首页> 美国卫生研究院文献>Applied and Environmental Microbiology >The Chlorocatechol-Catabolic Transposon Tn5707 of Alcaligenes eutrophus NH9 Carrying a Gene Cluster Highly Homologous to That in the 124-Trichlorobenzene-Degrading Bacterium Pseudomonas sp. Strain P51 Confers the Ability To Grow on 3-Chlorobenzoate
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The Chlorocatechol-Catabolic Transposon Tn5707 of Alcaligenes eutrophus NH9 Carrying a Gene Cluster Highly Homologous to That in the 124-Trichlorobenzene-Degrading Bacterium Pseudomonas sp. Strain P51 Confers the Ability To Grow on 3-Chlorobenzoate

机译:拟南芥NH9的氯邻苯二酚-转座子Tn5707携带与在124-三氯苯降解细菌假单胞菌中高度同源的基因簇。 P51菌株具有3-氯苯甲酸酯的生长能力

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摘要

Alcaligenes eutrophus (Ralstonia eutropha) NH9, isolated in Japan, utilizes 3-chlorobenzoate as its sole source of carbon and energy. Sequencing of the relevant region of plasmid pENH91 from strain NH9 revealed that the genes for the catabolic enzymes were homologous to the genes of the modified ortho-cleavage pathway. The genes from strain NH9 (cbnR-ABCD) showed the highest homology (89 to 100% identity at the nucleotide level) to the tcbR-CDEF genes on plasmid pP51 of the 1,2,4-trichlorobenzene-degrading bacterium Pseudomonas sp. strain P51, which was isolated in The Netherlands. The structure of the operon, including the lengths of open reading frames and intervening sequences, was completely conserved between the cbn and tcb genes. Most nucleotide substitutions were localized within and proximal to the cbnB (tcbD) gene. The difference in the chloroaromatics that the two strains could use as growth substrates seemed to be due to differences in enzymes that convert substrates to chlorocatechols. The restriction map of plasmid pENH91 was clearly different from that of pP51 except in the regions that contained the cbnR-ABCD and tcbR-CDEF genes, respectively, suggesting that the chlorocatechol gene clusters might have been transferred as units. Two homologous sequences, present as direct repeats in both flanking regions of the cbnR-ABCD genes on pENH91, were found to be identical insertion sequences (ISs), designated IS1600, which formed a composite transposon designated Tn5707. Although the tcbR-CDEF genes were not associated with similar ISs, a DNA fragment homologous to IS1600 was cloned from the chromosome of strain P51. The sequence of the fragment suggested that it might be a remnant of an IS. The two sequences, together with IS1326 and nmoT, formed a distinct cluster on a phylogenetic tree of the IS21 family. The diversity of the sources of these IS or IS-like elements suggests the prevalence of ISs of this type.
机译:在日本分离的嗜碱拟南芥(Ralstonia eutrophas)NH9利用3-氯苯甲酸酯作为唯一的碳和能源。从菌株NH9对质粒pENH91的相关区域进行测序表明,分解代谢酶的基因与修饰的邻位切割途径的基因同源。来自NH9菌株的基因(cbnR-ABCD)与降解1,2,4-三氯苯的细菌Pseudomonas sp。的质粒pP51上的tcbR-CDEF基因具有最高的同源性(在核苷酸水平上具有89%至100%的同一性)。 P51菌株,在荷兰分离。操纵子的结构,包括开放阅读框的长度和插入序列的长度,在cbn和tcb基因之间是完全保守的。大多数核苷酸取代位于cbnB(tcbD)基因内或附近。两种菌株可以用作生长底物的氯代芳香烃的差异似乎是由于将底物转化为氯邻苯二酚的酶的差异所致。质粒pENH91的限制性酶切图谱与pP51的限制性酶切图谱明显不同,除了分别包含cbnR-ABCD和tcbR-CDEF基因的区域外,这表明氯邻苯二酚基因簇可能已作为单位转移。发现在pENH91上cbnR-ABCD基因的两个侧翼区域直接重复出现的两个同源序列是相同的插入序列(IS),称为IS1600,形成了一个复合转座子,命名为Tn5707。尽管tcbR-CDEF基因与相似的IS无关,但从菌株P51的染色体上克隆了与IS 1600 同源的DNA片段。该片段的序列表明它可能是IS的残余。这两个序列与IS 1326 nmoT 一起在IS 21 家族的系统树上形成了独特的簇。这些IS或类似IS的元素来源的多样性表明这种IS的流行。

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