Isolation and reconstitution of the heme-thiolate protein obtusifoliol 14 alpha-demethylase from Sorghum bicolor (L.) Moench

被引:42
作者
Kahn, RA
Bak, S
Olsen, CE
Svendsen, I
Moller, BL
机构
[1] ROYAL VET & AGR UNIV,DEPT PLANT BIOL,PLANT BIOCHEM LAB,DK-1871 FREDERIKSBERG C,COPENHAGEN,DENMARK
[2] ROYAL VET & AGR UNIV,DEPT CHEM,DK-1871 FREDERIKSBERG C,COPENHAGEN,DENMARK
[3] CARLSBERG LAB,DEPT CHEM,DK-2500 VALBY,DENMARK
关键词
D O I
10.1074/jbc.271.51.32944
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 heme-thiolate (cytochrome P450) enzyme which catalyzes the 14 alpha-demethylation of obtusifoliol has been isolated from microsomes prepared from etiolated seedlings of Sorghum bicolor (L.) Moench. The obtusifoliol 14 alpha-demethylase is a key enzyme in plant sterol biosynthesis and a target for the design of phyla-specific sterol 14 alpha-demethylase inhibitors. Microsomal cytochrome P450s were solubilized by using the detergents Renex 690 and reduced Triton X-100, and the obtusifoliol 14 alpha-demethylase was isolated by DEAE ion exchange and dye affinity column chromatography. The isolated enzyme has an absorption spectrum characteristic for low spin cytochrome P450s and produces a Type I binding spectrum with obtusifoliol as substrate. Binding spectra were not obtained with lanosterol, campesterol, sitosterol, or stigmasterol. Obtusifoliol 14 alpha-demethylase has an apparent molecular mass of 53 kDa and is estimated to constitute approximate to 20% of the total cytochrome P450 content of the microsomal membranes and about 0.2% of the total microsomal protein. Gas chromatography-mass spectrometry analysis of reconstitution experiments with dilauroylphosphatidylcholine micelles containing isolated obtusifoliol 14 alpha-demethylase and sorghum NADPH-cytochrome P450 oxidoreductase demonstrated the conversion of obtusifoliol (4 alpha,14 alpha-dimethyl-5 alpha-ergosta-8,24-(28)-dien-3 beta-ol) to 4 alpha-methyl-5 alpha-ergosta-8,14,24(28)-trien-3 beta-ol, the 14 alpha-demethylated product of obtusifoliol with a double bond introduced at the Delta(14) position. The N-terminal amino acid sequence of the protein is MDLADIPQ/KQQRLMAGXALVV. Five internal sequences were obtained after endoproteinase Lys-C and Glu-C digestion. The fragment AAGAFSYISFGGGRH aligns with the unique heme binding domain of mammalian and yeast sterol 14 alpha-demethylases which belong to the CYP51 family, Therefore it is conceivable that the obtusifoliol 14 alpha-demethylase from plants also belongs to the CYP51 family, the only P450 family so far known to be conserved across the phyla.
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页码:32944 / 32950
页数:7
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