首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Role of fadR and atoC(Con) mutations in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthesis in recombinant pha+ Escherichia coli.
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Role of fadR and atoC(Con) mutations in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthesis in recombinant pha+ Escherichia coli.

机译:fadR和atoC(Con)突变在重组pha +大肠杆菌中的聚(3-羟基丁酸酯-co-3-羟基戊酸酯)合成中的作用。

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摘要

Recombinant Escherichia coli fadR atoC(Con) mutants containing the polyhydroxyalkanoate (PHA) biosynthesis genes from Alcaligenes eutrophus are able to incorporate significant levels of 3-hydroxyvalerate (3HV) into the copolymer poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(3HB-co-3HV)]. We have used E. coli fadR (FadR is a negative regulator of fatty acid oxidation) and E. coli atoC(Con) (AtoC is a positive regulator of fatty acid uptake) mutants to demonstrate that either one of these mutations alone can facilitate copolymer synthesis but that 3HV levels in single mutant strains are much lower than in the fadR atoC(Con) strain. E. coli atoC(Con) mutants were used alone and in conjunction with atoA and atoD mutants to determine that the function of the atoC(Con) mutation is to increase the uptake of propionate and that this uptake is mediated, at least in part, by atoD+. Similarly, E. coli fadR mutants were used alone and in conjunction with fadA, fadB, and fadL mutants to show that the effect of the fadR mutation is dependent on fadB+ and fadA+ gene products. Strains that were mutant in the fadB or fadA locus were unable to complement a PHA biosynthesis pathway that was mutant at the phaA locus (thiolase), but a strain containing a fadR mutation and which was fadA+ fadB+ was able to complement the phaA mutation and incorporated 3HV into P(3HB-co-3HV) to a level of 29 mol%.
机译:包含来自嗜碱产碱杆菌的多羟基链烷酸酯(PHA)生物合成基因的重组大肠杆菌fadR atoC(Con)突变体能够将显着水平的3-羟基戊酸酯(3HV)掺入共聚物聚(3-羟基丁酸酯-co-3-羟基戊酸酯)[P (3HB-co-3HV)]。我们已经使用了大肠杆菌fadR(FadR是脂肪酸氧化的负调节剂)和大肠杆菌atoC(Con)(AtoC是脂肪酸摄取的正调节剂)突变体来证明单独使用这些突变之一可以促进共聚物合成,但单个突变株中的3HV水平远低于fadR atoC(Con)株。单独使用大肠杆菌atoC(Con)突变体,并与atoA和atoD突变体结合使用,以确定atoC(Con)突变的功能是增加丙酸的吸收,并且至少部分地介导了这种吸收。通过atoD +。同样,大肠杆菌fadR突变体单独使用,也与fadA,fadB和fadL突变体结合使用,以表明fadR突变的作用取决于fadB +和fadA +基因产物。在fadB或fadA位点突变的菌株无法补充在phaA位点突变的PHA生物合成途径(硫解酶),但是含有fadR突变且fadA + fadB +的菌株能够补充phaA突变并掺入将3HV转化为P(3HB-co-3HV)的含量为29摩尔%。

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