Functional activity of the modA sub(2 )gene in Methylobacterium dichloromethanicum DM4
The putative METDI2644 (modA sub(2 )) gene of Methylobacterium dichloromethanicum DM4, present in the 126-kb chromosomal fragment associated with dichloromethane (DCM) degradation, was investigated. While this gene is presumed to encode the periplasmic substrate-binding subunit of a molybdate ABC tr...
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Published in | Microbiology (New York) Vol. 83; no. 3; pp. 205 - 210 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
01.05.2014
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Subjects | |
Online Access | Get full text |
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Summary: | The putative METDI2644 (modA sub(2 )) gene of Methylobacterium dichloromethanicum DM4, present in the 126-kb chromosomal fragment associated with dichloromethane (DCM) degradation, was investigated. While this gene is presumed to encode the periplasmic substrate-binding subunit of a molybdate ABC transporter, its conceptual translation also exhibits similarity to proteins containing the ostA conservative domain and responsible for resistance of gram-negative bacteria to organic solvents. Reverse transcription polymerase chain reaction (RT-PCR) revealed RNA transcripts of this gene in the cells grown on either DCM or cells grown on methanol. The mobilizable suicide vector pK18mob was used to obtain a knockout mutant with the METDI2644 gene inactivated by insertion of the gentamycin cassette. The mutant pregrown on methanol exhibited lower growth rate on DCM than the wild-type strain DM4. The difference was not alleviated by the addition of sodium molybdate. Our results demonstrate that the METDI2644 gene product plays a role in cell adaptation to DCM degradation. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0026-2617 1608-3237 |
DOI: | 10.1134/S0026261714030060 |