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Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release
Yeasts undergo intensive metabolic changes during the early stages of fermentation. Previous reports suggest the early production of hydrogen sulfide (H(2)S) is associated with the release of a range of volatile sulfur compounds (VSCs), as well as the production of varietal thiol compounds 3-sulfany...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569440/ https://www.ncbi.nlm.nih.gov/pubmed/37279910 http://dx.doi.org/10.1093/femsyr/foad031 |
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author | Hou, Ruoyu Jelley, Rebecca E van Leeuwen, Katryna A Pinu, Farhana R Fedrizzi, Bruno Deed, Rebecca C |
author_facet | Hou, Ruoyu Jelley, Rebecca E van Leeuwen, Katryna A Pinu, Farhana R Fedrizzi, Bruno Deed, Rebecca C |
author_sort | Hou, Ruoyu |
collection | PubMed |
description | Yeasts undergo intensive metabolic changes during the early stages of fermentation. Previous reports suggest the early production of hydrogen sulfide (H(2)S) is associated with the release of a range of volatile sulfur compounds (VSCs), as well as the production of varietal thiol compounds 3-sulfanylhexan-1-ol (3SH) and 3-sulfanylhexyl acetate (3SHA) from six-carbon precursors, including (E)-hex-2-enal. In this study, we investigated the early H(2)S potential, VSCs/thiol output, and precursor metabolism of 11 commonly used laboratory and commercial Saccharomyces cerevisiae strains in chemically defined synthetic grape medium (SGM) within 12 h after inoculation. Considerable variability in early H(2)S potential was observed among the strains surveyed. Chemical profiling suggested that early H(2)S production correlates with the production of dimethyl disulfide, 2-mercaptoethanol, and diethyl sulfide, but not with 3SH or 3SHA. All strains were capable of metabolizing (E)-hex-2-enal, while the F15 strain showed significantly higher residue at 12 h. Early production of 3SH, but not 3SHA, can be detected in the presence of exogenous (E)-hex-2-enal and H(2)S. Therefore, the natural variability of early yeast H(2)S production contributes to the early output of selected VSCs, but the threshold of which is likely not high enough to contribute substantially to free varietal thiols in SGM. |
format | Online Article Text |
id | pubmed-10569440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105694402023-10-13 Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release Hou, Ruoyu Jelley, Rebecca E van Leeuwen, Katryna A Pinu, Farhana R Fedrizzi, Bruno Deed, Rebecca C FEMS Yeast Res Research Article Yeasts undergo intensive metabolic changes during the early stages of fermentation. Previous reports suggest the early production of hydrogen sulfide (H(2)S) is associated with the release of a range of volatile sulfur compounds (VSCs), as well as the production of varietal thiol compounds 3-sulfanylhexan-1-ol (3SH) and 3-sulfanylhexyl acetate (3SHA) from six-carbon precursors, including (E)-hex-2-enal. In this study, we investigated the early H(2)S potential, VSCs/thiol output, and precursor metabolism of 11 commonly used laboratory and commercial Saccharomyces cerevisiae strains in chemically defined synthetic grape medium (SGM) within 12 h after inoculation. Considerable variability in early H(2)S potential was observed among the strains surveyed. Chemical profiling suggested that early H(2)S production correlates with the production of dimethyl disulfide, 2-mercaptoethanol, and diethyl sulfide, but not with 3SH or 3SHA. All strains were capable of metabolizing (E)-hex-2-enal, while the F15 strain showed significantly higher residue at 12 h. Early production of 3SH, but not 3SHA, can be detected in the presence of exogenous (E)-hex-2-enal and H(2)S. Therefore, the natural variability of early yeast H(2)S production contributes to the early output of selected VSCs, but the threshold of which is likely not high enough to contribute substantially to free varietal thiols in SGM. Oxford University Press 2023-06-05 /pmc/articles/PMC10569440/ /pubmed/37279910 http://dx.doi.org/10.1093/femsyr/foad031 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hou, Ruoyu Jelley, Rebecca E van Leeuwen, Katryna A Pinu, Farhana R Fedrizzi, Bruno Deed, Rebecca C Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title | Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title_full | Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title_fullStr | Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title_full_unstemmed | Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title_short | Hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
title_sort | hydrogen sulfide production during early yeast fermentation correlates with volatile sulfur compound biogenesis but not thiol release |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569440/ https://www.ncbi.nlm.nih.gov/pubmed/37279910 http://dx.doi.org/10.1093/femsyr/foad031 |
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