TARTRATE DEHYDROGENASE, A NEW MEMBER OF THE FAMILY OF METAL-DEPENDENT DECARBOXYLATING R-HYDROXYACID DEHYDROGENASES

被引:34
作者
TIPTON, PA
BEECHER, BS
机构
[1] Department of Biochemistry, University of Missouri-Columbia, Columbia
关键词
D O I
10.1006/abbi.1994.1352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene encoding tartrate dehydrogenase has been cloned from Pseudomonas putida and sequenced. The gene is 1098 nucleotides long and encodes a protein 365 amino acids in length with a calculated M(r) of 40,636. The gene and the protein encoded by it show strong homology to prokaryotic isopropylmalate dehydrogenases and, to a lesser extent, isocitrate dehydrogenase. Thus, tartrate dehydrogenase is the third member to be identified of the family of metal-dependent decarboxylating R-hydroxyacid dehydrogenases which have an evolutionarily distinct NAD(+)-binding domain. The poor catalytic properties of tartrate dehydrogenase suggest that it has not been under strong selective pressure to maximize its ability to turn over (+)-tartrate for very long; the homology with isopropylmalate dehydrogenase makes it an attractive candidate for a recent progenitor of tartrate dehydrogenase. beta-Isopropylmalate is a substrate for tartrate dehydrogenase with a K-m of 14 +/- 2 mu M; it is turned over with a V-max that is 35% of V-max in the (+)-tartrate reaction. The gene encoding tartrate dehydrogenase has been expressed in Escherichia coli and large quantities of soluble enzyme can be obtained. (C) 1994 Academic Press, Inc.
引用
收藏
页码:15 / 21
页数:7
相关论文
共 30 条