芳香菌EbN1T的分解代谢网络。

IF 0.1 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Physiology Pub Date : 2024-01-01 Epub Date: 2023-10-10 DOI:10.1159/000534425
Patrick Becker, Daniel Wünsch, Lars Wöhlbrand, Meina Neumann-Schaal, Dietmar Schomburg, Ralf Rabus
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引用次数: 0

摘要

反硝化β蛋白细菌芳香菌EbN1T是一种兼性厌氧降解专家,属于在蛋白基因组水平上研究得最好的环境细菌。这篇综述总结了47种有机生长底物(23种芳香酸、21种脂肪族和3种氨基酸)的厌氧和好氧降解(转化为CO2)以及呼吸节能模式(反硝化与O2呼吸)的知识现状。构建的分解代谢网络由256个基因组成,占基因组编码区的约7.5%。通过差异蛋白质组学共鉴定出219种编码蛋白质,蛋白质组覆盖率约为网络的74%。其降解区段由31个外围通路和4个中心通路组成,仅在完整基因组[Rabus等人,Arch Microbiol 2005 Jan;183(1):27-36]和a.aromicum EbN1T的第一次蛋白质组学调查[Wöhlbrand等人,Proteomics 2007 Jun;7(13):22222-39]之后才发现几个外围模块(例如,4-乙基苯酚、2-苯基乙胺、吲哚乙酸盐和苯丙素)。难降解芳香族化合物的活化涉及一系列生物化学上有趣的反应,从C通过羧化(如苯乙酮羧化酶)到氧化脱氨(如苄胺)、还原脱芳(苯甲酰基CoA)和形成环氧的加氧酶(如苯乙酰基CoA)的氢键活化(如乙苯脱氢酶)。外周反应序列是底物特异性诱导的,由体内反应阈值在纳摩尔范围内的特异性转录调节因子介导。亲脂性底物(如酚类)通过被动扩散进入细胞,而极性底物需要由特定转运蛋白驱动的主动摄取。除了经典复合物I-III、脱氮和O2呼吸(低亲和力和高亲和力氧化酶)的蛋白质库外,基因组编码一个Ndh II、一个四硫酸还原酶、两个ETF:醌氧化还原酶和两个Rnf型复合物,拓宽了菌株的电子转移灵活性。总之,这里提供的详细分解代谢网络为未来对a.aromicum EbN1T进行系统生物学水平的研究奠定了坚实的基础。
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The Catabolic Network of Aromatoleum aromaticum EbN1T.

The denitrifying betaproteobacterium Aromatoleum aromaticum EbN1T is a facultative anaerobic degradation specialist and belongs to the environmental bacteria studied best on the proteogenomic level. This review summarizes the current state of knowledge about the anaerobic and aerobic degradation (to CO2) of 47 organic growth substrates (23 aromatic, 21 aliphatic, and 3 amino acids) as well as the modes of respiratory energy conservation (denitrification vs. O2-respiration). The constructed catabolic network is comprised of 256 genes, which occupy ∼7.5% of the coding regions of the genome. In total, 219 encoded proteins have been identified by differential proteomics, yielding a proteome coverage of ∼74% of the network. Its degradation section is composed of 31 peripheral and 4 central pathways, with several peripheral modules (e.g., for 4-ethylphenol, 2-phenylethylamine, indoleacetate, and phenylpropanoids) discovered only after the complete genome [Arch Microbiol. 2005 Jan;183(1):27-36] and a first proteomic survey [Proteomics. 2007 Jun;7(13):2222-39] of A. aromaticum EbN1T were reported. The activation of recalcitrant aromatic compounds involves a suite of biochemically intriguing reactions ranging from C-H-bond activation (e.g., ethylbenzene dehydrogenase) via carboxylation (e.g., acetophenone carboxylase) to oxidative deamination (e.g., benzylamine), reductive dearomatization (benzoyl-CoA), and epoxide-forming oxygenases (e.g., phenylacetyl-CoA). The peripheral reaction sequences are substrate-specifically induced, mediated by specific transcriptional regulators with in vivo response thresholds in the nanomolar range. While lipophilic substrates (e.g., phenolics) enter the cells via passive diffusion, polar ones require active uptake that is driven by specific transporters. Next to the protein repertoire for canonical complexes I-III, denitrification, and O2-respiration (low- and high-affinity oxidases), the genome encodes an Ndh-II, a tetrathionate reductase, two ETF:quinone oxidoreductases, and two Rnf-type complexes, broadening the electron transfer flexibility of the strain. Taken together, the detailed catabolic network presented here forms a solid basis for future systems biology-level studies with A. aromaticum EbN1T.

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