the isolated furanoids to the known antifungal agent, nystatin. An activity against Saccharomyces cerevisiae with 74% inhibition at 250 µg/mL was observed, which is weak in comparison to the control nystatin, which achieved complete inhibition at 10 µg/mL.

The endophytic fungus H. investiens was isolated from the plant Blumea balsamifera in a recent work [110]. Cultivation and subsequent purification yielded the novel α-pyrones hypotiens A (80) to D, but assessment of the antimicrobial and cytotoxic activities was unsuccessful.

Miscellaneous secondary metabolites from Hypoxylaceae (Fig. 14)

From a mantis gut-derived D. eschscholtzii that also produced the dalescones, cultures supplemented with indole-3-carbinol yielded two (bis-)indole natural products named dalesindoloids A (81) to B [111]. Assessment of their cytotoxicity showed that 81 was strongly active against HL-60 cells (IC50 1.0 µM), while being less active against several other cell lines. Dalesindoloid B, however, was less active in comparison, but showed a broader spectrum of cytotoxicity.

Fig. 14

Recently reported miscellaneous secondary metabolites from species of the Hypoxylaceae

Polythetic taxonomic, chemoecological, and phylogenomic studies on endophytic Xylariales (Fig. 15)

Recently, several papers have been published that illustrated the importance of secondary metabolites for classification or were dealing with the elucidation of the life cycle of important fungal endophytes that are members of the Xylariales. Some of these organisms have been isolated as endophytes several decades ago and were found to be producers of molecules that served as lead candidates for developmental pharmaceuticals and agrochemicals, or as promising biocontrol agents. However, their taxonomic affinities remained unclear until recently and their life cycle remained to be elucidated by means of polythetic taxonomy. A fair example for such a fungal endophyte is H. pulicicidum, which represents the sexual state of the endophytic Nodulisporium spp. that are able to produce the insecticidal and antiparasitic agent, nodulisporic acid (82) [112]. Cultures derived from ascospores of this fungus, which is apparently rare and forms stromata on wood, were shown to produce the compound that has been found in various endophytes that were derived from plant material collected in various tropical countries [113]. The biosynthesis of the compound has recently been elucidated [114], which offers various opportunities, e.g. to study its production in planta using quantitative PCR and transcriptomics and shed some light on the natural function of the molecule.

Fig. 15

Some prominent secondary metabolites from members of Xylariales

The life cycle of the producer of the cyclodepsipeptide “PF-1022A” (83) [115] has also recently been elucidated in the course of the abovementioned study that also resulted in the segregation of the plant-pathogenic genus Dematophora from Rosellinia [8]. This compound is up-to-date the only one derived from an endophytic fungus that was further developed into a marketed drug. The semisynthetic emodepside (84), which is derived from “PF-1022A”, and can be produced in large amounts by fermentation, has been used in veterinary medicine for many years to combat worm diseases. In this case, the production is not restricted to a single species, but several strains of Rosellinia and the related genus Astrocystis were identified as producers of “PF-1022A”.

The life cycle of another important endophyte genus that contains several species which have been evaluated as biocontrol agents and so called “mycofumigants” has also recently been elucidated: the genus Muscodor was erected almost 20 years ago for a tropical endophyte that produces volatile antibiotics with which it kills a number of bacteria, fungal pathogens, and animal pests [116]. Over 20 species had been identified until recently and all of them were recognized on the basis of cultural morphology, volatile profiles, and molecular phylogenetic data, until recently the sexual state has been discovered from two specimens in Thailand. The ascospore-derived cultures of these fungi were able to produce volatile antibiotics, and they were found to correspond to the genus Induratia based on a multi-locus phylogeny. Moreover, this study also resulted in the recognition of Muscodor/Induratia and the related genus Emarcea as a unique phylogenetic lineage for which the new family Induratiaceae has been erected [117]. Interestingly, these fungi were never studied for the production of nonvolatile secondary metabolites and even the identity of the compounds that were detected by database aided GC-MS analytics often remains dubious [103, 118,119,120]. The Induratiaceae certainly deserve further studies of their secondary metabolome, including the identification of metabolites that show pronounced production in dual antagonist cultures.

Endophytes belonging to the genus Hypoxylon and its associated asexual stage Nodulisporium have also been repeatedly reported to produce biologically active volatiles [121, 122], even though the taxonomy of most of these strains and the identity of many of the volatile antibiotics produced by these fungi remain to be settled. Recently, an endophytic isolate that was unambiguously identified as H. rubiginosum was found to possess striking activities in dual culture against the Ash dieback pathogen, Hymenoscyphus fraxineus, and the active principles were identified after preparative isolation and classical structure elucidation (NMR spectroscopy and HR mass spectrometry) as phomopsidin derivatives [123, 124]. In a follow-up study, the production of phomopsidins (8586) in presence of the pathogen was observed in various strains of species that are phylogenetically related to H. rubiginosum including the new species, H. guilanense, but not in some distantly related species like H. fuscum. Interestingly the production of the compounds, which are known to be antifungal β-tubulin inhibitors, was enhanced in the presence of the pathogen.

Future outlook

The recent progress in “-OMICS” technology and bioinformatics has resulted in various options to further explore the secondary metabolism of filamentous fungi, which would have been unthinkable only 5 years ago. We wish to mention some recent highlights that concern the Xylariales and in particular the Hypoxylaceae, which have recently become a “model family” to study the correlations between phylogenomics and functional biodiversity within the fungal kingdom.

Genome sequences of their species had until recently been scarce and the few datasets that were published were mostly “shotgun” sequences based on Illumina sequencing, resulting in considerable gaps. However, the recent advent of third generation sequencing techniques like PacBio and Oxford nanopore (which still need to be complemented by “Illumina polishing” to reduce the number of sequencing errors) have substantially improved the data quality and made the generation of genome sequences much less expensive. From such high-quality genomes, it is now possible to draw much better conclusions, also because the bioinformatics tools have substantially improved in parallel. A recent study based on 13 high-quality genomes has for instance revealed for the first time that ITS sequences are present in multiple copies that may vary considerable in the same genome. These polymorphisms may in some cases explain why it is not feasible to “identify” a fungal species merely based on ITS data [125]. A larger study using these full genomes has provided the backbone for a phylogenomic study for the first time, which was based on the amino acid sequences of 4912 core genes and reflected the current accepted taxonomic concept of the family [81]. Furthermore, Percentage of Conserved Proteins analysis revealed that 70% of the proteins are conserved within the family, a value with potential application for the definition of family boundaries within the order Xylariales. Also, Hypomontagnella spongiphila was proposed as a new marine-derived species related to the terrestrial Hypomontagnella monticulosa (the type species of this recently erected genus [109]) based on in-depth genomic comparison and morphological differences of the cultures. This is the first time that high-quality genome sequence data were used to characterize species boundaries in the fungal kingdom. However, for the current topic it is more important to note that the abovementioned protein encoding genes included the complete BGCs encoding for secondary metabolites of the respective fungi, and the data can be used for synthetic biotechnology approaches. Recent studies have already made use of these data, and aside from the identification of the gene clusters by bioinformatic comparisons based on homology searches [87], it was even possible to express the BGC for cytochalasans in M. grisea as a heterologous host [82]. Various follow-up studies are now under way, based on these data, and exciting findings can be expected in the future from such genome mining approaches. The prerequisites to fully explore the secondary metabolome of the Hypoxylaceae and other Xylariales have therefore been created. Since the xylarialean endophyte Pestalotiopsis fici has already been found to contain almost 100 genes and BGC encoding for secondary metabolites using less sophisticated genome sequencing methodology [126], it can be imagined that this kind of work will result in many new discoveries of unprecedented compounds. Since the sequencing costs are steadily decreasing, the new techniques will soon be available for sequencing of large strain contingents, but skilled bioinformaticians who must continue to handle the data will never become dispensable.


  1. 1.

    Blackwell M. The fungi: 1, 2, 3… 5.1 million species? Am J Bot. 2011;98:426–38.

    PubMed  PubMed Central  Google Scholar 

  2. 2.

    Nilsson RH, Anslan S, Bahram M, Wurzbacher C, Baldrian P, Tedersoo L. Mycobiome diversity: high-throughput sequencing and identification of fungi. Nat Rev Microbiol. 2019;17:95–109.

    CAS  PubMed  Google Scholar 

  3. 3.

    Jamy M, Foster R, Barbera P, Czech L, Kozlov A, Stamatakis A, et al. Long-read metabarcoding of the eukaryotic rDNA operon to phylogenetically and taxonomically resolve environmental diversity. Mol Ecol Resour. 2020;20:429–43.

    CAS  PubMed  Google Scholar 

  4. 4.

    Helaly SE, Thongbai B, Stadler M. Diversity of biologically active secondary metabolites from endophytic and saprotrophic fungi of the ascomycete order Xylariales. Nat Prod Rep. 2018;35:992–1014.

    CAS  PubMed  Google Scholar 

  5. 5.

    Hyde KD, Norphanphoun C, Maharachchikumbura SSN, Bhat DJ, Jones EBG, Bundhun D, et al. Refined families of Sordariomycetes. Mycosphere. 2020;11:305–1059.

    Google Scholar 

  6. 6.

    Wijayawardene NN, Hyde KD, Al-Ani LKT, Tedersoo L, Haelewaters D, Rajeshkumar KC, et al. Outline of fungi and fungus-like taxa. Mycosphere. 2020;11:1060–456.

    Google Scholar 

  7. 7.

    Daranagama DA, Hyde KD, Sir EB, Thambugala KM, Tian Q, Samarakoon MC, et al. Towards a natural classification and backbone tree for Graphostromataceae, Hypoxylaceae, Lopadostomataceae and Xylariaceae. Fungal Divers. 2017;88:1–165.

    Google Scholar 

  8. 8.

    Wittstein K, Cordsmeier A, Lambert C, Wendt L, Sir EB, Weber J, et al. Identification of Rosellinia species as producers of cyclodepsipeptide PF1022 A and resurrection of the genus Dematophora as inferred from polythetic taxonomy. Stud Mycol. 2020;96:1–16.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Song F, Wu SH, Zhai YZ, Xuan QC, Wang T. Secondary metabolites from the genus Xylaria and their bioactivities. Chem Biodivers. 2014;11:673–94.

    CAS  PubMed  Google Scholar 

  10. 10.

    Macias-Rubalcava ML, Sanchez-Fernandez RE. Secondary metabolites of endophytic Xylaria species with potential applications in medicine and agriculture. World J Microbiol Biotechnol. 2017;33:15.

    PubMed  Google Scholar 

  11. 11.

    Nguyen HT, Kim S, Yu NH, Park AR, Yoon H, Bae CH, et al. Antimicrobial activities of an oxygenated cyclohexanone derivative isolated from Amphirosellinia nigrospora JS-1675 against various plant pathogenic bacteria and fungi. J Appl Microbiol. 2019;126:894–904.

    CAS  PubMed  Google Scholar 

  12. 12.

    Shiono Y, Murayama T, Takahashi K, Okada K, Katohda S, Ikeda M. Three oxygenated cyclohexenone derivatives produced by an endophytic fungus. Biosci Biotechnol Biochem. 2005;69:287–92.

    CAS  PubMed  Google Scholar 

  13. 13.

    Xu XM, Li DY, Hua HM, Li ZL, Liu Q. Two new threitol orsellinates from a sea mud-derived fungus, Ascotricha sp. ZJ-M-5. J Asian Nat Prod Res. 2017;19:673–7.

    CAS  PubMed  Google Scholar 

  14. 14.

    Mali PR, Chirke SS, Meshram HM. A common approach for the synthesis of (R)-ethyl 2,4-dihydroxy-6-(8-hydroxynonyl) benzoate, ethyl 2,4-dihydroxy-6-nonylbenzoate and (2R,3R)-1,2,3,4-butanetetraol-1,4-diorsellinate. ChemistrySelect. 2017;2:10718–21.

    CAS  Google Scholar 

  15. 15.

    Medina RP, Araujo AR, Batista JM Jr, Cardoso CL, Seidl C, Vilela AFL, et al. Botryane terpenoids produced by Nemania bipapillata, an endophytic fungus isolated from red alga Asparagopsis taxiformis - Falkenbergia stage. Sci Rep. 2019;9:12318.

    PubMed  PubMed Central  Google Scholar 

  16. 16.

    Kuhnert E, Surup F, Wiebach V, Bernecker S, Stadler M. Botryane, noreudesmane and abietane terpenoids from the ascomycete Hypoxylon rickii. Phytochemistry. 2015;117:116–22.

    CAS  PubMed  Google Scholar 

  17. 17.

    Qin XD, Shao HJ, Dong ZJ, Liu JK. Six new induced sesquiterpenes from the cultures of ascomycete Daldinia concentrica. J Antibiot. 2008;61:556–62.

    CAS  Google Scholar 

  18. 18.

    Kretz R, Wendt L, Wongkanoun S, Luangsa-Ard JJ, Surup F, Helaly SE, et al. The effect of cytochalasans on the actin cytoskeleton of eukaryotic cells and preliminary structure-activity relationships. Biomolecules. 2019;9:73.

    CAS  PubMed Central  Google Scholar 

  19. 19.

    Kumarihamy M, Ferreira D, Croom EM Jr, Sahu R, Tekwani BL, Duke SO, et al. Antiplasmodial and cytotoxic cytochalasins from an endophytic fungus, Nemania sp. UM10M, isolated from a diseased Torreya taxifolia leaf. Molecules. 2019;24:777.

    PubMed Central  Google Scholar 

  20. 20.

    Yuyama KT, Wendt L, Surup F, Kretz R, Chepkirui C, Wittstein K, et al. Cytochalasans act as inhibitors of biofilm formation of Staphylococcus aureus. Biomolecules. 2018;8:129.

    PubMed Central  Google Scholar 

  21. 21.

    Narmani A, Pichai S, Palani P, Arzanlou M, Surup F, Stadler M. Daldinia sacchari (Hypoxylaceae) from India produces the new cytochalasins saccalasins A and B and belongs to the D. eschscholtzii species complex. Mycol Prog. 2018;18:175–85.

    Google Scholar 

  22. 22.

    Sharma N, Kushwaha M, Arora D, Jain S, Singamaneni V, Sharma S, et al. New cytochalasin from Rosellinia sanctae-cruciana, an endophytic fungus of Albizia lebbeck. J Appl Microbiol. 2018;125:111–20.

    CAS  PubMed  Google Scholar 

  23. 23.

    Becker K, Wongkanoun S, Wessel AC, Bills GF, Stadler M, Luangsa-Ard JJ. Phylogenetic and chemotaxonomic studies confirm the affinities of Stromatoneurospora phoenix to the coprophilous Xylariaceae. J Fungi. 2020;6:144.

    Google Scholar 

  24. 24.

    Skellam E. The biosynthesis of cytochalasans. Nat Prod Rep. 2017;34:1252–63.

    CAS  PubMed  Google Scholar 

  25. 25.

    Scherlach K, Boettger D, Remme N, Hertweck C. The chemistry and biology of cytochalasans. Nat Prod Rep. 2010;27:869–86.

    CAS  PubMed  Google Scholar 

  26. 26.

    Wang WX, Lei X, Ai HL, Bai X, Li J, He J, et al. Cytochalasans from the endophytic fungus Xylaria cf. curta with resistance reversal activity against fluconazole-resistant Candida albicans. Org Lett. 2019;21:1108–11.

    CAS  PubMed  Google Scholar 

  27. 27.

    Wang WX, Li ZH, Feng T, Li J, Sun H, Huang R, et al. Curtachalasins A and B, two cytochalasans with a tetracyclic skeleton from the endophytic Fungus Xylaria curta E10. Org Lett. 2018;20:7758–61.

    CAS  PubMed  Google Scholar 

  28. 28.

    Wang WX, Lei X, Yang YL, Li ZH, Ai HL, Li J, et al. Xylarichalasin A, a halogenated hexacyclic cytochalasan from the fungus Xylaria cf. curta. Org Lett. 2019;21:6957–60.

    CAS  PubMed  Google Scholar 

  29. 29.

    Wang J, Sang Y, Tang S, Zhang P. New curtachalasin from the Xylaria sp. DO 1801. Nat Prod Res. 2020.

  30. 30.

    Chen Z, Chen Y, Huang H, Yang H, Zhang W, Sun Y, et al. Cytochalasin P1, a new cytochalasin from the marine-derived fungus Xylaria sp. SOF11. Z Naturforsch C J Biosci. 2017;72:129–32.

    CAS  PubMed  Google Scholar 

  31. 31.

    Han WB, Zhai YJ, Gao Y, Zhou HY, Xiao J, Pescitelli G, et al. Cytochalasins and an abietane-type diterpenoid with allelopathic activities from the endophytic fungus Xylaria species. J Agric Food Chem. 2019;67:3643–50.

    CAS  PubMed  Google Scholar 

  32. 32.

    Biasetto C, Somens A, Abdalla V, Abreu L, Gualtieri S, Pfenning L, et al. Phytotoxic constituents from endophytic fungus Xylaria cubensis associated with Eugenia brasiliensis. Química Nova. 2019;42:485–8.

  33. 33.

    Wang WX, Li ZH, He J, Feng T, Li J, Liu JK. Cytotoxic cytochalasans from fungus Xylaria longipes. Fitoterapia. 2019;137:104278.

    CAS  PubMed  Google Scholar 

  34. 34.

    Wang P, Cui Y, Cai CH, Kong FD, Chen HQ, Zhou LM, et al. A new cytochalasin derivative from the mangrove-derived endophytic fungus Xylaria sp. HNWSW-2. J Asian Nat Prod Res. 2018;20:1002–7.

    CAS  PubMed  Google Scholar 

  35. 35.

    Noppawan S, Mongkolthanaruk W, Suwannasai N, Senawong T, Moontragoon P, Boonmak J, et al. Chemical constituents and cytotoxic activity from the wood-decaying fungus Xylaria sp. SWUF08-37. Nat Prod Res. 2020;34:464–73.

    CAS  PubMed  Google Scholar 

  36. 36.

    Chang JC, Hsiao G, Lin RK, Kuo YH, Ju YM, Lee TH. Bioactive constituents from the termite nest-derived medicinal fungus Xylaria nigripes. J Nat Prod. 2017;80:38–44.

    CAS  PubMed  Google Scholar 

  37. 37.

    Chen HP, Zhao ZZ, Cheng GG, Zhao K, Han KY, Zhou L, et al. Immunosuppressive nor-isopimarane diterpenes from cultures of the fungicolous fungus Xylaria longipes HFG1018. J Nat Prod. 2020;83:401–12.

    CAS  PubMed  Google Scholar 

  38. 38.

    Chen HP, Li J, Zhao ZZ, Li X, Liu SL, Wang QY, et al. Diterpenes with bicyclo[2.2.2]octane moieties from the fungicolous fungus Xylaria longipes HFG1018. Org Biomol Chem. 2020;18:2410–5.

    CAS  PubMed  Google Scholar 

  39. 39.

    Chen Y-S, Chang H-S, Cheng M-J, Chan H-Y, Wu M-D, Hsieh S-Y, et al. New chemical constituents from the endophytic fungus Xylaria papulis cultivated on Taiwanese Lepidagathis stenophylla. Rec Nat Prod. 2016;10:735–43.

    CAS  Google Scholar 

  40. 40.

    Yang NN, Kong FD, Ma QY, Huang SZ, Luo DQ, Zhou LM, et al. Drimane-type sesquiterpenoids from cultures of the fungus Xylaria polymorpha. Phytochemistry Lett. 2017;20:13–16.

    CAS  Google Scholar 

  41. 41.

    Liang Y, Xu W, Liu C, Zhou D, Liu X, Qin Y, et al. Eremophilane sesquiterpenes from the endophytic fungus Xylaria sp. GDG-102. Nat Prod Res. 2019;33:1304–9.

    CAS  PubMed  Google Scholar 

  42. 42.

    Tang GH, Lu N, Li W, Wu M, Chen YY, Zhang HY, et al. Mannosylxylarinolide, a new 3,4-seco-ergostane-type steroidal saponin featuring a β-D-mannose from the endophytic fungus Xylaria sp. J Asian Nat Prod Res. 2020;22:397–403.

    CAS  PubMed  Google Scholar 

  43. 43.

    McCloskey S, Noppawan S, Mongkolthanaruk W, Suwannasai N, Senawong T, Prawat U. A new cerebroside and the cytotoxic constituents isolated from Xylaria allantoidea SWUF76. Nat Prod Res. 2017;31:1422–30.

    CAS  PubMed  Google Scholar 

  44. 44.

    Choi J-H, Ogawa A, Abe N, Masuda K, Koyama T, Yazawa K, et al. Chaxines B, C, D, and E from the edible mushroom Agrocybe chaxingu. Tetrahedron. 2009;65:9850–3.

    CAS  Google Scholar 

  45. 45.

    Ibrahim A, Tanney JB, Fei F, Seifert KA, Cutler GC, Capretta A, et al. Metabolomic-guided discovery of cyclic nonribosomal peptides from Xylaria ellisii sp. nov., a leaf and stem endophyte of Vaccinium angustifolium. Sci Rep. 2020;10:4599.

    CAS  PubMed  PubMed Central  Google Scholar 

  46. 46.

    Xu WF, Hou XM, Yao FH, Zheng N, Li J, Wang CY, et al. Xylapeptide A, an antibacterial cyclopentapeptide with an uncommon L-pipecolinic acid moiety from the associated fungus Xylaria sp. (GDG-102). Sci Rep. 2017;7:6937.

    PubMed  PubMed Central  Google Scholar 

  47. 47.

    Ai H, Wang W, Zhang X, Feng T, He J, Li Z. Preparation of compound E1011 from potato endophytic fungi fermentation product. Chinese patent, 2018 (CN1091180635).

  48. 48.

    Grabley S, Hammann P, Thiericke R, Wink J, Philipps S, Zeeck A. Secondary metabolites by chemical screening. 21. Clonostachydiol, a novel anthelmintic macrodiolide from the fungus Clonostachys cylindrospora (strain FH-A 6607). J Antibiot. 1993;46:343–5.

    CAS  Google Scholar 

  49. 49.

    Ojima KI, Yangchum A, Laksanacharoen P, Tasanathai K, Thanakitpipattana D, Tokuyama H, et al. Cordybislactone, a stereoisomer of the 14-membered bislactone clonostachydiol, from the hopper pathogenic fungus Cordyceps sp. BCC 49294: revision of the absolute configuration of clonostachydiol. J Antibiot. 2018;71:351–8.

    CAS  Google Scholar 

  50. 50.

    Wang J, Xu CC, Tang H, Su L, Chou Y, Soong K et al. Osteoclastogenesis inhibitory polyketides from the sponge-associated fungus Xylaria feejeensis. Chem Biodivers. 2018;15.

  51. 51.

    Chen MC, Wang GJ, Kuo YH, Chiang YR, Cho TY, Ju YM, et al. Isoprenyl phenolic ethers from the termite nest-derived medicinal fungus Xylaria fimbriata. J Food Drug Anal. 2019;27:111–7.

    CAS  PubMed  Google Scholar 

  52. 52.

    Zhang J, Liang JH, Zhao JC, Wang YL, Dong PP, Liu XG, et al. Xylarianins A−D from the endophytic fungus Xylaria sp. SYPF 8246 as natural inhibitors of human carboxylesterase 2. Bioorg Chem. 2018;81:350–5.

    CAS  PubMed  Google Scholar 

  53. 53.

    Yu G, Sun Z, Peng J, Zhu M, Che Q, Zhang G, et al. Secondary metabolites produced by combined culture of Penicillium crustosum and a Xylaria sp. J Nat Prod. 2019;82:2013–7.

    CAS  PubMed  Google Scholar 

  54. 54.

    Rudiyansyah, Alimuddin AH, Masriani, Muharini R, Liu Z, Lin W, et al. Arugosins O−Q, new fungal metabolites from the fungus Xylariaceae sp. isolated from leaves of Lansium domesticum (Meliaceae). Nat Prod Commun. 2019;14:125–8.

  55. 55.

    Hein SM, Gloer JB, Koster B, Malloch D. Arugosin F: a new antifungal metabolite from the coprophilous fungus Ascodesmis sphaerospora. J Nat Prod. 1998;61:1566–7.

    CAS  PubMed  Google Scholar 

  56. 56.

    Kralj A, Kehraus S, Krick A, Eguereva E, Kelter G, Maurer M, et al. Arugosins G and H: prenylated polyketides from the marine-derived fungus Emericella nidulans var. acristata. J Nat Prod. 2006;69:995–1000.

    CAS  PubMed  Google Scholar 

  57. 57.

    Lin Z, Zhu T, Fang Y, Gu Q, Zhu W. Polyketides from Penicillium sp. JP-1, an endophytic fungus associated with the mangrove plant Aegiceras corniculatum. Phytochemistry. 2008;69:1273–8.

    CAS  PubMed  Google Scholar 

  58. 58.

    Arunrattiyakorn P, Kuno M, Aree T, Laphookhieo S, Sriyatep T, Kanzaki H, et al. Biotransformation of β-mangostin by an endophytic fungus of Garcinia mangostana to furnish xanthenes with an unprecedented heterocyclic skeleton. J Nat Prod. 2018;81:2244–50.

    CAS  PubMed  Google Scholar 

  59. 59.

    Guo CJ, Wu P, Xue JH, Li HX, Wei XY. Xylarodons A and B, new hexaketides from the endophytic fungus Xylaria sp. SC1440. J Asian Nat Prod Res. 2019;21:343–50.

    CAS  PubMed  Google Scholar 

  60. 60.

    Patjana T, Jantaharn P, Katrun P, Mongkolthanaruk W, Suwannasai N, Senawong T, et al. Anti-inflammatory and cytotoxic agents from Xylaria sp. SWUF09-62 fungus. Nat Prod Res. 2019.

  61. 61.

    Maha A, Rukachaisirikul V, Phongpaichit S, Poonsuwan W, Sakayaroj J. Dimeric chromanone, cyclohexenone and benzamide derivatives from the endophytic fungus Xylaria sp. PSU-H182. Tetrahedron. 2016;72:2874–9.

    CAS  Google Scholar 

  62. 62.

    Guo C, Wu P, Xue J, Li H, Wei X. Xylaropyrones B and C, new γ-pyrones from the endophytic fungus Xylaria sp. SC1440. Nat Prod Res. 2018;32:1525–31.

    CAS  PubMed  Google Scholar 

  63. 63.

    Siriwach R, Kinoshita H, Kitani S, Igarashi Y, Pansuksan K, Panbangred W, et al. Xylaropyrone, a new γ-pyrone from the endophytic fungus Xylaria feejeensis MU18. J Antibiot. 2011;64:217–9.

    CAS  Google Scholar 

  64. 64.

    Chen R, Tang JW, Li XR, Liu M, Ding WP, Zhou YF, et al. Secondary metabolites from the endophytic fungus Xylaria sp. hg1009. Nat Prod Bioprospect. 2018;8:121–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  65. 65.

    Zheng N, Liu Q, He D-L, Liang Y, Li J, Yang R-Y. A new compound from the endophytic fungus Xylaria sp. from Sophora tonkinensis. Chem Nat Compd. 2018;54:447–9.

    CAS  Google Scholar 

  66. 66.

    Zheng N, Yao F, Liang X, Liu Q, Xu W, Liang Y, et al. A new phthalide from the endophytic fungus Xylaria sp. GDG-102. Nat Prod Res. 2018;32:755–60.

    CAS  PubMed  Google Scholar 

  67. 67.

    Paguigan ND, Al-Huniti MH, Raja HA, Czarnecki A, Burdette JE, Gonzalez-Medina M, et al. Chemoselective fluorination and chemoinformatic analysis of griseofulvin: natural vs. fluorinated fungal metabolites. Bioorg Med Chem. 2017;25:5238–46.

    CAS  PubMed  PubMed Central  Google Scholar 

  68. 68.

    Knowles SL, Raja HA, Isawi IH, Flores-Bocanegra L, Reggio PH, Pearce CJ, et al. Wheldone: characterization of a unique scaffold from the coculture of Aspergillus fischeri and Xylaria flabelliformis. Org Lett. 2020;22:1878–82.

    CAS  PubMed  PubMed Central  Google Scholar 

  69. 69.

    Itoh H, Matsui M, Miyamura Y, Takeda I, Ishii J, Kumagai T, et al. Biosynthesis of novel statins by combining heterologous genes from Xylaria and Aspergillus. ACS Synth Biol. 2018;7:2783–9.

    CAS  PubMed  Google Scholar 

  70. 70.

    Schneider G, Anke H, Sterner O. Xylarin, an antifungal Xylaria metabolite with an unusual tricyclic uronic acid moiety. Nat Prod Lett. 1995;7:309–16.

    CAS  Google Scholar 

  71. 71.

    Schneider G, Anke H, Sterner O. Xylaramide, a new antifungal compound, and other secondary metabolites from Xylaria longipes. Z Naturforsch C J Biosci. 1996;51:802–6.

    CAS  PubMed  Google Scholar 

  72. 72.

    Whalley AJS, Edwards RL. Secondary metabolites and systematic arrangement within the Xylariaceae. Can J Bot. 1995;73:802–10.

    Google Scholar 

  73. 73.

    Rusch M, Spielmeyer A, Zorn H, Hamscher G. Biotransformation of ciprofloxacin by Xylaria longipes: structure elucidation and residual antibacterial activity of metabolites. Appl Microbiol Biotechnol. 2018;102:8573–84.

    CAS  PubMed  Google Scholar 

  74. 74.

    Rusch M, Kauschat A, Spielmeyer A, Rompp A, Hausmann H, Zorn H, et al. Biotransformation of the antibiotic danofloxacin by Xylaria longipes leads to an efficient reduction of its antibacterial activity. J Agric Food Chem. 2015;63:6897–904.

    CAS  PubMed  Google Scholar 

  75. 75.

    Rusch M, Spielmeyer A, Meissner J, Kietzmann M, Zorn H, Hamscher G. Efficient reduction of antibacterial activity and cytotoxicity of fluoroquinolones by fungal-mediated N-oxidation. J Agric Food Chem. 2017;65:3118–26.

    CAS  PubMed  Google Scholar 

  76. 76.

    Li J, Wang WX, Chen HP, Li ZH, He J, Zheng YS, et al. (±)-Xylaridines A and B, highly conjugated alkaloids from the fungus Xylaria longipes. Org Lett. 2019;21:1511–4.

    CAS  PubMed  Google Scholar 

  77. 77.

    Li J, Wang WX, Li ZH, He J, Huang R, Zheng YS, et al. Xylaridines C and D, unusual thiopyranodipyridine alkaloids from the fungus Xylaria longipes. Org Lett. 2019;21:6145–8.

    CAS  PubMed  Google Scholar 

  78. 78.

    Brown CE, Liscombe DK, McNulty J. Three new polyketides from fruiting bodies of the endophytic ascomycete Xylaria polymorpha. Nat Prod Res. 2018;32:2408–17.

    CAS  PubMed  Google Scholar 

  79. 79.

    Stadler M, Fournier J, Læssøe T, Lechat C, Tichy H-V, Piepenbring M. Recognition of hypoxyloid and xylarioid Entonaema species and allied Xylaria species from a comparison of holomorphic morphology, HPLC profiles, and ribosomal DNA sequences. Mycol Prog. 2008;7:53–73.

    Google Scholar 

  80. 80.

    Sawadsitang S, Suwannasai N, Mongkolthanaruk W, Ahmadi P, McCloskey S. A new amino amidine derivative from the wood-decaying fungus Xylaria cf. cubensis SWUF08-86. Nat Prod Res. 2018;32:2260–7.

    CAS  PubMed  Google Scholar 

  81. 81.

    Wendt L, Sir EB, Kuhnert E, Heitkämper S, Lambert C, Hladki AI, et al. Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales. Mycol Prog. 2018;17:115–54.

    Google Scholar 

  82. 82.

    Wang C, Becker K, Pfütze S, Kuhnert E, Stadler M, Cox RJ, et al. Investigating the function of cryptic cytochalasan cytochrome P450 monooxygenases using combinatorial biosynthesis. Org Lett. 2019;21:8756–60.

    CAS  PubMed  Google Scholar 

  83. 83.

    Trung HV, Kuo P-C, Tuan NN, Ngan NT, Trung NQ, Thanh NT, et al. Characterization of cytochalasins and steroids from the ascomycete Daldinia concentrica and their cytotoxicity. Nat Prod Commun. 2019.

  84. 84.

    Hashimoto T, Tahara S, Takaoka S, Tori M, Asakawa Y. Structures of daldinins A–C, three novel azaphilone derivatives from ascomycetous fungus Daldinia concentrica. Chem Pharm Bull. 1994;42:2397–9.

    CAS  Google Scholar 

  85. 85.

    Surup F, Narmani A, Wendt L, Pfütze S, Kretz R, Becker K, et al. Identification of fungal fossils and novel azaphilone pigments in ancient carbonised specimens of Hypoxylon fragiforme from forest soils of Châtillon-sur-Seine (Burgundy). Fungal Divers. 2018;92:345–56.

    Google Scholar 

  86. 86.

    Gao JM, Yang SX, Qin JC. Azaphilones: chemistry and biology. Chem Rev. 2013;113:4755–811.

    CAS  PubMed  Google Scholar 

  87. 87.

    Becker K, Pfütze S, Kuhnert E, Cox RJ, Stadler M, Surup F. Hybridorubrins A−D, novel azaphilone heterodimers from stromata of Hypoxylon fragiforme and insights into the biosynthetic machinery for azaphilone diversification. Chemistry Eur J. 2020. (in press).

  88. 88.

    Chepkirui C, Yuyama KT, Wanga LA, Decock C, Matasyoh JC, Abraham WR, et al. Microporenic acids A−G, biofilm inhibitors, and antimicrobial agents from the Basidiomycete Microporus species. J Nat Prod. 2018;81:778–84.

    CAS  PubMed  Google Scholar 

  89. 89.

    Intaraudom C, Bunbamrung N, Dramae A, Boonyuen N, Kongsaeree P, Srichomthong K, et al. Terphenyl derivatives and drimane-phathalide/isoindolinones from Hypoxylon fendleri BCC32408. Phytochemistry. 2017;139:8–17.

    CAS  PubMed  Google Scholar 

  90. 90.

    Intaraudom C, Punyain W, Bunbamrung N, Dramae A, Boonruangprapa T, Pittayakhajonwut P. Antimicrobial drimane-phthalide derivatives from Hypoxylon fendleri BCC32408. Fitoterapia. 2019;138:104353.

    CAS  PubMed  Google Scholar 

  91. 91.

    Basnet BB, Chen B, Suleimen YM, Ma K, Guo S, Bao L, et al. Cytotoxic secondary metabolites from the endolichenic fungus Hypoxylon fuscum. Planta Med. 2019;85:1088–97.

    CAS  PubMed  Google Scholar 

  92. 92.

    Feng J, Surup F, Hauser M, Miller A, Wennrich J-P, Stadler M, et al. Biosynthesis of oxygenated brasilane terpene glucosides involves a promiscuous N-acetylglucosamine transferase. Chem Commun. 2020.

  93. 93.

    Wibberg D, Stadler M, Lambert C, Bunk B, Spröer C, Rückert C et al. High quality genome sequences of thirteen Hypoxylaceae (Ascomycota) strengthen the phylogenetic family backbone and enable the discovery of new taxa. Fungal Divers. 2020. (in press).

  94. 94.

    Liu Y, Kurtán T, Mándi A, Weber H, Wang C, Hartmann R, et al. A novel 10-membered macrocyclic lactone from the mangrove-derived endophytic fungus Annulohypoxylon sp. Tetrahedron Lett. 2018;59:632–6.

    CAS  Google Scholar 

  95. 95.

    Kuhnert E, Sir EB, Lambert C, Hyde KD, Hladki AI, Romero AI, et al. Phylogenetic and chemotaxonomic resolution of the genus Annulohypoxylon (Xylariaceae) including four new species. Fungal Divers. 2017;85:1–43.

    Google Scholar 

  96. 96.

    Becker K, Wessel AC, Luangsa-Ard JJ, Stadler M. Viridistratins A−C, antimicrobial and cytotoxic benzo[j]fluoranthenes from stromata of Annulohypoxylon viridistratum (Hypoxylaceae, Ascomycota). Biomolecules. 2020;10:805.

    CAS  PubMed Central  Google Scholar 

  97. 97.

    Kamauchi H, Shiraishi Y, Kojima A, Kawazoe N, Kinoshita K, Koyama K. Isoindolinones, phthalides, and a naphthoquinone from the fruiting body of Daldinia concentrica. J Nat Prod. 2018;81:1290–4.

    CAS  PubMed  Google Scholar 

  98. 98.

    Kuhnert E, Surup F, Herrmann J, Huch V, Muller R, Stadler M. Rickenyls A−E, antioxidative terphenyls from the fungus Hypoxylon rickii (Xylariaceae, Ascomycota). Phytochemistry. 2015;118:68–73.

    CAS  PubMed  Google Scholar 

  99. 99.

    Zhang AH, Liu W, Jiang N, Wang XL, Wang G, Xu Q, et al. Sequestration of guest intermediates by dalesconol bioassembly lines in Daldinia eschscholzii. Org Lett. 2017;19:2142–5.

    CAS  PubMed  Google Scholar 

  100. 100.

    Zhang AH, Jiang N, Wang XQ, Tan RX. Galewone, an anti-fibrotic polyketide from Daldinia eschscholzii with an undescribed carbon skeleton. Sci Rep. 2019;9:14316.

    PubMed  PubMed Central  Google Scholar 

  101. 101.

    Liao HX, Zheng CJ, Huang GL, Mei RQ, Nong XH, Shao TM, et al. Bioactive polyketide derivatives from the mangrove-derived fungus Daldinia eschscholtzii HJ004. J Nat Prod. 2019;82:2211–9.

    CAS  PubMed  Google Scholar 

  102. 102.

    Fournier J. Two new species of Hypoxylon (Xylariaceae) from French Central Pyrénées occurring on Fagus sylvatica. 2014;6:53–60.

    Google Scholar 

  103. 103.

    Dickschat JS, Wang T, Stadler M. Volatiles from the xylarialean fungus Hypoxylon invadens. Beilstein J Org Chem. 2018;14:734–46.

    CAS  PubMed  PubMed Central  Google Scholar 

  104. 104.

    Becker K, Lambert C, Wieschhaus J, Stadler M. Phylogenetic assignment of the fungicolous Hypoxylon invadens (Ascomycota, Xylariales) and investigation of its secondary metabolites. Microorganisms. 2020;8:1397.

    PubMed Central  Google Scholar 

  105. 105.

    Wheeler MH, Stipanovic RD. Melanin biosynthesis in Thielaviopsis basicola. Exp Mycol. 1979;3:340–50.

    CAS  Google Scholar 

  106. 106.

    Hu M, Yang XQ, Zhou QY, Li SQ, Wang BY, Ruan BH, et al. Benzopyran derivatives from endophytic Daldinia eschscholzii JC-15 in Dendrobium chrysotoxum and their bioactivities. Nat Prod Res. 2019;33:1431–5.

    CAS  PubMed  Google Scholar 

  107. 107.

    Wang BY, Yang YB, Yang XQ, Zhu CH, Yang S, Xu TT, et al. Inducing secondary metabolite production from Daldinia eschscholzii JC-15 by red ginseng medium. Nat Prod Res. 2019.

  108. 108.

    Burgess KMN, Ibrahim A, Sørensen D, Sumarah MW. Trienylfuranol A and trienylfuranone A-B: metabolites isolated from an endophytic fungus, Hypoxylon submoniticulosum, in the raspberry Rubus idaeus. J Antibiot. 2017;70:721–5.

    CAS  Google Scholar 

  109. 109.

    Lambert C, Wendt L, Hladki AI, Stadler M, Sir EB. Hypomontagnella (Hypoxylaceae): a new genus segregated from Hypoxylon by a polyphasic taxonomic approach. Mycol Prog. 2018;18:187–201.

    Google Scholar 

  110. 110.

    Yuan C, Yang H-X, Guo Y-H, Fan L, Zhang Y-B, Li G. New α-pyrones from an endophytic fungus, Hypoxylon investiens J2. RSC Adv. 2019;9:27419–23.

    CAS  Google Scholar 

  111. 111.

    Lin LP, Tan RX. Bioactive alkaloids from indole-3-carbinol exposed culture of Daldinia eschscholzii. Chin J Chem. 2018;36:749–53.

    CAS  Google Scholar 

  112. 112.

    Bills GF, Gonzalez-Menendez V, Martin J, Platas G, Fournier J, Peršoh D, et al. Hypoxylon pulicicidum sp. nov. (Ascomycota, Xylariales), a pantropical insecticide-producing endophyte. PLoS One. 2012;7:e46687.

    CAS  PubMed  PubMed Central  Google Scholar 

  113. 113.

    Polishook JD, Ondeyka JG, Dombrowski AW, Peláez F, Platas G, Teran AM. Biogeography and relatedness of Nodulisporium strains producing nodulisporic acid. Mycologia. 2019;93:1125–37.

    Google Scholar 

  114. 114.

    Van de Bittner KC, Nicholson MJ, Bustamante LY, Kessans SA, Ram A, van Dolleweerd CJ, et al. Heterologous biosynthesis of nodulisporic acid F. J Am Chem Soc. 2018;140:582–5.

    PubMed  Google Scholar 

  115. 115.

    Sasaki T, Takagi M, Yaguchi T, Miyadoh S, Okada T, Koyama M. A new anthelmintic cyclodepsipeptide, PF1022A. J Antibiot. 1992;45:692–7. Corrected in: J Antibiot 1996; 49(9):C-2

    CAS  Google Scholar 

  116. 116.

    Strobel GA, Dirkse E, Sears J, Markworth C. Volatile antimicrobials from Muscodor albus, a novel endophytic fungus. Microbiology. 2001;147:2943–50.

    CAS  PubMed  Google Scholar 

  117. 117.

    Samarakoon MC, Thongbai B, Hyde KD, Brönstrup M, Beutling U, Lambert C, et al. Elucidation of the life cycle of the endophytic genus Muscodor and its transfer to Induratia in Induratiaceae fam. nov., based on a polyphasic taxonomic approach. Fungal Divers. 2020;101:177–210.

    Google Scholar 

  118. 118.

    Rinkel J, Babczyk A, Wang T, Stadler M, Dickschat JS. Volatiles from the hypoxylaceous fungi Hypoxylon griseobrunneum and Hypoxylon macrocarpum. Beilstein J Org Chem. 2018;14:2974–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  119. 119.

    Lauterbach L, Wang T, Stadler M, Dickschat JS. Volatiles from the ascomycete Daldinia cf. childiae (Hypoxylaceae), originating from China. Medchemcomm. 2019;10:726–34.

    CAS  PubMed  PubMed Central  Google Scholar 

  120. 120.

    Wang T, Mohr KI, Stadler M, Dickschat JS. Volatiles from the tropical ascomycete Daldinia clavata (Hypoxylaceae, Xylariales). Beilstein J Org Chem. 2018;14:135–47.

    CAS  PubMed  PubMed Central  Google Scholar 

  121. 121.

    Tomsheck AR, Strobel GA, Booth E, Geary B, Spakowicz D, Knighton B, et al. Hypoxylon sp., an endophyte of Persea indica, producing 1,8-cineole and other bioactive volatiles with fuel potential. Micro Ecol. 2010;60:903–14.

    CAS  Google Scholar 

  122. 122.

    Riyaz-Ul-Hassan S, Strobel G, Geary B, Sears J. An endophytic Nodulisporium sp. from Central America producing volatile organic compounds with both biological and fuel potential. J Microbiol Biotechnol. 2013;23:29–35.

    CAS  PubMed  Google Scholar 

  123. 123.

    Halecker S, Wennrich J-P, Rodrigo S, Andrée N, Rabsch L, Baschien C, et al. Fungal endophytes for biocontrol of ash dieback: the antagonistic potential of Hypoxylon rubiginosum. Fungal Ecol. 2020;45,

  124. 124.

    Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, et al. Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the ash dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys. 2020;66:105–33.

    PubMed  PubMed Central  Google Scholar 

  125. 125.

    Stadler M, Lambert C, Wibberg D, Kalinowski J, Cox RJ, Kolařík M, et al. Intragenomic polymorphisms in the ITS region of high-quality genomes of the Hypoxylaceae (Xylariales, Ascomycota). Mycol Prog. 2020;19:235–45.

    Google Scholar 

  126. 126.

    Wang X, Zhang X, Liu L, Xiang M, Wang W, Sun X, et al. Genomic and transcriptomic analysis of the endophytic fungus Pestalotiopsis fici reveals its lifestyle and high potential for synthesis of natural products. BMC Genomics. 2015;16:28.

    PubMed  PubMed Central  Google Scholar 

Download references


We are grateful to Dr. Esteban B. Sir (Tucuman, Argentina) for kindly providing the illustrations for Fig. 1.


Open access funding provided by Open Access funding enabled and organized by Projekt DEAL.

Author information



Corresponding author

Correspondence to Marc Stadler.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

This paper is dedicated to the memory of our friend and colleague, Prof. Dr. Soleiman E. Helaly, who was the lead author of the preceding review on the same topic and passed away much too early in June of 2020.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Becker, K., Stadler, M. Recent progress in biodiversity research on the Xylariales and their secondary metabolism. J Antibiot 74, 1–23 (2021).

Download citation

Further reading


Quick links