Adrian Lorenz, Sawers R Gary, Deobald Darja
Helmholtz Centre for Environmental Research - UFZ, Department Molecular Environmental Biotechnology, Leipzig, Germany; Chair of Geobiotechnology, Technische Universität Berlin, Berlin, Germany.
Institute for Biology/Microbiology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Adv Microb Physiol. 2025;86:141-173. doi: 10.1016/bs.ampbs.2024.12.001. Epub 2025 Feb 6.
Dehalococcoides strains grow obligately by respiration with hydrogen as an electron donor and halogenated compounds as terminal electron acceptors, catalysed by a single membrane-integrated protein supercomplex. Many insights have been gained into the respiratory complex based on physiological experiments, biochemical analyses, genome sequencing, and proteomics. Recent data acquired from activity tests with deuterated water and whole cells revealed the mode of energy conservation by this respiratory complex. The data shows that the proton required for periplasmic dehalogenation originates from inside the cell, suggesting an electrogenic protonation of the electron acceptor, while two protons are released into the periplasm by hydrogen oxidation. This surprisingly simple mechanism of pmf generation aligns with the subunit composition of the respiratory complex, the orientation of the subunits in the membrane, the absence of quinones as electron mediators, the rigidity of the cell membrane, as evidenced by its phospholipid fatty acid composition, and with proton channels formed by protonatable amino acid residues identified in the AlphaFold2-predicted structure of one of the membrane-spanning subunits. The respiration model is characterised by: (i) electrogenic protonation of the electron acceptor; (ii) reliance on a single protein complex for pmf generation without quinones; (iii) lack of transmembrane cytochromes; (iv) presence of both redox-active centres on the same side of the membrane, both facing the periplasm; and (v) restriction of the electron flow to periplasmic subunits of the respiratory complex. This type of respiration may represent an ancestral, quinone-free mechanism, offering inspiring new biotechnological applications.
脱卤球菌菌株通过以氢气作为电子供体、卤代化合物作为末端电子受体进行呼吸作用来专性生长,这一过程由单一的膜整合蛋白超复合体催化。基于生理学实验、生化分析、基因组测序和蛋白质组学,人们对这种呼吸复合体有了许多深入了解。最近从使用重水和全细胞的活性测试中获得的数据揭示了这种呼吸复合体的能量守恒模式。数据表明,周质脱卤所需的质子源自细胞内部,这表明电子受体发生了产电质子化,而通过氢氧化作用有两个质子被释放到周质中。这种令人惊讶的简单质子动力势(pmf)产生机制与呼吸复合体的亚基组成、亚基在膜中的方向、不存在作为电子介质的醌、细胞膜的刚性(由其磷脂脂肪酸组成证明)以及在其中一个跨膜亚基的AlphaFold2预测结构中鉴定出的由可质子化氨基酸残基形成的质子通道相一致。该呼吸模型的特点是:(i)电子受体的产电质子化;(ii)依赖单一蛋白复合体产生质子动力势而无需醌;(iii)缺乏跨膜细胞色素;(iv)氧化还原活性中心都在膜的同一侧,均面向周质;(v)电子流限于呼吸复合体的周质亚基。这种呼吸类型可能代表了一种无醌的原始机制,为生物技术应用提供了新的启发。