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在蓝藻天然产物生物合成中脂肪酸的掺入和修饰。

Incorporation and modification of fatty acids in cyanobacterial natural products biosynthesis.

机构信息

Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, 4450-208 Matosinhos, Portugal.

ICBAS - Institute of Biomedical Sciences Abel Salazar, University of Porto, 4050-313 Porto, Portugal.

出版信息

Chem Commun (Camb). 2023 Apr 11;59(30):4436-4446. doi: 10.1039/d3cc00136a.

Abstract

Fatty acid-derived alkyl chains are often found in natural products, where they can exert a number of different functions, most notably biological membrane interactions. Such alkyl chains are difficult to modify regio- and stereoselectively, since most positions are distant from any directing functional group. Chemical and biochemical diversification of these moieties is therefore a challenge, and most organisms do not modify alkyl moieties to a great extent. Still, one particular group of microorgansims - cyanobacteria - display not only a large number of fatty acid-incorporating natural products, but also modify these to a great extent. Here, we provide an overview of the unique fatty acid metabolism of cyanobacteria in the context of natural products biosynthesis. We cover the diverse range of fatty acid incorporation mechanisms that these organisms use to recruit and commit fatty acids to natural products biosynthetic pathways. A variety of alkyl chain decorations and modifications that are found in cyanobacterial natural products are highlighted, illustrating the rich enzymatic arsenal that these organisms have evolved to diversify fatty acid-derived alkyl chains.

摘要

脂肪酸衍生的烷基链通常存在于天然产物中,它们可以发挥多种不同的功能,最显著的是生物膜相互作用。由于大多数位置远离任何导向官能团,因此很难对这些烷基链进行区域和立体选择性修饰。因此,对这些部分进行化学和生化多样化是一个挑战,而且大多数生物体不会在很大程度上修饰烷基部分。然而,一类特殊的微生物 - 蓝藻 - 不仅显示出大量含有脂肪酸的天然产物,而且还在很大程度上对这些天然产物进行修饰。在这里,我们提供了蓝藻天然产物生物合成背景下独特脂肪酸代谢的概述。我们涵盖了这些生物体用于招募脂肪酸并将其纳入天然产物生物合成途径的多种不同的脂肪酸掺入机制。强调了在蓝藻天然产物中发现的各种烷基链修饰和修饰,说明了这些生物体为多样化脂肪酸衍生的烷基链而进化出的丰富酶武器库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dce/10088813/1d05dfa36565/d3cc00136a-f1.jpg

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