{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T14:00:47Z","timestamp":1791986447559,"version":"4.4.0"},"reference-count":63,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2018,2,1]],"date-time":"2018-02-01T00:00:00Z","timestamp":1517443200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Antioxidants &amp; Redox Signaling"],"published-print":{"date-parts":[[2018,2]]},"abstract":"<jats:sec>\n                    <jats:title>Aims:<\/jats:title>\n                    <jats:p>\n                      The transsulfuration pathway enzymes cystathionine beta-synthase (CBS) and cystathionine gamma-lyase are thought to be the major source of hydrogen sulfide (H\n                      <jats:sub>2<\/jats:sub>\n                      S). In this study, we assessed the role of CBS in H\n                      <jats:sub>2<\/jats:sub>\n                      S biogenesis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      We show that despite discouraging enzyme kinetics of alternative H\n                      <jats:sub>2<\/jats:sub>\n                      S-producing reactions utilizing cysteine compared with the canonical condensation of serine and homocysteine, our simulations of substrate competitions at biologically relevant conditions suggest that cysteine is able to partially compete with serine on CBS, thus leading to generation of appreciable amounts of H\n                      <jats:sub>2<\/jats:sub>\n                      S. The leading H\n                      <jats:sub>2<\/jats:sub>\n                      S-producing reaction is condensation of cysteine with homocysteine, while cysteine desulfuration plays a dominant role when cysteine is more abundant than serine and homocysteine is limited. We found that the serine-to-cysteine ratio is the main determinant of CBS H\n                      <jats:sub>2<\/jats:sub>\n                      S productivity. Abundance of cysteine over serine, for example, in plasma, allowed for up to 43% of CBS activity being responsible for H\n                      <jats:sub>2<\/jats:sub>\n                      S production, while excess of serine typical for intracellular levels effectively limited such activity to less than 1.5%. CBS also produced lanthionine from serine and cysteine and a third of lanthionine coming from condensation of two cysteines contributed to the H\n                      <jats:sub>2<\/jats:sub>\n                      S pool.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Innovation:<\/jats:title>\n                    <jats:p>\n                      Our study characterizes the H\n                      <jats:sub>2<\/jats:sub>\n                      S-producing potential of CBS under biologically relevant conditions and highlights the serine-to-cysteine ratio as the main determinant of H\n                      <jats:sub>2<\/jats:sub>\n                      S production by CBS\n                      <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>\n                      Our data clarify the function of CBS in H\n                      <jats:sub>2<\/jats:sub>\n                      S biogenesis and the role of thioethers as surrogate H\n                      <jats:sub>2<\/jats:sub>\n                      S markers.\n                      <jats:italic toggle=\"yes\">Antioxid. Redox Signal.<\/jats:italic>\n                      28, 311\u2013323.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1089\/ars.2017.7009","type":"journal-article","created":{"date-parts":[[2017,9,6]],"date-time":"2017-09-06T03:50:23Z","timestamp":1504669823000},"page":"311-323","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":69,"title":["Biogenesis of Hydrogen Sulfide and Thioethers by Cystathionine Beta-Synthase"],"prefix":"10.1177","volume":"28","author":[{"given":"Tomas","family":"Majtan","sequence":"first","affiliation":[{"name":"University of Colorado"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jakub","family":"Krijt","sequence":"additional","affiliation":[{"name":"Charles University-First Faculty of Medicine and General University Hospital in Prague","place":["Czech Republic"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jitka","family":"Sokolov\u00e1","sequence":"additional","affiliation":[{"name":"Charles University-First Faculty of Medicine and General University Hospital in Prague","place":["Czech Republic"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michaela","family":"K\u0159\u00ed\u017ekov\u00e1","sequence":"additional","affiliation":[{"name":"Charles University-First Faculty of Medicine and General University Hospital in Prague","place":["Czech Republic"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria A.","family":"Ralat","sequence":"additional","affiliation":[{"name":"University of Florida"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jana","family":"Kent","sequence":"additional","affiliation":[{"name":"University of Colorado"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"suffix":"III","given":"Jesse F.","family":"Gregory","sequence":"additional","affiliation":[{"name":"University of Florida"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Viktor","family":"Ko\u017eich","sequence":"additional","affiliation":[{"name":"Charles University-First Faculty of Medicine and General University Hospital in Prague","place":["Czech Republic"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jan P.","family":"Kraus","sequence":"additional","affiliation":[{"name":"University of Colorado"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2018,2,1]]},"reference":[{"key":"e_1_3_4_2_2","doi-asserted-by":"publisher","DOI":"10.1523\/JNEUROSCI.16-03-01066.1996"},{"key":"e_1_3_4_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.abb.2004.08.024"},{"key":"e_1_3_4_4_2","doi-asserted-by":"publisher","DOI":"10.1111\/bph.12171"},{"key":"e_1_3_4_5_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0300-9084(76)80351-3"},{"key":"e_1_3_4_6_2","first-page":"1","article-title":"The beta-replacement-specific pyridoxal-P-dependent lyases","volume":"56","author":"Braunstein AE","year":"1984","unstructured":"Braunstein AE, and Goryachenkova EV. 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