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含血红素A的呼吸氧化酶起源于铁氧化细菌的祖先。

Respiratory Heme A-Containing Oxidases Originated in the Ancestors of Iron-Oxidizing Bacteria.

作者信息

Degli Esposti Mauro, Moya-Beltrán Ana, Quatrini Raquel, Hederstedt Lars

机构信息

Center for Genomic Sciences, Universidad Nacional Autónoma de México (UNAM), Cuernavaca, Mexico.

Fundación Ciencia & Vida, Santiago, Chile.

出版信息

Front Microbiol. 2021 Jun 15;12:664216. doi: 10.3389/fmicb.2021.664216. eCollection 2021.

DOI:10.3389/fmicb.2021.664216
PMID:34211444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8239418/
Abstract

Respiration is a major trait shaping the biology of many environments. Cytochrome oxidase containing heme A (COX) is a common terminal oxidase in aerobic bacteria and is the only one in mammalian mitochondria. The synthesis of heme A is catalyzed by heme A synthase (CtaA/Cox15), an enzyme that most likely coevolved with COX. The evolutionary origin of COX in bacteria has remained unknown. Using extensive sequence and phylogenetic analysis, we show that the ancestral type of heme A synthases is present in iron-oxidizing Proteobacteria such as spp. These bacteria also contain a deep branching form of the major COX subunit (COX1) and an ancestral variant of CtaG, a protein that is specifically required for COX biogenesis. Our work thus suggests that the ancestors of extant iron-oxidizers were the first to evolve COX. Consistent with this conclusion, acidophilic iron-oxidizing prokaryotes lived on emerged land around the time for which there is the earliest geochemical evidence of aerobic respiration on earth. Hence, ecological niches of iron oxidation have apparently promoted the evolution of aerobic respiration.

摘要

呼吸作用是塑造许多环境生物学特性的主要特征。含有血红素A的细胞色素氧化酶(COX)是需氧细菌中常见的末端氧化酶,也是哺乳动物线粒体中唯一的末端氧化酶。血红素A的合成由血红素A合酶(CtaA/Cox15)催化,该酶很可能与COX共同进化。细菌中COX的进化起源一直未知。通过广泛的序列和系统发育分析,我们表明血红素A合酶的原始类型存在于铁氧化变形菌中,如 属细菌。这些细菌还含有主要COX亚基(COX1)的一种深度分支形式以及CtaG的原始变体,CtaG是COX生物合成特别需要的一种蛋白质。因此,我们的研究表明现存铁氧化菌的祖先最早进化出了COX。与这一结论一致的是,嗜酸性铁氧化原核生物在地球上最早有有氧呼吸地球化学证据的时期生活在露出水面的陆地上。因此,铁氧化的生态位显然促进了有氧呼吸的进化。

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Thermodynamic efficiency, reversibility, and degree of coupling in energy conservation by the mitochondrial respiratory chain.
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