EXPRESSION OF RECOMBINANT HUMAN METHYLMALONYL-COA MUTASE - IN PRIMARY MUT FIBROBLASTS AND SACCHAROMYCES-CEREVISIAE

被引:33
作者
ANDREWS, E
JANSEN, R
CRANE, AM
CHOLIN, S
MCDONNELL, D
LEDLEY, FD
机构
[1] BAYLOR COLL MED, DEPT CELL BIOL, HOUSTON, TX 77030 USA
[2] BAYLOR COLL MED, DEPT PEDIAT, HOUSTON, TX 77030 USA
来源
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY | 1993年 / 50卷 / 02期
关键词
D O I
10.1006/bmmb.1993.1055
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
Methylmalonyl-CoA mutase is an adenosylcobalamin-dependent enzyme which catalyzes isomerization of methylmalonyl-CoA to succinyl-CoA. Previous reports have described cloning and sequencing of a cDNA for human methylmalonyl-CoA mutase. This clone does not express an active apoenzyme after gene transfer into primary MCM-deficient fibroblasts and contains several sequences which differ from the consensus sequence of other cDNA clones. We describe reconstruction of a functional MCM cDNA and expression of recombinant enzyme activity in primary fibroblasts and Saccharomyces cerevisiae. This consensus human MCM cDNA is capable of complementing the inherited defect in mut MMA and overexpressing an enzyme in yeast with kinetic properties indistinguishable from the enzyme in murine or human tissues. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:135 / 144
页数:10
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