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| School of Medicine • University of Washington • Box 357735 • 1705 NE Pacific St • Seattle WA 98195 | ||||||
| About Amy Schaefer |
Amy Schaefer, Ph.D. Email: Phone: Location: Mailing Address: Shipping Address: |
Research | ||||
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Dr. Schaefer has a long-standing interest in understanding how bacteria sense and respond to their environment. Working with Drs. Harwood and Greenberg, she has discovered a new chemical ‘dialect’ of the homoserine lactone (HSL) quorum sensing ‘language’ used by many Proteobacteria. Quorum sensing is a term used to describe cell-to-cell communication that allows cell density-dependent gene expression. Prior to our discovery, all known HSL quorum-sensing signals consisted of a fatty acid acyl group (derived from bacterial fatty acid biosynthetic pathways) linked to a homoserine lactone group (derived from S-adenosylmethionine). The fatty acid tail provides signal specificity, but the variety of possible signals that can be generated is limited. Recently, we identified a novel HSL quorum sensing system in Rhodopseudomonas palustris (Nature 2008 454:595). This phototrophic bacterium uses a LuxI-type HSL synthase to produce p-coumaroyl-HSL. Unlike previously described fatty acyl-HSLs, the p-coumaroyl side chain is derived from an exogenously provided plant metabolite, p-coumarate, rather than from endogenous bacterial fatty acid synthesis intermediates. The use of p-coumarate for quorum sensing signal production results in a single signal that integrates two distinct cues: sufficiently high bacterial population densities and the availability of a particular exogenous substrate. |
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