Thermophilic fungi can represent a rich source of industrially relevant enzymes. Here, 105 fungal strains capable of growing at 50 °C and pH 2.0 were isolated from compost and decaying plant matter. Maximum growth temperatures of the strains were in the range 50 °C to 60 °C. Sequencing of the internal transcribed spacer (ITS) regions indicated that 78 fungi belonged to 12 species of Ascomycota and 3 species of Zygomycota, while no fungus of Basidiomycota was detected. The remaining 27 strains could not be reliably assigned to any known species. Phylogenetically, they belonged to the genus Thielavia, but they represented 23 highly divergent genetic groups different from each other and from the closest known species by 12 to 152 nucleotides in the ITS region. Fungal secretomes of all 105 strains produced during growth on untreated rice straw were studied for lignocellulolytic activity at different pH and temperatures. The endoglucanase and xylanase activities differed substantially between the different species and strains, but in general, the enzymes produced by the novel Thielavia spp. strains exhibited both higher thermal stability and tolerance to acidic conditions. The study highlights the vast potential of an untapped diversity of thermophilic fungi in the tropics.
Thermotolerance is not very common among eukaryotes. While the upper temperature limit for the growth of prokaryotes has been reported to be 121 °C1, the highest growth temperature of eukaryotes is around 60–62 °C2, and only a small number of fungal species thrive at such high temperatures. Among the estimated 3.0 million fungal species existing in nature, and approximately 100 000 species described, only about 50 species have been found to be able to grow at 50–60 °C3. These species are limited to the Sordariales, Eurotiales, and Onygenales in the Ascomycota and the Mucorales of the Zygomycota. No representative of thermophilic Basidiomycota has yet been confirmed4. Fungi capable of growing at elevated temperatures are classified into thermophilic and thermotolerant groups. There is no consensus on the demarcation between the two groups, but typically, a fungus that has a thermal maximum near 50 °C and a minimum below 20 °C is regarded as thermotolerant, while those that grow at 50 °C or above, but not grow at 20 °C or above5 are regarded as thermophilic. In the present study, the cultivation temperature was maintained at 50 °C during initial screening for thermophilic fungi.
Earlier reports of thermophilic fungi were the result of accidental contamination of organic materials incubated at elevated temperatures. These include the isolation of Mucor pusillus (=Rhizomucor pusillus) from bread in 1886, and Humicola lanuginosa (=Thermomyces lanuginosus) from potato slices in 1899 (from Johri et al.6). It was later found that thermophilic fungi are a regular microbial component of self-heating decomposing hay7. In natural environments, thermophilic fungi are most commonly found in rapidly decomposing plant residues, where heat is generated through exothermic microbial activity. Heat accumulation in a 5-cm layer of leaf litter is sufficient to create favourable conditions for thermophilic fungi, and temperature increase may even lead to ignition in stockpiles of hay, oil seeds or manure. Most thermophilic fungi also grow well at moderate temperatures and can be found in various substrates, including soils, composts, piles of hay, stored grains, wood chip piles, nesting materials of birds and animals or in municipal refuse8.
While thermotolerant/thermophilic fungi appear to be exceedingly rare, fungi able to tolerate acidic conditions are frequently encountered in nature, and many species have been shown to be capable of growing at pH levels as low as 29. There is no clear demarcation between acidophilic and acid-tolerant fungi, but it is often assumed that acidophilic fungi are those that can grow at pH 1.0 and have optimum growth at pH 3.0 or below10. Hereafter, we refer to acidophilic species as those optimally growing at pH values below 3, while acidotolerant species refer to species able to grow in acidic environments but with growth optima above pH 3. The earliest description of acidophilic fungi dates back to 1943, when a strain of Acontium velatum and a “Fungus D” were shown to be capable of growing in glucose medium containing 1.25 M sulphuric acid at pH 011. Unfortunately, the strain of Acontium velatum appears to have been lost since the initial publication, but “Fungus D” is now believed to be a strain of Acidomyces acidophilus which is commonly found in extremely acidic environments12. Until now, acidophility has been shown for only 6 fungal species, including Acidomyces acidophilus (MB#511856) (=Scytalidium acidophilum = Acidomyces richmondensis = Fungus D), Acidomyces acidothermus (MB#564520), Acidothrix acidophila (MB#805424), Acidea extrema (MB#805425), Acontium velatum (MB#142596, no living specimen available) and Hortaea acidophila (MB#367373) (=Neohortaea acidophila). The strain Bispora sp. MEY-1, well-known for the production of a range of thermophilic and acid-tolerant lignocellulolytic enzymes13, probably belongs to the species Acidomyces acidothermus14. Phylogenetically, all acidophilic species are Ascomycota, and the teleomorphic state is known only for Acidomyces acidothermus (described as Teratosphaeria acidotherma, MB#517415)14.
Thermophilic and acid-tolerant fungi have received considerable attention, as their thermostable enzymes can be employed in industrial processes at elevated temperatures. Increasing the process temperature can have advantages, for example, increasing the rate of chemical reactions, decreasing the viscosity of substrates and reducing the risk of contamination by mesophilic microorganisms15. A number of enzymes such as amylases, cellulases, xylanases, lipases and proteases from thermophilic fungi have been found to be thermostable6. The lipase and rennet from Rhizomucor miehei are commercial enzymes that find wide applications in the food industry16. A range of genes encoding lignocellulolytic enzymes in the acidophilic fungus Acidomyces acidothermus MEY-1 has been cloned and expressed. The enzymes were found to be thermotolerant and functional under acidic conditions13.
As a result of increased interest in renewable sources of energy and biomaterials, fungi that are adapted to extreme environmental conditions have recently received special interest as sources of novel hydrolytic enzymes suitable for various technological applications. Genome sequences have been obtained for a large number of thermophilic fungi, such as Myceliophthora thermophila, Thielavia terrestris, Thielavia heterothallica, Chaetomium thermophilum, Thermomyces lanuginosus, T. thermophilus, Rhizomucor miehei, Talaromyces cellulolyticus and Malbranchea cinnamomea, as well as for acidophilic fungi, including Acidothrix acidophila, Acidomyces acidophilus and Hortaea acidophila17.
Genomes of thermophilic lignocellulose-degrading fungi such as Thermothelomyces thermophila18, Thielavia terrestris18, and Malbranchea cinnamomea19 have been found to harbour large numbers of carbohydrate-active enzymes (CAZymes). For examples, Thielavia terrestris genome encodes 473 CAZymes, including 212 glycoside hydrolases (GHs), 91 glycosyl transferases (GTs), 4 polysaccharide lyases (PLs), 28 carbohydrate esterases (CEs), 58 enzymes with auxiliary activities (AAs) and 80 carbohydrate-binding modules (CBMs). Compared to the well-known cellulase-producer Trichoderma reesei, Thielavia terrestris has a similar setup of GHs18. Through studies of the genomes of thermophilic fungi compared to related mesophiles, it appears that common strategies for thermal adaptation include a reduction of the genome size and an increased frequency of the amino acids Ile, Val, Tyr, Trp, Arg, Glu, and Leu (IVYWREL) in proteins20. Although high GC mol% is often assumed to contribute to the genome stability at elevated temperatures, the correlation between GC content and thermophilicity in fungi remains inconclusive21.
To take advantage of the high fungal biodiversity in the tropics, we have conducted a search in Vietnam for novel fungi for the production of lignocellulolytic enzymes applicable in agriculture and the bioconversion of plant biomass. In a previous study, we reported on the screening of 1100 mesophilic fungal isolates from decaying plant tissue for cellulase, xylanase and accessory enzyme activities22. In the present work, we aimed to explore the biodiversity in northern Vietnam to identify filamentous fungi able to grow at elevated temperatures (50 °C) under extremely acidic conditions (pH 2.0) using untreated rice straw as the sole carbon source. The underlying hypothesis was that the enzymes produced by the isolated fungi would be thermostable and functional under acidic conditions. Such enzymes are highly relevant for the feed industry, especially to improve the nutritional content of animal feed, where the enzymes must be stable at high temperatures during the pelleting process and also be functional in the acidic conditions of the animal’s stomach.
Results and Discussion
After 7–10 days of incubation of pre-washed plant debris on medium containing rice straw as sole carbon source at 50 °C, the proliferation of fungal hyphae was observed at pH 2.0 and 3.0, but not at pH 1.0. Moderate selection power was achieved at pH 2.0 and typically each plate contained one or rarely two macroscopically (colour and texture) distinctive types of fungi. This pH was employed for the whole study. A total of 105 fungal strains were obtained from 78 samples of compost and various kinds of decaying plant matter. The list of isolates and isolation source are presented in the Supplementary Dataset S1.
Although the fungi were isolated at pH 2.0, when inoculated in liquid media with different pHs they did not grow at pH 2.0 and showed only weak growth at pH 2.5, whereas growth at pH 3.0 and 5.0 was strong. Therefore, all the isolates were regarded as acidotolerant. We assume that, during initial isolation, the pH inside the inoculants (plant residues) might have been higher than that in the medium due to mechanical barrier or pH buffer capacity of the inoculants.
On the basis of the ITS sequence similarity to the published type/reference strains, 78 strains were closely affiliated with 15 known taxa, while the remaining 27 strains could not be reliably identified. Most of the isolates belonged to Ascomycota (89 strains), and the remaining belonged to Zygomycota (16 strains). Regarding species richness among these genera, the diversity of Thielavia was striking. As will be discussed below, among 42 isolated strains, 24 genetic groups of Thielavia that differed from each other at the species level were detected (Fig. 1). The less diverse genera were those that have been reported to occur commonly in compost, such as Thermomyces, Rhizomucor, Mycothermus and Aspergillus21. A relatively high number of isolates was found for one or two species within these genera. In term of frequency, the species could be listed in following decreasing order: Thielavia terrestris (15 strains), Thermomyces lanuginosus (12 strains), Rasamsonia emersonii (9 strains), Rhizomucor miehei (7 strains), Aspergillus fumigatus (6 strains), Mycothermus thermophilus (=Scytalidium thermophilum) (6 strains), Rhizomucor pusillus (5 strains), Thermothelomyces thermophila (=Myceliophthora thermophila) (4 strains), Rhizopus microsporus (4 strains), Thermomyces dupontii (=Talaromyces thermophilus) (4 strains), Thermothelomyces heterothallica (=Myceliophthora heterothallica) (2 strains), Chaetomium thermophilum (1 strain), Malbranchea cinnamomea (1 strain), Crassicarpon thermophilum (=Myceliophthora fergusii) (1 strain), and Rasamsonia byssochlamydoides (=Talaromyces byssochlamydoides) (1 strain) (Table 1). Apart from Aspergillus fumigatus, which is known to be thermotolerant21, all species found in this study were thermophilic and among the frequent inhabitants of compost and decomposing hay21.
It is interesting to note that the species with the highest occurrence showed little genetic variation between the strains. For example, all 12 Thermomyces langinosus strains were identical to the type strain in their ITS regions. Similarly, the species Thielavia terrestris (15 strains) and Rasamsonia emersonii (9 strains) also showed only 1–2 nucleotide (nuc) (or 0.16–0.32%) internal variation in the ITS sequences. However, high variation was observed in some species with lower occurrence. The 4 strains of Thermomyces dupontii were unique, and differed from each other by 1 to 5 nuc (or 0.18–0.91% variation) in their ITS sequences. Similarly, the 6 Mycothermus thermophilus strains represent 4 genetic groups with up to 5 nuc (or 0.94%) variations. In total, 59 unique genetic groups were detected within the 105 isolates (Table 1).
The assignment of 78 strains to 15 known species was considered reliable. The studied strains formed well supported clades (bootstrap confidence above 93%) with the type/reference strains of the corresponding taxa (Fig. 1) and nucleotide differences were less than 1%. Exceptions were LPHT 246 and FCH 7.1; the ITS sequence of LPHT 246 was closest to the GenBank sequence NR_119933 of the type strain of Rasamsonia byssochlamydoides, but differed from the latter by 10 nuc (1.81% variation). Similarly, the ITS sequence of the strain FCH 7.1 differed from the type strain of Chaetomium thermophilum by 8 nuc (1.35% variation). The differences are close to the limit for species delimitation, which is considered to be 1.96% for Ascomycota23, and the specific assignments of the strains are therefore provisional. Due to rapid changes, and confusion, in the taxonomy of thermophilic fungi3, all species names in this study are listed together with the corresponding MycoBank numbers and synonyms (Table 1).
In this study, 15 isolates were identified as Thielavia terrestris based on the ITS sequence similarity (less than 2 nuc difference) to the GenBank sequence KU729090 of the well-studied Thielavia terrestris ATCC 38088 strain. The genome of Thielavia terrestris ATCC 38088 has been sequenced and analysed18. Strictly speaking, the type strain of Thielavia terrestris is CBS 355.66 and not ATCC 38088. However, the ITS sequence of CBS 355.66 (CBS Record id: 16190616) differs from ATCC 38088 by only 1 nuc (542/543), and thus, the strains are considered conspecific.
As mentioned above, 27 strains could not be assigned to any known fungal species. Phylogenetically, the strains were found to be related to the genus Thielavia, and formed a well-supported clade (97% confidence) with Thielavia terrestris (Fig. 1). In the ITS sequences, they were also most close to Thielavia terrestris but differed from the latter by 12 to 152 nuc (or 2.16–27.39% variation), and are thus apparently far from being of the same species. Internally, these strains were highly heterogeneous in their ITS sequences, and belonged to 23 genetic groups. Another surprising fact is that each of the new genetic groups was represented by only 1 or 2 strains (19 groups with 1 strain and 4 groups with 2 strains) (Table 1). These 19 groups were nearly independent as indicated by low bootstrap values (Fig. 1). This may imply that the segregation of these genetic groups took place very recently and by some singular events. Otherwise, we might have found more isolates for a certain genetic group or some relatedness among them. The driving force for such rapid segregation is still unclear.
The unidentified Thielavia strains had optimum growth temperatures in the range 35 °C to 50 °C, and showed no or only limited growth at 20 °C and 60 °C (Fig. 2). Given these thermal growth patterns, these strains have been designated as thermophilic3. Bearing in mind the fact that only about 50 species of thermophilic fungi were known previously3, the discovery of these 23 new genetic groups is striking. Thielavia spp. isolates (both Thielavia terrestris and the new genetic groups) were similar in colony appearance (texture, colour) and conidiogenesis. On PDA at 50 °C, Thielavia strains formed white cottoneous spreading colonies that gradually changed to pinkish, yellow or light brown. Some strains formed diffused yellow pigment in the medium (Fig. 2). The strains produced rare holoblastic conidia (Fig. 3). No ascomata formation was observed. The genus Thielavia (MB#5450) comprises 41 validly described species and among them only 2 are thermophilic, namely Thielavia australiensis and Thielavia terrestris21.
No basidiomycetous fungus was found in the present study. The presence of thermophilic Basidiomycota has long been debated. Two unidentified basidiomycetous isolates have been shown to be able to grow at 45 °C in a study by Straatsma et al. 24, but no additional studies on growth at different temperatures were conducted, making it impossible to classify the isolates as thermophilic or thermotolerant. The thermophilic species Myriococcum thermophilum previously listed as a mitosporic basidiomycete is now classified as Crassicarpon hotsonii (MB#816112) under Ascomycota25.
Although ITS has been used widely as the primary marker for fungal barcoding23, the interpretation of data should be made with caution. ITS might be a poor choice for a certain group of fungi. For example, due to the presence of highly divergent non-orthologous copies of the ITS2 in Fusarium, ITS sequences cannot resolve species boundaries in the genus26. Protein-coding genes, such as translation elongation factor 1-alpha (tef1), RNA polymerase II largest (RPB1) and second largest subunit (RPB2), provided much better resolution for species of Fusarium26. Even though ITS was successfully utilised for discrimination of Thielavia species27, additional markers might be needed for understanding the taxonomic positions of the genetically highly divergent Thielavia isolates obtained in this study.
An overall significant correlation was found between lignocellulolytic activities and the amount of extracellular protein produced when the isolates were grown on rice straw (Fig. 4). Presumably, the fungi that possess a more effective lignocellulolytic machinery exhibit faster growth and hence excrete more enzymes into the medium. The low lignocellulase activities of several of the fungal species may be explained by the recalcitrance of the untreated rice straw that was used as the cultivation substrate. Zymograms of fungal secretomes were found to correlate well with the liquid enzyme activity assays. Species/strains that demonstrated high enzymatic activities also produced a wider range of enzymes, as indicated by a more varied band pattern on the zymograms (Figs 4 and 5). A combination of phylogenetic and enzymatic analyses indicated that the lignocellulose degradation patterns of closely related species/genera were similar. This could allow the provisional prediction of the ecology and lignocellulose degradation characteristics of a fungus based on its taxonomic position.
The isolated strains belonging to the Zygomycota (Rhizomucor miehei, Rhizomucor pusillus and Rhizopus microsporus) exhibited low xylanase and no carboxymethyl cellulase (CMCase) activities (Fig. 4). These species are not known as strong lignocellulose degraders and their genomes contain only about a half of the number of the CAZymes identified in the lignocellulolytic fungus Thielavia terrestris28,29. These fast-growing Mucoraceae are widespread in nature; they are often the first fungi to occupy moist plant debris30 and are known for their ability to degrade starch, proteins and lipids, which are much less recalcitrant substrates compared to lignocellulose. Accordingly, while the genome of Rhizomucor miehei harbours only 110 GHs, it encodes 155 proteases and 254 ester hydrolases29.
Low lignocellulolytic activities were also observed for the strains of Rasamsonia emersonii, Mycothermus thermophilus, Thermomyces lanuginosus and Thermomyces dupontii (Fig. 4). An exception was R. emersonii strain LPH 129, which exhibited both xylanase and CMCase activities; the CMCase activity being higher at pH 3.0 than at pH 5.0 or pH 7.0. Rasamsonia emersonii is an industrially important fungus that produces enzymes (β-glucanase, cellobiohydrolase, β-glucosidase) used in baking31 and beer production32. The fungus Mycothermus thermophilus is an important fungus in mushroom composting33.
Low lignocellulolytic activity of the strains assigned to the genus Thermomyces may seem counterintuitive as the genus has been extensively studied in biomass bioenergy research. The relatively low production of xylanase by Thermomyces strains when grown on untreated rice straw might be explained by the recalcitrance of the substrate34 and a corresponding low release of enzyme-inducing mono- or oligosaccharides. Genome analysis of Thermomyces lanuginosus revealed that it encodes few CAZy proteins (224) compared to other filamentous fungi (average 400)35. Glycoside hydrolases were significantly fewer in Thermomyces lanuginosus (94), whilst lignocellulosic fungi typically encode more than 200. Surprisingly, although Thermomyces lanuginosus is known as a xylanase superproducer, only a single β-1,4 xylanase was identified in its genome35. The zymography in our study indicated that strains of both Thermomyces lanuginosus and Thermomyces dupontii produce only one xylanase (xylanolytic band) when grown on untreated rice straw (Fig. 5). With its relatively small genome size, the percentage of CAZy proteins versus the total number of predicted proteins in Thermomyces lanuginosus is 4.38% and among the highest in fungi. Small genome size, and efficient gene regulation and enzyme transport are thought to be important factors in lowering the energy expenditure in fungi, which in turn is crucial in high-temperature environments35.
It is interesting to note that, the group of strains showing low CMCase activities exhibited a rather high maximum growth temperature (Fig. 4). Species like Rhizomucor pusillus, Rhizomucor miehei, Rasamsonia emersonii, Thermomyces dupontii, Thermomyces lanuginosus are known to involved in phase I of composting process, where readily accessible nutrients, microbial activity, and heat accumulation are at their maximum21.
Among the group of strains demonstrating high CMCase activity were species previously assigned to the genus Myceliophthora (Crassicarpon thermophilum, Thermothelomyces heterothallica and Thermothelomyces thermophila), species of Thielavia and the thermotolerant fungus Aspergillus fumigatus (Fig. 4). When cultivated on untreated rice straw, the strains produced high amounts of extracellular proteins. These strains also demonstrated relatively lower maximum growth temperatures, which indicates that they might be involved in the later stages of plant biomass degradation when more readily accessible nutrients have been exhausted and temperatures have dropped. Thielavia species and species previously under the genus Myceliophthora share such a high morphological resemblance during vegetative growth that several species of Myceliophthora were previously regarded as anamorphs of Thielavia36. In the present study, the two groups showed rather contrasting lignocellulolytic activity profiles. While Thielavia species exhibited both xylanase and CMCase activities, Myceliophthora species showed almost exclusively CMCase activity. The Myceliophthora genus was recently restructured based on ITS, translation elongation factor 1-α (TEF1) and RPB1 gene sequences. The species Myceliophthora heterothallica and Myceliophthora thermophila were placed under Thermothelomyces and Myceliophthora fergusii under Crassicarpon. Currently, Myceliophthora comprises only mesophilic species37. The thermotolerant Aspergillus fumigatus strains also demonstrated high CMCase and xylanase activities. This species is a human pathogen38 and its direct use in technical applications is therefore questionable. Among the thermophilic and thermotolerant fungi, Aspergillus fumigatus encodes the highest number of CAZymes35, and the genes encoding thermostable cellulases from this species might be worth pursuing39.
By using a very acidic medium at high temperature for isolation, we aimed to isolate fungi able to produce thermostable enzymes that can function under acidic conditions. Most of the isolates produced CMCases that exhibited higher activities at pH 3 than at pH 5 or pH 7, and were also thermostable. CMCase-exhibiting enzymes of 31 and 14 isolates retained more than 75% and 90% of their activity, respectively, after treatment at 70 °C for 20 min. Xylanases were generally less thermostable and showed lower activity under acidic conditions than CMCases (Fig. 4).
Heat treatment at 70 °C effectively denatured most of the xylanases, although xylanase produced by Rasamsonia emersonii LPH 067 was not affected, and xylanases produced by R. emersonii LPHT 227, R. emersonii LPHT 234, Rhizopus microsporus LPH 143 and Mycothermus thermophilus LPH 128 retained more than 75% of their initial activity. Similarly, 7 isolates (Rh. microsporus LPH 143, Thielavia terrestris FCH 9.4, T. terrestris LPHT 226, Thielavia sp. LPHT 232, Thielavia sp. LPHT 225, Thielavia sp. LPHT 235 and Thielavia sp. LPH 182) showed higher xylanase activities at pH 3 than at pH 5 and pH 7. Overall, the fungal secretomes produced by Thielavia spp. are of special interest because of their high enzymatic activity, thermostability, and the possibility of functioning under acidic conditions (Fig. 4).
In this study, rice straw was chosen as the substrate for lignocellulolytic enzyme production because it represents the most important lignocellulosic waste stream in Vietnam and other Southeast Asian countries34. Instead of pretreating rice straw and adding substrates facilitating optimal enzyme production, we chose minimum mineral medium with untreated rice straw as the medium for solid state fermentation. The ability of fungal isolates to colonize and degrade untreated rice straw provides insight into the natural process of plant biomass degradation by the fungi. Rice straw is especially recalcitrant to biodegradation, partly due to its high silica content34.
Fungal biodiversity in the tropics is high, but remains largely unstudied. Metagenomic analysis of soil samples collected around the globe has indicated that the highest fungal diversity is found in northwest Latin America, the southwest coast of India, on the Kalimantan island and in the triangle between Vietnam, Laos and China40. Characterisation of fungal diversity by isolation is often problematic since the real diversity may be masked by cosmopolitan species that occur at high frequency and cell density. By using a moderate selection pressure (elevated temperature, low pH and lignocellulosic substrate), we have here discovered numerous previously undocumented thermophilic fungi in the genus Thielavia which exhibited high genetic divergence. The selection medium was proven to be useful in finding fungi and enzymes with targeted properties. Studying secretomes produced by fungi on native substrates can provide new information on their roles in the natural processes of plant biomass degradation.
Isolation and cultivation of fungi
Various types of samples containing decaying plant residues (compost, grasses, rice straw, mushroom ground, wood, soil) were collected from different provinces in the northern part of Vietnam during the years 2012–2016. Fungi were isolated in a newly formulated medium containing untreated rice straw as the sole carbon source at pH 2.0 and 50 °C. For fungal isolation, samples were washed 3 times with sterile Czapek Dox mineral base ((NH4)2SO4 1.0 g L-1; K2HPO4.3H2O 0.5 g L−1; KCl 0.25 g L−1; MgSO4.7H2O 0.25 g L−1, FeSO4.7H2O 5 mg L−1) with the pH adjusted to 2.0 using 1.0 M H2SO4. Washing was performed to adjust the pH of samples that may have buffering capacity, and to enhance the fungal diversity by removing the overload of aerial spores while retaining substrate mycelia. For the preparation of the isolation medium, rice straw (variety Japonica J02) was hammer-milled and passed through an 18-mesh sieve. It was then rinsed with acidified Czapek Dox mineral base, autoclaved at 121 °C for 15 min and spread on plastic Petri dishes to form a 5–8 mm semi-solid layer. The pre-washed samples were sprinkled over the rice-straw plates and incubated at 50 °C. To avoid evaporation, the incubation chamber was humidified by inserting large trays of water. After 7–10 days of incubation, the fungal colonies formed were transferred to potato dextrose agar (PDA) plates (HiMedia, India) and purified by hyphal tip culture. After cultivation in PDA slants at 50 °C, the isolates were maintained in a refrigerator at 2–8 °C. For long-term storage, a loop-full of fungal biomass was transferred to neutral glass tubes containing sterile washed sand. The contents were freeze-dried and the tubes were vacuum sealed. Fungal isolates can be stored in this way for several years.
To assess the growth profiles at different temperatures, fungi were inoculated on PDA plates and incubated at 20, 30, 35, 40, 45, 50, 55, and 60 °C for 7 days. The growth was assessed in terms of colony diameter. Growth at different pH was tested at 50 °C in liquid YM broth (glucose 10 g L−1, malt extract 3 g L−1, peptone 5 g L−1, yeast extract 3 g L−1) with the pH adjusted to 2.0, 2.5, 3.0, 3.5, 4.0, 4.5 and 5.0 using 1.0 M H2SO4. Growth was evaluated visually after 7 days of incubation.
Solid state cultivation and enzyme extraction
For enzyme production, fungi were cultivated in a solid medium using untreated rice straw as the sole carbon source. Precultures were made by growing the fungi on PDA plates at 50 °C for 5 days. Surface mycelia and spores were scalped off and suspended in 4 mL of sterile 0.05% Tween 80 solution. One mililiter of the cell suspension was added to a 100 mL Erlenmeyer flask containing 5 g of milled rice straw and 10 mL of standard Czapek Dox mineral base (pH 5.0). The flasks were capped with SILICOSEN® C-type lids (Shin-Etsu Polymer, Japan) and incubated at 50 °C for 7 days in a humidified chamber. The flask contents were mixed once per day by manual shaking. For enzyme extraction, 45 mL of 50 mM sodium citrate buffer at pH 5.0 was added to the flask. It was then shaken for 2 h at 30 °C in a rotary shaker at 160 rpm. The supernatant was obtained by centrifugation at 7 000 g for 10 min at 10 °C and stored at −30 °C until use.
For the determination of xylanase or CMCase activity, 0.1 mL of crude culture filtrate was mixed with 0.2 mL of a 10 g L−1 xylan (from beechwood, Cas: 9014–63–5, Apollo Scientific) or 10 g L−1 CMC (Cas: 9004-32-4, Sigma) solution. After incubation at 50 °C for 20 min, 0.6 mL of DNS Reagent (water, 1416 mL; 3,5 dinitrosalicylic acid, 10.6 g; sodium hydroxide, 19.8 g; sodium potassium tartrate, 306 g; phenol, 7.6 mL; sodium metabisulphite, 8.3 g) was added and incubated at 100 °C for 5 min. The contents were cooled down, and 0.4 mL was mixed with 1.8 mL water, and the absorbance was measured at 540 nm41. Calibration curves were constructed using xylose and glucose for xylanase and CMCase activities, respectively. Britton-Robinson buffer (40 mM H3BO3, 40 mM H3PO4 and 40 mM CH3COOH) titrated to the desired pH with 0.2 M NaOH was used to determine the enzymatic activity at different pH (pH 3.0, 5.0, and 7.0). Crude culture filtrates were incubated at 70 °C for 20 min and the residual activity was measured to assess the thermostability.
Zymography was performed based on conventional denaturing SDS-PAGE42,43 using a 10% polyacrylamide gel containing 1% CMC or 1% xylan. After electrophoresis, to renature the protein fractions, the gel was rinsed twice in 2% Triton X-100 for 30 min at room temperature, and then twice with ice-cold 50 mM sodium citrate buffer, pH 5.0 for 15 min. In-gel hydrolysis was carried out by incubating the gel in 50 mM sodium citrate buffer, pH 5.0 at 50 °C for 1 h. The gel was then rinsed 4–5 times with distilled water and stained with 0.1% Congo Red solution at 50 °C for 1 h. De-staining was carried out with 1 M NaCl. Active CMCase or xylanase fractions appeared as transparent bands on the red background. Images were obtained using a digital camera (Nikon D7000) and converted into grayscale images. The images were overlaid as yellow (CMCase) and dark-blue (xylanase) channels in a new RGB image using Adobe Photoshop CS6 to display both the CMCase and xylanase activity.
Identification of fungi
Fungi were identified by sequencing of the internally transcribed spacer (ITS) region. This region has been found to be among the markers with the highest probability of correct identification for a very broad group of fungi23. Since there is no definitive percentage of sequence similarity that precisely indicates conspecific taxa, we adopted the average weighted infraspecific ITS variability value of 2.51% for the fungi kingdom (1.96% for Ascomycota, and 3.24% for Zygomycota)44 as guidance in species assignment.
Fungi were grown on PDA for 3–5 days at 50 °C. For DNA extraction, a loopful of mycelium was transferred to a micro-tube containing 1 mL of 2 × SSC (15 mM sodium citrate, 150 mM NaCl, pH 7.0). The tubes were incubated at 99 °C for 10 min using a dry heating block (Grant-bio, England). Cells were collected by centrifugation at 10 000 g for 1 min. About 100 μL of glass beads (0.2–0.5 mm in diameter; Roth, Germany), 100 μL of phenol-chloroform (1:1, v/v) and 150 μL of water were added to the cell pellet. The cells were disrupted using a Mini-Beadbeater-8 (Biospec, USA) for 45 s. The tubes were centrifuged at 14 000 g at 4 °C for 10 min, and the upper layer was transferred to a new micro-tube. The DNA solution was further purified using a Silica Bead DNA Gel Extraction kit (Thermo Scientific) according to the manufacturer’s instruction.
PCR amplification and sequencing of the ITS region were done using one of the forward primers ITS1 (TCC GTA GGT GAA CCT GCG G)45, ITS5 (GGA AGT AAA AGT CGT AAC AAG G)45, ITS1F (CTT GGT CAT TTA GAG GAA GTA A)46 or SR6R (AAG WAA AAG TCG TAA CAA GG)47, and one of the reverse primers ITS4 (TCC TCC GCT TAT TGA TAT GC)45 or LR1 (GGT TGG TTT CTT TTC CT)47. The PCR cycle was as follows: 94 °C for 3 min; 30 cycles of 94 °C for 40 s, 52 °C for 40 s and 72 °C for 60 s; 72 °C for 10 min. The DNA sequencing service provided by the First BASE Laboratories Sdn Bhd (Selangor, Malaysia) was used. The sequences obtained have been deposited in GenBank with consecutive accession numbers from MH305194 to MH305299. The sequences were compared with the available databases using BLAST at the National Center for Biotechnology Information (https://blast.ncbi.nlm.nih.gov), the sequence-based identification tool at UNITE Community (https://unite.ut.ee) and the CBS-KNAW Pairwise sequence alignment identification tool (http://www.westerdijkinstitute.nl). For phylogenetic analysis, sequences were aligned with a fast Fourier transform algorithm using the online version of MAFFT48 (http://www.ebi.ac.uk/Tools/msa/mafft/) hosted at the European Bioinformatics Institute (Hinxton, Cambridgeshire, UK). Phylogenetic trees were constructed using MEGA749. The graphical combination of enzymatic activities in the form of heat maps and a phylogenetic tree was performed using iTOL50.
Kashefi, K. & Lovley, D. R. Extending the upper temperature limit for life. Science 301, 934–934 (2003).
Tansey, M. R. & Brock, T. D. The upper temperature limit for eukaryotic organisms. Proc. Natl. Acad. Sci. 69, 2426–2428 (1972).
de Oliveira, T. B., Gomes, E. & Rodrigues, A. Thermophilic fungi in the new age of fungal taxonomy. Extremophiles 19, 31–37 (2015).
Morgenstern, I. et al. A molecular phylogeny of thermophilic fungi. Fungal Biol. 116, 489–502 (2012).
Cooney, D. G. & Emerson, R. Thermophilic fungi. An account of their biology, activities, and classification. Thermophilic fungi. An Acc. their Biol. Act. Classif (1964).
Johri, B. N., Satyanarayana, T. & Olsen, J. Thermophilic moulds in biotechnology. (Springer Science & Business Media 1999).
Miehe, H. Die selbsterhitzung des heus: Eine biologische studie. (G. Fischer 1907).
Singh, B. & Satyanarayana, T. Thermophilic molds in environmental management. Prog. Mycol. Res. 1, 352–375 (2009).
Magan, N. Fungi in extreme environments. The Mycota 4, 85–103 (2007).
Hujslová, M., Kubátová, A., Kostovčík, M. & Kolařík, M. Acidiella bohemica gen. et sp. nov. and Acidomyces spp. (Teratosphaeriaceae), the indigenous inhabitants of extremely acidic soils in Europe. Fungal Divers. 58, 33–45 (2013).
Starkey, R. L. & Waksman, S. A. Fungi tolerant to extreme acidity and high concentrations of copper sulfate. J. Bacteriol. 45, 509 (1943).
Selbmann, L. et al. Drought meets acid: three new genera in a dothidealean clade of extremotolerant fungi. Stud. Mycol. 61, 1–20 (2008).
Luo, H. et al. A thermophilic and acid stable family-10 xylanase from the acidophilic fungus Bispora sp. MEY-1. Extremophiles 13, 849–857 (2009).
Yamazaki, A., Toyama, K. & Nakagiri, A. A new acidophilic fungus Teratosphaeria acidotherma (Capnodiales, Ascomycota) from a hot spring. Mycoscience 51, 443–455 (2010).
Fernandez, S., Murry, P. G. & Tuohy, M. G. Enzyme systems from the thermophilic fungus Talaromyces emersonii for sugar beet bioconversion. BioResources 3, 898–909 (2008).
Trivedi, M., Singh, R., Shukla, M. & Tiwari, R. K. GMO and Food Security. in Ecofriendly Pest Management for Food Security 703–726 (Elsevier 2016).
Grigoriev, I. V. et al. MycoCosm portal: Gearing up for 1000 fungal genomes. Nucleic Acids Res. 42 (2014).
Berka, R. M. et al. Comparative genomic analysis of the thermophilic biomass-degrading fungi Myceliophthora thermophila and Thielavia terrestris. Nat. Biotechnol. 29, 922–929 (2011).
Hüttner, S. et al. Combined genome and transcriptome sequencing to investigate the plant cell wall degrading enzyme system in the thermophilic fungus Malbranchea cinnamomea. Biotechnol. Biofuels 10, 265 (2017).
van Noort, V. et al. Consistent mutational paths predict eukaryotic thermostability. BMC Evol. Biol. 13, 7 (2013).
Salar, R. K. Thermophilic Fungi: Basic Concepts and Biotechnological Applications. (CRC Press 2018).
Anasontzis, G. E. et al. Rice straw hydrolysis using secretomes from novel fungal isolates from Vietnam. Biomass and Bioenergy 99, 11–20 (2017).
Schoch, C. L. et al. Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi. Proc. Natl. Acad. Sci. USA 109, 6241–6246 (2012).
Straatsma, G. et al. Ecology of thermophilic fungi in mushroom compost, with emphasis on Scytalidium thermophilum and growth stimulation of Agaricus bisporus mycelium. Appl. Environ. Microbiol. 60, 454–458 (1994).
Koukol, O. Myriococcum revisited: a revision of an overlooked fungal genus. Plant Syst. Evol. 302, 957–969 (2016).
Hibbett, D. et al. Sequence-based classification and identification of Fungi. Mycologia 108, 1049–1068 (2016).
Stchigel, A. M., Figuera, L., José, C. & Guarro, J. New species of Thielavia, with a molecular study of representative species of the genus. Mycol. Res. 106, 975–983 (2002).
Hüttner, S. et al. Genome sequence of Rhizomucor pusillus FCH 5.7, a thermophilic zygomycete involved in plant biomass degradation harbouring putative GH9 endoglucanases. Biotechnol. Reports 20, e00279 (2018).
Zhou, P. et al. Genome sequence and transcriptome analyses of the thermophilic zygomycete fungus Rhizomucor miehei. BMC Genomics 15, 294 (2014).
Walther, G. et al. DNA barcoding in Mucorales: an inventory of biodiversity. Persoonia 30, 11–47 (2013).
Waters, D. M., Murray, P. G., Ryan, L. A., Arendt, E. K. & Tuohy, M. G. Talaromyces emersonii thermostable enzyme systems and their applications in wheat baking systems. J. Agric. Food Chem. 58, 7415–7422 (2010).
Briggs, D. E., Brookes, P. A., Stevens, R. & Boulton, C. A. Brewing: science and practice. (Elsevier 2004).
Straatsma, G. et al. Inoculation of Scytalidium thermophilum in button mushroom compost and its effect on yield. Appl. Environ. Microbiol. 60, 3049–3054 (1994).
Satlewal, A., Agrawal, R., Bhagia, S., Das, P. & Ragauskas, A. J. Rice straw as a feedstock for biofuels: Availability, recalcitrance, and chemical properties. Biofuels, Bioprod. Biorefining 12, 83–107 (2018).
Mchunu, N. P. Xylanase hyper-producer: Genome of the thermophilic fungus Thermomyces lanuginosus. PhD thesis, Durban University of Technology, Durban, South Africa (2014).
Van Den Brink, J., Samson, R. A., Hagen, F., Boekhout, T. & De Vries, R. P. Phylogeny of the industrial relevant, thermophilic genera Myceliophthora and Corynascus. Fungal Divers. 52, 197–207 (2012).
Marin-Felix, Y., Stchigel, A. M., Miller, A. N., Guarro, J. & Cano-Lira, J. F. A re-evaluation of the genus Myceliophthora (Sordariales, Ascomycota): its segregation into four genera and description of Corynascus fumimontanus sp. nov. Mycologia 107, 619–632 (2015).
Dagenais, T. R. T. & Keller, N. P. Pathogenesis of Aspergillus fumigatus in invasive aspergillosis. Clin. Microbiol. Rev. 22, 447–465 (2009).
Rungrattanakasin, B., Premjet, S., Thanonkeo, S., Klanrit, P. & Thanonkeo, P. Cloning and expression of an endoglucanase gene from the thermotolerant fungus Aspergillus fumigatus DBiNU-1 in Kluyveromyces lactis. Brazilian J. Microbiol. (2018).
Tedersoo, L. et al. Global diversity and geography of soil fungi. Science 346, 1256688 (2014).
Miller, G. L. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal. Chem. 31, 426–428 (1959).
Sambrook, J., Fritsch, E. F., Maniatis, T. Molecular cloning: a laboratory manual. (New York: Cold Spring Harbor Laboratory Press 1989).
Cano-Ramírez, C. et al. One-step zymogram method for the simultaneous detection of cellulase/xylanase activity and molecular weight estimation of the enzyme. Electrophoresis 38, 447–451 (2017).
Raja, H. A., Miller, A. N., Pearce, C. J. & Oberlies, N. H. Fungal Identification Using Molecular Tools: A Primer for the Natural Products Research Community. Journal of Natural Products 80, 756–770 (2017).
White, T., Bruns, T., Lee, S. & Taylor, J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In PCR Protocols: A Guide to Methods and Applications (eds Innis, M., Gelfand, D., Shinsky, J. & White, T.) 315–322 (Academic Press 1990).
Gardes, M. & Bruns, T. D. ITS primers with enhanced specificity for basidiomycetes–application to the identification of mycorrhizae and rusts. Mol. Ecol. 2, 113–118 (1993).
Vilgalys, R. & Hester, M. Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J. Bacteriol. 172, 4238–4246 (1990).
Katoh, K. & Standley, D. M. MAFFT multiple sequence alignment software version 7: Improvements in performance and usability. Mol. Biol. Evol. 30, 772–780 (2013).
Kumar, S., Stecher, G. & Tamura, K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 33, 1870–1874 (2016).
Letunic, I. & Bork, P. Interactive tree of life (iTOL)v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res. 44, W242–W245 (2016).
This work was funded by the Swedish Research Council (Vetenskapsrådet) through VR grant 2014–3523 “Enzyme discovery and production in Vietnam for the production of sustainable biofuels and biochemicals” (PI: LO). SH, JL and LO acknowledge funding from Wallenberg Wood Science Center (Knut and Alice Wallenberg Foundation).
The authors declare no competing interests.
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Thanh, V.N., Thuy, N.T., Huong, H.T.T. et al. Surveying of acid-tolerant thermophilic lignocellulolytic fungi in Vietnam reveals surprisingly high genetic diversity. Sci Rep 9, 3674 (2019). https://doi.org/10.1038/s41598-019-40213-5
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