{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,24]],"date-time":"2026-06-24T23:57:31Z","timestamp":1782345451198,"version":"3.54.5"},"reference-count":47,"publisher":"Microbiology Society","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,4,1]]},"abstract":"<jats:p>\n                    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,\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.19993\" xlink:type=\"simple\">Pusillimonas ginsengisoli<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    SBSA, which is found to oxidize thiosulfate via the formation of tetrathionate as an intermediate. The 4.7\u2009Mb SBSA genome was found to encompass a\n                    <jats:italic>soxCDYZAXOB<\/jats:italic>\n                    operon, plus single thiosulfate dehydrogenase (\n                    <jats:italic>tsdA<\/jats:italic>\n                    ) and sulfite\u202f:\u202facceptor oxidoreductase (\n                    <jats:italic>sorAB<\/jats:italic>\n                    ) genes. Recombination-based knockout of\n                    <jats:italic>tsdA<\/jats:italic>\n                    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\n                    <jats:italic>sox<\/jats:italic>\n                    genes. The \u2206\n                    <jats:italic>soxYZ<\/jats:italic>\n                    and \u2206\n                    <jats:italic>soxXA<\/jats:italic>\n                    knockout mutants exhibited a wild-type-like phenotype for thiosulfate\/tetrathionate oxidation, whereas \u2206\n                    <jats:italic>soxB,<\/jats:italic>\n                    \u2206\n                    <jats:italic>soxCD<\/jats:italic>\n                    and\n                    <jats:italic>soxO<\/jats:italic>\n                    ::Kan\n                    <jats:sup>R<\/jats:sup>\n                    mutants only oxidized thiosulfate up to tetrathionate intermediate and had complete impairment in tetrathionate oxidation. The substrate-dependent O\n                    <jats:sub>2<\/jats:sub>\n                    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\u202f:\u202ftetrathionate coupling in\n                    <jats:italic>\n                      <jats:named-content content-type=\"species\">\n                        <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/doi.org\/10.1601\/nm.19993\" xlink:type=\"simple\">P. ginsengisoli<\/jats:ext-link>\n                      <\/jats:named-content>\n                    <\/jats:italic>\n                    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\u202f:\u202fsulfodisulfane molecules) may proceed via the iterative action of\n                    <jats:italic>soxBCD<\/jats:italic>\n                    .\n                  <\/jats:p>","DOI":"10.1099\/mic.0.000890","type":"journal-article","created":{"date-parts":[[2020,1,30]],"date-time":"2020-01-30T12:12:51Z","timestamp":1580386371000},"page":"386-397","source":"Crossref","is-referenced-by-count":12,"title":["Molecular mechanism of sulfur chemolithotrophy in the betaproteobacterium Pusillimonas ginsengisoli SBSA"],"prefix":"10.1099","volume":"166","author":[{"given":"Subhrangshu","family":"Mandal","sequence":"first","affiliation":[{"name":"Department of Microbiology, Bose Institute, P-1\/12 CIT Scheme VIIM, Kolkata-700054, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Moidu Jameela","family":"Rameez","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Bose Institute, P-1\/12 CIT Scheme VIIM, Kolkata-700054, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sumit","family":"Chatterjee","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Bose Institute, P-1\/12 CIT Scheme VIIM, Kolkata-700054, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jagannath","family":"Sarkar","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Bose Institute, P-1\/12 CIT Scheme VIIM, Kolkata-700054, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2339-8686","authenticated-orcid":false,"given":"Prosenjit","family":"Pyne","sequence":"additional","affiliation":[{"name":"Present address: National Institute of Cholera and Enteric Diseases (NICED), P- C.I.T. 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