Inoue Y, Yano H, Ginya H, Tsuchiyama H, Murata K, Kimura A
Research Institute for Food Science, Kyoto University, Japan.
Biotechnol Appl Biochem. 1991 Dec;14(3):391-4.
A DNA fragment carrying a part of the structural gene for yeast (Saccharomyces cerevisiae) glyoxalase I was cloned from a lambda gt11 expression library using anti-glyoxalase IIgG as a probe. By Northern blotting analysis, the amount of glyoxalase I mRNA was found to increase in yeast cells containing plasmids carrying the GAC gene, which is a positive regulator for yeast glyoxalase I activity. This suggests that the GAC gene product may accelerate the transcription of glyoxalase I gene or may have some positive effects on the accumulation of glyoxalase I mRNA in yeast cells.
利用抗乙二醛酶II IgG作为探针,从λgt11表达文库中克隆出一段携带酵母(酿酒酵母)乙二醛酶I部分结构基因的DNA片段。通过Northern印迹分析发现,在含有携带GAC基因质粒的酵母细胞中,乙二醛酶I mRNA的量增加,GAC基因是酵母乙二醛酶I活性的正调控因子。这表明GAC基因产物可能加速乙二醛酶I基因的转录,或者对酵母细胞中乙二醛酶I mRNA的积累有一些积极作用。