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Microbiology 150 (2004), 2497-2502; DOI  10.1099/mic.0.27099-0
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Microbiology 150 (2004), 2497-2502; DOI  10.1099/mic.0.27099-0
© 2004 Society for General Microbiology


Mini-Review

Cyclic di-GMP as a bacterial second messenger

David A. D'Argenio1 and Samuel I. Miller1,2,3

1 Department of Microbiology, University of Washington, Seattle, WA 98195, USA
2 Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA
3 Department of Medicine, University of Washington, Seattle, WA 98195, USA

Correspondence
Samuel I. Miller
millersi{at}u.washington.edu

Environmental signals trigger changes in the bacterial cell surface, including changes in exopolysaccharides and proteinaceous appendages that ultimately favour bacterial persistence and proliferation. Such adaptations are regulated in diverse bacteria by proteins with GGDEF and EAL domains. These proteins are predicted to regulate cell surface adhesiveness by controlling the level of a second messenger, the cyclic dinucleotide c-di-GMP. Genetic evidence suggests that the GGDEF domain acts as a nucleotide cyclase for c-di-GMP synthesis while the EAL domain is a good candidate for the opposing activity, a phosphodiesterase for c-di-GMP degradation.




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