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J. Bacteriol., 01 1998, 167-170, Vol 180, No. 1
P Chen, J Novak, F Qi and PW Caufield
Genetic characterization of a Tn916 transposon mutant, Streptococcus mutans
T8-1, defective in mutacin II production, revealed that the transposon was
inserted into the 3' region of a diacylglycerol kinase (dgk) gene. The
insertion occurred in the same region as described for another S. mutans
mutant, GS5Tn1, which was altered in its ability to respond to
environmental stress (Y. Yamashita, T. Takehara, and H. K. Kuramitsu, J.
Bacteriol. 175:6220-6228, 1993). Quantitative primer extension from the
mutacin structural gene mutA showed a decreased level (about eightfold) of
mutA transcription for mutant T8-1. Mutacin production was restored by
transforming mutant T8-1 with integration vector pVA891 containing an
intact dgk gene. These data indicated that the full-length dgk gene product
along with the mutacin biosynthetic operon are required for the production
of the mutacin II lantibiotic.
Copyright © 1998, American Society for Microbiology
Diacylglycerol kinase is involved in regulation of expression of the lantibiotic mutacin II of Streptococcus mutans [In Process Citation]
Department of Oral Biology, School of Dentistry, University of Alabama at Birmingham, 35294, USA.
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