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Isolation and Characterization of the Epoxide Hydrolase-Encoding Gene from Xanthophyllomyces dendrorhous

机译:枯草芽孢杆菌环氧化物水解酶编码基因的分离与鉴定

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摘要

The epoxide hydrolase (EH)-encoding gene (EPH1) from the basidiomycetous yeast Xanthophyllomyces dendrorhous was isolated. The genomic sequence has a 1,236-bp open reading frame which is interrupted by eight introns that encode a 411-amino-acid polypeptide with a calculated molecular mass of 46.2 kDa. The amino acid sequence is similar to that of microsomal EH and belongs to the α/β hydrolase fold family. The EPH1 gene was not essential for growth of X. dendrorhous in rich medium under laboratory conditions. The Eph1-encoding cDNA was functionally expressed in Escherichia coli. A sixfold increase in specific activity was observed when we used resting cells rather than X. dendrorhous. The epoxides 1,2-epoxyhexane and 1-methylcyclohexene oxide were substrates for both native and recombinant Eph1. Isolation and characterization of the X. dendrorhous EH-encoding gene are essential steps in developing a yeast EH-based epoxide biotransformation system.
机译:从担子菌酵母菌黄单胞菌树突状细胞中分离出了环氧水解酶(EH)的编码基因(EPH1)。该基因组序列具有一个1,236 bp的开放阅读框,被八个内含子打断,这些内含子编码一个411个氨基酸的多肽,计算的分子量为46.2 kDa。氨基酸序列与微粒体EH相似,属于α/β水解酶折叠家族。在实验室条件下,EPH1基因对于X. dendrorhous在丰富培养基中的生长不是必需的。编码Eph1的cDNA在大肠杆菌中功能性表达。当我们使用静息细胞而不是X. dendrorhous时,观察到比活增加了六倍。环氧1,2-环氧己烷和1-甲基环己烯氧化物是天然和重组Eph1的底物。 X. dendrorhous EH编码基因的分离和表征是开发基于酵母EH的环氧化物生物转化系统的重要步骤。

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