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首页> 外文期刊>Biotechnology Progress >An efficient enzymatic baeyr-villiger oxidation by engineered escherichia coli cells under non-growing conditions
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An efficient enzymatic baeyr-villiger oxidation by engineered escherichia coli cells under non-growing conditions

机译:工程菌细胞在非生长条件下的高效酶促拜耶-维利格氧化

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Econcomical methods of supplying NADPH must be developed before biotransformations involving this cofactor can be considered for large-scale applications.We have studied the enzymatic Baeyer-Villiger oxidation of cyclohezanone as a model for this class of reactions and developed a simple approach that uses whole,non-growing Escherichia coli cells to provide high productivity(0.79 g #epsilon#-caprolactone/L/h ident to 18#mu#mol #epsilon#-caprolactone/min/g dcw)and an 88% yield.Glucose supplied the reducing equivalents for non-growing cells was an order of magnitude greater than that achieved with growing cells of the same strain.Cells of an engineered E.coli strain that overexpresses Acinetobacter sp.cyclohexanone monooxygenase were grown under inducing conditions in rich medium until the entry to stationary phase;the subsequent cyclohexanone oxidation was carried out in minimal salte medium lacking a nitrogen source.After the biotransformation was complete,the lactone product was adsorbed to a solid support and recovered by washing with an organic solvent.
机译:在考虑将涉及这种辅因子的生物转化用于大规模应用之前,必须先开发出提供NADPH的经济方法。非生长的大肠杆菌细胞可提供高生产率(0.79 g#epsilon#-己内酯/ L / h等同于18#mu#mol#epsilon#-己内酯/ min / g dcw),收率为88%。非生长细胞的当量当量要比相同菌株的生长细胞大一个数量级。在诱导条件下,在富营养培养基中培养过量表达不动杆菌环己酮单加氧酶的工程大肠杆菌菌株的细胞,直到进入固定相;随后的环己酮氧化反应在缺乏氮源的基本盐溶液中进行。生物转化完成后,内酯产物吸附床至固体支持物并通过用有机溶剂洗涤而回收。

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