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首页> 外文期刊>Applied and Environmental Microbiology >Influence of Calcium Ion on Ethanol Tolerance of Saccharomyces bayanus and Alcoholic Fermentation by Yeasts
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Influence of Calcium Ion on Ethanol Tolerance of Saccharomyces bayanus and Alcoholic Fermentation by Yeasts

机译:钙离子对酵母菌耐乙醇性和酵母酒精发酵的影响

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The addition of Ca2+ (as CaCl2) in optimal concentrations (0.75 to 2.0 mM) to a fermentation medium with a trace contaminating concentration of Ca2+ (0.025 mM) led to the rapid production of higher concentrations of ethanol by Saccharomyces cerevisiae, Saccharomyces bayanus, and Kluyveromyces marxianus. The positive effect of calcium supplementation (0.75 mM) on alcoholic fermentation by S. bayanus was explained by the increase in its ethanol tolerance. The ethanol inhibition of growth and fermentation followed the equation μxi = μoi [1 - (X/Xmi)]ni, where μoi and μxi are, respectively, the specific growth (i = g) and fermentation (i = f) rates in the absence or presence of a concentration (X) of added ethanol, and Xmi is the maximal concentration of ethanol which allows growth or fermentation. The toxic power is given by ni. In Ca2+ - supplemented medium (0.75 mM), ng = 0.42 for growth and nf = 0.43 for fermentation compared with 0.52 and 0.55, respectively, in unsupplemented medium; for both media, Xmg = 10% (vol/vol) and Xmf = 13% (vol/vol). For lethal concentrations of ethanol, the specific death rates were minimal for cells that were grown and incubated with ethanol in medium with an optimal concentration of Ca2+, maximal for cells grown and incubated with ethanol in unsupplemented medium, and intermediate for cells grown in unsupplemented medium and incubated with ethanol in calcium-supplemented medium. The effect of Ca2+ on the acidification curve of energized cells in the presence of ethanol was found to be closely associated with its protective effect on growth, fermentation, and viability.
机译:向具有微量污染浓度的Ca2 +(0.025 mM)的发酵培养基中添加最适浓度(0.75至2.0 mM)的Ca2 +(作为CaCl2)导致酿酒酵母,巴氏酵母和马克斯克鲁维酵母。补钙(0.75 mM)对巴氏链球菌酒精发酵的积极作用可以通过其对乙醇的耐受性增加来解释。乙醇对生长和发酵的抑制作用遵循方程μxi=μoi[1--(X / Xmi)] ni,其中μoi和μxi分别是发酵罐中比生长(i = g)和发酵(i = f)的速率。不存在或不存在添加的乙醇浓度(X),且Xmi是允许生长或发酵的最大乙醇浓度。毒性是由ni给出的。在添加Ca2 +的培养基(0.75 mM)中,生长的ng = 0.42,发酵的nf = 0.43,而未添加的培养基分别为0.52和0.55;对于两种介质,Xmg = 10 %(体积/体积)和Xmf = 13 %(体积/体积)。对于致死浓度的乙醇,对于在具有最佳Ca2 +浓度的培养基中生长并与乙醇一起培养的细胞,单位死亡率是最小的;对于在未补充培养基中与乙醇一起培养并培养的细胞,单位死亡率是最高的;对于在未补充培养基中生长的细胞,中间体的死亡率是最高的。并在添加钙的培养基中与乙醇一起孵育。发现在乙醇存在下,Ca2 +对通电细胞酸化曲线的影响与其对生长,发酵和生存能力的保护作用密切相关。

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