Source:http://linkedlifedata.com/resource/pubmed/id/10510239
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1999-11-4
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pubmed:abstractText |
In cell-free Pseudomonas aeruginosa culture supernatants, we identified two compounds capable of activating an N-acylhomoserine lactone (AHL) biosensor. Mass spectrometry and NMR spectroscopy revealed that these compounds were not AHLs but the diketopiperazines (DKPs), cyclo(DeltaAla-L-Val) and cyclo(L-Pro-L-Tyr) respectively. These compounds were also found in cell-free supernatants from Proteus mirabilis, Citrobacter freundii and Enterobacter agglomerans [cyclo(DeltaAla-L-Val) only]. Although both DKPs were absent from Pseudomonas fluorescens and Pseudomonas alcaligenes, we isolated, from both pseudomonads, a third DKP, which was chemically characterized as cyclo(L-Phe-L-Pro). Dose-response curves using a LuxR-based AHL biosensor indicated that cyclo(DeltaAla-L-Val), cyclo(L-Pro-L-Tyr) and cyclo(L-Phe-L-Pro) activate the biosensor in a concentration-dependent manner, albeit at much higher concentrations than the natural activator N-(3-oxohexanoyl)-L-homoserine lactone (3-oxo-C6-HSL). Competition studies showed that cyclo(DeltaAla-L-Val), cyclo(L-Pro-L-Tyr) and cyclo(L-Phe-L-Pro) antagonize the 3-oxo-C6-HSL-mediated induction of bioluminescence, suggesting that these DKPs may compete for the same LuxR-binding site. Similarly, DKPs were found to be capable of activating or antagonizing other LuxR-based quorum-sensing systems, such as the N-butanoylhomoserine lactone-dependent swarming motility of Serratia liquefaciens. Although the physiological role of these DKPs has yet to be established, their activity suggests the existence of cross talk among bacterial signalling systems.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0950-382X
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pubmed:author |
pubmed-author:BaintonN JNJ,
pubmed-author:BycroftB WBW,
pubmed-author:EnglandDD,
pubmed-author:GivskovMM,
pubmed-author:HillP JPJ,
pubmed-author:HoldenM TMT,
pubmed-author:KjellebergSS,
pubmed-author:KumarNN,
pubmed-author:LabatteMM,
pubmed-author:ManefieldMM,
pubmed-author:Ram ChhabraSS,
pubmed-author:RiceSS,
pubmed-author:SalmondG PGP,
pubmed-author:SteadPP,
pubmed-author:StewartG SGS,
pubmed-author:WilliamsPP,
pubmed-author:de NysRR
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pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1254-66
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10510239-4-Butyrolactone,
pubmed-meshheading:10510239-Biosensing Techniques,
pubmed-meshheading:10510239-Cell Communication,
pubmed-meshheading:10510239-Dipeptides,
pubmed-meshheading:10510239-Escherichia coli,
pubmed-meshheading:10510239-Gram-Negative Bacteria,
pubmed-meshheading:10510239-Luminescent Measurements,
pubmed-meshheading:10510239-Molecular Structure,
pubmed-meshheading:10510239-Peptides, Cyclic,
pubmed-meshheading:10510239-Phenotype,
pubmed-meshheading:10510239-Pseudomonas aeruginosa
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pubmed:year |
1999
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pubmed:articleTitle |
Quorum-sensing cross talk: isolation and chemical characterization of cyclic dipeptides from Pseudomonas aeruginosa and other gram-negative bacteria.
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pubmed:affiliation |
School of Pharmaceutical Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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