首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Molecular Characterization of the Genes pcaG and pcaH Encoding Protocatechuate 34-Dioxygenase Which Are Essential for Vanillin Catabolism in Pseudomonas sp. Strain HR199
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Molecular Characterization of the Genes pcaG and pcaH Encoding Protocatechuate 34-Dioxygenase Which Are Essential for Vanillin Catabolism in Pseudomonas sp. Strain HR199

机译:编码原儿茶酸34-双加氧酶的基因pcaG和pcaH的分子表征这对于假单胞菌属中的香兰素代谢而言是必不可少的。应变HR199

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摘要

Pseudomonas sp. strain HR199 is able to utilize eugenol (4-allyl-2-methoxyphenol), vanillin (4-hydroxy-3-methoxybenzaldehyde), or protocatechuate as the sole carbon source for growth. Mutants of this strain which were impaired in the catabolism of vanillin but retained the ability to utilize eugenol or protocatechuate were obtained after nitrosoguanidine mutagenesis. One mutant (SK6169) was used as recipient of a Pseudomonas sp. strain HR199 genomic library in cosmid pVK100, and phenotypic complementation was achieved with a 5.8-kbp EcoRI fragment (E58). The amino acid sequences deduced from two corresponding open reading frames (ORF) identified on E58 revealed high degrees of homology to pcaG and pcaH, encoding the two subunits of protocatechuate 3,4-dioxygenase. Three additional ORF most probably encoded a 4-hydroxybenzoate 3-hydroxylase (PobA) and two putative regulatory proteins, which exhibited homology to PcaQ of Agrobacterium tumefaciens and PobR of Pseudomonas aeruginosa, respectively. Since mutant SK6169 was also complemented by a subfragment of E58 that harbored only pcaH, this mutant was most probably lacking a functional β subunit of the protocatechuate 3,4-dioxygenase. Since this mutant was still able to grow on protocatechuate and lacked protocatechuate 4,5-dioxygenase and protocatechuate 2,3-dioxygenase, the degradation had to be catalyzed by different enzymes. Two other mutants (SK6184 and SK6190), which were also impaired in the catabolism of vanillin, were not complemented by fragment E58. Since these mutants accumulated 3-carboxy muconolactone during cultivation on eugenol, they most probably exhibited a defect in a step of the catabolic pathway following the ortho cleavage. Moreover, in these mutants cyclization of 3-carboxymuconic acid seems to occur by a syn absolute stereochemical course, which is normally only observed for cis,cis-muconate lactonization in pseudomonads. In conclusion, vanillin is degraded through the ortho-cleavage pathway in Pseudomonas sp. strain HR199 whereas protocatechuate could also be metabolized via a different pathway in the mutants.
机译:假单胞菌菌株HR199能够利用丁子香酚(4-烯丙基-2-甲氧基苯酚),香兰素(4-羟基-3-甲氧基苯甲醛)或原儿茶酸酯作为唯一的碳源进行生长。在亚硝基胍诱变后获得了该菌株的突变体,其突变体的香兰素分解代谢受损,但保留了利用丁香酚或原儿茶酸的能力。一种突变体(SK6169)被用作假单胞菌属sp的接收者。质粒pVK100中的HR199基因组文库,并用5.8 kbp EcoRI片段(E58)实现了表型互补。从在E58上鉴定的两个相应的开放阅读框(ORF)推导的氨基酸序列显示出与pcaG和pcaH的高度同源性,它们编码原儿茶酸3,4-二加氧酶的两个亚基。另外三个ORF最有可能编码4-羟基苯甲酸酯3-羟化酶(PobA)和两个推定的调节蛋白,它们分别与根癌农杆菌的PcaQ和铜绿假单胞菌的PobR具有同源性。由于突变体SK6169也被仅包含pcaH的E58亚片段所补充,因此该突变体很可能缺少原儿茶酸3,4-双加氧酶的功能性β亚基。由于该突变体仍然能够在原儿茶酸上生长并且缺乏原儿茶酸4,5-二加氧酶和原儿茶酸2,3-二加氧酶,因此降解必须由不同的酶催化。香草醛分解代谢也受损的另外两个突变体(SK6184和SK6190)没有片段E58的互补。由于这些突变体在丁香酚上培养期间积累了3-羧基粘康内酯,因此它们很可能在邻位裂解后的分解代谢途径步骤中表现出缺陷。而且,在这些突变体中,3-羧基粘康酸的环化似乎是通过顺式绝对立体化学过程发生的,通常仅在假单胞菌中观察到顺式,顺式-粘康酸酯内酯化。总之,香兰素通过假单胞菌属物种中的邻位裂解途径降解。菌株HR199,而原儿茶酸也可以通过突变体中的不同途径代谢。

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