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酵母中编码胞质NADP特异性异柠檬酸脱氢酶的基因的分离、特性鉴定及破坏

Isolation, characterization, and disruption of the yeast gene encoding cytosolic NADP-specific isocitrate dehydrogenase.

作者信息

Loftus T M, Hall L V, Anderson S L, McAlister-Henn L

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Irvine 92717.

出版信息

Biochemistry. 1994 Aug 16;33(32):9661-7. doi: 10.1021/bi00198a035.

Abstract

The cytosolic isozyme of NADP-specific isocitrate dehydrogenase (IDP2) was purified from a Saccharomyces cerevisiae mutant containing a chromosomal disruption in the gene encoding the mitochondrial isozyme (IDP1). IDP2 was shown to be a homodimer with a subunit molecular weight of approximately 45,000 and an isoelectric point of 5.5. Amino acid sequences were obtained for tryptic peptides of IDP2 and used to plan polymerase chain reactions. A resulting 400 bp DNA fragment was used as a hybridization probe to isolate the IDP2 gene from a yeast genomic DNA library. The complete nucleotide sequence of the IDP2 coding region was determined and translated into a 412-residue amino acid sequence. IDP2 and IDP1 were found to be identical in 71% of the aligned residue positions. The identity of the IDP2 gene was confirmed by genomic replacement with a disrupted IDP2 coding region. Haploid yeast strains lacking either or both IDP2 and IDP1 were constructed by genetic crosses of mutant strains containing disruptions in chromosomal IDP2 and IDP1 loci. No dramatic differences in growth rates with common carbon sources could be attributed to these disruptions.

摘要

从一个在编码线粒体异柠檬酸脱氢酶(IDP1)的基因中存在染色体缺失的酿酒酵母突变体中纯化出了NADP特异性异柠檬酸脱氢酶的胞质同工酶(IDP2)。结果表明,IDP2是一种同型二聚体,亚基分子量约为45,000,等电点为5.5。获得了IDP2胰蛋白酶肽段的氨基酸序列,并用于设计聚合酶链反应。所得的400 bp DNA片段用作杂交探针,从酵母基因组DNA文库中分离出IDP2基因。确定了IDP2编码区的完整核苷酸序列,并将其翻译成一个412个残基的氨基酸序列。发现IDP2和IDP1在71%的比对残基位置上是相同的。通过用破坏的IDP2编码区进行基因组替换,证实了IDP2基因的身份。通过对在染色体IDP2和IDP1位点含有缺失的突变菌株进行遗传杂交,构建了缺乏IDP2或IDP1或两者的单倍体酵母菌株。这些缺失并未导致在使用常见碳源时生长速率出现显著差异。

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