Modulation of aldosterone biosynthesis by adrenodoxin mutants with different electron transport efficiencies

被引:21
作者
Cao, PR [1 ]
Bernhardt, R [1 ]
机构
[1] Univ Saarlandes, Fachrichtung Biochem 12 4, D-66041 Saarbrucken, Germany
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1999年 / 265卷 / 01期
关键词
adrenodoxin; aldosterone synthesis; bovine CYP11B1; human CYP11B1; human CYP11B2;
D O I
10.1046/j.1432-1327.1999.00704.x
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
Aldosterone biosynthesis is highly regulated on different levels by hormones, potassium, lipid composition of the membrane and the molecular structure of its gene. Here, the influence of the electron transport efficiency from adrenodoxin (Adx) to CYP11B1 on the activities of bovine CYP11B1 has been investigated using a liposomal reconstitution System with truncated mutants of Adx. It could be clearly demonstrated that Adx mutants Adx 4-114 and Adx 4-108, possessing enhanced electron transfer abilities, produce increases in corticosterone and aldosterone biosynthesis. Based on the V-max values of corticosterone and aldosterone formation, Adx 4-108 and Adx 4-114 enhance corticosterone synthesis 1.3-fold and aldosterone formation threefold and twofold, respectively. The production of 18-hydroxycorticosterone was changed only slightly in these Adx mutants. The effect of Adx 1-108 on the product patterns of bovine CYP11B1, human CYP11B1 and human CYP11B2 was confirmed in COS-1 cells by cotransfection of CYP11B- and Adx-containing expression vectors. It could be shown that Adx 1-108 enhances the formation of aldosterone by bovine CYP11B1 and by human CYP11B2, and stimulates the production of corticosterone by bovine CYP11B1 and human CYP11B1 and CYP11B2 also.
引用
收藏
页码:152 / 159
页数:8
相关论文
共 43 条
[1]  
AKHREM AA, 1979, ACTA BIOL MED GER, V38, P257
[2]  
BECKERT V, 1994, J BIOL CHEM, V269, P2568
[3]   Specific aspects of electron transfer from adrenodoxin to cytochromes P450scc and P45011 beta [J].
Beckert, V ;
Bernhardt, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :4883-4888
[4]   Cytochrome P450: Structure, function, and generation of reactive oxygen species [J].
Bernhardt, R .
REVIEWS OF PHYSIOLOGY BIOCHEMISTRY AND PHARMACOLOGY, VOL 127, 1996, 127 :137-221
[5]   Conferring aldosterone synthesis to human CYP11B1 by replacing key amino acid residues with CYP11B2-specific ones [J].
Böttner, B ;
Denner, K ;
Bernhardt, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 252 (03) :458-466
[6]   Molecular cloning and functional expression of the cytochrome p450 11B-hydroxylase of the guinea pig [J].
Bulow, HE ;
Mobius, K ;
Bahr, V ;
Bernhardt, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (02) :304-312
[7]   Interaction of CYP11B1 (cytochrome P-45011β) with CYP11A1 (cytochrome P-450scc) in COS-1 cells [J].
Cao, PR ;
Bernhardt, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 262 (03) :720-726
[8]   THE DISTRIBUTION OF CHOLESTEROL AND PHOSPHOLIPID-COMPOSITION IN SUBMITOCHONDRIAL MEMBRANES FROM BOVINE ADRENAL-CORTEX - FUNDAMENTAL-STUDIES OF STEROIDOGENIC MITOCHONDRIA [J].
CHENG, B ;
KIMURA, T .
LIPIDS, 1983, 18 (09) :577-584
[9]  
CHU JW, 1973, J BIOL CHEM, V248, P2089
[10]  
COGHLAN VM, 1991, J BIOL CHEM, V266, P18606