Novel polyoxins generated by heterologously expressing polyoxin biosynthetic gene cluster in the sanN inactivated mutant of Streptomyces ansochromogenes.

BACKGROUND: Polyoxins are potent inhibitors of chitin synthetases in fungi and insects. The gene cluster responsible for biosynthesis of polyoxins has been cloned and sequenced from Streptomyces cacaoi and tens of polyoxin analogs have been identified already.
RESULTS: The polyoxin biosynthetic gene cluster from Streptomyces cacaoi was heterologously expressed in the sanN inactivated mutant of Streptomyces ansochromogenes as a nikkomycin producer. Besides hybrid antibiotics (polynik A and polyoxin N) and some known polyoxins, two novel polyoxin analogs were accumulated. One of them is polyoxin P that has 5-aminohexuronic acid with N-glycosidically bound thymine as the nucleoside moiety and dehydroxyl-carbamoylpolyoxic acid as the peptidyl moiety. The other analog is polyoxin O that contains 5-aminohexuronic acid bound thymine as the nucleoside moiety, but recruits polyoximic acid as the sole peptidyl moiety. Bioassay against phytopathogenic fungi showed that polyoxin P displayed comparatively strong inhibitory activity, whereas the inhibitory activity of polyoxin O was weak under the same testing conditions.
CONCLUSION: Two novel polyoxin analogs (polyoxin P and O) were generated by the heterologous expression of polyoxin biosynthetic gene cluster in the sanN inactivated mutant of Streptomyces ansochromogenes. Polyoxin P showed potent antifungal activity,while the activity of polyoxin O was weak. The strategy presented here may be available for other antibiotics producers.

Introduction

Polyoxinspan> (A-M), a group of peptidyl nucleoside antibiotics (Figure 1), were isolated from the culture broth of Streptomyces cacaoi[1]. Due to their structural similarity to UDP-N-acetylglucosamine, polyoxins act as competitive inhibitors of chitin synthetases and display potent inhibitory activity against phytopathogenic fungi and insects [2-4]. Polyoxins were composed of nucleoside moiety and peptidyl moiety connected via a peptide bond. In different polyoxin analogs, the nucleoside moiety could be a 5-aminohexuronic acid with N-glycosidically bounded different bases, such as uracil, thymine, 5-carboxyl-uracil or 5-hydroxylmethyl-uracil; the peptidyl moiety includes C-5 linked carbamoylpolyoxamic acid (CPOAA) or dehydroxyl-carbamoylpolyoxamic acid (DHCPOAA) and C-6 linked polyoximic acid (POIA) [5-8]. Studies on the structure-activity relationship (SAR) of polyoxins showed that the thymine derived polyoxins (polyoxin H and J) have higher inhibitory activity of chitin synthetase compared with polyoxin A, B, D, F and L, indicating that thymine is better than the other bases at bioactivity [3].

Figure 1

Structures of polyoxins, nikkomycins, hybrid antibiotics and their biosynthetic gene clusters.A, structures of polyoxin analogs; B, structures of two representative nikkomycins; C, structures of two hybrid antibiotics; D, gene organization of polyoxin and nikkomycin biosynthetic gene clusters. The red arrows indicate genes related to the nucleoside moiety biosynthesis, and the homolog genes are linked by oblique lines.

Structures of polyoxinspan>, nikkomycins, hybrid antibiotics and their biosynthetic gene clusters.A, structures of polyoxin analogs; B, structures of two representative nikkomycins; C, structures of two hybrid antibiotics; D, gene organization of polyoxin and nikkomycin biosynthetic gene clusters. The red arrows indicate genes related to the nucleoside moiety biosynthesis, and the homolog genes are linked by oblique lines.

The genes respopan class="Chemical">nsible for the biosynthesis of polyoxins have been cloned from class="Chemical">pan> class="Species">S. cacaoi[9]. It was suggested that seven genes polA, B, D, H, I, J and K were involved in polyoxin nucleoside moiety biosynthesis (Figure 1). Among them, polB, a proposed thymidylate synthase coding gene, likely governs the methylation of C-5′ position of uracil to afford thymine base. Genes encoding enzymes for subsequent oxidation at C-7′ are out of the cloned polyoxin biosynthetic cluster and may locate at other positions of chromosome. Previous efforts of heterologously expressing the polyoxin biosynthetic gene cluster in S. lividans TK24 obtained only polyoxin H [9].

To expand the diversity of papan class="Chemical">n class="Chemical">polyoxins by combinpan>atorial biosynthetic strategy, the pan> class="Chemical">nikkomycin producer was considered as a host for heterologous expression of polyoxin. Nikkomycins (Figure 1) are peptidyl nucleoside antibiotics produced by S. ansochromogenes or S. tendae[10,11]. The peptidyl moiety of nikkomycin is hydroxypyridylhomothreonine; while its nucleoside moiety is 5-aminohexuronic acid N-glycosidically bounded uracil in nikkomycin Z (the same as polyoxin K, L and M) or 5-aminohexuronic acid N-glycosidically bounded imidazolone in nikkomycin X. The gene cluster responsible for biosynthesis of nikkomycins has already been cloned and sequenced from S. ansochromogenes (Figure 1) [12]. Previous combinatorial biosynthesis attempts resulted in polyoxin N and a novel compound polynik A by expressing the polyoxin peptidyl moiety genes in sanN inactivated mutant (ΔsanN) [13]. SanN catalyzes the conversion from benzoate-CoA to benzaldehyde, which is a precursor of nikkomycin peptidyl moiety [14]. The resulting ΔsanN strain lost its ability to synthesize hydroxypyridylhomothreonine, but it can accumulate 5-aminohexuronic acid bounded uracil or 5-aminohexuronic acid bounded imidazole. Considering the yield of nikkomycins produced by S. ansochromogenes is quite high [12], the ΔsanN strain can supply not only the 5-aminohexuronic acid bounded imidazole for hybrid polynik compounds but also 5-aminohexuronic acid bounded uracil for more polyoxin production, which may lead to the production of novel polyoxin analogs.

Therefore, we introduced the papan class="Chemical">n class="Chemical">polyoxin biosynclass="Chemical">pan>thetic gene cluster inpan>to the Δpan> class="Chemical">sanN strain of S. ansochromogenes in this study. Here, we report that two new polyoxins (polyoxin O and P) were isolated from this constructed recombinant strain and the production of hybrid compounds, polynik A and polyoxin N, were also observed. Bioactive investigations revealed that polyoxin P displayed strong antifungal activity, whereas polyoxin O displayed weak antifungal activity. The strategy we have taken in this study is significant to obtain novel antibiotics or their derivatives with potential value in application.

Results

Construction of S. ansochromogenes ΔsanN/pPOL

Cosmid 9A, contaipan class="Chemical">ning the clustered polyoxin biosynthetic genes, was screenpan>ed by PCR from the genomic cosmid library preserved inpan> our lab. To construct a recombinpan>anpan>t plasmid for heterologous expression of genes, the clustered pan> class="Chemical">polyoxin genes in cosmid 9A were transferred to pSET152 via Red/ET recombination technology to result in pPOL, which could be integrated into the chromosome in Streptomyces.

Plasmid pPOL was introduced ipan class="Chemical">nto the ΔsanN strainpan> of class="Chemical">pan> class="Species">S. ansochromogenes by E. coli-Streptomyces intergenic conjugation, the resulting conjugates were verified by PCR (Additional file 1: Figure S1). The exconjugate ΔsanN/pPOL was then incubated in SP liquid medium. After 5 days, the fermentation broth was used to detect bioactivity against phytopathogenic fungus. Growth inhibition of A. kikuchiana was clearly observed (Additional file 1: Figure S2).

Isolation and characterization of polyoxin P

To identify the apan class="Chemical">ntifungal antibiotics produced by the recombinant strain ΔsanN/pPOL, the fermentation broth was processed by usinpan>g a macroporous absorption resinpan> HP-20 column. Thenpan>, it was subjected to HPLC analysis (Figure 2). Compared with the host strainpan>, the newly emerged peaks inpan> the recombinpan>anpan>t strainpan> were collected anpan>d further anpan>alyzed by LC-MS anpan>d MS/MS (Additional file 1: Figure S3). As anpan>ticipated, the hybrid compounds pan> class="Chemical">polynik A and polyoxin N were observed along with several known polyoxins including thymine polyoxin C and polyoxin J. Besides those, a new compound with retention time at 17.1 min was discovered. Preliminary MS analysis afforded an [M+H]+ ion at m/z 476.2 (Figure 3), which was inconsistent with any known polyoxins. The new compound was designated as polyoxin P. The production of polyoxin P is about 90 μg ml-1.

Figure 2

HPLC analyses of the antibiotics produced by ΔsanN/pPOL. The corresponding peaks of different compounds are marked by arrows. A, HPLC traces identifying as polyoxin P; B, HPLC traces identifying as polyoxin O. Polyoxin N and thymine polyoxin C had the similar retention time at about 11.8 min, the retention times of polynik A, polyoxin J and P were 12.9 min, 15.2 min and 17.2 min, respectively. The retention times for polyoxin O and H were about 19.5 min and 22 min, respectively.

Figure 3

MS and NMR analyses of polyoxin P and O.A, structure of polyoxin P. The fragmentation pattern of MS/MS is marked in dash lines. The bold lines indicate COSY correlations, and the HMBC correlations are showed by arrows; B, structure of polyoxin O. The fragmentation pattern of MS/MS is marked in dash lines; C, MS and MS/MS spectra of polyoxin P; D, MS and MS/MS spectra of polyoxin O.

HPLC analyses of the apan class="Chemical">ntibiotics produced by ΔsanN/pPOL. The correspondinpan>g peaks of different compounds are marked by arrows. A, HPLC traces identifyinpan>g as pan> class="Chemical">polyoxin P; B, HPLC traces identifying as polyoxin O. Polyoxin N and thymine polyoxin C had the similar retention time at about 11.8 min, the retention times of polynik A, polyoxin J and P were 12.9 min, 15.2 min and 17.2 min, respectively. The retention times for polyoxin O and H were about 19.5 min and 22 min, respectively.

MS and pan class="Chemical">NMR analyses of polyoxin P anpan>d O.A, structure of pan> class="Chemical">polyoxin P. The fragmentation pattern of MS/MS is marked in dash lines. The bold lines indicate COSY correlations, and the HMBC correlations are showed by arrows; B, structure of polyoxin O. The fragmentation pattern of MS/MS is marked in dash lines; C, MS and MS/MS spectra of polyoxin P; D, MS and MS/MS spectra of polyoxin O.

Polyoxin Ppan> was then purified by HPLC anpan>d further anpan>alyzed by high resolution electrospray pan> class="Disease">ionization mass spectrometry (HR-ESI-MS) and NMR. HR-ESI-MS results showed an [M+H]+ ion at m/z 476.1647 (Additional file 1: Figure S4), corresponding to the molecular formula C17H25O11N5 (476.1629 calculated). Subsequent MS/MS fragmentation pattern indicated that the polyoxin P contains a thymine base and DHCPOAA as peptidyl moiety (Figure 3). Based on the NMR results (Table 1 and Additional file 1: Figure S5), the chemical structure of polyoxin P was determined (Figure 3). The C-7′ methyl group can be assigned by the correlation from H-7′ (1.828 ppm) to C-5′ (111.7 ppm); and the DHCPOAA moiety can be determined by 1H, 13C, COSY and HMBC data. Structural elucidation of polyoxin P adds a new member of polyoxins with thymine besides polyoxin H and J.

Table 1

H andC NMR data of polyoxin P

Position	1H (δ, mult.,J)	13C (δ)
1	5.734(1H, d, 4.8)	90.6
2	4.366(1H, m)	72.2
3	4.467 (1H, m)	69.9
4	4.224(1H, m)	82.5
5	4.780(1H, d, 4.2)	54.4
6		171.4
2′		151.7
4′		166.4
5′		111.7
6′	7.331(1H, s)	138.2
7′	1.828 (3H, s)	11.5
1″		169.4
2″	4.194(1H, t, 7.2)	51.7
3″	1.919- 2.107(2H, m)	33.5
4″	4.097-4.086(1H, m)	66.8
5″	3.926-4.030(2H, m)	68.1
6″		159.1

*Polyoxin P in D2O,δ in ppm, J in Hz.

H andC NMR data of n class="Chemical">polyoxin P

*n class="Chemical">Polyoxin P in pan> class="Chemical">D2O,δ in ppm, J in Hz.

Isolation and characterization of polyoxin O

The fermentatiopan class="Chemical">n broth of ΔsanN/pPOL strainpan> was processed anpan>d subjected to HPLC anclass="Chemical">pan>alysis. Two compounds with retention time at about 19.4 anpan>d 22 minpan> were distinpan>guished inpan> comparison with the host strainpan> as a control (Figure 2). The compounds were collected anpan>d subjected to LC-MS anpan>d MS/MS anpan>alysis (Figure 3). Results showed that the compound has [M+H]+ ion at m/z 411.1, anpan>d containpan>s pan> class="Chemical">aminohexuronic acid with N-glycosidically bound thymine as the nucleoside moiety, polyoximic acid as the peptidyl moiety (Figure 3). So far as we know, this compound has not been reported, and was named as polyoxin O. In contrast to the standard compound, the peak at 22 min was identified as polyoxin H.

Bioassay of polyoxin P and polyoxin O

To characterize the antifupan class="Chemical">ngal activities of the two novel polyoxins, pan> class="Chemical">polyoxin P and O were subjected to bioassay against Alternaria kikuchiana, Aspergillus fumigates, Rhizoctonia solani, Botrytis cinerea and Trichoderma viride using polyoxin H as a control (Figure 4). It was shown that polyoxin P displayed potent inhibitory activity, whereas the activity of polyoxin O was very weak.

Figure 4

Bioassay of polyoxin H, polyoxin P and polyoxin O against fungi.A, Alternaria kikuchiana; B, Aspergillus fumigates; C,Rhizoctonia solani; D, Botrytis cinerea; E, Trichoderma viride. 1, polyoxin H; 2, polyoxin P; 3, polyoxin O.

Discussion

Given more apan class="Chemical">nd more biosynthetic machineries of natural products are elucidated, combinatorial biosynthesis has been developed as an optional way to generate novel antibiotics. A large number of successful examples demonstrated that the method was available [15-17]. In this study, we constructed a Δpan> class="Chemical">sanN/pPOL strain that provides a 5-aminohexuronic uracil and 5-aminohexuronic imidazolone as precursors for novel polyoxins formation. Two novel polyoxins (polyoxin P and O) were obtained together with two hybrid compounds (polynik A and polyoxin N) and several known polyoxins (polyoxin H, J and thymine polyoxin C).

All the uracilpan> derived polyoxins accumulated in the ΔsanN/pPOL were added a C-5′ methyl to form thymine base, which should be catalyzed by the thymidylate synthase PolB. Since the genes encoding enzymes to modify C-7′ methyl group into hydroxylmethyl and carboxylic acid are not in pPOL, ΔsanN/pPOL is an ideal strain to produce thymine derived polyoxins. Previous SAR (structure-activity relationships) research revealed that thymine derived polyoxins have better antifungal activity [3]. The bioassay against phytopathogenic fungi showed that the polyoxin P possesses comparatively strong bioactivity as polyoxin H (Figure 4), while polyoxin O has very weak bioactivity, indicating that components containing different peptidyl moieties possess different biological activity (DHCPOAA is important, whereas POIA is not necessary).

Our results proved that the pecies">S. ansochromogenespan> has capacity to supply enough pan> class="Chemical">5-aminohexuronic uracil for polyoxin biosynthesis. To generate more thymine derived polyoxins, blocking the 5-aminohexuronic imidazolone pathway and increasing the production of polyoxin peptidyl moieties are considered to optimize this heterologous expression system. The strategy in this study is efficient to obtain novel antibiotics or their derivatives and it may be available for other bacteria to result in new compounds.

Conclusion

Includipan class="Chemical">ng two new members (polyoxin P anpan>d O), variety of pan> class="Chemical">thymine derived polyoxins and hybrid compounds were generated by hererologous expression of polyoxin biosynthetic gene cluster in the sanN disruption mutant of S. ansochromogenes. Polyoxin P showed inhibitory activity against A. kuchiana, A. fumigates, R. solani, B. cinerea and T. viride, whereas the bioactivity of polyoxin O was quite weak against above five indicator strains under the same testing conditions. The strategy presented here may be available for other antibiotics producers.

Materials and methods

Stains and culture conditions

For spores collection, papan class="Chemical">n class="Species">S. cacaoi subsp. asoensis class="Chemical">pan> class="Species">AS4.1602 and S. ansochromogenes sanN disruption mutant were grown on mannitol/soya medium (MS) and minimal medium (MM), respectively [18]. For genomic DNA extraction, Streptomyces were grown in liquid YEME medium containing 20% sucrose, which was also used as seed culture for fermentation. For antibiotics production, the seed culture was inoculated into fresh SP medium at 1% ratio and further incubated for 5 days at 28°C, and then the culture broth was collected. Alternaria kikuchiana, Aspergillus fumigates, Rhizoctonia solani, Botrytis cinerea and Trichoderma viride obtained from the China General Microbiological Culture Collection Center (CGMCC) were grown at 28°C and used as indicator strains for bioassay. E. coli JM109 and DH5α were used as the hosts for propagating plasmids. Methylation-deficient E. coli ET12567 (pUZ8002) was used as a host for transferring DNA from E. coli to Streptomyces by intergeneric conjugation [18].

When pan class="Chemical">necessary, antibiotics were used at the following final concentrations: 100 μg ml-1 ampicillin (pan> class="Chemical">Amp), 100 μg ml-1 kanamycin (Kan), 100 μg ml-1 apramycin (Apr), 15 μg ml-1 tetracycline and 12.5 μg ml-1 chloramphenicol in LB for E. coli; 10 μg ml-1 Apr or Kan in MM, MS and YEME for Streptomyces.

Plasmids and DNA manipulations

Isolation of plasmids and chromosomal DNA were carried out according to the standard methods [18,19]. Conjugal transfer from E. coli to pan> class="Species">Streptomyces and Red/ET recombination were performed as described elsewhere [18,20]. Cosmid 9A containing the polyoxin biosynthetic gene cluster was screened by PCR from the genomic cosmid library preserved in our lab. Then, cosmid cos9A was digested with BamHI and the resulting 10.6 kb lineared vector fragment was self-ligated to create cosAfl. CosAfl was digested with EcoRI and the excised DNA fragment (about 4.1 kb) was inserted into the same site of pSET152 to generate pSET152::Afl. Plasmid pSET152::polR[21,22] was digested with EcoRI/XbaI and the 3.4 kb DNA fragment containing polR was inserted into pIJ2925 to give pIJ2925::polR. A 3.4 kb XbaI/BglII DNA fragment was excised from pIJ2925::polR and then inserted into the XbaI/BamHI site of pSET152::Afl to result in pSET152::polR::Afl. pSET152::polR::Afl was linearized with NdeI/SpeI digestion and introduced into E. coli BW25113/pIJ790 containing cosmid cos9A. Then pPOL was generated after λ-Red-mediated recombination.

Detection of polyoxins and antifungal bioassays

The fermentatiopan class="Chemical">n broth was chromatographed on a macroporous absorption resin HP-20 column, and the flow-through was collected and concentrated in vacuum. Then, 6 volumes of cold ethanol were added anpan>d kept at 4°C overnpan>ight, the precipitate was collected by centrifugation anpan>d dried at room temperature. The crude powder was dissolved inpan> pan> class="Chemical">water. Polyoxins are monitored by HPLC analysis with Agilent 1100 HPLC system. Two different HPLC conditions were used to identify different compounds. For detection of polyoxin P: ZORBAX SB-AQ was used as the column, 95% H2O (containing 0.1% trifluoroacetic acid) and 5% methanol were used as the mobile phase, the flow rate was 0.3 ml/min, and the absorption wavelength was 260nm. For detection of polyoxin O: ZORBAX SB-C18 column was used for analysis, and mobile phase conditions were the same as those for detecting nikkomycins described elsewhere [23]. The detection wavelength was 260 nm. Bioassay against A. kikuchiana, A. fumigates, R. solani, B. cinerea and T. viride was carried out according to the method used in previous study [24], and 100μl polyoxins solution (about 100 μg ml-1) was added.

Isolation of polyoxins

The method for isolating papan class="Chemical">n class="Chemical">polyoxin P was similar to that for class="Chemical">pan> class="Chemical">polynik A [13]. The fermentation broth was harvested by centrifugation and the pH was adjusted to 4.5 with acetic acid. Then, it was chromatographed on a macroporous absorption resin HP-20 (Mitsubishi) column, and the flow-through was collected and subjected to a Dowex 50WX2 (Sigma) column. The column was eluted with 0.4 N ammonia solution and the samples with antifungal activity was collected and concentrated to a small volume (less than 10 ml). About 6 volumes of cold ethanol were added and the precipitated sample was dried and dissolved in water, subsequently it was further purified by HPLC and identified as a pure polyoxin P. Polyoxin O was first purified by the ion pair HPLC program [23], lyophilized and dissolved in water. The sample was subsequently subjected to HPLC to remove salts with following conditions: ZORBAX SB-C18 was used as the column with 1 ml min-1 flow rate at 40°C, a liner gradient of 10%-50% solution B (solution A = 0.1% trifluoroacetic acid; solution B = methanol) over 30 min was used as the elution profile.

Spectrometric analyses

MS and Tapan class="Chemical">ndem Mass Spectrometry analyses were carried out on LCQ Deca XP Plus (Thermo-Finnigan) with the electrospray n class="Disease">ionization source inpan> positive mode. For high resolution mass spectrometry anpan>alysis, anpan> Aligent 1200 HPLC system anpan>d 6520 QTF-MS system were used inpan> positive mode. NMR analyses were subjected with a Bruker spectrometer (AV600 MHz).

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

JL and LL carried out experimepan class="Chemical">nts, analyzed the primary data and wrote the draft manuscript. CF assisted with experiments. YC assisted with data analysis and revised the manuscript. HT supervised the whole research work and revised the manuscript. All authors read and approved the final manuscript.

Additional file 1

Figure S1. Analysis of copan class="Chemical">njugated ΔsanN/pPol strainpan>s by PCR. A, RTS-afsR (5’-CCTCTACCGCAGTCTCCT-3’) anpan>d RTA-afsR (5′-TGTCCTCGTCCTCCAGTT-3′) were used as primers for PCR class="Chemical">pan> class="Chemical">amplification; B, RTS-26 (5′-CCGCTCGCTCCACATCAAC-3′) and RTA-26 (5′-AGCCAGGAGTGGGTGAGGT-3′) were used as primers for PCR amplification. Lane 1, S. cacaoi;lane 2, S. ansochromogenes 7100; lanes 3-8, different clones from conjugated ΔsanN/pPol;lane 9, ΔsanN mutant; lane 10, DNA marker. Figure S2, Bioassay of the fermentation broth of ΔsanN/pPOL. 1, the fermentation broth of S. ansochromgenes 7100; 2, the fermentation broth of sanN disruption mutant; 3, the fermentation broth of S. cacaoi; 4-9, the fermentation broth of ΔsanN/pPOL. Figure S3, MS and MS/MS spectra of polyoxin N, polynik A, polyoxin J and thymine-polyoxin C. A, MS and MS/MS spectra of polyoxin N; B, MS and MS/MS spectra of polynik A; C, MS and MS/MS spectra of polyoxin J; D, MS and MS/MS spectra of thymine polyoxin C. Figure S4, HR-ESI-MS spectrum of polyoxin P. Figure S5, NMR spectrum of polyoxin P. A, The 1H-NMR spectrum of polyoxin P; B, The 13C-NMR spectrum of polyoxin P; C, The DEPT spectrum of polyoxin P; D, The COSY spectrum of polyoxin P; E, The HMQC spectrum of polyoxin P; F, The HMBC spectrum of polyoxin P.

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