Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.598191
Title: The genetic regulation of pigment and antibiotic synthesis in Serratia sp.
Author: Crow, M. A.
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2002
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Abstract:
Serratia sp. strain ATCC 39006 ('39006') produces a bright red pigment prodigiosin (Pig), and a carbapenem antibiotic, 1-carbapen-2-em-3-carboxylic acid (Car). Recently it was shown that 39006 also produced N-acylhomoserine lactones (AHL), which act as quorum sensing (QS) signalling molecules. The notion that 39006 used a QS system to regulate phenotypes according to cell-density was investigated and characterised here. N-butanoyl-L-homoserine lactone (BHL) and N-hexanoyl-L-homoserine lactone (HHL) were identified as the QS signalling molecules by thin-layer chromatography. Ahl- mutants carrying mini-transposon insertions in a single ORF (smaI) were concomitantly deficient in the production of Pig, Car, 'white-opaque phenotype' and the synthesis of the extracellular enzymes pectate lyase and cellulase, all of which were restored by the addition of synthetic AHLs. All five phenotypes were also restored in the smaI- mutant when grown with or near a BHL/HHL-producing strain. It was therefore concluded that 39006 possessed a previously uncharacterised QS system that played a central role in exoenzyme and secondary metabolite production. The smaI gene was sequenced and found to encode a protein (SmaI) similar to members of the LuxI family of AHL synthases. DNA sequencing also revealed another ORF, smaR, which encoded a protein (SmaR) similar to the LuxR family of QS response regulator proteins. The regulation of Pig and Car production with respect to quorum sensing was investigated in this study using lacZ transcriptional fusions to pigA, pigH (pig biosynthetic gene cluster) and carA (car biosynthetic gene cluster). Data supported a model in which the smaIR locus formed a complete regulatory switch where SmaR acted as a repressor of gene transcription at low cell density. At high cell-density, in the presence of AHLs, SmaR-mediated repression was lifted thus allowing transcription.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.598191  DOI: Not available
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