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Optimizing the Production of 5-Aminolevulinic Acid by Recombinant Escherichia coli Containing the Rhodobacter capsulatus hemA Gene

机译:含有荚膜红细菌hemA基因的重组大肠杆菌优化5-氨基乙酰丙酸的生产

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摘要

Recombinant Escherichia coli BLR(DE3) harboring the hemA gene from Rhodobacter capsulatus under the control of a constitutive promoter, which we constructed previously, was used for the extracellular production of 5-aminolevulinic acid (ALA). The effects of several factors on ALA production were investigated in flask culture. ALA production by the recombinant E. coli was more efficient at 30°C than 37°C. The glycine concentration had an important effect on cell growth. Glycine and succinic acid concentration of 5-10 and 10-20 g/L, respectively, resulted in high ALA production. In addition, the partial replacement of succinic acid by sodium glutamate increased the ALA production. The ALA production was inhibited by the presence of glucose in the medium. Using the optimal conditions, an ALA concentration of 8.2 g/L was achieved in jar fermentation without an added inducer or ALA dehydratase inhibitor; this is the highest reported concentration.
机译:在我们先前构建的组成型启动子的控制下,携带来自荚膜红球菌的hemA基因的重组大肠杆菌BLR(DE3)用于细胞外产生5-氨基乙酰丙酸(ALA)。在烧瓶培养中研究了几种因素对ALA产生的影响。在30°C时,重组大肠杆菌生产ALA比在37°C时效率更高。甘氨酸浓度对细胞生长有重要影响。甘氨酸和琥珀酸的浓度分别为5-10 g / L和10-20 g / L,导致高的ALA产量。另外,用谷氨酸钠部分替代琥珀酸增加了ALA的产生。培养基中葡萄糖的存在抑制了ALA的产生。使用最佳条件,在不添加诱导剂或ALA脱水酶抑制剂的广口瓶发酵中,ALA浓度达到8.2 g / L。这是报告的最高浓度。

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