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基于基因组挖掘和前体肽诱变对线性环肽天然产物的生物合成见解

Biosynthetic Insights into Linaridin Natural Products from Genome Mining and Precursor Peptide Mutagenesis.

作者信息

Mo Tianlu, Liu Wan-Qiu, Ji Wenjuan, Zhao Junfeng, Chen Tuo, Ding Wei, Yu Shaoning, Zhang Qi

机构信息

Department of Chemistry, Fudan University , Shanghai 200433, China.

Key Laboratory of Extreme Environmental Microbial Resources and Engineering, Northwest Institute of Eco-environment and Resource, Chinese Academy of Sciences , Lanzhou, Gansu 730000, China.

出版信息

ACS Chem Biol. 2017 Jun 16;12(6):1484-1488. doi: 10.1021/acschembio.7b00262. Epub 2017 May 3.

Abstract

Linaridin is a small class of peptide natural products belonging to the ribosomally synthesized and post-translationally modified peptides (RiPPs) superfamily. By an extensive genome-wide survey of linaridin biosynthetic genes, we show that this class of natural products is widespread in nature and possesses vast structural diversity. The linaridin precursor peptides are relatively conserved in the N-termini but have diverse sequences in the core region, which appear to have coevolved with the biosynthetic enzymes. Using the prototypic linaridin cypemycin as a model, we have explored the structure-activity relationships involved in precursor peptide maturation and generated a diverse set of novel cypemycin variants, among which the T2S variant exhibits enhanced activity against Micrococcus luteus. Our results reveal valuable insights into linaridin biosynthesis and highlight the potential to explore this class of natural products by genome mining and by biosynthetic engineering studies.

摘要

线性菌素是一类小分子肽天然产物,属于核糖体合成及翻译后修饰肽(RiPPs)超家族。通过对线性菌素生物合成基因进行广泛的全基因组调查,我们发现这类天然产物在自然界广泛存在且具有巨大的结构多样性。线性菌素前体肽在N端相对保守,但核心区域具有不同的序列,这些序列似乎与生物合成酶共同进化。以典型的线性菌素环霉素为模型,我们探索了前体肽成熟过程中的构效关系,并产生了一系列不同的新型环霉素变体,其中T2S变体对藤黄微球菌的活性增强。我们的结果揭示了线性菌素生物合成的宝贵见解,并突出了通过基因组挖掘和生物合成工程研究探索这类天然产物的潜力。

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