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Production in Escherichia coli of Poly(3-Hydroxybutyrate-co-3-Hydroxyvalerate) with Differing Monomer Compositions from Unrelated Carbon Sources

机译:在大肠杆菌中生产不相关碳源的不同单体组成的聚(3-羟基丁酸酯-co-3-羟基戊酸酯)

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摘要

The industrial production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) has been hindered by high cost and a complex control strategy caused by the addition of propionate. In this study, based on analysis of the PHBV biosynthesis process, we developed a PHBV biosynthetic pathway from a single unrelated carbon source via threonine biosynthesis in Escherichia coli. To accomplish this, we (i) overexpressed threonine deaminase, which is the key factor for providing propionyl-coenzyme A (propionyl-CoA), from different host bacteria, (ii) removed the feedback inhibition of threonine by mutating and overexpressing the thrABC operon in E. coli, and (iii) knocked out the competitive pathways of catalytic conversion of propionyl-CoA to 3-hydroxyvaleryl-CoA. Finally, we constructed a series of strains and mutants which were able to produce the PHBV copolymer with differing monomer compositions in a modified M9 medium supplemented with 20 g/liter xylose. The largest 3-hydroxyvalerate fraction obtained in the copolymer was 17.5 mol%.
机译:聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV)的工业化生产因成本高以及添加丙酸酯引起的复杂控制策略而受到阻碍。在这项研究中,基于对PHBV生物合成过程的分析,我们从单一无关碳源通过苏氨酸生物合成开发了一种PHBV生物合成途径。为此,我们(i)过表达苏氨酸脱氨酶,这是从不同宿主细菌中提供丙酰辅酶A(propionyl-CoA)的关键因素,(ii)通过突变和过表达thrABC操纵子来消除对苏氨酸的反馈抑制作用(iii)消除了丙酰辅酶A催化转化为3-羟基戊酰辅酶A的竞争途径。最后,我们构建了一系列菌株和突变体,它们能够在添加了20 g /升木糖的改良M9培养基中生产具有不同单体组成的PHBV共聚物。在该共聚物中获得的最大的3-羟基戊酸酯分数为17.5mol%。

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