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Expression of the gum Operon Directing Xanthan Biosynthesis in Xanthomonas campestris and Its Regulation In Planta

June 2001 , Volume 14 , Number  6
Pages  768 - 774

Adrian A. Vojnov , Holly Slater , Michael J. Daniels , and J. Maxwell Dow

The Sainsbury Laboratory, John Innes Centre, Colney Lane, Norwich NR4 7UH, U.K.

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Accepted 1 March 2001.

The gum gene cluster of Xanthomonas campestris pv. campestris comprises 12 genes whose products are involved in the biosynthesis of the extracellular polysaccharide xanthan. These genes are expressed primarily as an operon from a promoter upstream of the first gene, gumB. Although the regulation of xanthan synthesis in vitro has been well studied, nothing is known of its regulation in planta. A reporter plasmid was constructed in which the promoter region of the gum operon was fused to gusA. In liquid cultures, the expression of the gumgusA reporter was correlated closely with the production of xanthan, although a low basal level of β-glucuronidase activity was seen in the absence of added carbon sources when xanthan production was very low. The expression of the gumgusA fusion also was subject to positive regulation by rpfF, which is responsible for the synthesis of the diffusible signal factor (DSF). The expression of the gumgusA fusion in bacteria recovered from inoculated turnip leaves was maximal at the later phases of growth and was subject to regulation by rpfF. These results provide indirect support for the operation of the DSF regulatory system in bacteria in planta.

Additional keyword: black rot.

© 2001 The American Phytopathological Society