Genome Mining and Metabolic Profiling Uncover Polycyclic Tetramate Macrolactams from Streptomyces koyangensis SCSIO 5802

We have previously shown deep-sea-derived SCSIO 5802 to produce two types of active secondary metabolites, abyssomicins and candicidins. Here, we report the complete genome sequence of SCSIO 5802 employing bioinformatics to highlight its potential to produce at least 21 categories of natural product...

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Veröffentlicht in:Marine drugs 2021-07, Vol.19 (8), p.440
Hauptverfasser: Ding, Wenjuan, Tu, Jiajia, Zhang, Huaran, Wei, Xiaoyi, Ju, Jianhua, Li, Qinglian
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Sprache:eng
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Zusammenfassung:We have previously shown deep-sea-derived SCSIO 5802 to produce two types of active secondary metabolites, abyssomicins and candicidins. Here, we report the complete genome sequence of SCSIO 5802 employing bioinformatics to highlight its potential to produce at least 21 categories of natural products. In order to mine novel natural products, the production of two polycyclic tetramate macrolactams (PTMs), the known 10- -HSAF ( ) and a new compound, koyanamide A ( ), was stimulated via inactivation of the abyssomicin and candicidin biosynthetic machineries. Detailed bioinformatics analyses revealed a PKS/NRPS gene cluster, containing 6 open reading frames (ORFs) and spanning ~16 kb of contiguous genomic DNA, as the putative PTM biosynthetic gene cluster (BGC) (termed herein ). We furthermore demonstrate, via gene disruption experiments, that the cluster encodes the biosynthesis of 10- -HSAF and koyanamide A. Finally, we propose a plausible biosynthetic pathway to 10- -HSAF and koyanamide A. In total, this study demonstrates an effective approach to cryptic BGC activation enabling the discovery of new bioactive metabolites; genome mining and metabolic profiling methods play key roles in this strategy.
ISSN:1660-3397
1660-3397
DOI:10.3390/md19080440