3.8 Article

Polysulfide metabolizing enzymes influence SqrR-mediated sulfide-induced transcription by impacting intracellular polysulfide dynamics

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PNAS NEXUS
卷 2, 期 3, 页码 -

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OXFORD UNIV PRESS
DOI: 10.1093/pnasnexus/pgad048

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polysulfide; sulfur metabolism; signal transduction; proteobacteria

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Sulfide plays crucial roles in physiological activities, and recent studies have shown its endogenous generation and metabolism into polysulfides inside cells. However, the relationship between polysulfide metabolism and sensing mechanisms is not well understood. This study investigates the role of polysulfide-metabolizing enzyme SQR on cellular polysulfide speciation and transcriptional regulation in Rhodobacter capsulatus. The results reveal a novel association between polysulfide metabolism and sensing mechanisms inside cells.
Sulfide plays essential roles in controlling various physiological activities in almost all organisms. Although recent evidence has demonstrated that sulfide is endogenously generated and metabolized into polysulfides inside the cells, the relationship between polysulfide metabolism and polysulfide-sensing mechanisms is not well understood. To better define this interplay between polysulfide metabolism and sensing in cells, we investigated the role of polysulfide-metabolizing enzymes such as sulfide:quinone oxidoreductase (SQR) on the temporal dynamics of cellular polysulfide speciation and on the transcriptional regulation by the persulfide-responsive transcription factor SqrR in Rhodobacter capsulatus. We show that disruption of the sqr gene resulted in the loss of SqrR repression by exogenous sulfide at longer culture times, which impacts the speciation of intracellular polysulfides of Delta sqr vs. wild-type strains. Both the attenuated response of SqrR and the change in polysulfide dynamics of the Delta sqr strain is fully reversed by the addition to cells of cystine-derived polysulfides, but not by glutathione disulfide (GSSG)-derived polysulfides. Furthermore, cysteine persulfide (CysSSH) yields a higher rate of oxidation of SqrR relative to glutathione persulfide (GSSH), which leads to DNA dissociation in vitro. The oxidation of SqrR was confirmed by a mass spectrometry-based kinetic profiling strategy that showed distinct polysulfide-crosslinked products obtained with CysSSH vs. GSSH. Taken together, these results establish a novel association between the metabolism of polysulfides and the mechanisms for polysulfide sensing inside the cells.

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