Moran J W, Witter L D
J Bacteriol. 1979 Jun;138(3):823-31. doi: 10.1128/jb.138.3.823-831.1979.
The effect of sugars on the production of d-arabitol and on the glucose catabolic pathways was investigated in the osmotrophic yeast Saccharomyces rouxii. The activity of d-arabitol dehydrogenase, which served as a measure of total d-arabitol production, increased when cells were grown in the presence of increasing glucose concentrations. Growth in sucrose had no effect on the enzyme activity. A high intracellular concentration of d-arabitol could be demonstrated when the cells were grown in a 60% glucose medium and could be eliminated by anaerobic growth or growth in the presence of 4 mg of chloramphenicol per ml. A mutant was isolated that would not grow in 60% glucose; although the regulation of d-arabitol dehydrogenase was altered in this strain, the production of d-arabitol was not eliminated. The activity of d-arabitol dehydrogenase followed the growth phases of the parent strain when the cells were preadapted to 30% glucose. If the cells were adapting from 1 to 30% glucose, a large increase in enzyme activity was detected before growth occurred. Protein synthesis was found to be involved in this increase in activity. There was an increased participation of the pentose phosphate pathway when the cells were grown in the presence of increasing glucose concentrations. The mutant strain had only an 11% pentose phosphate pathway participation compared with 20% for the parent strain in glucose. The results suggest that the active pentose phosphate pathway is involved in glucose tolerance by providing a plentiful supply of reduced nicotinamide adenine dinucleotide phosphate which is necessary for cell survival.
在渗透营养型酵母鲁氏酵母中研究了糖类对D-阿拉伯糖醇产生及葡萄糖分解代谢途径的影响。作为总D-阿拉伯糖醇产生量衡量指标的D-阿拉伯糖醇脱氢酶活性,在细胞于葡萄糖浓度不断增加的环境中生长时会升高。在蔗糖中生长对该酶活性没有影响。当细胞在60%葡萄糖培养基中生长时,可证明细胞内D-阿拉伯糖醇浓度很高,且通过厌氧生长或在每毫升含4毫克氯霉素的环境中生长可使其消除。分离出一个在60%葡萄糖中无法生长的突变体;尽管该菌株中D-阿拉伯糖醇脱氢酶的调节发生了改变,但D-阿拉伯糖醇的产生并未消除。当细胞预先适应30%葡萄糖时,D-阿拉伯糖醇脱氢酶活性随亲本菌株的生长阶段而变化。如果细胞从1%葡萄糖适应到30%葡萄糖,在生长发生之前会检测到酶活性大幅增加。发现蛋白质合成参与了这种活性增加。当细胞在葡萄糖浓度不断增加的环境中生长时,磷酸戊糖途径的参与度增加。与在葡萄糖中亲本菌株的20%相比,突变菌株的磷酸戊糖途径参与度仅为11%。结果表明,活跃的磷酸戊糖途径通过提供细胞存活所需的大量还原型烟酰胺腺嘌呤二核苷酸磷酸参与葡萄糖耐受性。