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Publisert 2006

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Publikasjonsdetaljer

Tidsskrift : Journal of Microbiological Methods , vol. 67 , p. 193–201–9 , 2006

Utgiver : Elsevier

Internasjonale standardnummer :
Trykt : 0167-7012
Elektronisk : 1872-8359

Publikasjonstype : Vitenskapelig artikkel

Bidragsytere : Straume, Daniel; Axelsson, Lars; Nes, Ingolf F.; Diep, Dzung Bao

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Kjetil Aune
Bibliotekleder
kjetil.aune@nofima.no

Sammendrag

The response regulator PlnC is part of the signal transduction system that plays a key role in the regulation of bacteriocin production in Lactobacillus plantarum C11. In this study, we wanted to express high levels of the response regulator PlnC in a soluble and native form for purification and further studies. The protein was expressed as a fusion protein (fPlnC) containing an N-terminal Flag-tag to facilitate detection and purification. When the fusion gene, fplnC, was expressed in Escherichia coli BL2l, nearly all (99%) of the recombinant protein ended up inside inclusion bodies as an incorrectly folded protein. By utilizing two different Gram-positive expression systems (SIP and NICE) in L. plantarum NC8 and Lactobacillus sakei Lb790, the expression of the soluble fPlnC was significantly increased, being 20-40 times more than that in E. coli BL2l. Using the N-terminal tag, the expressed protein was purified by immunoprecipitation. By DNA-binding study (EMSA), we demonstrated that the fusion protein purified from the soluble pool was correctly folded as judged by its ability to bind specifically on regulated promoters. Using our approach, we estimate that about 1 mg of fPlnC can be purified from 1 1 of the bacterial culture. (c) 2006 Elsevier B.V. All rights reserved.

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