首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Futile cycles in Saccharomyces cerevisiae strains expressing the gluconeogenic enzymes during growth on glucose.
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Futile cycles in Saccharomyces cerevisiae strains expressing the gluconeogenic enzymes during growth on glucose.

机译:酿酒酵母菌株在葡萄糖生长期间表达糖异生酶的无效循环。

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摘要

The systems which control the levels of the gluconeogenic enzymes in Saccharomyces cerevisiae have been bypassed to ascertain their physiological significance. The coding regions of the genes FBP1 and PCK1, which encode fructose-1,6-bisphosphatase and phosphoenolpyruvate carboxykinase, have been put under the control of the promoter of ADC1 (alcohol dehydrogenase I), a gene not repressed by glucose, and introduced into yeast in multicopy plasmids. The transformed yeast cells show high levels of the gluconeogenic enzymes during growth on glucose. Generation time and growth yield of yeast expressing either fructose-1,6-bisphosphatase or phosphoenolpyruvate carboxykinase are not significantly different from those of the wild-type strain. For a strain expressing both enzymes the increase in generation time is about 20% and the decrease in growth yield around 30%. The concentration of ATP is about 1.5 mM in the growing cells of the different strains. The extent of in vivo cycling was measured by 13C NMR in cell-free extracts from yeast growing on [6-13C]glucose. Cycling between fructose-6-phosphate and fructose-1,6-bisphosphate is < 2%, most likely due to the very strong inhibition of fructose-1,6-bisphosphatase by fructose 2,6-bisphosphate. Cycling between phosphoenolpyruvate and pyruvate is low, but a precise figure could not be obtained due to poor equilibration of label between carbons 2 and 3 of oxaloacetate.
机译:控制啤酒酵母中糖原异生酶水平的系统已被绕过以确定其生理学意义。编码果糖-1,6-双磷酸酶和磷酸烯醇丙酮酸羧化激酶的基因FBP1和PCK1的编码区已置于不受葡萄糖抑制的基因ADC1(酒精脱氢酶I)的启动子的控制之下,并被引入多拷贝质粒中的酵母。转化的酵母细胞在葡萄糖上生长期间显示出高水平的糖异生酶。表达果糖-1,6-双磷酸酶或磷酸烯醇丙酮酸羧化激酶的酵母的生成时间和生长产量与野生型菌株没有显着差异。对于同时表达两种酶的菌株,世代时间的增加约为20%,而生长产量的减少则约为30%。在不同菌株的生长细胞中,ATP的浓度约为1.5 mM。通过13 C NMR测定在[6-13C]葡萄糖上生长的酵母的无细胞提取物中的体内循环程度。果糖6-磷酸和果糖-1,6-双磷酸之间的循环<2%,最有可能是由于果糖2,6-双磷酸非常强烈地抑制了果糖-1,6-双磷酸酶。磷酸烯醇丙酮酸和丙酮酸之间的循环很低,但是由于草酰乙酸的碳2和3之间标记的平衡差,因此无法获得精确的数字。

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