Arreguin de Lorencez M, Käppeli O
Institute of Biotechnology, Swiss Federal Institute of Technology, Zürich.
J Gen Microbiol. 1987 Sep;133(9):2517-22. doi: 10.1099/00221287-133-9-2517.
Oscillation of the activities of gluconeogenic enzymes (malate dehydrogenase, phosphoenolpyruvate carboxykinase and fructose-1,6-bisphosphatase) was observed during the cell cycle of chemostat cultures of Saccharomyces cerevisiae. Since ethanol is released by the cells at the beginning of the division cycle, its effect on enzyme expression was determined. Pulsing ethanol to a synchronously dividing yeast culture led to a prolongation of the metabolically active phase as indicated by the course of oxygen uptake and carbon dioxide production rates (concomitant ethanol and glucose assimilation). Enzyme activities also remained elevated as long as ethanol was available to the cells. After a substrate shift from glucose to ethanol during cell division, ethanol was used without a lag phase and enzyme induction increased from the level reached at the point of the substrate change. The data confirmed that the small amount of ethanol produced when the cells begin active reproduction acts as an inducer of gluconeogenic enzymes.
在酿酒酵母恒化器培养的细胞周期中,观察到糖异生酶(苹果酸脱氢酶、磷酸烯醇式丙酮酸羧激酶和果糖-1,6-二磷酸酶)活性的振荡。由于细胞在分裂周期开始时会释放乙醇,因此测定了其对酶表达的影响。向同步分裂的酵母培养物中脉冲添加乙醇导致代谢活跃期延长,这由氧气摄取和二氧化碳产生速率(伴随乙醇和葡萄糖同化)的变化过程表明。只要细胞有乙醇可用,酶活性也会保持升高。在细胞分裂过程中从葡萄糖向乙醇进行底物转换后,乙醇无需滞后阶段即可被利用,并且酶诱导从底物变化点达到的水平开始增加。数据证实,细胞开始活跃繁殖时产生的少量乙醇充当糖异生酶的诱导剂。