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影响酿酒酵母棕榈酰辅酶A去饱和酶的因素。

Factors affecting the palmitoyl-coenzyme A desaturase of Saccharomyces cerevisiae.

作者信息

Klein H P, Volkmann C M

出版信息

J Bacteriol. 1975 Nov;124(2):718-23. doi: 10.1128/jb.124.2.718-723.1975.

Abstract

The activity and stability of the palmitoyl-coenzyme A (CoA) desaturase complex of Saccharomyces cerevisiae was influenced by several factors. Cells, grown nonaerobically and then incubated with glucose, either in air or under N2, showed a marked increase in desaturase activity. Cycloheximide, added during such incubations, prevented the increase in activity, suggesting de novo synthesis. The stability of the desaturase from cells grown nonaerobically was affected by subsequent treatment of the cells; enzyme from freshly harvested cells, or from cells that were then shaken under nitrogen, readily lost activity upon washing or during density gradient analysis, whereas aerated cells, in the presence or absence of glucose, yielded stable enzyme preparations. The loss of activity in nonaerobic preparations could be reversed by adding soluble supernatant from these homogenates and could be prevented by growing the cells in the presence of palmitoleic acid and ergosterol, but not with several other lipids tested.

摘要

酿酒酵母的棕榈酰辅酶A(CoA)去饱和酶复合体的活性和稳定性受到多种因素的影响。在无氧条件下生长然后在空气中或氮气下与葡萄糖一起孵育的细胞,其去饱和酶活性显著增加。在这种孵育过程中添加放线菌酮可阻止活性增加,提示有从头合成。无氧生长细胞的去饱和酶稳定性受细胞后续处理的影响;新鲜收获细胞或随后在氮气下振荡的细胞中的酶,在洗涤或密度梯度分析过程中容易丧失活性,而通气细胞,无论有无葡萄糖,均可产生稳定的酶制剂。无氧制剂中活性的丧失可通过添加这些匀浆的可溶性上清液来逆转,并且通过在棕榈油酸和麦角固醇存在下培养细胞可防止活性丧失,但其他几种测试的脂质则不能。

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