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聚酮合酶在 dynemicin 烯二炔和蒽醌生物合成中的双重作用。

A dual role for a polyketide synthase in dynemicin enediyne and anthraquinone biosynthesis.

机构信息

Department of Chemistry, The Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218, USA.

出版信息

Nat Chem. 2018 Feb;10(2):231-236. doi: 10.1038/nchem.2876. Epub 2017 Nov 20.

Abstract

Dynemicin A is a member of a subfamily of enediyne antitumour antibiotics characterized by a 10-membered carbocycle fused to an anthraquinone, both of polyketide origin. Sequencing of the dynemicin biosynthetic gene cluster in Micromonospora chersina previously identified an enediyne polyketide synthase (PKS), but no anthraquinone PKS, suggesting gene(s) for biosynthesis of the latter were distant from the core dynemicin cluster. To identify these gene(s), we sequenced and analysed the genome of M. chersina. Sequencing produced a short list of putative PKS candidates, yet CRISPR-Cas9 mutants of each locus retained dynemicin production. Subsequently, deletion of two cytochromes P450 in the dynemicin cluster suggested that the dynemicin enediyne PKS, DynE8, may biosynthesize the anthraquinone. Together with O-labelling studies, we now present evidence that DynE8 produces the core scaffolds of both the enediyne and anthraquinone, and provide a working model to account for their formation from the programmed octaketide of the enediyne PKS.

摘要

dynemicin A 是烯二炔类抗肿瘤抗生素的一个亚家族成员,其特征是 10 元碳环与来自聚酮体的蒽醌融合。先前在 Micromonospora chersina 中对 dynemicin 生物合成基因簇进行测序,鉴定出一种烯二炔聚酮合酶(PKS),但没有蒽醌 PKS,这表明后者的生物合成基因与核心 dynemicin 簇相距较远。为了鉴定这些基因,我们对 M. chersina 的基因组进行了测序和分析。测序产生了一系列短的推定 PKS 候选基因,但每个基因座的 CRISPR-Cas9 突变体仍保留 dynemicin 的产生。随后,dynemicin 簇中两个细胞色素 P450 的缺失表明,dynemicin 烯二炔 PKS(DynE8)可能生物合成蒽醌。结合 O 标记研究,我们现在提供了证据表明 DynE8 产生了烯二炔和蒽醌的核心支架,并提供了一个工作模型来解释它们是如何从烯二炔 PKS 的程序化八酮体形成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/685a/5944350/633b094cf8d0/nihms908085f1.jpg

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