ISOLATION OF A GENE FOR A REGULATORY 15-KDA SUBUNIT OF MITOCHONDRIAL F1F0-ATPASE AND CONSTRUCTION OF MUTANT YEAST LACKING THE PROTEIN

被引:22
|
作者
YOSHIDA, Y
SATO, T
HASHIMOTO, T
ICHIKAWA, N
NAKAI, S
YOSHIKAWA, H
IMAMOTO, F
TAGAWA, K
机构
[1] OSAKA UNIV, SCH MED, DEPT PHYSIOL CHEM, KITA KU, OSAKA 530, JAPAN
[2] KYOTO PHARMACEUT UNIV, INST MOLEC & CELLULAR BIOL, KYOTO 607, JAPAN
[3] OSAKA UNIV, SCH MED, DEPT GENET, OSAKA 530, JAPAN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1990年 / 192卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1990.tb19193.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A gene coding for yeast 15‐kDa protein, a regulatory factor of mitochondrial F1F0‐ATPase, was isolated. The cloned gene was disrupted in vitro and mutant strains that did not contain the 15‐kDa protein were constructed by transformation of yeast cells with the disrupted gene. The ATP‐synthesizing activity of the mutant mitochondria was the same as that of wild‐type cells, suggesting that the 15‐kDa protein is not required for mitochondrial oxidative phosphorylation. Collapse of the membrane potential induced ATP‐hydrolyzing activity of F1F0‐ATPase of the mutant mitochondria but not of normal mitochondria. Activation of the enzyme was also observed during incubation of submitochondrial particles from mutant cells, but not of those from wild‐type cells. Thus, it is inferred that the 15‐kDa protein supports the action of an intrinsic ATPase inhibitor of the ATP‐hydrolyzing activity of the enzyme upon de‐energization of mitochondrial membranes. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:49 / 53
页数:5
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