Research Support, Non-U.S. Gov't
- Development of a Suicidal Vector-Cloning System Based on Butanal Susceptibility Due to an Expression of YqhD Aldehyde Reductase
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Changhan Lee , Chankyu Park
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J. Microbiol. 2012;50(2):249-255. Published online April 27, 2012
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DOI: https://doi.org/10.1007/s12275-012-1438-5
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Abstract
- Previously, we observed butanal/propanal sensitivity of
Escherichia coli K-12 when cells overexpress YqhD protein,
a NADPH dependent aldehyde reductase, possibly due to
an accumulation of butanol/propanol in vivo as the reaction
products. Based on this finding, we developed a suicidal
vector-cloning system derived from pUC19, in which lacZ
was substituted with the yqhD gene. As a result, when foreign
DNA was inserted into its multiple cloning sites by disrupting
an expression of YqhD, the recombinants survived on
butanal/propanal containing plate, whereas cells containing
the YqhD vector died because of the alcohol production
by YqhD. The cloning efficiency, estimated based on colony
PCR and enzyme digestion, was achieved more than 90%
when the suicidal vector system was used. Moreover, the
plasmid vector itself was stably maintained in the cell, presumably
due to its ability to remove toxic aldehydes being
accumulated in E. coli cell by metabolic stress.