HyfF subunit of hydrogenase 4 is crucial for regulating FOF1 dependent proton/potassium fluxes during fermentation of various concentrations of glucose.
{"title":"HyfF subunit of hydrogenase 4 is crucial for regulating F<sub>O</sub>F<sub>1</sub> dependent proton/potassium fluxes during fermentation of various concentrations of glucose.","authors":"Liana Vanyan, Karen Trchounian","doi":"10.1007/s10863-022-09930-x","DOIUrl":null,"url":null,"abstract":"<p><p>Escherichia coli anaerobically ferment glucose and perform proton/potassium exchange at pH 7.5. The role of hyf (hydrogenase 4) subunits (HyfBDF) in sensing different concentrations of glucose (2 g L<sup>-1</sup> or 8 g L<sup>-1</sup>) via regulating H<sup>+</sup>/K<sup>+</sup> exchange was studied. HyfB, HyfD and HyfF part of a protein family of NADH-ubiquinone oxidoreductase ND2, ND4 and ND5 subunits is predicted to operate as proton pump. Specific growth rate was optimal in wild type and mutants grown on 2 g L<sup>-1</sup> glucose reaching ~ 0.8 h<sup>-1</sup>. It was shown that in wild type cells proton but not potassium fluxes were stimulated ~ 1.7 fold reaching up to 1.95 mmol/min when cells were grown in the presence of 8 g L<sup>-1</sup> glucose. Interestingly, cells grown on peptone only had similar proton/potassium fluxes as grown on 2 g L<sup>-1</sup>glucose. H<sup>+</sup>/K<sup>+</sup> fluxes of the cells grown on 2 g L<sup>-1</sup> but not 8 g L<sup>-1</sup> glucose depend on externally added glucose concentration in the assays. DCCD-sensitive H<sup>+</sup> fluxes were tripled and K<sup>+</sup> fluxes doubled in wild type cells grown on 8 g L<sup>-1</sup> glucose compared to 2 g L<sup>-1</sup> when in the assays 2 g L<sup>-1</sup>glucose was added. Interestingly, in hyfF mutant when cells were grown on 2 g L<sup>-1</sup>glucose and in 2 g L<sup>-1</sup> assays DCCD-sensitive fluxes were not determined compared to wild type while in hyfD mutant it was doubled reaching up to 0.657 mmol/min. In hyf mutants DCCD-sensitive K<sup>+</sup> fluxes were stimulated in hyfD and hyfF mutants compared to wild type but depend on external glucose concentration. DCCD-sensitive H<sup>+</sup>/K<sup>+</sup> ratio was equal to ~ 2 except hyfF mutant grown and assayed on 2 g L<sup>-1</sup>glucose while in 8 g L<sup>-1</sup> conditions role of hyfB and hyfD is considered. Taken together it can be concluded that Hyd-4 subunits (HyfBDF) play key role in sensing glucose concentration for regulation of DCCD-sensitive H<sup>+</sup>/K<sup>+</sup> fluxes for maintaining proton motive force generation.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10863-022-09930-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/2/2 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 4
Abstract
Escherichia coli anaerobically ferment glucose and perform proton/potassium exchange at pH 7.5. The role of hyf (hydrogenase 4) subunits (HyfBDF) in sensing different concentrations of glucose (2 g L-1 or 8 g L-1) via regulating H+/K+ exchange was studied. HyfB, HyfD and HyfF part of a protein family of NADH-ubiquinone oxidoreductase ND2, ND4 and ND5 subunits is predicted to operate as proton pump. Specific growth rate was optimal in wild type and mutants grown on 2 g L-1 glucose reaching ~ 0.8 h-1. It was shown that in wild type cells proton but not potassium fluxes were stimulated ~ 1.7 fold reaching up to 1.95 mmol/min when cells were grown in the presence of 8 g L-1 glucose. Interestingly, cells grown on peptone only had similar proton/potassium fluxes as grown on 2 g L-1glucose. H+/K+ fluxes of the cells grown on 2 g L-1 but not 8 g L-1 glucose depend on externally added glucose concentration in the assays. DCCD-sensitive H+ fluxes were tripled and K+ fluxes doubled in wild type cells grown on 8 g L-1 glucose compared to 2 g L-1 when in the assays 2 g L-1glucose was added. Interestingly, in hyfF mutant when cells were grown on 2 g L-1glucose and in 2 g L-1 assays DCCD-sensitive fluxes were not determined compared to wild type while in hyfD mutant it was doubled reaching up to 0.657 mmol/min. In hyf mutants DCCD-sensitive K+ fluxes were stimulated in hyfD and hyfF mutants compared to wild type but depend on external glucose concentration. DCCD-sensitive H+/K+ ratio was equal to ~ 2 except hyfF mutant grown and assayed on 2 g L-1glucose while in 8 g L-1 conditions role of hyfB and hyfD is considered. Taken together it can be concluded that Hyd-4 subunits (HyfBDF) play key role in sensing glucose concentration for regulation of DCCD-sensitive H+/K+ fluxes for maintaining proton motive force generation.
大肠杆菌在pH 7.5条件下厌氧发酵葡萄糖并进行质子/钾交换。研究了氢化酶4亚基(HyfBDF)通过调节H+/K+交换来感知不同浓度葡萄糖(2 g L-1或8 g L-1)的作用。HyfB, HyfD和HyfF是nadh -泛醌氧化还原酶ND2, ND4和ND5亚基蛋白家族的一部分,预计作为质子泵起作用。野生型和突变体在2 g L-1葡萄糖条件下生长,达到~ 0.8 h-1,比生长率最佳。结果表明,在8 g L-1葡萄糖的作用下,野生型细胞的质子通量增加1.7倍,达到1.95 mmol/min。有趣的是,在蛋白胨上生长的细胞与在2g l -1葡萄糖上生长的细胞具有相似的质子/钾通量。在2 g L-1而不是8 g L-1葡萄糖环境中生长的细胞H+/K+通量取决于外部添加的葡萄糖浓度。与添加2 g L-1葡萄糖时相比,在8 g L-1葡萄糖中生长的野生型细胞对dccd敏感的H+通量增加了两倍,K+通量增加了一倍。有趣的是,在hyfF突变体中,当细胞在2 g L-1葡萄糖上生长时,在2 g L-1试验中,与野生型相比,dccd敏感通量没有测定,而在hyfD突变体中,dccd敏感通量增加了一倍,达到0.657 mmol/min。在hyf突变体中,与野生型相比,hyfD和hyfF突变体对dccd敏感的K+通量受到刺激,但依赖于外部葡萄糖浓度。除hyfF突变体在2 g L-1葡萄糖条件下生长和测定外,对dccd敏感的H+/K+比值均为~ 2,而在8 g L-1葡萄糖条件下则考虑hyfB和hyfD的作用。综上所述,可以得出结论,氢-4亚基(HyfBDF)在感知葡萄糖浓度中发挥关键作用,调节dccd敏感的H+/K+通量,维持质子动力的产生。