Kirino H, Oshima T
Department of Life Science, Tokyo Institute of Technology, Kanagawa.
J Biochem. 1991 Jun;109(6):852-7. doi: 10.1093/oxfordjournals.jbchem.a123470.
A gene (leuB) coding for 3-isopropylmalate dehydrogenase [EC 1.1.1.85] from an extreme thermophile, Thermus aquaticus YT-1 was cloned in Escherichia coli and the nucleotide sequence was determined. It contains an open reading frame of 1,035 bp encoding 344 amino acid residues. The homology with that from T. thermophilus HB8 is 87.0% in nucleotide and 91.3% in amino acid sequences. No overlapped gene was found in the present leuB gene, in contrast to the previous prediction that Thermus leuD gene is overlapped with leuB [Croft et al. (1987) Mol. Gen. Genet. 210, 490-497]. Substitutions in the primary structure which are unique for the thermophile sequences are discussed in relation to the unusual stability of the thermophile dehydrogenase based on amino acid sequence comparison of 9 microorganisms including thermophiles and mesophiles.
从嗜热栖热菌YT-1中克隆出编码3-异丙基苹果酸脱氢酶[EC 1.1.1.85]的基因(leuB),并在大肠杆菌中进行了克隆,同时测定了其核苷酸序列。该基因含有一个1035 bp的开放阅读框,编码344个氨基酸残基。与嗜热栖热菌HB8的相应基因相比,核苷酸序列同源性为87.0%,氨基酸序列同源性为91.3%。与之前预测嗜热栖热菌leuD基因与leuB重叠不同,在目前的leuB基因中未发现重叠基因[克罗夫特等人(1987年),《分子遗传学与普通遗传学》210,490 - 497]。基于包括嗜热菌和嗜温菌在内的9种微生物的氨基酸序列比较,讨论了嗜热菌序列特有的一级结构中的取代与嗜热菌脱氢酶异常稳定性的关系。