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Originally published In Press as doi:10.1074/jbc.M010567200 on January 31, 2001

J. Biol. Chem., Vol. 276, Issue 17, 13875-13880, April 27, 2001
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Differential Expression of Vibrio vulnificus Elastase Gene in a Growth Phase-dependent Manner by Two Different Types of Promoters*

Hye Sook JeongDagger , Kwang Cheol JeongDagger , Hyun Kyung ChoiDagger , Kyung-Je Park§, Kyu-Ho Lee§, Joon Haeng Rhee, and Sang Ho ChoiDagger ||

From the Dagger  Department of Food Science and Technology, Department of Molecular Biotechnology, Institute of Biotechnology, Chonnam National University, Kwang-Ju 500-757, the § Department of Environmental Science, Hankuk University of Foreign Studies, Yongin, Kyunggi-Do 449-791, and the  Department of Microbiology, Chonnam National University Medical School, Kwang-Ju 500-190, South Korea

Elastase activity of Vibrio vulnificus was highly dependent on growth phase, reached a maximum during the stationary phase, and was regulated at the level of transcription. The stationary phase production of elastase in crp or rpoS mutants, which were constructed by allelic exchanges, decreased about 3- and 10-fold, respectively. However, the promoter activity of vvpE encoding elastase was unaffected by those mutations in the log phase when analyzed using a vvpE-lux fusion. A primer extension analysis revealed that the transcription of vvpE begins at two different sites, consisting of putative promoter L (PL) and promoter S (PS). The PL activity was constitutive through the log and stationary phases, lower than the PS activity, and unaffected by the crp or rpoS mutations. The transcription of PS, induced only in the stationary phase, was dependent on RpoS. The mutation in crp reduced the activity of PS; however, the additional inactivation of crp did not influence the PS activity in the rpoS mutant, indicating that CRP exerted its effects through PS requiring RpoS. These results demonstrate that vvpE expression is differentially directed by PL and PS depending on the growth phase and elevated by RpoS and CRP in the stationary phase.


* This work was supported by a grant to S. H. C. from the Korea Research Foundation (2000-041-G00101), Republic of Korea.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

|| To whom correspondence should be addressed: Dept. of Food Science and Technology, Inst. of Biotechnology, Chonnam National University, Kwang-Ju 500-757, S. Korea. Tel.: 82-62-530-2146; Fax: 82-62-530-2149; E-mail: shchoi@chonnam.chonnam.ac.kr.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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