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Journal of Bacteriology, July 2009, p. 4152-4157, Vol. 191, No. 13
0021-9193/09/$08.00+0 doi:10.1128/JB.00227-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Agricultural Biotechnology and Center for Agricultural Biomaterials, Seoul National University, Seoul 151-921, Republic of Korea,1 Plant Genome Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-633, Republic of Korea2
Received 19 February 2009/ Accepted 21 April 2009
Quorum sensing (QS) plays important roles in the pathogenicity of Burkholderia glumae, the causative agent of bacterial rice grain rot. We determined how QS is involved in catalase expression in B. glumae. The QS-defective mutant of B. glumae exhibited less catalase activity than wild-type B. glumae. A β-glucuronidase assay of a katG::Tn3-gusA78 reporter fusion protein revealed that katG expression is under the control of QS. Furthermore, katG expression was upregulated by QsmR, a transcriptional activator for flagellar-gene expression that is regulated by QS. A gel mobility shift assay confirmed that QsmR directly activates katG expression. The katG mutant produced toxoflavin but exhibited less severe disease than BGR1 on rice panicles. Under visible light conditions and a photon flux density of 61.6 µmol–1 m–2, the survival rate of the katG mutant was 105-fold lower than that of BGR1. This suggests that KatG is a major catalase that protects bacterial cells from visible light, which probably results in less severe disease caused by the katG mutant.
Published ahead of print on 24 April 2009.
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