Greening Chris, Biswas Ambarish, Carere Carlo R, Jackson Colin J, Taylor Matthew C, Stott Matthew B, Cook Gregory M, Morales Sergio E
Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
The Commonwealth Scientific and Industrial Research Organisation, Land and Water Flagship, Acton, Australian Capital Territory, Australia.
ISME J. 2016 Mar;10(3):761-77. doi: 10.1038/ismej.2015.153. Epub 2015 Sep 25.
Recent physiological and ecological studies have challenged the long-held belief that microbial metabolism of molecular hydrogen (H2) is a niche process. To gain a broader insight into the importance of microbial H2 metabolism, we comprehensively surveyed the genomic and metagenomic distribution of hydrogenases, the reversible enzymes that catalyse the oxidation and evolution of H2. The protein sequences of 3286 non-redundant putative hydrogenases were curated from publicly available databases. These metalloenzymes were classified into multiple groups based on (1) amino acid sequence phylogeny, (2) metal-binding motifs, (3) predicted genetic organisation and (4) reported biochemical characteristics. Four groups (22 subgroups) of [NiFe]-hydrogenase, three groups (6 subtypes) of [FeFe]-hydrogenases and a small group of [Fe]-hydrogenases were identified. We predict that this hydrogenase diversity supports H2-based respiration, fermentation and carbon fixation processes in both oxic and anoxic environments, in addition to various H2-sensing, electron-bifurcation and energy-conversion mechanisms. Hydrogenase-encoding genes were identified in 51 bacterial and archaeal phyla, suggesting strong pressure for both vertical and lateral acquisition. Furthermore, hydrogenase genes could be recovered from diverse terrestrial, aquatic and host-associated metagenomes in varying proportions, indicating a broad ecological distribution and utilisation. Oxygen content (pO2) appears to be a central factor driving the phylum- and ecosystem-level distribution of these genes. In addition to compounding evidence that H2 was the first electron donor for life, our analysis suggests that the great diversification of hydrogenases has enabled H2 metabolism to sustain the growth or survival of microorganisms in a wide range of ecosystems to the present day. This work also provides a comprehensive expanded system for classifying hydrogenases and identifies new prospects for investigating H2 metabolism.
最近的生理学和生态学研究对长期以来认为分子氢(H₂)的微生物代谢是一个小众过程的观点提出了挑战。为了更全面地了解微生物H₂代谢的重要性,我们全面调查了氢化酶的基因组和宏基因组分布,氢化酶是催化H₂氧化和生成的可逆酶。从公开可用的数据库中整理出3286个非冗余假定氢化酶的蛋白质序列。这些金属酶根据以下因素分为多个组:(1)氨基酸序列系统发育,(2)金属结合基序,(3)预测的基因组织,以及(4)报道的生化特性。鉴定出了四组(22个亚组)[NiFe] - 氢化酶、三组(6个亚型)[FeFe] - 氢化酶和一小组[Fe] - 氢化酶。我们预测,这种氢化酶的多样性除了支持各种H₂传感、电子分叉和能量转换机制外,还在有氧和无氧环境中支持基于H₂的呼吸、发酵和碳固定过程。在51个细菌和古菌门中鉴定出了氢化酶编码基因,这表明垂直和横向获取都面临强大压力。此外,氢化酶基因可以从不同比例的各种陆地、水生和宿主相关宏基因组中回收,这表明其具有广泛的生态分布和利用。氧含量(pO₂)似乎是驱动这些基因在门和生态系统水平分布的核心因素。除了越来越多的证据表明H₂是生命的第一个电子供体外,我们的分析表明,氢化酶的巨大多样化使H₂代谢能够维持微生物在广泛生态系统中的生长或生存直至今日。这项工作还提供了一个全面扩展的氢化酶分类系统,并确定了研究H₂代谢的新前景。