Kinetics and intensity of the expression of genes involved in the stress response tightly induced by phenolic acids in Lactobacillus plantarum

Journal of Molecular Microbiology and Biotechnology

Volumn 14, Issue 1-3, 2007, Pages 41-47

  Licandro Seraut, Hélène ^a   Gury, Jérôme ^b   Tran, Ngoc Phuong ^a   Barthelmebs, Lise ^c   Cavin, Jean François ^a,d  

^a UNIVERSITÉ DE BOURGOGNE   (France)

^b UNIV GRENOBLE ALPES   (France)

^c UNIVERSITÉ DE PERPIGNAN   (France)

^d UNIVERSITÉ DE BOURGOGNE   (France)

Author keywords

Gene expression; Lactobacillus plantarum; PadA; PadR; Phenolic acid; Stress

Indexed keywords

BACTERIAL PROTEIN; CARBOXYLYASE; MESSENGER RNA; PADA PROTEIN; PADR PROTEIN; PARA COUMARIC ACID; PHENOL DERIVATIVE; PHENOLIC ACID; UNCLASSIFIED DRUG; USP1 PROTEIN;

ARTICLE; BACTERIAL GROWTH; CONTROLLED STUDY; CULTURE MEDIUM; ENZYME ACTIVITY; GENE EXPRESSION; GENETIC TRANSCRIPTION; KINETICS; LACTOBACILLUS PLANTARUM; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN STRUCTURE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY; STRESS;

BACTERIAL PROTEINS; CARBOXY-LYASES; COUMARIC ACIDS; CULTURE MEDIA; GENE EXPRESSION REGULATION, BACTERIAL; HEAT-SHOCK PROTEINS; HEAT-SHOCK RESPONSE; HYDROXYBENZOIC ACIDS; KINETICS; LACTOBACILLUS PLANTARUM; REPRESSOR PROTEINS;

BACTERIA (MICROORGANISMS); LACTOBACILLUS PLANTARUM;

EID: 35649007770     PISSN: 14641801     EISSN: None     Source Type: Journal    
DOI: 10.1159/000106081     Document Type: Article

References (24)

1. Arendt, B.M., Ellinger, S., Kekic, K., Geus, L., Fimmers, R., Spengler, U., Muller, W.U., Goerlich, R. 2005. Single and repeated moderate consumption of native or dealcoholized red wine show different effects on antioxidant parameters in blood and DNA strand breaks in peripheral leukocytes in healthy volunteers: a randomized controlled trial (ISRCTN68505294). Nutr J 4: 33.
2. Barthelmebs, L., Diviès, C., Cavin, J.-F. 2000a. Knockout of the p-coumarate decarboxylase gene from Lactobacillus plantarum reveals the existence of two other inducible enzymatic activities involved in phenolic acid metabolism. Appl Environ Microbiol 66:3368-3375.
3. Barthelmebs, L., Lecomte, B., Diviès, C., Cavin, J.-F. 2000b. Inducible metabolism of phenolic acids in Pediococcus pentosaceus is encoded by an autoregulated operon which involves a new class of negative transcriptional regulator. J Bacteriol 182:6724-6731.
4. Cavin, J.-F., Barthelmebs, L., Diviès, C. 1997. Molecular characterization of an inducible p-coumaric acid decarboxylase from Lactobacillus plantarum: gene cloning, transcriptional analysis, overexpression in Escherichia coli, purification, and characterization. Appl Environ Microbiol 63:1939-1944.
5. Cavin, J.-F., Dartois, V., Diviès, C. 1998. Gene cloning, transcriptional analysis, purification, and characterization of phenolic acid decarboxylase from Bacillus subtilis. Appl Environ Microbiol 64:1466-1471.
6. Degrassi, G., Polverino De Laureto, P., Bruschi, C.V. 1995. Purification and characterization of ferulate and p-coumarate decarboxylase from Bacillus pumilus. Appl Environ Microbiol 61:326-332.
7. De Man, P.J., M. Rogosa, M. Sharpe. 1960. A medium for the cultivation of Lactobacilli. J Appl Bacteriol 23:130-135.
8. De Silva, R.S., Kovacikova, G., Lin, W., Taylor, R.K., Skorupski, K., Kull, F. J. 2005. Crystal structure of the virulence gene activator AphA from Vibrio cholerae reveals it is a novel member of the winged helix transcription factor superfamily. J Biol Chem 280:13779-13783.
9. Gury, J., Barthelmebs, L., Tran, N.P., Diviès, C., Cavin, J.-F. 2004. Cloning, deletion, and characterization of PadR, the transcriptional repressor of the phenolic acid decarboxylase-encoding padA gene of Lactobacillus plantarum. Appl Environ Microbiol 70:2146-2153.
10. Huillet, E., Velge, P., Vallaeys, T., Pardon, P. 2006. LadR, a new PadR-related transcriptional regulator from Listeria monocytogenes, negatively regulates the expression of the multidrug efflux pump MdrL. FEMS Microbiol Lett 254:87-94.
11. Kleerebezem, M., Boekhorst, J., van Kranenburg, R., Molenaar, D., Kuipers, O.P., Leer, R., Tarchini, R., Peters, S.A., Sandbrink, H. M., Fiers, M.W., et al. 2003. Complete genome sequence of Lactobacillus plantarum WCFS1. Proc Natl Acad Sci USA 100:1990-1995.
12. Kovacikova, G., Lin, W., Skorupski, K. 2005. Dual regulation of genes involved in acetoin biosynthesis and motility/biofilm formation by the virulence activator AphA and the acetate-responsive LysR-type regulator AlsR in Vibrio cholerae. Mol Microbiol 57:420-433.
13. Kvint, K., Nachin, L., Diez, A., Nyström, T. 2003. The bacterial universal stress protein: function and regulation. Curr Opin Microbiol 6:140-145.
14. -ΔΔCT method. Methods 25:402-408.
15. Nachin, L., Nannmark, U., Nyström, T. 2005. Differential roles of the universal stress proteins of Escherichia coli in oxidative stress resistance, adhesion, and mobility. J Bacteriol 187:6265-6272.
16. Nyström, T., Neidhardt, F.C. 1996. Effects of overproducing the universal stress protein, UspA, in Escherichia coli K-12. J Bacteriol 178:927-930.
17. Pavan, S., Hols, P., Delcour, J., Geoffroy, M.C., Grangette, C., Kleerebezem, M., Mercenier, A. 2000. Adaptation of the nisin-controlled expression system in Lactobacillus plantarum: a tool to study in vivo biological effects. Appl Environ Microbiol 66:4427-4432.
18. Prytz, I., Sanden, A.M., Nystrom, T., Farewell, A., Wahlstrom, A., Forberg, C., Pragai, Z., Barer, M., Harwood, C., Larsson, G. 2003. Fed-batch production of recombinant β-galactosidase using the universal stress promoters uspA and uspB in high cell density cultivations. Biotechnol Bioeng 83:595-603.
19. Roberts, C., Anderson, K.L., Murphy, E., Projan, S.J., Mounts, W., Hurlburt, B., Smeltzer, M., Overbeek, R., Disz, T., Dunman, P.M. 2006. Characterizing the effect of the Staphylococcus aureus virulence factor regulator, SarA, on log-phase mRNA half-lives. J Bacteriol 188:2593-2603.
20. Santapaola, D., Casalino, M., Petrucca, A., Presutti, C., Zagaglia, C., Berlutti, F., Colonna, B., Nicoletti, M. 2002. Enteroinvasive Escherichia coli virulence-plasmid-carried apyrase (apy) and ospB genes are organized as a bicistronic operon and are subject to differential expression. Microbiology 148:2519-2529.
21. Sorvig, E., Mathiesen, G., Naterstad, K., Eijsink, V.G., Axelsson, L. 2005. High-level, inducible gene expression in Lactobacillus sakei and Lactobacillus plantarum using versatile expression vectors. Microbiology 151:2439-2449.
22. van de Guchte, M., Serror, P., Chervaux, C., Smokvina, T., Ehrlich, S.D., Maguin, E. 2002. Stress responses in lactic acid bacteria. Antonie Van Leeuwenhoek 82:187-216.
23. Zaldivar, J., Ingram, L.O. 1999. Effect of organic acids on the growth and fermentation of ethanologenic Escherichia coli LY01. Biotechnol Bioeng 66:203-210.
24. Zhang, C., Nietfeldt, J., Zhang, M., Benson, A.K. 2005. Functional consequences of genome evolution in Listeria monocytogenes: the lmo0423 and lmo0422 genes encode sigmaC and LstR, a lineage II-specific heat shock system. J Bacteriol 187:7243-7253.