Johnson C H, McEwen J E
D. W. Reynolds Department of Geriatrics, University of Arkansas for Medical Sciences, GRECC (Geriatrics Research and Education Clinical Center), John L. McClellan Memorial VA Hospital, Mail Slot 151/LR, 4300 West 7th Street, Little Rock, AR 72205, USA.
Yeast. 1999 Jun 30;15(9):799-804. doi: 10.1002/(SICI)1097-0061(19990630)15:9<799::AID-YEA419>3.0.CO;2-N.
A cDNA library was prepared from Histoplasma capsulatum strain G-217B yeast cells and an apparently full-length cDNA for a subunit of the citric acid cycle enzyme NAD(+)-isocitrate dehydrogenase was identified by sequence analysis. Its predicted amino acid sequence is more similar to the IDH1 regulatory subunit of S. cerevisiae NAD(+)-isocitrate dehydrogenase than to the IDH2 catalytic subunit. After expression in S. cerevisiae from an S. cerevisiae promoter, it was shown to functionally complement an S. cerevisiae idh1 mutant, but not an idh2 mutant, for growth on acetate as a carbon source and for production of NAD(+)-isocitrate dehydrogenase enzyme activity. These results confirm that the H. capsulatum cDNA encodes a homologue of subunit I of the S. cerevisiae mitochondrial isocitrate dehydrogenase isozyme that functions in the citric acid cycle.
从荚膜组织胞浆菌G-217B酵母细胞制备了一个cDNA文库,并通过序列分析鉴定出柠檬酸循环酶NAD(+)-异柠檬酸脱氢酶一个亚基的一个明显全长cDNA。其预测的氨基酸序列与酿酒酵母NAD(+)-异柠檬酸脱氢酶的IDH1调节亚基比与IDH2催化亚基更相似。在酿酒酵母中从一个酿酒酵母启动子表达后,它被证明在以乙酸盐作为碳源生长以及产生NAD(+)-异柠檬酸脱氢酶酶活性方面,能功能性互补酿酒酵母idh1突变体,但不能互补idh2突变体。这些结果证实荚膜组织胞浆菌cDNA编码酿酒酵母线粒体异柠檬酸脱氢酶同工酶亚基I的一个同源物,该同源物在柠檬酸循环中起作用。