Osmotic stress as a factor for regulating <i>E. coli</i> hydrogenase activity and enhancing H<sub>2</sub> production during mixed carbon sources fermentation
{"title":"Osmotic stress as a factor for regulating <i>E. coli</i> hydrogenase activity and enhancing H<sub>2</sub> production during mixed carbon sources fermentation","authors":"Anush Babayan, Anait Vassilian, Karen Trchounian","doi":"10.3934/microbiol.2023037","DOIUrl":null,"url":null,"abstract":"<abstract> <p><italic>Escherichia coli</italic> performs mixed-acid fermentation and produces molecular hydrogen (H<sub>2</sub>) via reversible hydrogenases (Hyd). H<sub>2</sub> producing activity was investigated during hyper- and hypo-osmotic stress conditions when a mixture of carbon sources (glucose and glycerol) was fermented at different pHs. Hyper-osmotic stress decreased H<sub>2</sub> production rate (V<sub>H2</sub>) ~30 % in wild type at pH 7.5 when glucose was supplemented, while addition of formate stimulated V<sub>H2</sub> ~45% compared to hypo-stress conditions. Only in <italic>hyfG</italic> in formate assays was V<sub>H2</sub> inhibited ~25% compared to hypo-stress conditions. In hypo-stress conditions addition of glycerol increased V<sub>H2</sub> ~2 and 3 fold in <italic>hybC</italic> and <italic>hyfG</italic> mutants, respectively, compared to wild type. At pH 6.5 hyper-osmotic stress stimulated V<sub>H2</sub> ~2 fold in all strains except <italic>hyaB</italic> mutant when glucose was supplemented, while in formate assays significant stimulation (~3 fold) was determined in <italic>hybC</italic> mutant. At pH 5.5 hyper-osmotic stress inhibited V<sub>H2</sub> ~30% in wild type when glucose was supplemented, but in formate assays it was stimulated in all strains except <italic>hyfG</italic>. Taken together, it can be concluded that, depending on external pH and absence of Hyd enzymes in stationary-phase-grown osmotically stressed <italic>E. coli</italic> cells, H<sub>2</sub> production can be stimulated significantly which can be applied in developing H<sub>2</sub> production biotechnology.</p> </abstract>","PeriodicalId":46108,"journal":{"name":"AIMS Microbiology","volume":"27 1","pages":"0"},"PeriodicalIF":2.7000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIMS Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3934/microbiol.2023037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Escherichia coli performs mixed-acid fermentation and produces molecular hydrogen (H2) via reversible hydrogenases (Hyd). H2 producing activity was investigated during hyper- and hypo-osmotic stress conditions when a mixture of carbon sources (glucose and glycerol) was fermented at different pHs. Hyper-osmotic stress decreased H2 production rate (VH2) ~30 % in wild type at pH 7.5 when glucose was supplemented, while addition of formate stimulated VH2 ~45% compared to hypo-stress conditions. Only in hyfG in formate assays was VH2 inhibited ~25% compared to hypo-stress conditions. In hypo-stress conditions addition of glycerol increased VH2 ~2 and 3 fold in hybC and hyfG mutants, respectively, compared to wild type. At pH 6.5 hyper-osmotic stress stimulated VH2 ~2 fold in all strains except hyaB mutant when glucose was supplemented, while in formate assays significant stimulation (~3 fold) was determined in hybC mutant. At pH 5.5 hyper-osmotic stress inhibited VH2 ~30% in wild type when glucose was supplemented, but in formate assays it was stimulated in all strains except hyfG. Taken together, it can be concluded that, depending on external pH and absence of Hyd enzymes in stationary-phase-grown osmotically stressed E. coli cells, H2 production can be stimulated significantly which can be applied in developing H2 production biotechnology.