Kaiser B, Munder T, Saluz H P, Künkel W, Eck R
Hans-Knöll-Institut für Naturstoff-Forschung e.V., Jena, Germany.
Yeast. 1999 May;15(7):585-91. doi: 10.1002/(SICI)1097-0061(199905)15:7<585::AID-YEA401>3.0.CO;2-9.
In a screen for Candida albicans genes encoding transactivating proteins, a pyruvate decarboxylase (EC 4.1.1.1.) regulator gene was isolated. An open reading frame (ORF) of 2511 bp was identified encoding a predicted protein of 836 amino acids with a molecular weight of 94.4 kDa. The protein showed glutamine- and proline-rich stretches typical for transcriptional activators. The amino acid sequence comparisons between CaPdc2p of C. albicans and both Pdc2p of Saccharomyces cerevisiae and Rag3p of Kluyveromyces lactis, revealed similarities of 40% and 39%, respectively. The CaPDC2 gene was localized on chromosome 1. Southern blot analysis indicated that CaPDC2 might be a single copy gene. The growth defect of a S. cerevisiae pdc2 delta mutant on glucose was compensated by transformation of the C. albicans CaPDC2 gene.
在对编码反式激活蛋白的白色念珠菌基因进行的筛选中,分离出了一个丙酮酸脱羧酶(EC 4.1.1.1.)调节基因。鉴定出一个2511 bp的开放阅读框(ORF),其编码一个预测的含有836个氨基酸、分子量为94.4 kDa的蛋白质。该蛋白质显示出转录激活因子典型的富含谷氨酰胺和脯氨酸的区域。白色念珠菌的CaPdc2p与酿酒酵母的Pdc2p和乳酸克鲁维酵母的Rag3p之间的氨基酸序列比较分别显示出40%和39%的相似性。CaPDC2基因定位于1号染色体上。Southern印迹分析表明CaPDC2可能是一个单拷贝基因。白色念珠菌CaPDC2基因的转化补偿了酿酒酵母pdc2δ突变体在葡萄糖上的生长缺陷。