Molecular mechanism of sulfur chemolithotrophy in the betaproteobacterium Pusillimonas ginsengisoli SBSA
| Autor: | Sumit Chatterjee, Prosenjit Pyne, Rahul Shaw, Jagannath Sarkar, Sabyasachi Bhattacharya, Moidu Jameela Rameez, Subhrangshu Mandal, Wriddhiman Ghosh |
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| Rok vydání: | 2020 |
| Předmět: |
Tetrathionate
Thiosulfate chemistry.chemical_classification 0303 health sciences Pusillimonas ginsengisoli 030306 microbiology Operon chemistry.chemical_element Glutathione medicine.disease_cause Microbiology Thiosulfate dehydrogenase Sulfur 03 medical and health sciences chemistry.chemical_compound chemistry Biochemistry Oxidoreductase medicine 030304 developmental biology |
| Zdroj: | Microbiology. 166:386-397 |
| ISSN: | 1465-2080 1350-0872 |
| Popis: | Chemolithotrophic sulfur oxidation represents a significant part of the biogeochemical cycling of this element. Due to its long evolutionary history, this ancient metabolism is well known for its extensive mechanistic and phylogenetic diversification across a diverse taxonomic spectrum. Here we carried out whole-genome sequencing and analysis of a new betaproteobacterial isolate, Pusillimonas ginsengisoli SBSA, which is found to oxidize thiosulfate via the formation of tetrathionate as an intermediate. The 4.7 Mb SBSA genome was found to encompass a soxCDYZAXOB operon, plus single thiosulfate dehydrogenase (tsdA) and sulfite : acceptor oxidoreductase (sorAB) genes. Recombination-based knockout of tsdA revealed that the entire thiosulfate is first converted to tetrathionate by the activity of thiosulfate dehydrogenase (TsdA) and the Sox pathway is not functional in this bacterium despite the presence of all necessary sox genes. The ∆soxYZ and ∆soxXA knockout mutants exhibited a wild-type-like phenotype for thiosulfate/tetrathionate oxidation, whereas ∆soxB, ∆soxCD and soxO::KanR mutants only oxidized thiosulfate up to tetrathionate intermediate and had complete impairment in tetrathionate oxidation. The substrate-dependent O2 consumption rate of whole cells and the sulfur-oxidizing enzyme activities of cell-free extracts, measured in the presence/absence of thiol inhibitors/glutathione, indicated that glutathione plays a key role in SBSA tetrathionate oxidation. The present findings collectively indicate that the potential glutathione : tetrathionate coupling in P. ginsengisoli involves a novel enzymatic component, which is different from the dual-functional thiol dehydrotransferase (ThdT), while subsequent oxidation of the sulfur intermediates produced (e.g. glutathione : sulfodisulfane molecules) may proceed via the iterative action of soxBCD . |
| Databáze: | OpenAIRE |
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