Van Doorn J, Valkenburg J A, Scholte M E, Oehlen L J, Van Driel R, Postma P W, Nanninga N, Van Dam K
Laboratory of Biochemistry and Biotechnology Centre, University of Amsterdam, The Netherlands.
J Bacteriol. 1988 Oct;170(10):4808-15. doi: 10.1128/jb.170.10.4808-4815.1988.
Activity changes of a number of enzymes involved in carbohydrate metabolism were determined in cell extracts of fractionated exponential-phase populations of Saccharomyces cerevisiae grown under excess glucose. Cell-size fractionation was achieved by an improved centrifugal elutriation procedure. Evidence that the yeast populations had been fractionated according to age in the cell cycle was obtained by examining the various cell fractions for their volume distribution and their microscopic appearance and by flow cytometric analysis of the distribution patterns of cellular DNA and protein contents. Trehalase, hexokinase, pyruvate kinase, phosphofructokinase 1, and fructose-1,6-diphosphatase showed changes in specific activities throughout the cell cycle, whereas the specific activities of alcohol dehydrogenase and glucose-6-phosphate dehydrogenase remained constant. The basal trehalase activity increased substantially (about 20-fold) with bud emergence and decreased again in binucleated cells. However, when the enzyme was activated by pretreatment of the cell extracts with cyclic AMP-dependent protein kinase, no significant fluctuations in activity were seen. These observations strongly favor posttranslational modification through phosphorylation-dephosphorylation as the mechanism underlying the periodic changes in trehalase activity during the cell cycle. As observed for trehalase, the specific activities of hexokinase and phosphofructokinase 1 rose from the beginning of bud formation onward, finally leading to more than eightfold higher values at the end of the S phase. Subsequently, the enzyme activities dropped markedly at later stages of the cycle. Pyruvate kinase activity was relatively low during the G1 phase and the S phase, but increased dramatically (more than 50-fold) during G2. In contrast to the three glycolytic enzymes investigated, the highest specific activity of the gluconeogenic enzyme fructose-1, 6-diphosphatase 1 was found in fractions enriched in either unbudded cells with a single nucleus or binucleated cells. The observed changes in enzyme activities most likely underlie pronounced alterations in carbohydrate metabolism during the cell cycle.
在过量葡萄糖条件下生长的酿酒酵母指数生长期群体的分级细胞提取物中,测定了参与碳水化合物代谢的多种酶的活性变化。通过改进的离心淘析程序实现细胞大小分级。通过检查各个细胞级分的体积分布、微观外观以及对细胞DNA和蛋白质含量的分布模式进行流式细胞术分析,获得了酵母群体已根据细胞周期中的年龄进行分级的证据。海藻糖酶、己糖激酶、丙酮酸激酶、磷酸果糖激酶1和果糖-1,6-二磷酸酶在整个细胞周期中比活性发生变化,而乙醇脱氢酶和葡萄糖-6-磷酸脱氢酶的比活性保持恒定。基础海藻糖酶活性随着芽的出现大幅增加(约20倍)并在双核细胞中再次降低。然而,当用环磷酸腺苷依赖性蛋白激酶预处理细胞提取物来激活该酶时,未观察到活性有明显波动。这些观察结果强烈支持通过磷酸化-去磷酸化进行的翻译后修饰作为细胞周期中海藻糖酶活性周期性变化的潜在机制。正如对海藻糖酶所观察到的那样,己糖激酶和磷酸果糖激酶1的比活性从芽形成开始就上升,最终在S期结束时导致值高出八倍以上。随后,酶活性在周期的后期显著下降。丙酮酸激酶活性在G1期和S期相对较低,但在G2期急剧增加(超过50倍)。与所研究的三种糖酵解酶相反,糖异生酶果糖-1,6-二磷酸酶1的最高比活性在富含单核未出芽细胞或双核细胞的级分中发现。观察到的酶活性变化很可能是细胞周期中碳水化合物代谢明显改变的基础。