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Appl. Environ. Microbiol. doi:10.1128/AEM.00616-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Nucleotide sequence of plasmid pCNB1 from Comamonas strain CNB-1 reveals novel genetic organization and evolution for 4-chloronitrobenzene degradation

Ying-Fei Ma, Jian-Feng Wu, Sheng-Yue Wang, Cheng-Ying Jiang, Yun Zhang, Su-Wei Qi, Lei Liu, Guo-Ping Zhao*, and Shuang-Jiang Liu*

State Key Laboratory of Microbial Resource at Institute of Microbiology, Beijing, 100080; and Shanghai Institutes for Biological Sciences, Shanghai, 200031, P. R. China

* To whom correspondence should be addressed. Email: gpzhao{at}sibs.ac.cn. liusj{at}sun.im.ac.cn.


   Abstract

The nucleotide sequence of a new plasmid pCNB1 from Comamonas sp. strain CNB-1 that degrades 4-chloronitrobenzene (4CNB) was determined. pCNB1 belongs to IncP-1{beta} group and is 91,181-bp in length. A total of 95 open reading frames (ORFs) appear to be involved in (i) the replication, maintenance, and transfer of pCNB1, (ii) resistance to arsenate and chromate, and (iii) the degradation of 4CNB. The 4CNB degradative genes and arsenate resistance genes were located on an extraordinarily large transposon (44.5 kb), proposed as TnCNB1. TnCNB1 was flanked by two IS1071 sequences, and represents a new member of composite I transposon family. The 4CNB degradative genes within TnCNB1 were separated by various truncated genes and genetic homologs from other DNA molecules. Genes for chromate resistance were located on another transposon that was similar to Tn21 transposon of the class II replicative family that is frequently responsible for mobilization of mercury resistance genes. Resistance to arsenate and chromate were experimentally confirmed, and transcriptions of arsenate and chromate resistance genes were demonstrated by reverse transcription-PCR. These results described a new member of the IncP-1{beta} plasmid family and the findings suggest that gene deletion and acquisition as well as genetic rearrangement of DNA molecules happened during the evolution of the 4CNB degradation pathway on pCNB1.




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