Mattingly J R, Rodriguez-Berrocal F J, Gordon J, Iriarte A, Martinez-Carrion M
Division of Molecular Biology and Biochemistry, School of Basic Life Sciences, University of Missouri-Kansas City 64110.
Biochem Biophys Res Commun. 1987 Dec 31;149(3):859-65. doi: 10.1016/0006-291x(87)90487-6.
A 2.4 kilobase cDNA for rat mitochondrial aspartate aminotransferase (E.C. 2.6.1.1.) was isolated and sequenced. The predicted presequence is 93% homologous to the presequences of the enzyme from pig and mouse. The predicted amino acid sequence of the mature enzyme differs from that determined directly by amino acid sequencing (Huynh, Q.K., Sakakibara, R., Watanabe, T., and Wada, H. (1981) J. Biochem. (Tokyo) 90, 863-875) at 13 amino acids residues. The most important difference is at position 140 where the cDNA encodes a tryptophanyl residue rather than the previously reported glycine. This critical residue is now seen to be conserved in all aspartate aminotransferases. The coding region of this cDNA was inserted into the plasmid cloning vector pKK233-2 and used to stably express an unfused precursor in Escherichia coli JM105.
分离并测定了大鼠线粒体天冬氨酸氨基转移酶(E.C. 2.6.1.1.)的一段2.4千碱基的cDNA序列。预测的前导序列与猪和小鼠该酶的前导序列有93%的同源性。成熟酶的预测氨基酸序列与通过氨基酸测序直接测定的序列(Huynh, Q.K., Sakakibara, R., Watanabe, T., and Wada, H. (1981) J. Biochem. (Tokyo) 90, 863 - 875)在13个氨基酸残基处不同。最重要的差异在第140位,cDNA编码一个色氨酸残基,而不是先前报道的甘氨酸。现在发现这个关键残基在所有天冬氨酸氨基转移酶中都是保守的。将该cDNA的编码区插入质粒克隆载体pKK233 - 2中,并用于在大肠杆菌JM105中稳定表达未融合的前体。