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从大规模核苷酸数据库中获取的多样化 II 型聚酮合酶生物合成基因簇的更新目录。

An updated catalogue of diverse type II polyketide synthase biosynthetic gene clusters captured from large-scale nucleotide databases.

机构信息

Department of Chemistry, Haverford College, Haverford, PA, USA.

Department of Biology, Haverford College, Haverford, PA, USA.

出版信息

Microb Genom. 2023 Mar;9(3). doi: 10.1099/mgen.0.000965.

Abstract

Nature serves as a rich source of molecules with immense chemical diversity. Aptly named, these 'natural products' boast a wide variety of environmental, medicinal and industrial applications. Type II polyketides, in particular, confer substantial medicinal benefits, including antibacterial, antifungal, anticancer and anti-inflammatory properties. These molecules are produced by enzyme assemblies known as type II polyketide synthases (PKSs), which use domains such as the ketosynthase chain-length factor and acyl carrier protein to produce polyketides with varying lengths, cyclization patterns and oxidation states. In this work, we use a novel bioinformatic workflow to identify biosynthetic gene clusters (BGCs) that code for the core type II PKS enzymes. This method does not rely on annotation and thus was able to unearth previously 'hidden' type II PKS BGCs. This work led us to identify over 6000 putative type II PKS BGCs spanning a diverse set of microbial phyla, nearly double those found in most recent studies. Notably, many of these newly identified BGCs were found in non-actinobacteria, which are relatively underexplored as sources of type II polyketides. Results from this work lay an important foundation for future bioprospecting and engineering efforts that will enable sustainable access to diverse and structurally complex molecules with medicinally relevant properties.

摘要

自然界是具有巨大化学多样性的分子的丰富来源。这些“天然产物”恰如其名,具有广泛的环境、医学和工业应用。特别是 II 型聚酮化合物具有显著的药用价值,包括抗菌、抗真菌、抗癌和抗炎特性。这些分子是由称为 II 型聚酮合酶(PKS)的酶组装体产生的,它们使用酮合成酶链长因子和酰基载体蛋白等结构域来产生具有不同长度、环化模式和氧化态的聚酮化合物。在这项工作中,我们使用一种新颖的生物信息学工作流程来识别编码核心 II 型 PKS 酶的生物合成基因簇(BGC)。这种方法不依赖于注释,因此能够挖掘出以前“隐藏”的 II 型 PKS BGC。这项工作使我们确定了超过 6000 个假定的 II 型 PKS BGC,涵盖了多样化的微生物门,几乎是最近大多数研究中发现的两倍。值得注意的是,这些新鉴定的 BGC 中有许多存在于非放线菌中,它们作为 II 型聚酮化合物的来源相对未被充分探索。这项工作为未来的生物勘探和工程努力奠定了重要基础,这些努力将使我们能够可持续地获得具有药用相关特性的多样化和结构复杂的分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1265/10132072/9c8dbdb8cf89/mgen-9-965-g001.jpg

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