Construction and characterization of a Lactococcus lactis strain deficient in intracellular ClpP and extracellular HtrA proteases

1 Unité d'Ecologie et de Physiologie du Système Digestif, INRA, Domaine de Vilvert, 78352 Jouy en Josas cedex, France 2 Unité des Bactéries Lactiques et Pathogènes Opportunistes, INRA, Domaine de Vilvert, 78352 Jouy en Josas cedex, France 3 Institute of Biological Sciences, Federal University o...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2006-09, Vol.152 (9), p.2611-2618
Hauptverfasser: Cortes-Perez, N. G, Poquet, I, Oliveira, M, Gratadoux, J. J, Madsen, S. M, Miyoshi, A, Corthier, G, Azevedo, V, Langella, P, Bermudez-Humaran, L. G
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Sprache:eng
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Zusammenfassung:1 Unité d'Ecologie et de Physiologie du Système Digestif, INRA, Domaine de Vilvert, 78352 Jouy en Josas cedex, France 2 Unité des Bactéries Lactiques et Pathogènes Opportunistes, INRA, Domaine de Vilvert, 78352 Jouy en Josas cedex, France 3 Institute of Biological Sciences, Federal University of Minas Gerais (UFMG-ICB), Belo Horizonte, Minas Gerais, Brazil 4 Bioneer A/S, Hørsholm, Denmark Correspondence Philippe Langella philippe.langella{at}jouy.inra.fr A Lactococcus lactis strain deficient in both its major proteases, intracellular (ClpP) and extracellular (HtrA), was constructed and characterized. This strain, hereafter called clpP-htrA , could be obtained only by conjugation between a clpP donor strain and an htrA recipient strain in the NZ9000 context, allowing heterologous gene expression under the control of the NICE (nisin-controlled expression) system. The clpP-htrA double mutant showed both higher stress tolerance (e.g. high temperature and ethanol resistance) and higher viability than single clpP or htrA mutant strains. In addition, the secretion rate of two heterologous proteins (staphylococcal nuclease Nuc and Nuc-E7) was also higher in clpP-htrA than in the wild-type strain. This strain should be a useful host for high-level production and quality of stable heterologous proteins. Abbreviations: NICE, nisin-controlled expression
ISSN:1350-0872
1465-2080
DOI:10.1099/mic.0.28698-0