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鉴定和描述鲍曼不动杆菌醛戊糖降解的新途径。

Identification and characterization of a novel pathway for aldopentose degradation in Acinetobacter baumannii.

机构信息

Department of Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences, Goethe-University Frankfurt am Main, Frankfurt, Germany.

Department of Genomic and Applied Microbiology and Göttingen Genomics Laboratory, Institute of Microbiology and Genetics, University of Göttingen, Göttingen, Germany.

出版信息

Environ Microbiol. 2023 Nov;25(11):2416-2430. doi: 10.1111/1462-2920.16471. Epub 2023 Jul 31.

DOI:10.1111/1462-2920.16471
PMID:37522309
Abstract

The nosocomial pathogen Acinetobacter baumannii is well known for its extraordinary metabolic diversity. Recently, we demonstrated growth on L-arabinose, but the pathway remained elusive. Transcriptome analyses revealed two upregulated gene clusters that code for isoenzymes catalysing oxidation of a pentonate to α-ketoglutarate. Molecular, genetic, and biochemical experiments revealed one branch to be specific for L-arabonate oxidation, and the other for D-xylonate and D-ribonate. Both clusters also encode an uptake system and a regulator that acts as activator (L-arabonate) or repressor (D-xylonate and D-ribonate). Genes encoding the initial oxidation of pentose to pentonate were not part of the clusters, but our data are consistent with the hypothesis of a promiscous, pyrroloquinoline quinone (PQQ)-dependent, periplasmic pentose dehydrogenase, followed by the uptake of the pentonates and their degradation by specific pathways. However, there is a cross-talk between the two different pathways since the isoenzymes can replace each other. Growth on pentoses was found only in pathogenic Acinetobacter species but not in non-pathogenic such as Acinetobacter baylyi. However, mutants impaired in growth on pentoses were not affected in traits important for infection, but growth on L-arabinose was beneficial for long-term survival and desiccation resistance in A. baumannii ATCC 19606.

摘要

医院病原体鲍曼不动杆菌以其非凡的代谢多样性而闻名。最近,我们证明了它可以在 L-阿拉伯糖上生长,但该途径仍然难以捉摸。转录组分析显示,有两个上调的基因簇,它们编码同工酶,可将戊糖氧化为α-酮戊二酸。分子、遗传和生化实验表明,一个分支专门用于 L-阿拉伯酸盐的氧化,另一个分支用于 D-木糖酸盐和 D-核糖酸盐。这两个簇还编码一个摄取系统和一个调节剂,作为激活剂(L-阿拉伯酸盐)或抑制剂(D-木糖酸盐和 D-核糖酸盐)。编码戊糖初始氧化为戊糖的基因不是簇的一部分,但我们的数据与一个混杂的、吡咯喹啉醌 (PQQ) 依赖的、周质戊糖脱氢酶的假设一致,然后是戊糖的摄取及其通过特定途径的降解。然而,由于同工酶可以相互替代,因此两种不同的途径之间存在交叉对话。只有致病性鲍曼不动杆菌物种能够在戊糖上生长,而非致病性的如鲍曼不动杆菌 baylyi 则不能。然而,在戊糖生长中受损的突变体在感染的重要特征方面不受影响,但在 L-阿拉伯糖上的生长对 A.baumannii ATCC 19606 的长期存活和干燥抗性有益。

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