Suppr超能文献

编码酵母线粒体ATP酶复合体的核基因。对编码F1-ATP酶α亚基的ATP1及其组装的分析。

Nuclear genes encoding the yeast mitochondrial ATPase complex. Analysis of ATP1 coding the F1-ATPase alpha-subunit and its assembly.

作者信息

Takeda M, Chen W J, Saltzgaber J, Douglas M G

出版信息

J Biol Chem. 1986 Nov 15;261(32):15126-33.

PMID:2876995
Abstract

Mitochondria prepared from the yeast nuclear pet mutant N9-84 lack a detectable F1-ATPase activity. Genetic complementation of this mutant with a pool of yeast genomic DNA in the yeast Escherichia coli shuttle vector YEp13 restored its growth on a nonfermentable carbon source. Mitochondria prepared from the transformed host contained an 8-fold higher than normal level of the F1 alpha-subunit and restored ATPase activity to 50% that of the wild-type strain. Deletion and nucleotide sequence analysis of the complementing DNA on the plasmid revealed a coding sequence designated ATP1 for a protein of 544 amino acids which exhibits 60 and 54% direct protein sequence homology with the proton-translocating ATPase alpha-subunits from tobacco chloroplast and E. coli, respectively. In vitro expression and mitochondrial import experiments using this ATP1 sequence showed that additional amino-terminal sequences not present in the comparable plant and bacterial subunits function as transient sequences for import.

摘要

从酵母核pet突变体N9 - 84制备的线粒体缺乏可检测到的F1 - ATP酶活性。用酵母 - 大肠杆菌穿梭载体YEp13中的酵母基因组DNA库对该突变体进行遗传互补,恢复了其在非发酵碳源上的生长。从转化宿主制备的线粒体中F1α亚基的水平比正常水平高8倍,并将ATP酶活性恢复到野生型菌株的50%。对质粒上互补DNA的缺失和核苷酸序列分析揭示了一个编码序列,命名为ATP1,编码一种544个氨基酸的蛋白质,该蛋白质与烟草叶绿体和大肠杆菌的质子转运ATP酶α亚基分别具有60%和54%的直接蛋白质序列同源性。使用该ATP1序列进行的体外表达和线粒体导入实验表明,在可比的植物和细菌亚基中不存在的额外氨基末端序列作为导入的瞬时序列起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验