MICROSOMAL RETINAL SYNTHESIS - RETINOL VS HOLO-CRBP AS SUBSTRATE AND EVALUATION OF NADP, NAD AND NADPH AS COFACTORS

被引:35
作者
NAPOLI, JL
POSCH, KC
BURNS, RD
机构
[1] Department of Biochemistry, School of Medicine and Biomedical Sciences, The State University of New York at Buffalo, Buffalo, NY
关键词
RETINOL; RETINAL; RETINOIC ACID; MICROSOME; CELLULAR RETINOL BINDING PROTEIN; DEHYDROGENASE;
D O I
10.1016/0167-4838(92)90267-H
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
Holo-CRBP (cellular retinol binding protein) is recognized specifically by an NADP-dependent microsomal retinol dehydrogenase and protects retinol from conversion into retinal by NAD and NADPH dependent dehydrogenases. The synthesis of retinal from free retinol is catalyzed by both NADP- and NAD-dependent pathways, with the former being the preferred one (K(m) of 4 vs. 22-mu-M for retinol, and V(max)/K(m) of 33 vs. 9, respectively). NADPH does not support quantitatively significant retinal synthesis from physiological concentrations of retinol or holo-CRBP, if an NADPH regenerating system is used to prevent NADP formation.
引用
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页码:183 / 186
页数:4
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