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来自降解4-磺酸邻苯二酚的放射形土壤杆菌S2菌株的两种原儿茶酸3,4-双加氧酶基因的特性分析

Characterization of the genes for two protocatechuate 3, 4-dioxygenases from the 4-sulfocatechol-degrading bacterium Agrobacterium radiobacter strain S2.

作者信息

Contzen M, Stolz A

机构信息

Institut für Mikrobiologie, Universität Stuttgart, 70569 Stuttgart, Germany.

出版信息

J Bacteriol. 2000 Nov;182(21):6123-9. doi: 10.1128/JB.182.21.6123-6129.2000.

Abstract

The genes for two different protocatechuate 3,4-dioxygenases (P34Os) were cloned from the 4-sulfocatechol-degrading bacterium Agrobacterium radiobacter strain S2 (DSMZ 5681). The pcaH1G1 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 strain Agrobacterium 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.

摘要

从能够降解4-磺酸邻苯二酚的放射形土壤杆菌菌株S2(DSMZ 5681)中克隆出了两种不同原儿茶酸3,4-双加氧酶(P34O)的基因。pcaH1G1基因编码一种P34O(P34O-I),它能氧化原儿茶酸,但不能氧化4-磺酸邻苯二酚。这些基因是原儿茶酸降解操纵子的一部分,该操纵子与先前D. Parke描述的原儿茶酸降解菌株根癌土壤杆菌A348中的同功能操纵子极为相似(《FEMS微生物学快报》146:3 - 12, 1997)。由pcaH2G2基因编码的第二种P34O(P34O-II)经功能表达后显示能转化原儿茶酸和4-磺酸邻苯二酚。将PcaH-I和PcaH-II以及PcaG-I和PcaG-II的推导氨基酸序列彼此之间以及与来自其他细菌属的P34O的相应序列进行比较,结果表明菌株S2的P34O-II基因是通过横向基因转移获得的。编码P34O-II的基因与另外两个根据序列比对编码转运蛋白的基因一起存在于一个假定的操纵子中。在这个假定操纵子的更下游,鉴定出了两个开放阅读框,它们分别编码IclR家族的假定调节蛋白和假定的3-羧基粘康酸环异构酶。

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