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来自拟南芥的NAD(+)依赖性异柠檬酸脱氢酶。两种密切相关亚基的特性

NAD(+)-dependent isocitrate dehydrogenase from Arabidopsis thaliana. Characterization of two closely related subunits.

作者信息

Behal R H, Oliver D J

机构信息

Department of Botany, Iowa State University, Ames 50011-1020, USA.

出版信息

Plant Mol Biol. 1998 Mar;36(5):691-8. doi: 10.1023/a:1005923410940.

Abstract

Two cDNA clones which appear to encode different subunits of NAD(+)-dependent isocitrate dehydrogenase (IDH; EC 1.1.1.41) were identified by homology searches from the Arabidopsis EST database. These cDNA clones were obtained and sequenced; both encoded full-length messages and displayed 82.7% nucleotide sequence identity over the coding region. The deduced amino acid sequences revealed preprotein lengths of 367 residues, with an amino acid identity of 86.1%. Genomic Southern blot analysis showed distinct single-copy genes for both IDH subunits. Both IDH subunits were expressed as recombinant proteins in Escherichia coli, and polyclonal antibodies were raised to each subunit. The Arabidopsis cDNA clones were expressed in Saccharomyces cerevisiae mutants which were deficient in either one or both of the yeast NAD(+)-dependent IDH subunits. The Arabidopsis cDNA clones failed to complement the yeast mutations; although both IDH-I and IDH-II were expressed at detectable levels, neither protein was imported into the mitochondria.

摘要

通过对拟南芥EST数据库进行同源性搜索,鉴定出两个似乎编码NAD(+)依赖型异柠檬酸脱氢酶(IDH;EC 1.1.1.41)不同亚基的cDNA克隆。获得了这些cDNA克隆并进行了测序;两者均编码全长信息,且在编码区域显示出82.7%的核苷酸序列同一性。推导的氨基酸序列显示前体蛋白长度为367个残基,氨基酸同一性为86.1%。基因组Southern印迹分析表明,两个IDH亚基均有独特的单拷贝基因。两个IDH亚基均在大肠杆菌中表达为重组蛋白,并针对每个亚基制备了多克隆抗体。拟南芥cDNA克隆在缺乏酵母NAD(+)依赖型IDH亚基之一或两者的酿酒酵母突变体中表达。拟南芥cDNA克隆未能弥补酵母突变;尽管IDH-I和IDH-II均以可检测的水平表达,但两种蛋白均未导入线粒体。

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