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Construction of the expression vector based on the growth phase-and growth rate-dependent rmf promoter:use of cell growth rate to control the expression of cloned genes in Escherichia coli

机译:基于依赖于生长阶段和生长速率的rmf启动子的表达载体的构建:利用细胞生长速率来控制克隆基因在大肠杆菌中的表达

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A novel expression vector base don the rmf promoter(Wada et al.Proc,Natl.Acad.Sci.USA(1995) 87:2657-2661) was developed.Using lacZ gene as a model,protein production depending on cell growth pahse and growth rate was found.In addition,by subjecting therecombinant cells to temperature downshift and substrate famine,the strain was capable of producing 35000-40000 units of #beta#-galactosidase.These characteristics indicate the potential application of this expression vector to bioprocessing such as protein production in continuous or batch fermentation,biotransformation using entrapped cells,and in situ bioremediation.
机译:研发了一种新的表达载体,该载体具有rmf启动子(Wada等,Proc,Natl.Acad.Sci.USA(1995)87:2657-2661)。使用lacZ基因作为模型,蛋白质的产生取决于细胞的生长速度和此外,通过使重组细胞经历温度下降和底物饥荒,该菌株能够产生35000-40000单位的#beta#-半乳糖苷酶。这些特征表明了该表达载体在生物加工中的潜在应用,例如在连续或分批发酵中生产蛋白质,使用截留的细胞进行生物转化以及原位生物修复。

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