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草肽及其生物合成相关蛋白多样性的系统发育组学分析。

Phylogenomic analysis of the diversity of graspetides and proteins involved in their biosynthesis.

机构信息

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.

Tuberculosis Research Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

出版信息

Biol Direct. 2022 Mar 21;17(1):7. doi: 10.1186/s13062-022-00320-2.

Abstract

BACKGROUND

Bacteria and archaea produce an enormous diversity of modified peptides that are involved in various forms of inter-microbial conflicts or communication. A vast class of such peptides are Ribosomally synthesized, Postranslationally modified Peptides (RiPPs), and a major group of RiPPs are graspetides, so named after ATP-grasp ligases that catalyze the formation of lactam and lactone linkages in these peptides. The diversity of graspetides, the multiple proteins encoded in the respective Biosynthetic Gene Clusters (BGCs) and their evolution have not been studied in full detail. In this work, we attempt a comprehensive analysis of the graspetide-encoding BGCs and report a variety of novel graspetide groups as well as ancillary proteins implicated in graspetide biosynthesis and expression.

RESULTS

We compiled a comprehensive, manually curated set of graspetides that includes 174 families including 115 new families with distinct patterns of amino acids implicated in macrocyclization and further modification, roughly tripling the known graspetide diversity. We derived signature motifs for the leader regions of graspetide precursors that could be used to facilitate graspetide prediction. Graspetide biosynthetic gene clusters and specific precursors were identified in bacterial divisions not previously known to encode RiPPs, in particular, the parasitic and symbiotic bacteria of the Candidate phyla radiation. We identified Bacteroides-specific biosynthetic gene clusters (BGC) that include remarkable diversity of graspetides encoded in the same loci which predicted to be modified by the same ATP-grasp ligase. We studied in details evolution of recently characterized chryseoviridin BGCs and showed that duplication and horizonal gene exchange both contribute to the diversification of the graspetides during evolution.

CONCLUSIONS

We demonstrate previously unsuspected diversity of graspetide sequences, even those associated with closely related ATP-grasp enzymes. Several previously unnoticed families of proteins associated with graspetide biosynthetic gene clusters are identified. The results of this work substantially expand the known diversity of RiPPs and can be harnessed to further advance approaches for their identification.

摘要

背景

细菌和古菌产生了大量的修饰肽,这些肽参与了各种形式的微生物间冲突或通讯。这类肽的一个很大的类别是核糖体合成的、翻译后修饰的肽(RiPPs),而 RiPPs 的一个主要群体是graspetides,这个名称源于催化这些肽中环内酰胺和内酯键形成的 ATP-抓握连接酶。graspetides 的多样性、各自生物合成基因簇(BGCs)中编码的多个蛋白及其进化尚未得到全面详细的研究。在这项工作中,我们尝试对 graspetide 编码 BGCs 进行全面分析,并报告了各种新的 graspetide 群体以及参与 graspetide 生物合成和表达的辅助蛋白。

结果

我们编译了一个全面的、手动整理的 graspetide 数据集,其中包括 174 个家族,其中包括 115 个具有不同氨基酸模式的新家族,这些模式涉及大环化和进一步修饰,使已知的 graspetide 多样性增加了约两倍。我们为 graspetide 前体的 leader 区域推导了特征基序,可用于促进 graspetide 的预测。在以前未知编码 RiPPs 的细菌分类中,包括寄生和共生菌的候选门辐射中,发现了 graspetide 生物合成基因簇和特定前体。我们确定了拟杆菌属特有的生物合成基因簇(BGC),其中包括同一基因座编码的、预测由相同 ATP-抓握连接酶修饰的 graspetide 的显著多样性。我们详细研究了最近表征的 chryseoviridin BGCs 的进化,并表明在进化过程中,重复和水平基因交换都有助于 graspetide 的多样化。

结论

我们证明了 graspetide 序列的多样性,甚至是与密切相关的 ATP-抓握酶相关的多样性,以前都没有被怀疑过。还确定了几个与 graspetide 生物合成基因簇相关的以前未被注意到的蛋白家族。这项工作的结果大大扩展了已知的 RiPPs 多样性,可以用于进一步推进它们的鉴定方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf47/8939145/055308cbbbfc/13062_2022_320_Fig1_HTML.jpg

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