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细菌和古菌中吡哆醛 5′-磷酸的合成与回收:预测途径变体分布和空缺。

Pyridoxal 5'-phosphate synthesis and salvage in Bacteria and Archaea: predicting pathway variant distributions and holes.

机构信息

Department of Microbiology and Cell Sciences, Gainesville, USA.

Present address: APC Microbiome Ireland, University College Cork, Cork, Ireland.

出版信息

Microb Genom. 2023 Feb;9(2). doi: 10.1099/mgen.0.000926.

Abstract

Pyridoxal 5’-phosphate or PLP is a cofactor derived from B vitamers and essential for growth in all known organisms. PLP synthesis and salvage pathways are well characterized in a few model species even though key components, such as the vitamin B transporters, are still to be identified in many organisms including the model bacteria or . Using a comparative genomic approach, PLP synthesis and salvage pathways were predicted in 5840 bacterial and archaeal species with complete genomes. The distribution of the two known biosynthesis pathways and previously identified cases of non-orthologous displacements were surveyed in the process. This analysis revealed that several PLP pathway genes remain to be identified in many organisms, either because sequence similarity alone cannot be used to discriminate among several homologous candidates or due to non-orthologous displacements. Candidates for some of these pathway holes were identified using published TnSeq data, but many remain. We find that ~10 % of the analysed organisms rely on salvage but further analyses will be required to identify potential transporters. This work is a starting point to model the exchanges of B vitamers in communities, predict the sensitivity of a given organism to drugs targeting PLP synthesis enzymes, and identify numerous gaps in knowledge that will need to be tackled in the years to come.

摘要

吡哆醛 5’-磷酸酯或 PLP 是一种辅酶,来源于维生素 B 族,是所有已知生物生长所必需的。PLP 的合成和回收途径在少数模式生物中得到了很好的描述,尽管包括模式细菌 或 在内的许多生物中的关键成分,如维生素 B 转运体,仍有待确定。利用比较基因组学方法,预测了具有完整基因组的 5840 种细菌和古细菌中的 PLP 合成和回收途径。在此过程中,调查了两种已知的 生物合成途径和以前确定的非同源置换的分布情况。该分析表明,由于仅通过序列相似性无法区分几个同源候选物,或者由于非同源置换,许多生物中仍有几个 PLP 途径基因有待鉴定。使用已发表的 TnSeq 数据鉴定了其中一些途径缺失的候选基因,但仍有许多需要鉴定。我们发现,~10%的分析生物依赖于回收途径,但需要进一步分析才能确定潜在的转运体。这项工作是对社区中 B 族维生素交换进行建模、预测针对 PLP 合成酶的药物对特定生物体的敏感性以及确定未来需要解决的众多知识空白的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a18/9997740/36e3125f0116/mgen-9-926-g001.jpg

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