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首页> 外文期刊>Applied Microbiology and Biotechnology >Effect of inactivation of poly(hydroxyalkanoates) depolymerase gene on the properties of poly(hydroxyalkanoates) in Pseudomonas resinovorans
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Effect of inactivation of poly(hydroxyalkanoates) depolymerase gene on the properties of poly(hydroxyalkanoates) in Pseudomonas resinovorans

机译:聚羟基链烷酸酯解聚酶基因失活对树脂假单胞菌中聚羟基链烷酸酯性质的影响

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摘要

The phaZ gene of Pseudomonas resinovorans codes for a poly(hydroxyalkanoates) (PHA) depolymerase. Two phaZ mutants of Pseudomonas resinovorans NRRL B-2649, FOAC001 and FOAC002, were constructed by an in vitro transposition procedure followed by chromosomal integration via homologous recombination. A detailed mapping of the transposon insertion sites and an analysis of the resultant sequences showed that putative fusion polypeptides PhaZ(FOAC001) (239 amino-acid residues) and PhaZ(FOAC002) (85 amino-acid residues) could result from the mutant phaZ genes of FOAC001 and FOAC002, respectively. In vivo PHA degradation data indicated that PhaZ(FOAC001) might still retain a partial PHA depolymerization activity, while PhaZ(FOAC002) is completely devoid of this function. The cell yields and PHA contents of B-2649, FOAC001, and FOAC002 were similar when the cells were grown either under a limiting nitrogen-source (low-N) condition for up to 5 days or in excess N-source (high-N) for 3 days. A dramatic decrease in PHA content was observed in the PhaZ-active B-2649 and FOAC001 cells during prolonged cell growth (5 days) in high-N medium or in response to a shift-up in nitrogen-source. The repeat-unit compositions of the PHAs from FOAC001 and FOAC002 contained slightly lower amounts of beta-hydroxyoctanoate and higher beta-hydroxytetradecenoate than that of the wild-type B-2649 when grown under a high-N condition. While the molecular masses of the PHAs from FOAC001 and FOAC002 did not vary under any conditions used in this study, those of the wild-type B-2649 were markedly increased in cells either grown for 5 days under a high-N condition or subjected to a nitrogen-source shift-up. These phaZ mutants thus provide a valuable system to study the influence of PHA depolymerase on the accumulation and properties of medium-chain-length PHA. [References: 21]
机译:树脂假单胞菌的phaZ基因编码聚(羟基链烷酸酯)(PHA)解聚酶。通过体外转座程序,然后通过同源重组进行染色体整合,构建了树脂假单胞菌NRRL B-2649的两个phaZ突变体FOAC001和FOAC002。转座子插入位点的详细定位和所得序列的分析表明,突变的phaZ基因可能导致推定的融合多肽PhaZ(FOAC001)(239个氨基酸残基)和PhaZ(FOAC002)(85个氨基酸残基)分别为FOAC001和FOAC002。体内PHA降解数据表明,PhaZ(FOAC001)可能仍保留部分PHA解聚活性,而PhaZ(FOAC002)完全没有此功能。当细胞在有限氮源(低氮)条件下生长长达5天或过量氮源(高氮)下生长时,B-2649,FOAC001和FOAC002的细胞产量和PHA含量相似。 )的3天。在高氮培养基中延长的细胞生长(5天)过程中或响应氮源的上移,在PhaZ活性B-2649和FOAC001细胞中观察到PHA含量急剧下降。在高氮条件下生长时,来自FOAC001和FOAC002的PHA的重复单元组成比野生型B-2649的β-羟基辛酸酯含​​量略低,而β-羟基十四碳酸酯含量更高。尽管在本研究中使用的任何条件下,FOAC001和FOAC002的PHA的分子质量均没有变化,但野生型B-2649的分子在高氮条件下生长5天或受到氮源上移。因此,这些phaZ突变体提供了一个有价值的系统,可用于研究PHA解聚酶对中链PHA积累和性质的影响。 [参考:21]

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