Journal of Biochemistry Advance Access originally published online on July 27, 2006
Journal of Biochemistry 2006 140(3):429-438; doi:10.1093/jb/mvj168
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© 2006 The Japanese Biochemical Society.
ARTICLE |
Homologous Response Regulators KvgA, KvhA and KvhR Regulate the Synthesis of Capsular Polysaccharide in Klebsiella pneumoniae CG43 in a Coordinated Manner
Department of Biological Science and Technology, National Chiao Tung University, 75 Po-Ai Street, Hsin Chu 30050, Taiwan, Republic of China
* To whom correspondence should be addressed. Phone: +886 3 5712121 (Ext. 56916), Fax: +886 3 5729288, E-mail: hlpeng{at}cc.nctu.edu.tw
On the basis of phenotypic analysis, the Klebsiella pneumoniae CG43 derived mutants with deletions of the gene encoding respectively the response regulators KvgA, KvhA, and KvhR were classified into two groups. Group I bacteria carrying either kvgA or kvhR exhibited less mucoidy, lower level of capsular polysaccharide (CPS) synthesis and higher LD50 than the parental strain. No apparent change of the group II, including kvhA and kvhAkvhR mutants, was observed. However, the mucoidy of kvhAkvhR mutant was found to be diminished after introducing into a kvhA expressing plasmid. Via promoter-lacZ fusion analysis, kvhA deletion was found to reduce kvhR expression. A regulatory role of KvhA for the expression of kvhR was supported further by EMSA showing a specific binding of KvhA to the putative promoter of kvhR. The promoter activity measurement and EMSA also revealed that KvgA acted as an autoregulator and an activator for the expression of kvhAS and kvhR. In addition, deletion of kvgA suppressed slightly the promoter activity of the cps-orf16-17, and the expression of all three cps transcripts orf1-2, orf3-15, and orf16-17 were reduced in the kvhR mutant. These suggest that the three homologous response regulators interact to control, in coordination, the bacterial cps expression.
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C.-T. Lin and H.-L. Peng Regulation of the Homologous Two-Component Systems KvgAS and KvhAS in Klebsiella pneumoniae CG43 J. Biochem., November 1, 2006; 140(5): 639 - 648. [Abstract] [Full Text] [PDF] |
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