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首页> 外文期刊>Applied Microbiology and Biotechnology >Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyalkanoates) by recombinant bacteria expressing the PHA synthase gene phaC1 from Pseudomonas sp 61-3
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Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyalkanoates) by recombinant bacteria expressing the PHA synthase gene phaC1 from Pseudomonas sp 61-3

机译:表达假单胞菌sp 61-3的PHA合酶基因phaC1的重组细菌对聚(3-羟基丁酸酯-co-3-羟基链烷酸酯)的生物合成

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摘要

Pseudomonas sp. 61-3 accumulated a blend of poly(3-hydroxybutyrate) [P(3HB)] homopolymer and a random copolymer consisting of 3-hydroxyalkanoate (3HA) units of 4-12 carbon atoms. The genes encoding beta-ketothiolase (PhbAR(Re)) and NADPH-dependent acetoacetyl-CoA reductase (PhbB(Re)) from Ralstonia eutropha were expressed under the control of promoters for Pseudomonas sp. 61-3 pha locus or ii. eutropha phb operon together with phaCl(Ps) gene (PHA synthase 1 gene) from Pseudomonas sp. 61-3 in PHA-negative mutants P. putida GPp104 and R. eutropha PHB(-)4 to produce copolyesters [P(3HB-co-3HA)] consisting of 3HB and medium-chain-length 3HA units of 6-12 carbon atoms. The introduction of the three genes into GPp104 strain conferred the ability to synthesize P(3HB-co-3HA) with relatively high 3HB compositions (up to 49 mol%) from gluconate and alkanoates, although 3HB units were not incorporated at all or at a very low fraction (3 mol%) into copolyesters by the strain carrying phaCl(Ps) gene only. In addition, recombinant strains of R. eutropha PHB(-)4 produced P(3HB-co-3HA) with higher 3HB fractions from alkanoates and plant oils than those from recombinant GPp104 strains. One of the recombinant strains, R. eutropha PHB(-)4/ pJKSc46-pha, in which all the genes introduced were expressed under the control of the native promoter for Pseudomonas sp. 61-3 pha locus, accumulated P(3HB-co-3HA) copolyester with a very high 3HB fraction (85 mol%) from palm oil. The nuclear magnetic resonance analyses showed that the copolyesters obtained here were random copolymers of 3HB and 3HA units. [References: 37]
机译:假单胞菌61-3累积了聚(3-羟基丁酸酯)[P(3HB)]均聚物和由4-12个碳原子的3-羟基链烷酸酯(3HA)单元组成的无规共聚物的共混物。在富营养假单胞菌的启动子的控制下,表达了来自富营养小球藻的β-酮硫醇酶(PhbAR(Re))和NADPH依赖性乙酰乙酰辅酶A还原酶(PhbB(Re))的基因。 61-3相位或ii。富营养化phb操纵子与假单胞菌属的phaCl(Ps)基因(PHA合酶1基因)一起。在PHA阴性突变体恶臭假单胞菌GPp104和富营养假单胞菌PHB(-)4中产生61-3,以产生由3HB和6-12个碳原子的中链长度3HA单元组成的共聚酯[P(3HB-co-3HA)]原子。将三个基因引入GPp104菌株赋予了从葡萄糖酸和链烷酸酯合成具有相对较高3HB组成(最高49 mol%)的P(3HB-co-3HA)的能力,尽管3HB单元根本没有或根本没有结合。仅携带phaCl(Ps)基因的菌株可将极低的部分(3 mol%)转化为共聚酯。此外,富营养罗汉果PHB(-)4的重组菌株从链烷酸酯和植物油中产生的P(3HB-co-3HA)具有比重组GPp104菌株更高的3HB馏分。重组菌株之一,富营养古生菌PHB(-)4 / pJKSc46-pha,其中引入的所有基因在假单胞菌sp。的天然启动子的控制下表达。 61-3相位,从棕榈油中积累的P(3HB-co-3HA)共聚酯具有很高的3HB比例(85 mol%)。核磁共振分析表明,此处获得的共聚酯是3HB和3HA单元的无规共聚物。 [参考:37]

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