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Heterologous redox partners supporting the efficient catalysis of epothilone B biosynthesis by EpoK in Schlegelella brevitalea

机译:异源氧化还原合作伙伴支持EPOTHILONE B生物合成的高效催化BioSyneste在雪普利菌Brevitalea

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摘要

Highly efficient redox proteins support the catalytic activity of EpoK in DSM 7029. a Epothilone yield of strain H7029-2 with epoK expression. The data are presented as the means ± standard deviations of the values from three independent experiments (n = 3). b HPLC analysis of the standard sample (25 mg L−1) and the extracts from the parental strain H7029-1 and the mutant strain H7029-2. A, epothilone A; B, epothilone B; C, epothilone C; D, epothilone D. c Schematic diagram: EpoK efficiently catalysed the conversion of epothilone C and D to epothilone A and B, respectively, in the epothilone C/D high-yield strain H7029-1. The epothilone gene cluster from S. cellulosum So0157-2 was transposed into the genome of the heterologous host DSM 7029
机译:高效的氧化还原蛋白支持DSM 7029中的EPOK的催化活性。菌株H7029-2菌株H7029-2的催化活性。将数据呈现为来自三个独立实验的值的平均值±标准偏差(n = 3)。 B HPLC分析标准样品(25mg L-1)和来自亲本菌株H7029-1的提取物H7029-1 H7029-2。 a,epothilone a; B,EPOTHILONE B; C,EPOTHILONE C; D,EPOTHILONE D. C示意图:EPOK分别有效地将EPOTHILONE C和D的转化为EPOTHILONE A和B,在EPThiLONE C / D高收率菌株H7029-1中。将纤维素SO0157-2的EPOTHILONE基因簇转移到异源宿主DSM 7029的基因组中

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