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首页> 外文期刊>Molecular Microbiology >Two different pathways are involved in the beta-oxidation of n-alkanoic and n-phenylalkanoic acids in Pseudomonas putida U: genetic studies and biotechnological applications.
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Two different pathways are involved in the beta-oxidation of n-alkanoic and n-phenylalkanoic acids in Pseudomonas putida U: genetic studies and biotechnological applications.

机译:恶臭假单胞菌(Pseudomonas putida U)中正链烷酸和正苯基链烷酸的β-氧化涉及两种不同的途径:遗传研究和生物技术应用。

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摘要

In Pseudomonas putida U, the degradation of n-alkanoic and n-phenylalkanoic acids is carried out by two sets of beta-oxidation enzymes (betaI and betaII). Whereas the first one (called betaI) is constitutive and catalyses the degradation of n-alkanoic and n-phenylalkanoic acids very efficiently, the other one (betaII), which is only expressed when some of the genes encoding betaI enzymes are mutated, catabolizes n-phenylalkanoates (n > 4) much more slowly. Genetic studies revealed that disruption or deletion of some of the betaI genes handicaps the growth of P. putida U in media containing n-alkanoic or n-phenylalkanoic acids with an acyl moiety longer than C4. However, all these mutants regained their ability to grow in media containing n-alkanoates as a result of the induction of betaII, but they were still unable to catabolize n-phenylalkanoates completely, as the betaI-FadBA enzymes are essential for the beta-oxidation of certain n-phenylalkanoyl-CoA derivatives when they reach a critical size. Owing to the existence of the betaII system, mutants lacking betaIfadB/A are able to synthesize new poly 3-OH-n-alkanoates (PHAs) and poly 3-OH-n-phenylalkanoates (PHPhAs) efficiently. However, they are unable to degrade these polymers, becoming bioplastic overproducer mutants. The genetic and biochemical importance of these results is reported and discussed.
机译:在恶臭假单胞菌(Pseudomonas putida U)中,正链烷酸和正苯基链烷酸的降解通过两组β-氧化酶(βI和βII)进行。第一个(称为betaI)是组成型的并且非常有效地催化n-链烷酸和n-苯基链烷酸的降解,而另一个(betaII)(仅当某些编码betaI酶的基因发生突变时才表达)将n分解代谢。 -苯基链烷酸酯(n> 4)要慢得多。遗传研究表明,某些betaI基因的破坏或缺失会阻碍恶臭假单胞菌U在含有长于C4的酰基部分的正链烷酸或正苯基链烷酸的培养基中生长。然而,所有这些突变体由于βII的诱导而恢复了在含正链烷酸酯的培养基中生长的能力,但它们仍无法完全分解代谢正苯基链烷酸酯,因为βI-FadBA酶对于β氧化至关重要当某些n-苯基烷酰基-CoA衍生物达到临界尺寸时。由于存在betaII系统,缺乏betaIfadB / A的突变体能够有效地合成新的聚3-OH-n-链烷酸酯(PHA)和聚3-OH-n-苯基链烷酸酯(PHPhAs)。但是,它们无法降解这些聚合物,成为生物塑料生产过量的突变体。这些结果的遗传和生物化学重要性已被报道和讨论。

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