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首页> 外文期刊>Journal of bacteriology >Characterization of the Genes for Two Protocatechuate 3,4-Dioxygenases from the 4-Sulfocatechol-Degrading Bacterium Agrobacterium radiobacter Strain S2
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Characterization of the Genes for Two Protocatechuate 3,4-Dioxygenases from the 4-Sulfocatechol-Degrading Bacterium Agrobacterium radiobacter Strain S2

机译:从4-磺基邻苯二酚降解农杆菌放射细菌菌株S2的两个原儿茶酸3,4-双加氧酶的基因的表征。

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摘要

The genes for two different protocatechuate 3,4-dioxygenases (P34Os) were cloned from the 4-sulfocatechol-degrading bacteriumAgrobacterium radiobacter strain S2 (DSMZ 5681). ThepcaH1G1 genes encoded a P34O (P34O-I) which oxidized protocatechuate but not 4-sulfocatechol. These genes were part of a protocatechuate-degradative operon which strongly resembled the isofunctional operon from the protocatechuate-degrading strainAgrobacterium tumefaciens A348 described previously by D. Parke (FEMS Microbiol. Lett. 146:3–12, 1997). The second P34O (P34O-II), encoded by the pcaH2G2 genes, was functionally expressed and shown to convert protocatechuate and 4-sulfocatechol. A comparison of the deduced amino acid sequences of PcaH-I and PcaH-II, and of PcaG-I and PcaG-II, with each other and with the corresponding sequences from the P34Os, from other bacterial genera suggested that the genes for the P34O-II were obtained by strain S2 by lateral gene transfer. The genes encoding the P34O-II were found in a putative operon together with two genes which, according to sequence alignments, encoded transport proteins. Further downstream from this putative operon, two open reading frames which code for a putative regulator protein of the IclR family and a putative 3-carboxymuconate cycloisomerase were identified.
机译:从4-磺基邻苯二酚降解细菌 Agrobacterium radiobacter S2(DSMZ 5681)克隆了两种不同的原儿茶酸3,4-双加氧酶(P34Os)基因。 pcaH1G1 基因编码的P34O(P34O-I)氧化了原儿茶酸而不是4-磺基儿茶酚。这些基因是原儿茶酸降解操纵子的一部分,该操纵子非常类似于原先由D. Parke(FEMS Microbiol。Lett。146:3–12的原发根癌农杆菌A348的同功能操纵子)组成。 1997)。由 pcaH2G2 基因编码的第二个P34O(P34O-II)在功能上得到表达,并显示可以转化原儿茶酸和4-磺基儿茶酚。推导的PcaH-I和PcaH-II氨基酸序列以及PcaG-I和PcaG-II的氨基酸序列彼此之间以及与其他细菌属的P34Os相应序列的比较表明,P34O的基因通过侧向基因转移通过菌株S2获得-II。在推定的操纵子中发现了编码P34O-II的基因,以及两个根据序列比对编码转运蛋白的基因。在该推定操纵子的更下游,鉴定了两个开放阅读框,其编码IclR家族的推定调节蛋白和推定的3-羧基粘康酸酯环异构酶。

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