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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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摘要

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:将最佳浓度(0.75至2.0 mM)的Ca 2 + (以CaCl2的形式)添加到具有微量污染浓度的Ca 2 + (0.025 mM)的发酵培养基中导致酿酒酵母,巴氏酵母和马克斯克鲁维酵母迅速产生更高浓度的乙醇。补钙(0.75 mM)对巴氏链球菌酒精发酵的积极影响可以通过其乙醇耐受性的提高来解释。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分别是比生长(i = g)和发酵( i = f)在添加或不添加乙醇浓度(X)的情况下的速率,Xmi是允许生长或发酵的最大乙醇浓度。毒性力由 n i 给出。在Ca 2 + -补充培养基(0.75 mM)中, n g 的生长= 0.42, n f = 0.43,而未添加培养基的发酵分别为0.52和0.55;对于两种媒体, X mg = 10%(vol / vol), X mf = 13%(vol / vol)。对于致死浓度的乙醇,在具有最佳浓度Ca 2 + 的培养基中生长并与乙醇孵育的细胞的单位死亡率最低,而对于在未添加培养基的条件下与乙醇孵育并培养的细胞的单位死亡率最高。 ,以及用于在未补充培养基中生长并在钙补充培养基中与乙醇一起孵育的细胞的中间体。发现在乙醇存在下,Ca 2 + 对能量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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