Mercury resistance transposons of Gram-negative environmental bacteria and their classification
A total of 29 mercury resistance transposons were isolated from mercury-resistant environmental strains of proteobacteria collected in different parts of Eurasia and the USA and tested for hybridization with probes specific for transposase genes of known mercury resistance transposons. 9 were relate...
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Veröffentlicht in: | Research in microbiology 2001-11, Vol.152 (9), p.811-822 |
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Sprache: | eng |
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Zusammenfassung: | A total of 29 mercury resistance transposons were isolated from mercury-resistant environmental strains of proteobacteria collected in different parts of Eurasia and the USA and tested for hybridization with probes specific for transposase genes of known mercury resistance transposons. 9 were related to Tn
21 in this test, 12 were related to Tn
5053, 4 to Tn
5041 and 1 to Tn
5044; three transposons were negative in this test. Restriction mapping and DNA sequencing revealed that 12 transposons were identical or nearly identical to their corresponding relatives while the rest showed varying divergence from their closest relatives. Most of these previously unknown transposons apparently arose as a result of homologous or site-specific recombination. One of these, Tn
5046, was completely sequenced, and shown to be a chimera with the
mer operon and the transposition module derived from the transposons related to Tn
5041 and to Tn
5044, respectively. Transposon Tn
5070, showing no hybridization with the specific probes used in this study, was also completely sequenced. The transposition module of Tn
5070 was most closely related to that of Tn
3 while the
mer operon was most closely related to that of plasmid pMERPH. The
merR of Tn
5070 is transcribed in the same direction as the
mer structural genes, which is typical for
mer operons of Gram-positive bacteria. Our data suggest that environmental bacteria may harbor many not yet recognized mercury resistance transposons and warrant their further inventory. |
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ISSN: | 0923-2508 1769-7123 |
DOI: | 10.1016/S0923-2508(01)01265-7 |