Activation and Characterization of Cryptic Gene Cluster: Two Series of Aromatic Polyketides Biosynthesized by Divergent Pathways

One biosynthetic gene cluster (BGC) usually governs the biosynthesis of a series of compounds exhibiting either the same or similar molecular scaffolds. Reported here is a multiplex activation strategy to awaken a cryptic BGC associated with tetracycline polyketides, resulting in the discovery of co...

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Veröffentlicht in:Angewandte Chemie International Edition 2019-12, Vol.58 (50), p.18046-18054
Hauptverfasser: Ji, Zhen‐Yu, Nie, Qiu‐Yue, Yin, Yue, Zhang, Mei, Pan, Hai‐Xue, Hou, Xian‐Feng, Tang, Gong‐Li
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Sprache:eng
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Zusammenfassung:One biosynthetic gene cluster (BGC) usually governs the biosynthesis of a series of compounds exhibiting either the same or similar molecular scaffolds. Reported here is a multiplex activation strategy to awaken a cryptic BGC associated with tetracycline polyketides, resulting in the discovery of compounds having different core structures. By constitutively expressing a positive regulator gene in tandem mode, a single BGC directed the biosynthesis of eight aromatic polyketides with two types of frameworks, two pentacyclic isomers and six glycosylated tetracyclines. The proposed biosynthetic pathway, based on systematic gene inactivation and identification of intermediates, employs two sets of tailoring enzymes with a branching point from the same intermediate. These findings not only provide new insights into the role of tailoring enzymes in the diversification of polyketides, but also highlight a reliable strategy for genome mining of natural products. Breaking the silence: A silent gene cluster was engaged by the expression of a positive regulator gene in tandem mode, directing the biosynthesis of eight aromatic polyketides. These polyketides comprise two different frameworks, two pentacyclic isomers (1 and 2) and six glycosylated tetracyclines (3–8), which are proposed to arise from divergent pathways originating from a common intermediate.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201910882