Integrated Multiomics Elucidates Glutathione Metabolic Regulation in a Marine Aromatic Probiotic Yeast Meyerozyma guilliermondii GXDK6 under Salt Stress
{"title":"Integrated Multiomics Elucidates Glutathione Metabolic Regulation in a Marine Aromatic Probiotic Yeast Meyerozyma guilliermondii GXDK6 under Salt Stress","authors":"Zhenze Li, , , Hao Sun, , , Xinglin Chen, , , Pai Peng, , , Huijie Sun, , , Shipeng Chen, , , Muhammad Kashif, , , Ruilin Xie, , , Qi Liang, , , Yujia Luo, , , Tingmei Li, , , Qian Ou, , , Sheng Huang, , and , Chengjian Jiang*, ","doi":"10.1021/acsomega.5c07376","DOIUrl":null,"url":null,"abstract":"<p >High-salt environments impose significant oxidative stress on microorganisms by disrupting redox homeostasis, necessitating efficient adaptive mechanisms such as glutathione (GSH) metabolism. <i>Meyerozyma guilliermondii</i> GXDK6, a marine-derived multistress-tolerant probiotic yeast, exhibits robust salt tolerance; however, the molecular basis of its GSH-mediated regulatory networks under salt stress remains unexplored. In this study, a comprehensive multiomics approach, integrating whole-genome sequencing, transcriptomics, and proteomics profiling, along with targeted physiological assays, was employed to investigate GSH metabolic regulation under salt stress. Genome-wide analysis identified 55 genes involved in other amino acid metabolism, with transcriptomic and proteomic profiling revealing salt-induced upregulation of key GSH biosynthetic genes (<i>GSS</i>, <i>cysK</i>_2, and <i>glyA</i>) and downregulation of degradation-related gene <i>ggt</i>_2. Moreover, transcript and protein level analyses demonstrated the activation of the biosynthetic pathway. Intracellular GSH content exhibited a biphasic response, with a 39.75% reduction at 5% NaCl, followed by a 53.01% increase at 10% NaCl. Glutathione S-transferase enzyme activity was significantly increased under salt stress, highlighting its role in cellular detoxification. Furthermore, exogenous application of GSH (10 mg/L) markedly improved halotolerance, resulting in a 52.7-fold increase in colony-forming units under 10% NaCl conditions. These findings highlight the crucial role of GSH in maintaining redox homeostasis and provide valuable insights for engineering microbial resilience in hypersaline environments.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"10 41","pages":"48965–48975"},"PeriodicalIF":4.3000,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acsomega.5c07376","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsomega.5c07376","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
High-salt environments impose significant oxidative stress on microorganisms by disrupting redox homeostasis, necessitating efficient adaptive mechanisms such as glutathione (GSH) metabolism. Meyerozyma guilliermondii GXDK6, a marine-derived multistress-tolerant probiotic yeast, exhibits robust salt tolerance; however, the molecular basis of its GSH-mediated regulatory networks under salt stress remains unexplored. In this study, a comprehensive multiomics approach, integrating whole-genome sequencing, transcriptomics, and proteomics profiling, along with targeted physiological assays, was employed to investigate GSH metabolic regulation under salt stress. Genome-wide analysis identified 55 genes involved in other amino acid metabolism, with transcriptomic and proteomic profiling revealing salt-induced upregulation of key GSH biosynthetic genes (GSS, cysK_2, and glyA) and downregulation of degradation-related gene ggt_2. Moreover, transcript and protein level analyses demonstrated the activation of the biosynthetic pathway. Intracellular GSH content exhibited a biphasic response, with a 39.75% reduction at 5% NaCl, followed by a 53.01% increase at 10% NaCl. Glutathione S-transferase enzyme activity was significantly increased under salt stress, highlighting its role in cellular detoxification. Furthermore, exogenous application of GSH (10 mg/L) markedly improved halotolerance, resulting in a 52.7-fold increase in colony-forming units under 10% NaCl conditions. These findings highlight the crucial role of GSH in maintaining redox homeostasis and provide valuable insights for engineering microbial resilience in hypersaline environments.
ACS OmegaChemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍:
ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.