Affiliation:
1. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
Abstract
ABSTRACT
Many microbes use secreted peptide-signaling molecules to stimulate changes in gene expression in response to high population density, a process called quorum sensing. ComX pheromone is a modified 10-amino-acid peptide used by
Bacillus subtilis
to modulate changes in gene expression in response to crowding.
comQ
and
comX
are required for production of ComX pheromone. We found that accumulation of ComX pheromone in culture supernatant paralleled cell growth, indicating that there was no autoinduction of production of ComX pheromone. We overexpressed
comQ
and
comX
separately and together and found that overexpression of
comX
alone was sufficient to cause an increase in production of ComX pheromone and early induction of a quorum-responsive promoter. These results indicate that the extracellular concentration of ComX pheromone plays a major role in determining the timing of the quorum response and that expression of
comX
is limiting for production of ComX pheromone. We made alanine substitutions in the residues that comprise the peptide backbone of ComX pheromone. Analysis of these mutants highlighted the importance of the modification for ComX pheromone function and identified three residues (T50, G54, and D55) that are unlikely to interact with proteins involved in production of or response to ComX pheromone. We have also identified and mutated a putative isoprenoid binding domain of ComQ. Mutations in this domain eliminated production of ComX pheromone, consistent with the hypothesis that ComQ is involved in modifying ComX pheromone and that the modification is likely to be an isoprenoid.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference43 articles.
1. Ashby, M. N., D. H. Spear, and P. A. Edwards. 1990. Prenyltransferases: from yeast to man, p27–34. In A. D. Attie (ed.), Molecular biology of atherosclerosis. Elsevier, Inc., New York, N.Y.
2. Current protocols in molecular biology 1990
3. Caldwell, G. A., S. H. Wang, C. B. Xue, Y. Jiang, H. F. Lu, F. Naider, and J. M. Becker. 1994. Molecular determinants of bioactivity of the Saccharomyces cerevisiae lipopeptide mating pheromone. J. Biol. Chem.269:19817–19825.
4. Chen, A., P. A. Kroon, and C. D. Poulter. 1994. Isoprenyl diphosphate synthases: protein sequence comparisons, a phylogenetic tree, and predictions of secondary structure. Protein Sci.3:600–607.
5. Chen, P., S. K. Sapperstein, J. D. Choi, and S. Michaelis. 1997. Biogenesis of the Saccharomyces cerevisiae mating pheromone a-factor. J. Cell Biol.136:251–269.
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