Living GenoChemetics by hyphenating synthetic biology and synthetic chemistry in vivo

Marrying synthetic biology with synthetic chemistry provides a powerful approach toward natural product diversification, combining the best of both worlds: expediency and synthetic capability of biogenic pathways and chemical diversity enabled by organic synthesis. Biosynthetic pathway engineering can be employed to insert a chemically orthogonal tag into a complex natural scaffold affording the possibility of site-selective modification without employing protecting group strategies. Here we show that, by installing a sufficiently reactive handle (e.g., a C–Br bond) and developing compatible mild aqueous chemistries, synchronous biosynthesis of the tagged metabolite and its subsequent chemical modification in living culture can be achieved. This approach can potentially enable many new applications: for example, assay of directed evolution of enzymes catalyzing halo-metabolite biosynthesis in living cells or generating and following the fate of tagged metabolites and biomolecules in living systems. We report synthetic biological access to new-to-nature bromo-metabolites and the concomitant biorthogonal cross-coupling of halo-metabolites in living cultures.

B acterial natural products represent an unparalleled starting point for drug discovery 1 , and there is much interest in the generation of analogs of such compounds in order to explore modes of action, determine structure-activityrelationships and improve bioavailability and bioactivity. Natural products and their analogs may of course be accessed through total synthesis; excellent recent examples include the total synthesis of the antibiotic marinomycin 2 and generation of rifamycin and the structurally related metabolite salinisporamycin 3,4 . Such studies are invaluable in developing methodology, revealing potential biogenic mechanisms and providing the only access to molecules generated by rare or hard to culture organisms. However, the approach of total synthesis can be challenging, time consuming and costly. Analog generation through semi-synthesis is also limiting; with the selective chemical modification of complex molecules remaining as a longstanding challenge within chemical synthesis, and usually demanding the presence of innate chemical orthogonality within the molecule. To overcome such obstacles, Miller has pioneered the use of peptides to catalyze site-selective epoxidation 5 , acylation 6 and halogenation 7 of complex scaffolds, enabling access to novel antibiotic analogs; nevertheless, a range of regioisomers still results.
The enzymatic introduction of a halogen into a compound is regioselective and provides a chemically orthogonal handle to enable its further direct functionalization through cross-coupling methodologies; we have previously developed such a GenoChemetic strategy, but were limited in vivo to chlorination 8 . Analogous to our GenoChemetic approach, Miller has combined his peptide enabled selective bromination with diversification using Suzuki-Miyaura cross-coupling. This is exemplified in his regioselective functionalisation of vancomycin through a stepwise monodehalogenation/cross-coupling strategy of its native aryl chlorides 9 and his two step derivatization of teicoplanin 10 . In a complementary approach to Miller, Lewis has engineered the halogenase RebH to enable regioselective and late-stage in vitro bromination of synthetic scaffolds 11 . The use of a membrane-partitioned reactor, to segregate a stabilized halogenase enzyme aggregate (crosslinked enzyme aggregates (CLEAs)) from a palladium catalyst, enabled the 'almost one-pot' C-H functionalization of aryl compounds to be achieved at 50-80°C on a 3-indole propionate substrate 12 .
The cross-coupling of the highly reactive C-I bonds of 4-I-phenylalanine residues in modified proteins 13 and the cross-coupling of aryltriflates in living cells has also been demonstrated 14 . In these studies, the aryl iodide and triflate substrates utilized, were synthesized separately and exogenously supplied.
Building upon our GenoChemetics approach to generate natural product analogues 8 , we wished to explore the ambitious goal of genetically engineering the biosynthesis of a metabolite tagged with a sufficiently reactive, chemically orthogonal handle. Such an approach would allow the tagged metabolite to be a good substrate for subsequent palladium-mediated modification in the presence of the living cells that produced it. While the incorporation of a C-I bond provides a highly reactive site for functionalization, so far, no enzymes capable of iodination have been characterized and therefore other halogenases must be  Fig. 1 Biosynthetic halogenation enabling Suzuki-Miyaura cross-coupling. a in vivo generation of Cl-pacidamycin, by the natural producer, transformed with a halogenase, followed by in vitro cross-coupling of the compound as a component of cell free extract, at 80°C (in vivo: in vitro) 8 , b in vitro generation of reactive bromo-aromatics by RebH variant enzymes, followed by in vitro cross-coupling of the compound as a component of the crude extract (in vitro: in vitro) 11 , c in vitro generation of reactive bromo-aromatics by stabilized crosslinked enzyme aggregates ((CLEAs) of a series of flavin-dependent halogenases, membrane partitioned from anaerobic, palladium-mediated cross-coupling conditions (in vitro: in vitro) 12 , d in vivo incorporation of reactive, synthetic iodophenylalanine into peptides, followed by protein purification and cross-coupling of the iodinated protein (in vivo: in vitro) 13 , e in vivo Suzuki-Miyaura modification of synthetically generated, reactive triflate fluoran (synthetic: in vitro) 14 , f in vivo generation of reactive 7-Br-tryptophan 2 by engineered E. coli RG-1500 synchronous with the in-culture Suzuki-Miyaura cross-coupling of this reactive metabolite (in vivo: in vivo); and g generation of reactive Br-pacidamycin D 3 by engineered Streptomyces coelicolor RG-1104 concomitant with the in-culture Suzuki-Miyaura cross-coupling of this reactive metabolite (in vivo: in vivo) employed. The engineering of several pathways to enable the generation of new-to-nature fluoroand chloro-metabolites has been previously achieved 8,[15][16][17][18] . The C-F bond does not facilitate subsequent cross-coupling and the poor reactivity of C-Cl renders cross-coupling challenging as it requires harsher conditions 8 . Engineering the biosynthesis of brominated natural products represents a needed compromise between chemical reactivity and genetic install-ability. For our model system, we choose to focus toward diversification of tryptophan 1. This amino acid is a key component in many natural products and its presence in proteins and peptides is important to their structural integrity and fluorescent properties, its modulation is therefore attractive. Mild approaches to address the functionalization of halo-tryptophans are challenging as halo-indoles are shown to be less reactive than analogous heterocyclic aryl halides 19 .
Tryptophan inhibits L1-Pd catalyzed Suzuki-Miyaura coupling. We next investigated the cross-coupling of halo-tryptophan using mild, aqueous conditions. We previously reported the first Suzuki-Miyaura cross-coupling reaction of unprotected Br-and Cl-tryptophans, these reactions required heating at 80°C 25 . Under the optimal conditions for halo-indoles (described above), the cross-coupling of unprotected 5-or 7-Br-tryptophan (13 and 2, respectively) was unsuccessful, potentially due to their ability to coordinate to Pd and substrate could inhibit the catalysis under mild reaction conditions 10,26 . Hence, to explore the inhibition of the cross-coupling of halo-indoles by the amino acid, we investigated the reaction of 5-I-indole 4, doped with free tryptophan 1, with p-Tol-B(OH) 2 . An almost linear drop in conversion correlated with the increase in added tryptophan 1 (Fig. 3) was observed. To explore whether the drop in conversion is directly attributable to the carboxylate or primary amine functionality, we added one equiv. of either tryptophan 1, tryptophan methyl ester 9, N-acetyl tryptophan 10 (acylated primary amine) or the N-acetyl tryptophan methyl ester 11 (Fig. 3). The effect of addition of tryptophan methyl ester 9 or free tryptophan 1 on the reaction were comparable (conversions reduced to 12 and 15% respectively). However, in reactions where one equiv. of N-acetyl tryptophan 10 was added, as a potential inhibitor, a 41% conversion resulted. This indicates that the primary amine of tryptophan plays a key role in the inhibition of the reaction; however, the carboxylate may not be considered as completely innocent as when doubly protected tryptophan 11 was added, a conversion of 59% resulted under the same reaction conditions. It is possible, therefore, that N-and O-coordination complexes (NH 2 -Pd, COO-Pd) or N,O-Pd may be formed in situ, reducing the effective concentration of available Pd for catalysis [26][27][28][29] . Usefully, we observed that inhibition of cross-coupling by tryptophan 1 can be partially reversed by increasing the concentration of p-Tol-B(OH) 2 . These results indicate that chelation of Pd by the amino acid motif is not the sole possibility; but that heterodimeric complexation of amino acid with boronic acid is also present 30 . Together, these two equilibria could contribute towards inhibition of the cross-coupling reaction.

Suzuki-Miyaura coupling of Br-tryptophans and tripeptides.
In the light of our observations on the inhibitory effect of the amino acid, we next set out to explore mild conditions that could be translated to cross-coupling of unprotected halo-tryptophan or halo-tryptophan containing peptide. We screened series of catalysts and ligands for any that would provide reactivity at physiological temperature ( Supplementary Fig. 1). Recently, Ballet et al. 31 . reported that the palladium pre-catalyst of disodium 2-aminopyrimidine-4,6-diol 31-34 (L2-Pd, Fig. 2) was effective for cross-coupling of halo-tryptophans at 80°C under microwave irradiation. We further explored the utility of L2-Pd to perform cross-coupling at lower temperature. After optimizing reagent concentrations (3 equiv. p-Tol-B(OH) 2 and 6 equiv. K 2 CO 3 ), we successfully cross-coupled unprotected 7-Br- NATURE COMMUNICATIONS | DOI: 10.1038/s41467-017-00194-3 ARTICLE tryptophan 2, at 45°C (Fig. 4a). The reaction proceeded smoothly using 5 mol% of the L2-Pd catalyst and the product 7-p-tolyl-tryptophan 2a was isolated in high yield (85%). For 5-Br-tryptophan 13, a 90% NMR conversion and a lower 54% isolated yield of the product 13a, potentially due to product solubility issues, was observed. Moreover, a modest 32% conversion was observed for the significantly more challenging and less reactive unprotected 7-Cl-tryptophan 12 (Fig. 4a).
To assess the applicability of these cross-coupling conditions for the modification of small peptides, we explored the reaction with three tripeptides containing 7-Br-tryptophan 2 placed centrally 14 or at the N-terminal 15 or C-terminal 16 ( Fig. 4b) 35 (for syntheses, see Supplementary Methods). The reactions worked well in aqueous conditions without need for organic co-solvent and at relatively low catalyst loading (L2-Pd, 5 mol%). The cross-coupling products 14a-16a were isolated in good yields (62-71%, Fig. 4c). In general, this mild protocol is amenable for derivatisation of peptides and has potential to be applicable to higher polypetides/proteins possessing halo-aryl functionality.
Our ultimate and ambitious goal was to, for the first time, enable engineered production of a halogen tagged metabolite and its cross-coupling in living culture. This would be a significant breakthrough in the field. Such a combination of genetic engineering to generate tagged metabolites and both synchronous and sequential chemical modification of the tag has the exciting potential to pave the way to in vivo diversification, labeling and affinity tagging. To explore whether we could engineer biosynthetic halogenation and chemical cross-coupling in a living system, we chose to work toward two model systems of varying challenge: firstly, engineering Escherichia coli for biosynthesis of 7-Br-tryptophan 2, secondly engineering streptomycetes to produce Br-pacidamycin D. Pacidamycin represents a challenging model system; its selective functionalization is inherently difficult as it contains both a peptide chain and a modified nucleic acid moiety. Pacidamycin is produced, like many natural products, in  very low concentration and challenges any synthetic methodology to be efficient even at such high dilution. It also exemplifies a further demand in accessing the bromo-metabolite because the natural producer has poor tolerance to bromide, and the biosynthetic gene cluster would therefore need to be introduced into a more suitable host strain. We set out to engineer the two systems and to systematically and iteratively address the impact of the cross-coupling reagents on the two biological systems and assess how components from the fermentation media would impact upon cross-coupling efficiency. To undertake this ambitious task, we first explored and enabled the generation and cross-coupling of 7-Br-tryptophan 2 in E. coli culture.
Applying in-culture GenoChemetics to tryptophan. A plasmid carrying prnA encoding a tryptophan 7-halogenase from pyrrolnitrin biosynthesis 36 was constructed and introduced into E. coli PHL644 strain (engineered E. coli RG-1500), and upon supplementation of the culture with sodium bromide, resulted in production of 7-Br-tryptophan 2 (see Supplementary Figs 6-8 and Supplementary Methods for details).
We set out to establish conditions that would promote 7-Brtryptophan 2 production and be suitable for its corresponding cross-coupling in living cultures of E. coli. While cross-coupling of synthetic halogenated materials has been previously reported in buffer 37 there are no reports of reactions carried out in media that would be required to sustain growth and metabolite production. In parallel, we established the effect of Pd, ligand and boronic acid concentration, both separately and in combination, on E. coli viability; and explored the efficiency of cross-coupling of 7-Br-tryptophan 2 within a range of media and in the presence of individual media components. As an in vitro model reaction for this screening, we used 7-Br-tryptophan 2 (0.35 mM) 38 , p-Tol-B(OH) 2 (1.2 mM, 3.4 equiv.) and L2-Pd catalyst (0.1 mM) (for details of the media screening see Supplementary Discussion). In summary, key observations revealed that only trace conversion ( < 2%) occurred in the presence of series of standard culture media (e.g., Luria-Bertani (LB), 2xYT) or yeast/malt extracts (Supplementary Table 2). However, we observed that cross-coupling conditions were tolerant to phosphate buffer (100 mM with 50 mM NaCl/Br, pH 8) and citrate buffer (100 mM, pH 8). Provision of both a carbon and nitrogen source is essential for bacteria growth. Nitrogen is usually supplied from amino acids and/or ammonium salts in the media. Our investigations demonstrated both the free amine and carboxylate of tryptophan 1 had a detrimental effect on the reaction (discussed in earlier section). Unsurprisingly,  cross-coupling was strongly suppressed by the presence of amino acids (e.g., glycine 20 mM) as well as ammonium salts. Provision of a suitable carbon source could also prove a challenge, as poor conversions (~10%) were observed in the presence of glucose (22 mM, 0.4% w/v) or glycerol (217 mM, 2% w/v). Alternative carbon sources, that could either enter directly into the Krebs' cycle (such as citrate) or could be slowly metabolized so that inhibitory monosaccharide and glycerol concentrations would remain low, were also explored (see Supplementary Table 2). Following numerous iterative rounds of assessing media that would enable bacterial growth, 7-Br-tryptophan 2 production and be cross-coupling compatible, we determined that a minimal media containing potassium nitrate (20 mM) as the nitrogen source, glycerol (0.5% w/v, 55 mM) as the sole carbon source and supplemented with 50 mM NaBr ('cross-coupling media' (CCM)) could be employed. Aware that the bacteria would metabolize the media, thereby depleting the carbon and nitrogen sources initially supplied, we also considered that a dynamic living system would generate cofactors, bio-thiols and radical species with a potential to poison Pd-catalyst and be detrimental to the cross-coupling reactions. To determine the impact of such metabolites, cultures of the engineered E. coli RG-1500 were grown and bromination of tryptophan was performed; cells were then removed by centrifugation and the resultant cell free supernatant media containing in vivo generated 7-Br-tryptophan 2 ('spent media') was used for further screening of the cross-coupling reactions. Though series of metabolites that have the potential to interfere with the catalytic cycle, chelating to the Pd have been generated, encouragingly 82% conversion for the cross-coupling could be achieved, if first diluted 1:5 in phosphate buffer (Supplementary Table 4). The reactions in the spent CCM proceeded well to give high conversions; however, the reaction time was very long (60 h) upon using p-Tol-B(OH) 2 (1.2 mM) and L2-Pd (100 µM). Thus, we again looked further toward a more active Pd catalyst system. Pd-catalysts based on tetramethylguanidine (L4-Pd) 39 and 2-(dimethylamino)-pyrimidine-4,6-diol (L3-Pd) 40 ligands were recently reported to enable the expeditious cross-coupling of activated aryl iodides. Importantly, both are water-soluble and their lack of toxicity is attractive for in vivo applications. We were pleased to find both ligand variants (L3-Pd, L4-Pd) afforded increased catalytic activity with~2-fold increase in conversions (75% and 70% respectively) over L2-Pd catalyst (38%) using the spent CCM (Supplementary Fig. 3). Moreover, these conversions were obtained after 18 h using 100 µM Pd-catalyst and 1.2 mM boronic acid at 1:4 dilution. A time course experiment at 1:8 dilution revealed complete conversion of 2 within 4 h and high Ultra Performance Liquid Chromatography (UPLC) yields of cross-coupling product for both L3-Pd (76%) and L4-Pd (64%) were obtained for the spent CCM ( Supplementary Fig. 4). These results, achieved at a low Pd-concentration (50 µM) within 4 h, represented significant advancement towards our goal.
Having developed a suitable medium and improved catalytic system, we cultured E. coli RG-1500 in CCM supplemented with L-tryptophan (1.5 mM). By UPLC, we determined that optimal 7-Br-tryptophan 2 production was achieved after 24 h (see Supplementary Fig. 7-9); at this time point, the culture was mixed with phosphate buffer (10 mM, pH 8.5), followed by addition of p-Tol-B(OH) 2 (1 mM) and appropriate Pd-catalyst (50 µM) and incubated for a further 4 h to obtain a conversion of 61% of the desired product 2a (Fig. 5 Table 5). The slightly lower conversions of the product 2a in a matured living culture may be due to interference from the soluble cofactors required for halogenation as catalyzed by PrnA (e.g., redox active NAD + /NADH system), excreted amino acids/proteins (coordinating to Pd), carbohydrates (chelation with boronic acid) as well as bio-thiols (Pd-poisoning). The viability of cells was assessed by comparing the numbers of colony forming units. The cells from the in-culture crosscoupling remained fully viable ( Supplementary Fig. 12).

and Supplementary
Antibiotic analogue generation via in-culture GenoChemetics. The antibiotic pacidamycin is a challenging system demanding that any orthogonal derivatization chemistry developed must be nucleoside and peptide compatible. We previously demonstrated the first out of context use of a halogenase, introducing the gene encoding prnA to the wild-type pacidamycin producing strain Streptomyces coeruleorubidis in order to generate a strain (RG-5059) capable of producing chloropacidamycin 8 . Generation of the more reactive bromo-metabolite would be essential if we were to achieve compound generation and synthetic modification synchronously in live culture. However, supplementation of RG5059 culture media with various bromide salts including KBr, NaBr, NH 4 Br impaired culture growth and no brominated pacidamycin could be detected; it was clear that the natural pacidamycin producer could not be utilized for the generation of brominated metabolites. We investigated the tolerance of another streptomycete, S. coelicolor M1154 41 , to bromide salts (from 0 to 200 mM in 50 mM increments) and determined 100 mM KBr to be well tolerated. Next, we engineered the heterologous production of pacidamycin into this strain by conjugatively transforming the strain with S. coeruleorubidus cosmid 2H-5 42 , which carries pac1-pac22 as a 32.2 kb insert. This new synthetic strain (named RG-4242) was shown to produce pacidamycin, and its growth and production of pacidamycin not be compromised by bromide salts. Next, we installed prnA, encoding tryptophan 7-halogenase, into the genome (see Supplementary  Having utilized a synthetic biological approach to generate a strain capable of producing new-to-nature bromo-metabolites, the stage was set to determine whether synchronous biosynthetic bromo-natural product production and chemical diversification in living bacterial culture could be accomplished. This system further challenged the limits of the technology with the S. coelicolor culture being considerably more susceptible to palladium poisoning than the E. coli culture and the metabolic profile being rather more complex. Exploring the media (CCM) that was developed for the cross-coupling of 2 (Fig. 5) in living cultures of E. coli, we observed that it was both capable of supporting the growth of S. coelicolor (RG-1104) and production of Br-pacidamycin D 3 (Fig. 6). To implement the cross-coupling in the presence of the living cells, a mature (6 day old) culture grown in CCM was mixed with phosphate buffer, followed by addition of p-Tol-B(OH) 2 and appropriate L3-Pd/L4-Pd solutions and incubated at 37°C, 25 μM Palladium and 1 mM boronic acid proved to be optimal. The reaction mixture was analyzed after 4 h by LC-MS, revealing the complete consumption of Br-pacidamycin-D 3 and presence of the desired product p-tolyl-pacidamycin D 3a (Fig. 6 and Supplementary Figs 23-25). Again, we explored the viability of the engineered cells following the reaction and quenching with DTT at 4 h, little impact on the cell viability could be observed for L4-Pd ( > 96% viability Supplementary Fig. 26).   Fig. 6 In culture biosynthesis and cross-coupling of Br-pacidamycin-D. a S. coelicolor M1154 engineered to express the tryptophan 7-halogenase gene (prnA) and the entire pacidamycin gene cluster (pac1-pac22), which encodes the non-ribosomal peptide template/thiol tethered biosynthesis of pacidamycin (S. coelicolor RG-1104). b Cross-coupling of the Br-pacidamycin D 3 produced by the living culture. c Extracted Ion Chromatograms of Br-pacidamycin D 3 and the cross-coupled product p-tolyl-pacidamycin D 3a. This system exemplifies that this chemistry is not only compatible with less robust living cells but also that it is compatible with the very high dilutions and low titers that many natural products are present at. The engineering of bromo-metabolite production enables this exciting advance. Furthermore, the use of this model system exemplifies that the chemistry is compatible with both peptides and nucleosides NATURE COMMUNICATIONS | DOI: 10.1038/s41467-017-00194-3

Discussion
In summary, we have developed, in two different systems, the first synthetic biological generation of new-to-nature bromo-metabolites and their synchronous cross-coupling within a living aerated microbial fermentation, even at high dilution. As many natural products are generated at low concentration, this is essential. This pioneering approach and exceptionally mild conditions for Suzuki-Miyaura cross-coupling of challenging halo-metabolites have the potential to be broadly used for the GenoChemetic diversification of halogenated natural products and new-to-nature halo-natural products. This approach is powerful as it enables the generation and diversification of a natural product in the presence of the cells that produce it. Being able to perform this chemistry in the presence of living cells at 28 or 37°C, including on as challenging a system as free halo-tryptophan, opens up new possibilities, for example: assessing and screening, in vivo, the directed evolution of the biosynthetic enzymes like halogenases or multifunctional enzymes for example polyketide synthases (PKSs) and nonribosomal peptide synthetases (NRPSs). In such directed evolution studies, being able to assay in vivo is time efficient and maintaining the viability of the cells removes need for duplicate plating-a time consuming process when handling the large numbers of colonies required for such systems. Recently, Sewald reported the use of the fluorescence modulating cross-coupling chemistry, which we have previously developed 25 , as a screen for the directed evolution of a thermophilic halogenase 43 .
The cell compatible chemistry developed here has the potential to significantly open up this area, making this approach applicable to aryl halogenases that do not originate from thermophiles. One might also envisage utilizing the combination of synthetic biology and synthetic chemistry, which results in a change in fluorescence to enable cell sorting of particularly productive clones 25 . A further advantage of carrying out the chemistry in the presence of the living cells is that, with the provision of additional media, the cells can continuously produce their halo-metabolites, such an approach could potentially be applied to biofilms in flow, or possibly have dual utility in diversification and increasing metabolite flux 44 . From a technical viewpoint the ability to carry out the diversification without an additional purification step, in the presence of a continuously producing biosynthetic system is attractive. Furthermore, we find that the enhanced lipophilicity that the cross-coupling diversification confers, significantly simplifies the otherwise challenging extraction and purification from other media components. Being able to use synthetic biology to generate new-to-nature halo-natural products and carry out in-culture diversification of these metabolites also paves the way for chemical biological studies in which the interactions of the diversified natural product can be explored in the producing organisms, affinity or fluorescence labeling of microbial natural products and their subsequent tracking. For example, it would be interesting to see if this could be applied to determine the origin and distribution of halogenated signaling molecules. In the light of the potential power and applicability of this approach, it is our aim to expand the toolkit of potential orthogonal chemistries that can be translated into the living GenoChemetic context in order to provide new tools to monitor and better understand biological processes or manipulating natural product targets in a precise manner.

Methods
General information. All chemical reagents were used as received from commercial sources without further purification or prepared as described in the literature. The fully synthetic reactions were monitored by thin-layer chromatography and the products were purified using flash chromatography and characterized using NMR and mass spectrometry. For experimental details and characterization of all new compounds ( 1 H/ 13 C NMR and MS, see Supplementary Methods and Supplementary Figs 27-50). The reactions carried out in cell culture and involving the synthetic-biological/synthetic-chemical generation of materials in 1 µM-500 µM quantities were followed by UPLC and liquid chromatographytandem mass spectrometry and compared to known standards. Additional methods for all synthetic/biosynthetic preparations and associated references are available in the Supplementary Methods.
LC-HRMS analysis. Liquid chromatography-high resolution mass spectrometry (LC-HRMS) analysis of the cross-coupling reactions was conducted on a Thermo Scientific Dionex Ultimate 3000 Rapid Separation LC system using XBridge BEH C18 column (130 Å, 3.5 µm, 2.1 × 100 mm). The flow rate was set to 0.35 ml min −1 and the column temperature was maintained at 40°C. A generic binary gradient elution was carried out using different ratios of eluents A (water containing 0.1% formic acid) and B (acetonitrile). Following gradient was used: 0-0.5 min (5% B), 0.5-9.5 min (5% to 95% B), 9.5-11.5 min (95% B), 11.5-12.0 min (95% to 5% B) and 12.0-15.0 min (5% B). The mass spectrometric analysis was performed on an Orbitrap Velos Pro™ mass spectrometer system equipped with a Thermo Scientific Ion MAX API source housing. The MS conditions were as follows: heated electrospray ionization (HESI-II) probe, positive ionization mode, spray voltage 3.5 kV, capillary temperature 350°C, normalized collision energy 35% for collision induced dissociation, and sheath gas and auxiliary gas flow rates of 35 and 10 arbitrary units, respectively. Full scan MS spectra (from m/z 100-1000) were acquired in the orbitrap with resolution R = 60 K.
Production of 7-Br-tryptophan 2 by engineered E. coli RG-1500. Construction of recombinant plasmid of pSG36 for expression of the inserted halogenase system composed of the tryptophan 7-halogenase gene (prnA) and the flavin reductase gene (ssuE) is given in Supplementary Fig. 6. A single colony of the E. coli K-12 PHL644 harboring plasmid pSG36 designated as RG-1500, from the LB agar plates was inoculated in 5 ml of LB broth supplemented with 100 μg ml −1 ampicillin and 50 μg ml −1 kanamycin. This culture was incubated for 12 h (37°C, 200 r.p.m., incubator throw of 19 mm) and was subcultured (1:100) into 200 ml LB broth supplemented with 100 μg ml −1 ampicillin and 50 μg ml −1 kanamycin in 2 litre baffled flasks. These cultures were grown to an OD 600 of 0.6 (37°C, 200 r.p.m., incubator throw 19 mm). The growth temperature was then reduced to 16°C over 30 min. After cooling, the cell cultures were aliquoted into 100 ml in 2 litre baffled flasks. Sodium propionate was then added, as inducer, at a final concentration of 20 mM (from 2 M stock in water) for inducing expression of the inserted halogenase system. A 100 ml culture, without the addition of sodium propionate, was used as a control of the induction process. The cultures were incubated for a further 24 h (16°C, 200 r.p.m., incubator throw 19 mm). Following this incubation period the cultures were transferred aseptically into sterile 750 ml polypropylene centrifuge bottles (Beckman Coulter UK Ltd.). Cells from each 100 ml culture, were pelleted to remove LB growth media by centrifugation (8000 r.p.m., 15,970 × g, 10 min, 16°C), washed twice with 100 ml of 10 mM phosphate buffer (pH 8.5) and resuspended in 45 ml CCM. Each 45 ml of cell suspension was split into 15 ml aliquots, and 1.5 mM of L-tryptophan was added (i.e., addition of 957 μl of a 25 mM stock in 10 mM phosphate buffer (pH 8.5) to each 15 ml of cell suspension). The cultures were incubated for 24 h (28°C, 200 r.p.m., incubator throw 19 mm) to enable the generation of 7-Br-tryptophan 2.
Br-pacidamycin production by engineered S. coelicolor RG-1104. PCRtargeting 45 was used to replace the kanamycin resistance gene on cosmid 2H-5 42 containing the pacidamycin biosynthetic genes (pac1-pac22) with a cassette for conjugal transfer and site-specific integration into Streptomyces. The integration cosmid was introduced into S. coelicolor M1154 by conjugal transfer from E. coli ET12567/pUZ8002 to generate strain RG-4242, which had the expected apramycin-resistant, kanamycin-sensitive phenotype consistent with integration of the pacidamycin genes into the genome. Finally, plasmid pSG19, containing the halogenase gene (prnA), was introduced into E. coli ET12567 carrying pUZ8002 before transfer to RG-4242 by conjugation, as previously described for S. coeruleorubidus 8 . The resulting strain, designated as RG-1104, was used for production of brominated pacidamycins (for details, see Supplementary Methods and Supplementary . Streptomycetes culturing for metabolite production. Spore stocks of the streptomycetes to be cultured (40 µl) were used to inoculate starter culture (5 ml) containing appropriate antibiotics. The cultures were incubated for 20 h (28°C, 180-220 r.p.m., incubator throw 2.54 cm) before 10-fold dilution into fresh starter media containing antibiotics. The cultures were incubated for a further 20 h (28°C, 180-220 r.p.m., incubator throw 2.54 cm). The starter cultures were then used to inoculate the main culture (plus antibiotics, 20-fold dilution) which were incubated for 5-8 days (28°C, 180-220 r.p.m., incubator throw 19 mm). Starter cultures were grown in sterile baffled flasks (250 ml) whilst main cultures were grown in sterile 250 ml conical flasks (for 30 ml cultures) or sterile 2 litre conical flasks (for 0.5 litre cultures). Sterile springs were placed inside the flasks to prevent clumping of the mycelium.
Cell viability analysis for cultures after cross-coupling reaction. Samples from cross-coupling reactions of E. coli RG-1500 or S. coelicolor RG-1104 cultures, containing 7-Br-tryptophan 2 or Br-pacidamycin D 3, treated with p-Tol-B(OH) 2 (1 mM) and appropriate Pd-catalyst (50 or 25 µM, L3-Pd or L4-Pd) were incubated for 4 h (37°C, 200 r.p.m., incubator throw 19 mm). The cross-coupling reaction for S. coelicolor RG-1104 cultures was quenched by addition of DTT (25 µl of 1 M stock). An aliquot (1 ml) was used for cell viability assay. The reaction culture (30 µl) was transferred to a sterile 96-well plate containing 270 μl of sterile phosphate buffer (10 mM, pH 8.5) obtaining a 10-fold diluted cell solution (1 × 10 −1 dilution). In this fashion, a serial dilution was performed to give the final concentration 1 × 10 −6 ; 100 μl of the final dilution were spread on LB-agar plates containing 50 µg ml −1 kanamycin or ISP2 agar plates, respectively. The plates were incubated in a static incubator at 37°C overnight and colony forming units were counted. In parallel, this process was repeated for a control reaction culture, without treatment with both the Pd-catalyst and p-Tol-B(OH) 2. The experiments were performed in triplicate ( Supplementary Figs 12 and 26).
Data availability. Data supporting the findings in this study are available within the article (and its supplementary information files) and from the corresponding author upon reasonable request.