Youssef K A, Ghareib M, Khalil A A
Indian J Exp Biol. 1989 Feb;27(2):121-3.
Cells of S. cerevisiae strain "14-12" of different ages were immobilized in sodium alginate and used for conversion of glucose to ethanol. Immobilized cells of 48 hr old were the most potential. Employment of high counts of alginate-entrapped cells shortened the period required for production of the maximal alcohol yield. However, the percentage surviving cells decreased with increasing initial cell counts. Maximal accumulation of ethanol (4.18 g/100 ml) was obtained after 4 days of static fermentation with 1.8 X 10(8) immobilized yeast cells. The residual viable cell count was found to represent 3-fold the surviving percentage in a control experiment using an inoculum of the free yeast cells. Immobilized yeast cells could convert about 85% of the available sugars to ethanol over 28 days of the repeated-batch fermentation. The immobilized cells retained 50% of their viability for 16 days. After 48 days of repeated fermentation only 6% of the yeast cells were viable, and on the 52nd day no viable cells could be detected.
将不同菌龄的酿酒酵母菌株“14 - 12”的细胞固定在海藻酸钠中,并用于将葡萄糖转化为乙醇。48小时菌龄的固定化细胞最具潜力。使用大量海藻酸钠包埋的细胞缩短了达到最大酒精产量所需的时间。然而,存活细胞的百分比随着初始细胞数量的增加而降低。用1.8×10⁸个固定化酵母细胞进行4天静态发酵后,乙醇的最大积累量为4.18克/100毫升。发现残余活细胞数是使用游离酵母细胞接种物的对照实验中存活百分比的3倍。在重复分批发酵的28天内,固定化酵母细胞可将约85%的可用糖转化为乙醇。固定化细胞在16天内保持其50%的活力。经过48天的重复发酵后,只有6%的酵母细胞存活,在第52天未检测到活细胞。