Cytochrome P450 enzymes play important roles in the biosynthesis of macrolide antibiotics by mediating a vast variety of regio- and stereoselective oxidative modifications, thus improving their chemical diversity, biological activities, and pharmaceutical properties. Tremendous efforts have been made on engineering the reactivity and selectivity of these useful biocatalysts. However, the 20 proteinogenic amino acids cannot always satisfy the requirement of site-directed/random mutagenesis and rational protein design of P450 enzymes. To address this issue, herein, we practice the semi-rational non-canonical amino acid mutagenesis for the pikromycin biosynthetic P450 enzyme PikC, which recognizes its native macrolide substrates with a 12- or 14-membered ring macrolactone linked to a deoxyamino sugar through a unique sugar-anchoring mechanism. Based on a semi-rationally designed substrate binding strategy, non-canonical amino acid mutagenesis at the His238 position enables the unnatural activities of several PikC mutants towards the macrolactone precursors without any sugar appendix. With the aglycone hydroxylating activities, the pikromycin biosynthetic pathway is rewired by the representative mutant PikCH238pAcF carrying a p-acetylphenylalanine residue at the His238 position and a promiscuous glycosyltransferase. Moreover, structural analysis of substrate-free and three different enzyme-substrate complexes of PikCH238pAcF provides significant mechanistic insights into the substrate binding and catalytic selectivity of this paradigm biosynthetic P450 enzyme.
The ability of microorganisms to rapid evolve resistance to antibiotics warrants endless requirements for discovering and engineering new antimicrobial agents1. Macrolide antibiotics with the hallmark feature of a variably sized (≥12 carbons) macrolactone ring connected to a deoxy and/or amino-sugar moiety via glycosylic bond have demonstrated remarkable therapeutic applications as effective protein synthesis inhibitors2. To address the central issues of side effects and antibiotic resistance, three generations of macrolides have been developed in the past century. Nowadays, macrolide antibiotics are still widely used in the treatment of infectious2,3, respiratory4, digestive5, and other diseases. In particular, the third generation of macrolides, namely ketolides (with the 3-glycosylated hydroxyl group replaced by a 3-keto group), have shown enhanced activities against many macrolide-resistant pathogens6.
During the biosynthesis of diverse macrolide natural products, after assembly of the macrolactone core structure by modular type I polyketide synthases (PKSs), glycosylation and oxidation that are mediated by various glycosyltransferases (GTs; e.g., UGTs, UDP-dependent GTs) and cytochrome P450 monooxygenases (P450s), respectively, are among the most important post-PKS tailoring modifications7,8. Interestingly, the order of these two types of structural decoration largely varies in different macrolide biosynthetic pathways (Fig. 1, Supplementary Fig. 1). For example, the glycosylation step must occur prior to the P450-catalyzed oxidation in the biosynthesis of pikromycin7,9 (Fig. 1a) and rosamicin10 (Supplementary Fig. 1a). By contrast, the P450-mediated transformation precedes the glycosylation in many cases such as avermectins11 (Fig. 1b) and disciformycins12 (Supplementary Fig. 1b). More intriguingly, the monooxygenation and glycosylation steps even stagger in the mycinamicin13,14 (Fig. 1c) and erythromycin15 (Supplementary Fig. 1c) biosynthetic pathways. It is noteworthy that the biosynthetic order in most of these cases cannot be reversed, indicative of the stringent substrate specificities of the involved P450s and GTs. The irreversible order likely endows the antibiotic producer organisms with evolutionary benefit by directing the metabolic flux to a single or a limited number of product(s) with high potency. However, from the standpoint of structural diversification for new drug development, the frozen biosynthetic order is a limiting factor because it would hamper more extensive pathway reprogramming and combinatorial biosynthesis16. To resolve this problem, the substrate specificity of GTs and P450s need to be changed simultaneously, which represents a substantial biocatalytic challenge.
Comparatively, we reason that the order of oxidation-glycosylation might be advantageous over that of glycosylation-oxidation with respect to product structural diversification because the preceding oxidation (as a small structural modification) is unlikely to impede the following glycosylation(s). Moreover, the oxidation in some cases could generate a new chemical handle for further glycosylation(s), e.g., mycinamicins (Fig. 1c) and disciformycins (Supplementary Fig. 1b). However, the sugar attachment by GTs would cause a significant increase of both the size and polarity of the resulting macrolide, thus limiting the potential oxidation by a P450 enzyme that originally favors the smaller hydrophobic macrolactone substrate.
Cytochrome P450 PikC (CYP107L1) from Streptomyces venezuelae ATCC 15439 is an intriguing P450 monooxygenase with unusual innate substrate flexibility17,18. In the biosynthetic pathway of methymycin/neomethymycin (1/2) and pikromycin (3, the first discovered natural ketolide), the sole P450 enzyme recognizes both 12-membered ring macrolide YC-17 (4) and 14-membered ring macrolide narbomycin (5) as substrates (Fig. 1a). Comparatively, PikC catalyzes the hydroxylation of 4 at the C10 allylic position and the C12 methylene position with almost equal efficiency, while the PikC-mediated hydroxylation of 5 preferentially occurs at the C12 allylic position19,20. In the past two decades, Sherman and co-workers have made tremendous efforts on the structures, mechanisms, and engineering of PikC21,22,23,24, making this enzyme a paradigm of microbial P450 enzyme.
Although the substrate scope and product diversity of PikC have been dramatically expanded by enzyme engineering and substrate engineering21,22,23,24, to the best of our knowledge, there is no report of any PikC mutant that is able to directly oxidize the two native macrolactones including 10-deoxymethonolide (6) and narbonolide (7), likely due to the very poor binding of these two unglycosylated substrate precursors to PikC. This is mechanistically owing to the dependence of the dimethylamino sugar desosamine in both 4 and 5 during substrate recognition and productive binding by PikC. To date, it has been well known that the presence of the positively charged dialkylamino group as a substrate anchor is a prerequisite for PikC’s substrate recognition and catalytic activities17,21.
To further diversify the structures related to the 1/2/3 biosynthetic pathway by reversing the natural glycosylation-oxidation order, in this study, we challenge the unnatural activity of PikC against the macrolactones without any appendix. Taking advantage of the non-canonical amino acids (ncAAs), we successfully reshape the sugar binding pocket of PikC in a manner that the proteinogenic amino acid mutagenesis cannot achieve. A number of mutants with the pivotal residue His238 replaced by different ncAAs show significant hydroxylation activities towards the aglycones 6 and 7. X-ray crystal structures and molecular docking analyses of the optimal mutant PikCH238pAcF in substrate-free and substrate-bound forms provide significant insights into the mechanisms of PikC’s substrate recognition and regioselectivity. Furthermore, the oxidation activity towards 6 and 7 enable us to change the order of late pikromycin biosynthetic pathway, giving rise to unnatural mono- and di-glucosylated macrolide derivatives.
Semi-rational engineering of PikC into an aglycone hydroxylase by ncAA mutagenesis
According to the previous structural and mechanistic studies19,20,23, the sugar (desosamine) and aglycone (6 and 7) moieties of PikC’s natural substrates (4 and 5) adopt distinct binding pockets (Fig. 2a). To enable the productive binding of either 6 or 7 to PikC, we reasoned that the introduction of a rather bulky amino acid to occupy the accommodating space of desosamine might work. Moreover, this amino acid should endow the aglycones with some specific interactions, thereby increasing the substrate binding affinity to a productive level. Thus, we first identified the amino acids within 4.0 Å away from the desosamine of either substrate, including Glu85, Glu94, Phe178 and His238 (Fig. 2a). Next, the ncAA p-acetylphenylalanine (pAcF), which was previously reported to show beneficial effects on P450’s efficiency and regioselectivity25, was selected to individually replace the four residues by amber stop codon suppression and the well-established system of mutant Methanococcus jannaschii tyrosyl aaRS/tRNA pair in Escherichia coli26. We expected that the unnatural bulky acetylphenyl side chain with π-stacking and hydrogen bonding potential would not only sterically occupy the desosamine binding pocket, but also provide some favorable interactions with the macrolactone ring of 6 or 7, thus enabling the unnatural aglycone hydroxylation activities.
To our delight, pAcF was successfully incorporated into PikC with high efficiency as evidenced by tandem mass spectrometry (Supplementary Fig. 2) and electrospray ionization-quadrupole-time of flight-mass spectrometry (ESI-Q-TOF-MS) analysis of the purified mutant P450 enzyme PikCH238pAcF (Fig. 2b, c). The two macrolactone substrates 6 and 7 were prepared using the glycosyltransferase DesVII inactivated strain Sv-ΔdesVII (see Methods). Among the four confirmed pAcF mutants including PikCE85pAcF, PikCE94pAcF, PikCF178pAcF and PikCH238pAcF (Supplementary Figs. 3–5), PikCH238pAcF turned out to be the only mutant to show a low but detectable activity towards both 6 and 7 with the respective substrate conversion ratios of 17.9 ± 2.4% and 24.7 ± 3.0% (Supplementary Fig. 6). The low but significant activities of this ncAA mutant might result from the challenging nature of C-H bond activation and low binding affinity towards aglycones (see below). Upon high-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) analyses (Supplementary Figs. 9–22, 35–39), the structures of the two products from 6 were determined to be methynolide (8, the C10-hydroxylated product) and neomethynolide (9, the C12-hydroxylated product) (Fig. 3a) with a relative ratio of 19:1 (Fig. 3c). The single hydroxylation product of 7 was determined to be pikronolide (10, the C12-hydroxylated product) (Fig. 3a, d). Interestingly, tiny amounts of 8–10 were previously isolated from another S. venezuelae strain27 and a desI (the sugar dehydrase gene) knockout mutant28, perhaps due to the marginal activity of PikCWT or other unknown oxidase towards 6 and 7 in vivo. However, the hypothetical activities of PikCWT against 6 and 7 were not observed in vitro (Fig. 3c, d). Of note, all 20 natural amino acids at the His238 position were incapable of reproducing the aglycone hydroxylation activity caused by pAcF (Supplementary Fig. 7).
Unexpected discovery of the improved activities to native substrates by aromatic substitution at His238
Strikingly, compared with the activities of PikCWT towards 4 (45.0 ± 4.5% conversion) and 5 (54.4 ± 2.8%), PikCH238pAcF exhibited 0.9- and 0.7-fold increase in the hydroxylation activity towards the natural substrates 4 and 5, respectively (Fig. 3e, f). Unlike the wild-type enzyme that almost equally hydroxylates C10 and C12 positions of 4, PikCH238pAcF regioselectively hydroxylated the C10 C-H bond, producing 1 as the major product (Fig. 3e, 1 : 2 = 9 : 1). Inspired by these unexpected results, we examined the activities of twenty proteinogenic variants of His238 towards 4 and 5. As a result, these mutants exhibited varied activities and product distributions against 4 with H238F and H238Y being the most active mutants. Specifically, the substrate conversion ratios of PikCH238F and PikCH238Y towards 4 were 93.2 ± 5.3% and 83.8 ± 3.9%, respectively. However, these two mutants did not significantly change the product ratio as PikCH238pAcF did (Fig. 3e, Supplementary Fig. 51). As for 5, PikCH238F and PikCH238Y were also the most efficient mutants with the substrate conversion ratios of 96.3 ± 1.7% and 88.3 ± 3.3%, respectively (Fig. 3f, Supplementary Fig. 51). Taken together, we surmised that the presence of an aromatic side chain at the His238 position might be essential for the improvement of native activities of PikC. However, as mentioned above, PikCH238F and PikCH238Y were unable to oxidize 6 and 7 (Fig. 3c, d), suggesting that the aglycone hydroxylation activity of PikCH238pAcF should stem from a mechanism different from that for the enhanced activities towards 4 and 5.
Determination of substrate binding affinities
To rationalize the enhanced activity of PikCH238pAcF towards 4–7, we compared the substrate binding affinities of PikCWT and PikCH238pAcF by measuring the spectral changes upon different substrate titrations19,20. Similar to the previous report, 6 and 7 could not bind or only marginally bound to PikCWT so that their KD values could not be determined due to poor binding and limited substrate solubility (Supplementary Table 1). By contrast, the KD values of 6 and 7 towards PikCH238pAcF were determined as 207.5 µM and 236.9 µM, respectively, comparable to those of 4 and 5 towards PikCWT (177.6 µM and 373.6 µM). Compared with PikCWT, the binding affinities of PikCH238F and PikCH238Y to 4 increased by 14.9 and 9.6 times, respectively. The affinity of PikCH238pAcF to 4 also increased by 3.4-fold (KD = 40.2 µM). Similarly, the binding affinities of PikCH238F and PikCH238Y to 5 increased by 4.1 and 4.9 times, respectively. The affinity of PikCH238pAcF to 5 also increased by 3.3-fold (KD = 87.1 µM). All these results are well consistent with the corresponding enzymatic activities (Fig. 3), at least partially explaining the improved activities of the His238 mutants.
Extended ncAA mutagenesis analysis
Motivated by the above results, we tested more aromatic ncAAs with diverse para-substituents for His238 replacement, including p-ethynyl-L-phenylalanine (pENF)29, 4-phenyl-L-phenylalanine (BipA)30, p-propargyloxyphenylalanine (pPrF)30, p-azido-L-phenylalanine (pAzF)30, O-methyltyrosine (OMeY)31, O-tert-butyltyrosine (OtBuY)31, and p-bromophenylalanine (pBrF)31 (Fig. 3b). All purified mutants (Supplementary Table 4) except PikCH238BipA exhibited varied hydroxylation activities towards 6, with PikCH238pAcF giving the highest hydroxylation activity. Unlike 6 that could be accepted by almost all ncAA mutants to different extents, the 14-membered ring macrolactone 7 was only hydroxylated by PikCH238pAcF (Fig. 3b). We reasoned that these activity profiles might result from the complicated interplay of substrate structures and the size, shape and electronic property of the ncAA side chain. Essentially, all the active ncAA mutants have an aromatic side chain larger than tyrosine (Supplementary Fig. 8).
Crystallographic/mechanistic analyses of PikCH238pAcF
To understand the molecular mechanism of the unique catalytic activity of PikCH238pAcF, we first determined the high-resolution three-dimensional structure of substrate-free PikCH238pAcF (PDB ID code: 7XBM, 2.4 Å resolution, Supplementary Table 9). In each asymmetric unit, there are two molecules of PikCH238pAcF (named Chain A and Chain B) adopting the almost identical conformation with a root mean square deviation (rmsd) of 0.171 Å over 334 equivalent Cα atoms (Supplementary Fig. 52). Clear electron density corresponding to the ncAA pAcF was unambiguously observed at the amino acid residue 238 site, indicating that the His238 of PikCWT was replaced by pAcF with a very high incorporation efficiency (Fig. 4a), which is consistent with the results of ESI-Q-TOF-MS analysis (Fig. 2c) and tandem mass spectrometry (Supplementary Fig. 2). The overall structure of PikCH238pAcF is virtually identical to the previously determined PikCWT structure in a closed conformation (PDB ID code: 2BVJ, Chain A), with a rmsd of 0.323 Å over 345 Cα atoms, which indicates the incorporation of pAcF does not change the overall structure of PikC (Fig. 4a, Supplementary Fig. 52).
To further gain mechanistic insights into the unique substrate selectivity and hydroxylation pattern of PikCH238pAcF, we solved the crystal structures of 6-bound and 4-bound PikCH238pAcF (Supplementary Fig. 53). Similar to the substrate free PikCH238pAcF structure, in both structures, each crystallographic asymmetric unit has two protein chains (named Chain A and Chain B). There is basically no major conformational difference between Chains A and B (6-bound, rmsd = 0.169 Å; 4-bound, rmsd = 0.155 Å), all of which are in a closed conformation (Supplementary Fig. 55, Supplementary Figs. 60a, b). Therefore, structures of one representative chain (Chain A) were selected for further analysis.
In the crystal structure of PikCH238pAcF in complex with 6 (PDB ID code: 7XBO, 2.2 Å resolution, Supplementary Table 9), the 12-membered ring macrolactone is unambiguously positioned in the active site, and its electron density is well defined (Supplementary Fig. 53). Similar to the interactions between the macrolactone portion of 4 in PikCWT (PDB ID code: 2C6H), 6 hydrophobically interacts with the side chains of Leu93, Phe178, Val179, Val242, Ala243, Val290, and Ile395 (Fig. 4b). Consistent with the observation in the 4-bound PikCWT structure, upon binding of the ligand 6, the carboxyl group of Glu246 side chain is flipped away to better accommodate the macrolactone ring of 6 (Fig. 4b, c). Importantly, the carbonyl group of pAcF238 and the C3 hydroxyl group of 6 form a 2.9 Å hydrogen bond (Fig. 4b). Meanwhile, the terminal methyl group of pAcF238 hydrophobically contacts with the C3 carbon atom and C4 methyl group of 6. Essentially, these extra interactions would not exist without the incorporation of pAcF into PikC at the position of His238 (Fig. 4b). Therefore, the extra strong hydrogen bond and additional hydrophobic interactions mediated by ncAA in PikCH238pAcF simulate the interactions to some extent mediated by desosamine moiety of 4 in the 4-bound PikCWT structure (Fig. 4c) and likely play a vital role in the catalysis of PikCH238pAcF towards the non-natural substrate 6.
Compared with PikCWT, PikCH238pAcF showed a higher catalytic activity for 4 (Fig. 3e). In the crystal structure of 4-bound PikCH238pAcF (PDB ID code: 7XBN, 2.0 Å resolution, Supplementary Table 9), clear electron density corresponding to the 12-membered ring macrolide 4 is unambiguously observed at the active site (Supplementary Fig. 53). Upon replacement of His238 by the bulkier pAcF, the desosamine sugar is pushed away and tilts 40 degrees, comparing to the conformation of 4 in the substrate binding pocket of PikCWT, in the 4-bound PikCH238pAcF structure. This sugar relocation leads to the loss of the key salt bridge with Glu94 as observed in the 4-bound PikCWT structure, thereby leading 4 to be more perpendicular to the heme plane (Fig. 4d). The majority of hydrophobic interactions between 4 and PikC are conserved in the 4-bound PikCWT and PikCH238pAcF structures, such as the amino acids Trp74, Leu81, Glu85, Met191, and Phe178 to the desosamine moiety, and Leu93, Phe178, Val179, Val242, Ala243, Thr247, Val290, Thr294, Met394, and Ile395 to the macrolactone ring of 4. Due to the relative position change, 4 loses several hydrophobic contacts with PikCH238pAcF via Leu88, Gln89, and Ile239 (Fig. 4e, f). Although PikCH238pAcF loses some electrostatic and hydrophobic interactions with 4, the presence of pAcF238 also introduces several extra interactions for 4. Specifically, the carbonyl group of pAcF and the carboxyl group of Glu94 form a hydrogen bond network with the C3’ hydroxyl group of desosamine through two water molecules (Fig. 4g), and the methyl group of pAcF238 forms hydrophobic interactions with the C4 and C5’ methyl groups of 4 (Fig. 4e). In addition, the specific position of 4 in PikCH238pAcF also introduces the hydrophobic interaction between desosamine and Tyr295 (Fig. 4e). All these extra interactions likely contribute to the increased binding affinity of PikCH238pAcF towards 4. Further structural analysis revealed that in the 4-bound PikCH238pAcF structure, the loop between F and G helices and the A-B loop become less flexible than in the 4-bound PikCWT structure (Fig. 4h, i). We reason that the positive charge of the protonated C3’ dimethylamino group of desosamine in new position might better interact with the negative charges of the loop between F and G helices (Asp182-Asp183) and the A-B loop (Glu48-Gly49-Asp50-Glu51) in the 4-bound PikCH238pAcF structure. These structural features demonstrate a “tighter” binding mode of 4 in the productive substrate binding pocket of PikCH238pAcF, by which the binding affinity and activity of PikCH238pAcF towards 4 are significantly increased.
Due to continuous decomposition of 7 in aqueous solution and lower binding affinity than 6, we were unable to solve the crystal structure of 7-bound PikCH238pAcF. Thus, molecular docking with AutoDock vina was performed to explore the binding mode of 7 in PikCH238pAcF. According to the structural superimpositions of the 7-PikCH238pAcF docking model with the substrate free PikCWT (Fig. 5a) and with the previously determined structure of a PikC mutant in complex with 5 (i.e., the more active PikCD50N with a productive substrate binding conformation) (Fig. 5b), the 14-membered ring macrolactone is stabilized mainly through hydrophobic interactions between the macrolactone and the amino acids Leu93, Phe178, Val179, Ile239, Val242, Ala243, Thr247, Thr294, and Ile395. Importantly, the carbonyl group of pAcF238 and the C5 hydroxyl group of 7 form a 3.2 Å hydrogen bond. In addition, the C3 carbonyl group of 7 form a 3.5 Å hydrogen bond with the carboxy group of Glu94 (Fig. 5a). Taken together, we reason that the hydrophobic interactions and two extra hydrogen bonds likely enable the activity of PikCH238pAcF towards the non-natural substrate 7. Of note, the crystal structure of PikCD50N/5 showed the productive binding pose of the 14-membered ring substrate (PDB ID code: 2VZM, Chain B) rather than the non-productive binding mode seen in the PikCWT/5 complex structure (PDB ID code: 2C7X); therefore, we elected to use the PikCD50N/5 structure as a reference for the following analyses. Since the structures of PikCD50N/5 and PikCWT/5 are virtually identical to each other except for the different 50th residues and alternative substrate binding conformations (Supplementary Fig. 54), we deemed that the comparisons using PikCD50N/5 should be valid.
PikCH238pAcF also exhibited higher hydroxylation activity towards the 14-membered ring macrolide 5 than PikCWT (Fig. 3f). To elucidate the molecular basis for this observation, we further determined the crystal structure of PikCH238pAcF in complex with 5 in a closed conformation (PDB ID code: 8GUE, 1.9 Å resolution, Supplementary Table 9, Supplementary Figs. 55 and 60c). In the complex structure, clear electron density corresponding to the structure of 5 was unambiguously observed at the active site (Supplementary Fig. 53). The H238pAcF mutation pushes away the desosamine for about 60 degrees in the structure of 5-bound PikCH238pAcF. This substrate repositioning abolishes the salt bridge between desosamine and Glu94 as observed in the PikCWT/5 complex, and rebuilds a salt bridge between desosamine and Glu85 (Fig. 5c). Consistent with the substrate-enzyme interactions between 5 and PikCWT, 5 in PikCH238pAcF is also stabilized through a number of hydrophobic interactions with the amino acids Leu81, Leu93, Phe178, Val179, Ile239, Val242, Ala243, Thr247, Val290, Thr294, Met394, Ile395, Trp74, and Met191. Due to the relative position change, 5 loses several hydrophobic contacts with Leu88 and Gln89. Nevertheless, there in PikCH238pAcF/5 exists an extra hydrophobic contact between the desosamine moiety and Tyr295. Importantly, in the PikCH238pAcF structure in complex with 5, pAcF238 introduces more hydrophobic interactions through the methyl group of this ncAA with the C5’ methyl group of the desosamine moiety and the C6 methyl group of the macrolactone ring (Fig. 5d, e). Moreover, three water molecules were found to mediate a hydrogen bond network between the pAcF carbonyl, Glu94 carboxyl and C3’ hydroxyl group of desosamine in the co-crystal structure (Fig. 5f). Therefore, the hydrophobic interactions mediated by pAcF238, Tyr295 and the water-mediated hydrogen bond network likely make the main contribution to the increased binding affinity of PikCH238pAcF towards 5.
Probing the structural basis for the regioselectivity of PikCH238pAcF
In addition to the broadened substrate scope and increased catalytic activity, PikCH238pAcF also exhibits significantly improved regioselectivity for the C10 hydroxylation of both 4 (Fig. 3e) and 6 (Fig. 3c). As previously observed19, in the PikCWT/4 complex, the allylic C10 and methylene C12 positions are 7.2 Å and 5.1 Å away from the heme-iron reactive center, respectively (Fig. 4j, Supplementary Fig. 61a). This observation did not directly explain the equal distribution of the two hydroxylation products 1 and 2 because the hydroxylation pattern could be determined by multiple factors, such as the substrate repositioning resulted from the catalytic oxygen bonding and/or interaction with redox partner protein, differential bond dissociation energy of the C-H bonds to be oxidized, and protein dynamics that cannot be observed in crystal structures. Nonetheless, a correlation between the C10- and C12-to-iron distances and the hydroxylation product ratio could still be established. Upon examination of the complex structures of PikCH238pAcF/4 and PikCH238pAcF/6, we found that the distances between the C10 atom (of 4 and 6) and the heme-iron reactive center are significantly shortened to 6.7 and 6.8 Å, respectively, when compared to the corresponding distance of 7.2 Å observed in the PikCWT/4 complex structure; while the corresponding C12-to-iron distances are 5.3 and 5.4 Å (for 4 and 6, respectively), longer than the corresponding distance of 5.1 Å in the PikCWT/4 complex structure (Fig. 4j, Supplementary Figs. 61a–c). These distance changes might reflect the disruption of the original balance between the two hydroxylation sites of C10 and C12, thus leading to the shifted regio-preference to C10 position.
Unlike the different regioselectivity of PikCH238pAcF and PikCWT towards 4 and 6, PikCH238pAcF displayed similar regioselectivity to 5 and 7 as PikCWT and the more active mutant of PikCD50N20. Comparatively, the distances between the C12 atom and the heme-iron reactive center are 7.4 Å in both complex structures of PikCH238pAcF/5 and PikCD50N/5 (reflecting the productive binding of 5 to PikCWT20 as described above); while the corresponding C14-to-iron distances are 5.3 Å (PikCH238pAcF/5) and 5.5 Å (PikCD50N/5), respectively, basically remains unchanged (Supplementary Fig. 56, Supplementary Figs. 61d, e). Biochemically, the farther (relative to heme-iron) C12 C-H bond instead of the closer C14 C-H bond is the preferred hydroxylation site perhaps due to the lower bond dissociation energy of the C12 allylic C-H bond and the unfavorable orientation of the C14 C-H bond19,20. The docking analysis of PikCH238pAcF/7 demonstrates a similar C12-to-iron distance (7.3 Å) as observed in both complex structures (Supplementary Fig. 56). These observations may explain the same regioselectivity of PikCH238pAcF and PikCWT towards 5 and 7.
Engineering of a strict aglycone hydroxylase
Next, we attempted to engineer PikCH238pAcF to be a strict hydroxylase of 6 and 7 by aborting the activity towards both 4 and 5. Of note, a unique substrate anchoring mechanism of PikC has been unravelled by Sherman and co-workers19,20,21. Briefly, the acidic side chain of Glu94 is responsible for forming a salt bridge with the positively charged C3’-dimethylamino group of desosamine in 4 and 5. Glu85, another acidic residue to sandwich the C3’-dimethylamino group together with Glu94, is also critical for both 4- and 5-hydroxylating activities and shows some synergistic effect with Glu9419,20.
Thus, we elected to mutate Glu94 and/or Glu85 to either glutamine or alanine in combination with the H238pAcF mutation. Consistent with the previous reports19,20, the substrate conversion ratios of the four single mutants including PikCE85Q, PikCE85A, PikCE94Q, and PikCE94A towards 4/5 were reduced from 45.0 ± 4.5%/54.4 ± 2.8% (PikCWT) to 38.5 ± 3.1%/27.5 ± 4.4%, 43.3 ± 3.8%/25.8 ± 1.9%, 14.2 ± 4.7%/18.6 ± 4.6%, and 8.2 ± 2.7%/34.0 ± 4.8%, respectively; while the four double mutants PikCE85A/E94A, PikCE85A/E94Q, PikCE85Q/E94A, and PikCE85Q/E94Q almost entirely lost their activities. Unsurprisingly, all these single/double mutants were inactive to 6 and 7 (Supplementary Fig. 57). When the PikCH238pAcF mutation was introduced into these less active mutants, all double and triple mutants displayed the C10-hydroxylation activity towards 6 and C12-hydroxylation activity towards 7 (Fig. 3c, d, Supplementary Fig. 57). In particular, the triple mutant PikCH238pAcF/E85Q/E94Q almost entirely lost the activity towards both 4 and 5, but showed 12.0 ± 0.5% and 13.4 ± 2.4% conversion ratios for 6 and 7, respectively. Interestingly, compared with PikCH238pAcF, the double mutant PikCH238pAcF/E85Q exhibited 0.4- and 0.5-fold increase in the hydroxylation activity towards 6 and 7 (Fig. 3c, d) for unknown reasons. However, it retained significant activities towards 4 (52.2 ± 2.8% conversion) and 5 (94.3 ± 3.1% conversion) (Fig. 3e, f). Consistently, the binding affinities of PikCH238pAcF/E85Q to 6 and 7 increased by 0.3 and 0.4 times, respectively, compared to those of PikCH238pAcF (Supplementary Table 1).
Establishing an artificial enzyme cascade for unnatural macrolides
With the PikCH238pAcF/E85Q mutant, we sought to establish an artificial enzyme cascade in vitro with an oxidation-glycosylation order (Fig. 6a, b), which would reverse the natural glycosylation-oxidation order in the late pikromycin biosynthetic pathway, which is sequentially mediated by the glycosyltransferase DesVII and P450 PikC (Fig. 1a). First, the in vitro hydroxylation reactions of 6 and 7 by PikCH238pAcF/E85Q were optimized by adding glucose-6-phosphate dehydrogenase (GDH) and glucose for NADPH regeneration and extending the reaction time from 40 min to 4 h. As a result, the conversions of 6 and 7 achieved 75.3% and 78.0%, respectively (Fig. 6c, d). Second, we tested the glycosylation activities of six UDP-dependent glycosyltransferases towards the hydroxylated macrolactones 8 and 10 by using UDP-glucose as the sugar donor, including UGT85A132, RrUGT1733, RrUGT333, UGT72B1434, UGT73B6FS and BSGT-135,36. BSGT-1 turned out to be the only active enzyme, glucosylating 8 and 10 into methynolide-3-O-glucoside (11), O3,O2’-di-glucosyl-methynolide (12) and pikronolide-5-O-glucoside (13) (Fig. 6a, b; see Supplementary Figs. 23–39 for structural determination). Due to the incomplete oxidation of 6 and 7, the unreacted 6 and 7 were also glucosylated by BSGT-1, demonstrating the extraordinary substrate promiscuity of this UGT. Unsurprisingly, the resulting products 14 and 15 (i.e., 10-deoxymethynolide-3-O-glucoside and narbonolide-5-O-glucoside, see Supplementary Figs. 40–50 for structural determination) cannot be recognized by PikCH238pAcF/E85Q (Supplementary Fig. 58).
Selective C-H bond oxidation remains a central challenge in synthetic chemistry21,37. To address this issue, tremendous efforts on enzyme engineering of cytochrome P450 enzymes have been made in order to improve the activity, substrate scope, stability, robustness, and other catalytic properties of these selective biocatalysts for practical bio-oxidation7,38,39,40,41,42,43,44,45,46,47. To engineer the P450 mutants with desired properties, a variety of effective mutagenesis strategies such as CAST, CAST/ISM, and FRISM have been developed with great successes achieved48,49,50. However, the 20 proteinogenic amino acids cannot always satisfy the requirement of site-directed and/or random mutagenesis and rational protein design in terms of steric, topological and electronic properties or other inspiring reactivity. Therefore, appropriate ribosomal incorporation of ncAAs in a site-specific manner, which could be designed on demand theoretically, has shown significant possibilities to overcome the limit of conventional protein mutagenesis51,52,53,54.
Compared with extensive studies on ncAA-based protein engineering for protein labeling, crosslinking, photo-activation, bioorthogonal conjugation and other purposes52, the use of ncAA mutagenesis to tailor the catalytic activities of diverse enzymes, especially P450 enzymes, remains largely underexplored. Among few examples, NMR-active ncAAs were incorporated into P450 enzymes to illuminate the role of conformational dynamics55. Recently, Kolev et al. utilized four ncAAs to scan the 11 active-site positions of CYP102A1, leading to unusual changes in regioselectivity and catalytic efficiency25. This pioneering and inspiring exploration represents the first semi-rational engineering of P450 active site using ncAAs in a site-specific manner.
Aiming to change the substrate specificity of a biosynthetic P450 enzyme (PikC) from the sugar-appended macrolides (4 and 5) to the corresponding aglycones (6 and 7), in this study, we successfully engineered a number of ncAA-containing PikC mutants that are capable of selectively hydroxylating 6 at C10 position. PikCH238pAcF, as the most efficient C10-hydroxylase of 6, was also the only mutant enzyme to catalyze the C12-hydroxylation of 7 giving rise to 10. Further structural analysis provided mechanistic basis for the ability of PikCH238pAcF to selectively catalyze the hydroxylation of 6 and 7. We envision that our functional, crystallographic, and mechanistic study will advance the engineering of cytochrome P450 enzymes using ncAAs.
The relevant mechanisms were elucidated by comparative analysis of four crystal structures of PikCH238pAcF. As the best ncAA substituent, pAcF creates a specific binding strategy for 6 and 7. In PikCWT, the desosamine sugar acts as a substrate anchor by forming a key salt bridge between the dimethylamino group and the acidic amino acid residue and a network of hydrogen bonds with the native substrate 4 or 519,20. In PikCH238pAcF, the benzylic carbonyl group and terminal methyl groups respectively provide the hydrogen bond and hydrophobic contacts with the macrolactone ring of 6 or 7 without the desosamine anchor (Figs. 4 and 5). In this scenario, the methyl keto moiety of pAcF, which cannot be provided by any proteinogenic amino acids, is essential for productive binding of the two aglycones.
In natural product biosynthetic pathways, the order of enzymatic steps is usually fixed to prevent metabolic flux leaking. However, a locked pathway would limit pathway reprogramming for structural diversification. Using the ncAA-engineered macrolactone hydroxylase PikCH238pAcF, we successfully reversed the natural glycosylation-oxidation order of late pikromycin biosynthetic pathway, by which it becomes feasible to attach different sugars to the aforehand oxidized macrolactone (Fig. 6). Otherwise, the GT-mediated attachment of a non-desosamine sugar to 6 or 7, which was previously achieved by Borisova et al.56, would disable PikC since desosamine (or a dimethylamino group) is required for PikC’s activity19,20. Thus, we envision that the substrate flexibility of GTs could be better harnessed for generation of more macrolides through changing the macrolide-oxidizing P450s into macrolactone-tailoring P450s by similar ncAA mutagenesis approaches in the future. Since glycosylation and oxidation can improve the properties of a compound in terms of aqueous solubility, biological activity, bioavailability and hence druggability56, a better coordinated biosynthetic glycosylation and oxidation that is enabled by ncAA mutagenesis would likely benefit the future drug development.
In conclusion, herein we practiced the semi-rational ncAA mutagenesis for a natural product biosynthetic P450 enzyme. We conceived and realized a unique binding strategy for two unnatural substrates in PikC based on their structural characteristics, which also improved the catalytic performance towards natural substrates. With the unnatural macrolactone hydroxylating activities, PikCH238pAcF was employed to rewire the pikromycin biosynthetic pathway in vitro. The strategy of ncAA-based P450 enzyme engineering and the mechanisms gained from detailed structural analysis of enzyme-substrate complexes could be applied in more glycosylation-oxidation coupled systems in the future. Furthermore, this kind of biosynthetic pathway reprogramming may also be performed in vivo given that the required ncAA can be supplied by feeding or in situ biosynthesis57. With the useful toolkit of ncAAs, we anticipate that more fine-tuning enzymatic reactions or cascades will be created and more rationally designed natural product derivatives could be produced.
Unless otherwise specified, all ncAAs and antibiotics used in this study were purchased from Suzhou Amatek Biotechnology and Sigma Aldrich, respectively. All P450 enzymatic reactions were supported by NADPH from Qingdao Baisai Biotechnology. δ-Aminolevulinic acid (5-ALA) and isopropyl-β-D-thiogalactopyranoside (IPTG) were bought from Shanghai Aladdin Biochemical Technology. Taq DNA Polymerase and Agarose Gel DNA Recovery kit were purchased from Beijing Dingguo Changsheng Biotechnology. All plasmids were prepared in E. coli DH5α using MonPure™ Plasmid Mini-Prep Kit from Qingdao Baisai Biotechnology. MultiF Seamless Assembly Mix was purchased from Abclonal. All proteins were purified using Ni-NTA SefinoseTM Resin (Settled Resin) from Sangon Biotech. Iodoacetamide (IAA), dithiothreitol (DTT), and trypsin were obtained from Sigma Aldrich. C18 ZipTip was purchased from Millipore. Polypeptone and uridine 5’-diphosphoglucose (UDP-Glu, disodium salt) were bought from Beijing Solarbio Science & Technology. Primer synthesis and DNA sequencing were performed by Sangon Biotech.
The PikC expression vector pET28a-pikC19 and plasmid pULTRA-Ambrx (gifted by Professor Xiaozhou Luo at Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences) bearing the MjTyrRS/tRNACUA orthogonal system (pUltra-AcrFRS/tRNATyrCUA)58 were used for preparation of the ncAA-containing mutants of PikC. Briefly, pULTRA-Ambrx contains an amber suppressor M. jannaschii tRNATyrCUA (Mj tRNATyrCUA) and encodes a cognate tRNA synthetase mutant MjTyrRS carrying seven active-site mutations including Y32V, L65Y, F108H, Q109G, D158G, L162E, and D286R. The plasmid also contains the kanamycin resistance gene and regulatory gene lacI to encode the repressor of lactose operon. Incorporation of the amber codon into different positions of PikC was achieved by PCR reactions using pET28a-pikC as a template and the specific mutagenesis primers as listed in Supplementary Table 3. The plasmids pET28a-pikC with the amber codon incorporated and pULTRA-Ambrx were co-transformed into E. coli BL21(DE3) by electroporation. All constructed plasmids were verified by DNA sequencing.
Protein expression and purification
PikCWT and mutants were overexpressed in E. coli BL21(DE3) cells. A colony of each individual protein expression strains was inoculated into LB broth containing kanamycin (50 µg/mL) and spectinomycin (50 µg/mL) and grown at 37 °C and 220 rpm for 12 h. This culture was inoculated into 0.5 L TB medium containing kanamycin (50 µg/mL) and spectinomycin (50 µg/mL) at a ratio of 1:100 (v/v) in a 2 L conical flask, which was grown at 37 °C and 200 rpm for 4~6 h. When OD600 reached 0.6~0.7, a certain ncAA was added to the final concentration of 2 mM. When OD600 reached 0.8~0.9, IPTG was added to the final concentration of 0.5 mM to induce the expression of both P450 enzyme and orthogonal tRNA synthetase at 18 °C and 160 rpm for 18~20 h. Cells were harvested by centrifugation (6000 × g, 15 min). The target proteins were purified according to the procedure established previously17. Briefly, cells resuspended in lysis buffer (50 mM NaH2PO4, 300 mM NaCl, 10 mM imidazole, 10% glycerol, pH 8.0) were crushed by high-pressure homogenizor (ATS, Shanghai, China) at 4 °C. Cell lysates were prepared by high-speed centrifugation (10,000 × g, 60 min, 4 °C), to which Ni-NTA agarose was added and followed by gently mixing at 4 °C for 1 h. Then, the Ni-NTA agarose was loaded onto a gravity column and the impurity proteins were washed out with washing buffer (50 mM NaH2PO4, 300 mM NaCl, 20 mM imidazole, 10% glycerol, pH 8.0). The target proteins were eluted with elution buffer (50 mM NaH2PO4, 300 mM NaCl, 250 mM imidazole, 10% glycerol, pH 8.0). Finally, a suitable Amicon size-exclusion column was used for protein concentration, and a PD-10 desalting column was employed for buffer exchange to storage buffer (0.2 mM dithioerythritol, 1 mM EDTA, 50 mM NaH2PO4, 10% glycerol, pH 7.3). The purified proteins were flash frozen by liquid nitrogen and stored at −80 °C for later use. P450 concentrations were determined from the CO-reduced difference spectra using the extinction coefficient of 91,000 M−1 cm−1 (ref. 20).
Construction of the gene knockout plasmids
All primers used to construct the knockout plasmids are listed in Supplementary Table 2. The knockout plasmids were derived from the modification of the CRISPR/Cas9 gene editing plasmid pKCcas9dO59. To generate the pikC (5576176–5577426 bp) and desVII (5587287–5588567 bp) deletion plasmids, the sgRNA expressing cassettes were amplified with the primer pairs of PikCsgRNA-F/PikCsgRNA-R and DesVIIsgRNA-F/DesVIIsgRNA-R. The two homologous arms flanking pikC and desVII were amplified from S. venezuelae genomic DNA separately with the primer pairs of PikC-up-F/PikC-up-R and PikC-dn-F/PikC-dn-R, and DesVII-up-F/DesVII-up-R and DesVII-dn-F/DesVII-dn-R. These DNA fragments were individually ligated into the SpeI/HindIII linearized pKCcas9dO vector using MultiF Seamless Assembly Mix. Correct constructs were confirmed by DNA sequencing, and subsequently used for transforming S. venezuelae strains.
Preparation of substrates
PikC’s natural substrates 4 and 5 were prepared using the pikC knockout strain of S. venezuelae ATCC 15439 (Sv-ΔpikC). Aglycones 6 and 7 were obtained from the fermentation extract of the desVII knockout strain of S. venezuelae ATCC 15439 (Sv-ΔdesVII). As described above, the two gene deletion strains were generated using CRISPR-Cas9 gene editing technology60. Briefly, the E. coli ET12567/pUZ8002 strain harboring the knockout plasmid was mixed with S. venezuelae ATCC15439 in equal volume. The mixed bacterial solution was spread on the surface of MS agar containing 50 mM MgCl2 and 50 mM CaCl2. After incubation at 30 °C for 14–16 h, the MS plates were covered with 25 µg/mL nalidixic acid and 25 µg/mL apramycin, and further incubated until exconjugants appeared. To prepare the substrates, each strain was cultured at 30 °C and 220 rpm for 3 days. Then the seed culture was inoculated to 3 L of fermentation medium at a ratio of 1:10 (v/v). The fermentation was carried out at 30 °C and 220 rpm for 7 days (note: the acquisition of 7 only took two days of fermentation). Afterwards, the fermentation broth (with mycelia removed by centrifugation) was extracted twice with 2× volumes of ethyl acetate. The organic extracts were dried with a rotary evaporator and re-dissolved in methanol. All substrates were isolated and purified using semi-preparative HPLC. The composition of the fermentation medium is as follow: 10.0 g glucose, 10.0 g glycerol, 10.0 g polypeptone, 5.0 g meat extracts, 5.0 g NaCl, and 2.0 g CaCl2•H2O in 1 L tap water; pH was adjusted to 7.3 before autoclaving. The addition of 0.06 M sodium acetate led to significant increases in the macrolide antibiotics production61.
Substrate binding assay
Purified P450 enzymes were diluted to 1 µM with the storage buffer, which was titrated with the substrate dissolved in DMSO (20 mM) in 1 µL aliquots. The difference spectra were recorded at room temperature on a Molecular Devices Spectra Max M2 spectrometer in the wavelength range of 350–500 nm. The difference absorbance ∆A (Apeak 390 nm − Atrough 420 nm) calculated from at least duplicated data was plotted versus the substrate concentrations. Then, the data points were fit with the hyperbolic function ∆A = Amax [S] / (KD + [S]), where Amax is the maximum absorbance shift at saturation, [S] is the total concentration of substrate, and KD is the apparent dissociation constant for the enzyme-substrate complex20.
P450 enzymatic assays
The analytical scale P450 reactions were carried out with a volume of 100 μL in 1.5 mL centrifugation tubes, while the preparative scale reactions were conducted with a volume of 10 mL in 50 mL conical flasks. The analytical scale reaction containing 1 µM PikC (wild type or mutant), 1 mM NADPH, 10 µM Fdx1499, 5 µM FdR097814,62,63, and 0.5 mM substrate in 100 μL storage buffer was incubated at 30 °C for 40 min. To quench the reaction, 150 μL methanol was added into the reaction mixture. After thorough vortex mixing and high-speed centrifugation (12,000 × g, 15 min) to remove cell debris and precipitated proteins, the supernatant was subjected to HPLC analysis. The reaction samples were analyzed on an Agilent 1220 HPLC system under a linear gradient mobile phase at 230 nm. The mobile phase system consisted of solvent A (water with 0.1% trifluoroacetic acid, TFA) and solvent B (acetonitrile, ACN). The following gradient program was applied: 0–3 min, 10% solvent B; 3–30 min, 10~90% solvent B; and 30–31 min, 90~100% solvent B, at a flow rate of 1.0 mL/min. Boiled enzymes were used in all negative control experiments. The preparative scale reaction system containing 5 µM PikCH238pAcF/E85Q, 1 U glucose-6-phosphate dehydrogenase (GDH), 1 mM glucose, 1 mM NADPH, 10 µM Fdx1499, 5 µM FdR 0978, and 0.5 mM substrate in 10 mL storage buffer was incubated at 30 °C for 4 h. Three times extraction with an equal volume of ethyl acetate was performed to extract enzymatic products. The organic extracts were dried in vacuo and re-dissolved in methanol for products purification by semi-preparative HPLC. To determine the structures of substrates and products by NMR, 2.0 mg 6, 2.0 mg 7, 1.2 mg 8, 1.0 mg 9, 2.3 mg 11, 1.5 mg 12, 2.2 mg 13, 2.4 mg 14, and 1.8 mg 15 were prepared in >95% purity.
In vitro glycosylation reactions by BSGT-1
Expression and purification of glycosyltransferases (e.g., BSGT-1) basically followed the same protocol used for P450 enzymes with some slight modifications. In the end of the P450 reaction mediated by PikCH238pAcF/E85Q, 10 mM MgCl2, 3 mM UDP-Glu, and 9 µM BSGT-1 were added. The glycosylation reactions were performed at 37 °C for 2 h.
In gel digestion and LC-MS/MS analysis
The target proteins were analysed on SDS-PAGE gels, and the gel spots (2 × 2 mm) containing the interested protein band were cut from the gel. The gel spots were cleaned with 0.5 mL Buffer I (25 mM NH4HCO3, 50% ACN) until becoming colorless, and vacuum-centrifuged to dryness. Then, 0.1 mL of 10 mM DTT was added to break disulfide bonds at 56 °C for 1 h before colloidal particles were cleaned by ACN. To alkylate histidine and cysteine, 100 µL of 55 mM IAA was added at room temperature in the dark, and excess liquid was removed after 30 min. Then, the colloidal particle was washed twice by 25 mM NH4HCO3 and ACN respectively before drying. The dehydrated colloidal particles were digested by trypsin at a ratio of 1:20 (w/w, trypsin:protein) at 37 °C for 12 h. For analysis by Q Exactive mass, 20 µL of 0.1% TFA was added to terminate the reaction, and peptides were dissolved after desalination with C18 ZipTip. Samples were eluted on an Ultimate 3000 HPLC (Dionex). The mobile phase system of solvent A (water with 0.1% formic acid) and solvent B (ACN with 0.1% formic acid) was applied at a flow rate of 0.4 µL/min. The gradient program was as follow: 0–6 min, 5~8% solvent B; 6–40 min, 8~30% solvent B; 40–45 min, 30~60% solvent B; 45–48 min, 60~80% solvent B; and 48–60 min, 80% solvent B.
Proteome Discoverer (Thermo, version 1.4) was used for database search. The establishment of a reference database was achieved using the PikC amino acid sequence. The search parameters for PikCH238pAcF were set as follows: (1) The molecular weight of His238 (155.07 Da) was replaced by pAcF (207.09 Da); (2) Trypsin was selected as the digestive enzyme; and (3) The alkylation of cysteine was set as a fixed modification and the oxidation of methionine as a variable modification.
Crystallization and structure determination
The crystals of substrate-free PikCH238pAcF were grown by hanging-drop vapor diffusion at 16 °C, by mixing 1 µL of 6 mg/mL of protein and 1 µL of reservoir solution (0.2 M Li2SO4, 0.1 M sodium cacodylate pH 6.1, 16% PEG8000) according to the previous report21. The 6- and 4-bound PikCH238pAcF complexes were prepared by mixing 6 mg/mL PikCH238pAcF with 5 mM 6 or 4 at 25 °C for 30 min, respectively. Initial crystallization conditions of the 6- and 4-bound PikCH238pAcF complexes were screened by the sitting-drop vapor-diffusion method using commercial crystal screening kits at 16 °C. Optimization of conditions was carried out manually in 24-well plates by the hanging-drop vapor diffusion method. Crystals of 6-bound PikCH238pAcF complex were obtained from 0.2 M (NH4)2SO4, 0.1 M Bis-TRIS, pH 5.8, 19% PEG3350. Crystals of 4-bound PikCH238pAcF complex were obtained from 0.2 M Li2SO4, 0.1 M Bis-TRIS, pH 6.0, 18% PEG4000. The 5-bound PikCH238pAcF crystals were grown under the same crystalization conditions as 4-bound PikCH238pAcF. Before data collection, the crystals were cryo-protected by plunging them into a drop of reservoir solution supplemented with 25% glycerol. The data were collected at beamline BL19U (SSRF, China) under cryogenic conditions at 100 K. Data indexing, integration, and scaling were conducted using HKL3000 software suite64. Crystal structures were determined by molecular replacement using the atomic coordinates of the PDB ID code 2BVJ as a search model. The models were built into the electron density using COOT65 and refined in PHENIX66. The molecules of 4–6 were modeled at the final stage of refinement, and the model quality was verified using the program MolProbity in PHENIX. Structural models were drawn using the program PyMOL version 2.3.2 (https://pymol.org/2/).
The initial structures of 7 were generated by ChemDraw 17.0, followed by DFT optimization at the B3LYP-D3/def2SVP67 theoretical level with the Gaussian16 (Revision A.03) package68. Automated molecular docking was performed using the DFT optimized structure by running the AutoDock vina (version 1.5.7) program equipped with ADT. All side chains were set as rigid body and grid spacing was set to 0.5 Å. Other parameters remained as their default values. The top 9 lowest energy docking poses of 7 in PikCH238pAcF from 2,500,000 searching results were output, among which the ideal catalytic conformation was used for analysis as shown in Fig. 5. The docking models were analyzed and represented using ADT and PyMOL version 2.3.2 (https://pymol.org/2/).
Statistics and reproducibility
All experiments in this study were carried out in duplicate or triplicate, and statistical analyses were performed using the Student’s t test, two-sided. Basic statistical analysis was performed using Microsoft Excel 2016 (version 16.0.4266.1001).
Figures and schemes were prepared using Adobe Illustrator CC 2021 (version 25.2.1), ChemDraw (version 17.0), and PowerPoint 2016 (version 16.0.4266.1001).
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.
Atomic coordinates and structure factors for substrate-free PikCH238pAcF, 4-bound PikCH238pAcF, 5-bound PikCH238pAcF and 6-bound PikCH238pAcF have been deposited in the Protein Data Bank under the accession numbers 7XBM, 7XBN, 8GUE and 7XBO, respectively. Previously published structures used in this study include PDB IDs: 2BVJ (the crystal structure of ligand-free PikCWT), 2C6H (the crystal structure of 4-bound PikCWT), 2C7X (the crystal structure of 5-bound PikCWT), 2VZ7 (the crystal structure of 4-bound PikCD50N), and 2VZM (the crystal structure of 5-bound PikCD50N). All other relevant data supporting the findings of this study are available in Supplementary Information. Source data are provided with this paper.
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This work was supported by the National Natural Science Foundation of China (32025001), the National Key Research and Development Program (2019YFA0905100), the Natural Science Foundation of Shandong Province, China (ZR2019ZD20, ZR2021JQ09, and ZR2021QC043), the Key R&D Program of Shandong Province (2020CXGC011305), the Youth Interdisciplinary Innovative Research Group of Shandong University (2020QNQT009), and the China Postdoctoral Science Foundation (2021M701988). The authors thank Jingyao Qu, Jing Zhu, Fengzhi Li, Haiyan Sui, Guannan Lin, and Xiaoju Li of the Core Facilities for Life and Environmental Sciences, State Key laboratory of Microbial Technology at Shandong University for their assistance in collection of LC-MS, NMR, LC-MS/MS and XRD data. We also thank Prof. Xiaozhou Luo at Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences for providing the plasmid pULTRA-Ambrx.
The authors declare no competing interests.
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Pan, Y., Li, G., Liu, R. et al. Unnatural activities and mechanistic insights of cytochrome P450 PikC gained from site-specific mutagenesis by non-canonical amino acids. Nat Commun 14, 1669 (2023). https://doi.org/10.1038/s41467-023-37288-0
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