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Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) from glucose with elevated 3-hydroxyvalerate fraction via combined citramalate and threonine pathway in Escherichia coli

机译:通过结合柠檬酸和苏氨酸途径在大肠杆菌中从葡萄糖中提高3-羟基戊酸酯含量的生物合成聚(3-羟基丁酸酯-co-3-羟基戊酸酯)

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摘要

The biosynthesis of polyhydroxyalkanoate copolymers in Escherichia coli from unrelated carbon sources becomes attractive nowadays. We previously developed a poly(hydroxybutyrate-co-hydroxyvalerte) (PHBV) biosynthetic pathway from an unrelated carbon source via threonine metabolic route in E. coli(Chen et al.,Appl Environ Microbiol 77:4886-4893, 2011). In our study, a citramalate pathway was introduced in recombinant E. coliby cloning a cimAgene from Leptospira interrogans. By blocking the pyruvate and the propionyl-CoA catabolism and replacing the β-ketothiolase gene, the PHBV with 11.5 mol% 3HV fraction was synthesized. Further, the combination of citramalate pathway with the threonine biosynthesis pathway improved the 3HV fraction in PHBV copolymer to 25.4 mol%in recombinant E. coli.
机译:如今,从无关的碳源在大肠杆菌中生物合成聚羟基链烷酸酯共聚物变得很有吸引力。我们先前通过大肠杆菌中的苏氨酸代谢途径从不相关的碳源开发了聚羟基丁酸酯-共羟基戊酸酯(PHBV)生物合成途径(Chen等人,Appl Environ Microbiol 77:4886-4893,2011)。在我们的研究中,通过从询问钩端螺旋体克隆cimA基因,在重组大肠杆菌中引入了柠檬酸途径。通过阻断丙酮酸和丙酰辅酶A的分解代谢并替换β-酮硫解酶基因,合成了具有11.5mol%3HV部分的PHBV。此外,柠檬酸途径与苏氨酸生物合成途径的组合将重组大肠杆菌中PHBV共聚物中的3HV部分提高至25.4mol%。

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