Wu Genfu, Li Ning, Mao Yinting, Zhou Guangqi, Gao Haichun
Institute of Microbiology and College of Life Sciences, Zhejiang University Hangzhou, China.
Front Microbiol. 2015 Apr 28;6:374. doi: 10.3389/fmicb.2015.00374. eCollection 2015.
Hydrogen sulfide (H2S) has been recognized as a physiological mediator with a variety of functions across all domains of life. In this study, mechanisms of endogenous H2S generation in Shewanella oneidensis were investigated. As a research model with highly diverse anaerobic respiratory pathways, the microorganism is able to produce H2S by respiring on a variety of sulfur-containing compounds with SirACD and PsrABC enzymatic complexes, as well as through cysteine degradation with three enzymes, MdeA, SO_1095, and SseA. We showed that the SirACD and PsrABC complexes, which are predominantly, if not exclusively, responsible for H2S generation via respiration of sulfur species, do not interplay with each other. Strikingly, a screen for regulators controlling endogenous H2S generation by transposon mutagenesis identified global regulator Crp to be essential to all H2S-generating processes. In contrast, Fnr and Arc, two other global regulators that have a role in respiration, are dispensable in regulating H2S generation via respiration of sulfur species. Interestingly, Arc is involved in the H2S generation through cysteine degradation by repressing expression of the mdeA gene. We further showed that expression of the sirA and psrABC operons is subjected to direct regulation of Crp, but the mechanisms underlying the requirement of Crp for H2S generation through cysteine degradation remain elusive.
硫化氢(H₂S)已被公认为一种生理介质,在生命的各个领域都具有多种功能。在本研究中,我们调查了希瓦氏菌中内源性H₂S生成的机制。作为一种具有高度多样化厌氧呼吸途径的研究模型,该微生物能够通过SirACD和PsrABC酶复合物对多种含硫化合物进行呼吸作用来产生H₂S,以及通过三种酶MdeA、SO_1095和SseA进行半胱氨酸降解来产生H₂S。我们发现,主要(如果不是唯一)负责通过硫物种呼吸产生H₂S的SirACD和PsrABC复合物彼此之间没有相互作用。引人注目的是,通过转座子诱变筛选控制内源性H₂S生成的调节因子,发现全局调节因子Crp对所有H₂S生成过程至关重要。相比之下,另外两个在呼吸作用中起作用的全局调节因子Fnr和Arc在通过硫物种呼吸调节H₂S生成方面是可有可无的。有趣的是,Arc通过抑制mdeA基因的表达参与了通过半胱氨酸降解产生H₂S的过程。我们进一步表明,sirA和psrABC操纵子的表达受到Crp的直接调控,但Crp通过半胱氨酸降解产生H₂S的需求背后的机制仍然难以捉摸。