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Streptomyces coelicolor A3(2) CYP102 Protein, a Novel Fatty Acid Hydroxylase Encoded as a Heme Domain without an N-Terminal Redox Partner

机译:链霉菌coelicolor A3(2)CYP102蛋白,一种新型的脂肪酸羟化酶,编码为没有N端氧化还原伴侣的血红素域

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The gene from Streptomyces coelicolor A3(2) encoding CYP102B1, a recently discovered CYP102 subfamily which exists solely as a single P450 heme domain, has been cloned, expressed in Escherichia coli , purified, characterized, and compared to its fusion protein family members. Purified reconstitution metabolism experiments with spinach ferredoxin, ferredoxin reductase, and NADPH revealed differences in the regio- and stereoselective metabolism of arachidonic acid compared to that of CYP102A1, exclusively producing 11,12-epoxyeicosa-5,8,14-trienoic acid in addition to the shared metabolites 18-hydroxy arachidonic acid and 14,15-epoxyeicosa-5,8,11-trienoic acid. Consequently, in order to elucidate the physiological function of CYP102B1 , transposon mutagenesis was used to generate an S. coelicolor A3(2) strain lacking CYP102B1 activity and the phenotype was assessed.
机译:来自大肠杆菌链霉菌A3(2)的编码CYP102B1的基因已被克隆,在大肠杆菌中表达,纯化,鉴定并与其融合蛋白家族成员进行了比较,该基因是最近发现的CYP102亚家族,它仅以单个P450血红素结构域存在。用菠菜铁氧还蛋白,铁氧还蛋白还原酶和NADPH进行的纯净重组代谢实验显示,花生四烯酸的区域和立体选择性代谢与CYP102A1相比有所不同,除了CYP102A1以外,还独家生产11,12-环氧-5,8,14-三烯酸共有的代谢物18-羟基花生四烯酸和14,15-环氧二十碳五,8,11-三烯酸。因此,为了阐明CYP102B1的生理功能,使用转座子诱变产生缺乏CYP102B1活性的大肠杆菌S. coelicolor A3(2)菌株,并评估其表型。

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