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| Professor George Salmond | |
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University of Cambridge >
School of the Biological Sciences >
Department of Biochemistry
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Molecular Microbiology: Bacterial Quorum Sensing, Virulence, Protein Secretion, Antibiotic Regulation and Bacteriophage Abortive Infection Research Groupings: Structural and molecular cell biology | Infection and Immunity
Our research involves multiple aspects of molecular microbiology including quorum sensing (QS), molecular pathogenesis in plant and animal pathogens, regulation and biosynthesis of antibiotics and other secondary metabolites, protein secretion systems, bacteriophage exploitation and viral abortive infection systems. We work on various Gram-negative enterobacteria, including the phytopathogen, Erwinia (Pectobacterium), Serratia species, which can be opportunistic human pathogens, Citrobacter rodentium the murine pathogen, and a spectrum of phages infecting various bacteria of fundamental, medical, agricultural or industrial biotechnology interest. We are investigating the phenomenon of quorum sensing in which bacteria make small diffusible molecules (N-acyl homoserine lactones) as chemical communication signals reflecting cell population density status. The phenotypes regulated by quorum sensing include virulence, and exoenzyme and antibiotic production. Our research aims are to understand molecular mechanisms involved in quorum sensing, and dissect their physiological role(s), evolution and potential use in synthetic biology. We study the genetics and biochemistry of carbapenem and prodiginine antibiotic synthesis in Erwinia and Serratia. We use genetics, transcriptomics and proteomics to investigate the physiological impacts of environmental signaling in regulation to virulence and antibiotic production in Erwinia, Serratia and Citrobacter. We also investigate molecular processes involved in proteinaceous virulence factor secretion in Erwinia. We are investigating new bacteriophages that attack a range of enteric bacteria, both in terms of host range and for the development of new genetic tools for functional genomics. We are also studying phage abortive infection systems (with bifunctional toxin:antitoxin capacity) through which bacteria control the replication of their viral parasites. The latter project also involves collaborative structural biology work.
Lab members References
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