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Construction of Recombinant Escherichia coli Strains for Polyhydroxybutyrate Production Using Soy Waste as Nutrient

机译:以大豆废料为营养源的多羟基丁酸酯生产重组大肠杆菌的构建

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Construction and comparison of recombinant Escherichia coli strains harboring the polyhydroxybutyrate (PHB) operon from Ralstonia eutropha using vectors possessing different promotors, as well as the production of PHB from soy waste by the recombinant strain, are reported. The lac promotor was the most efficient on expression of the phb operon among the three promotors studied: i.e., lac promoter, T7 promotor and the normal σ~(70) pro-motor. The pKS/PHB was the most efficient plasmid for phb operon expression among the three plasmids used: i.e., pKS~-, pAED4, and pJM9131. It was observed that isopropyl-β-D-thiogalactopyranoside was not required for the induction of the expression of phb operon. The cell dry wt and polyhydroxy-alkanoate content by E. coli XL-1 Blue (pKS/PHB) were 3.025 g/L and 27.83%, respectively.
机译:报道了使用具有不同启动子的载体构建和比较具有富营养小球藻的多羟基丁酸酯(PHB)操纵子的重组大肠杆菌菌株,以及重组菌株从大豆废料中生产PHB的报道。在研究的三个启动子中,即lac启动子,T7启动子和正常σ〜(70)启动子中,lac启动子对phb操纵子的表达最有效。在使用的三种质粒中,即pKS-,pAED4和pJM9131中,pKS / PHB是用于phb操纵子表达的最有效的质粒。观察到不需要异丙基-β-D-硫代半乳糖吡喃糖苷来诱导phb操纵子的表达。大肠杆菌XL-1 Blue(pKS / PHB)测得的细胞干重和多羟基链烷酸酯含量分别为3.025 g / L和27.83%。

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