Previous Article | Next Article 
Journal of Bacteriology, February 2002, p. 928-935, Vol. 184, No. 4
0021-9193/01/$04.00+0 DOI: 10.1128/jb.184.4.928-935.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Regulation and Adaptive Evolution of Lactose Operon Expression in Lactobacillus delbrueckii
Luciane Lapierre, Beat Mollet, and Jacques-Edouard Germond*
Nestlé Research Center, Nestlé, Ltd., CH-1000 Lausanne 26, Switzerland
Received 21 August 2001/
Accepted 9 November 2001
Lactobacillus delbrueckii subsp. bulgaricus and L. delbrueckii subsp. lactis are both used in the dairy industry as homofermentative lactic acid bacteria in the production of fermented milk products. After selective pressure for the fast fermentation of milk in the manufacture of yogurts, L. delbrueckii subsp. bulgaricus loses its ability to regulate lac operon expression. A series of mutations led to the constitutive expression of the lac genes. A complex of insertion sequence (IS) elements (ISL4 inside ISL5), inserted at the border of the lac promoter, induced the loss of the palindromic structure of one of the operators likely involved in the binding of regulatory factors. A lac repressor gene was discovered downstream of the ß-galactosidase gene of L. delbrueckii subsp. lactis and was shown to be inactivated by several mutations in L. delbrueckii subsp. bulgaricus. Regulatory mechanisms of the lac gene expression of L. delbrueckii subsp. bulgaricus and L. delbrueckii subsp. lactis were compared by heterologous expression in Lactococcus lactis of the two lac promoters in front of a reporter gene (ß-glucuronidase) in the presence or absence of the lac repressor gene. Insertion of the complex of IS elements in the lac promoter of L. delbrueckii subsp. bulgaricus increased the promoter's activity but did not prevent repressor binding; rather, it increased the affinity of the repressor for the promoter. Inactivation of the lac repressor by mutations was then necessary to induce the constitutive expression of the lac genes in L. delbrueckii subsp. bulgaricus.
* Corresponding author. Mailing address: Nestlé Research Center, Nestlé, Ltd., Vers-chez-les-Blanc, P.O. Box 44, CH-1000 Lausanne 26, Switzerland. Phone: 41-21-785-88-35. Fax: 41-21-785-89-25. E-mail: jacques-edouard.germond{at}rdls.nestle.com.
Journal of Bacteriology, February 2002, p. 928-935, Vol. 184, No. 4
0021-9193/01/$04.00+0 DOI: 10.1128/jb.184.4.928-935.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
van de Guchte, M., Penaud, S., Grimaldi, C., Barbe, V., Bryson, K., Nicolas, P., Robert, C., Oztas, S., Mangenot, S., Couloux, A., Loux, V., Dervyn, R., Bossy, R., Bolotin, A., Batto, J.-M., Walunas, T., Gibrat, J.-F., Bessieres, P., Weissenbach, J., Ehrlich, S. D., Maguin, E.
(2006). The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution. Proc. Natl. Acad. Sci. USA
103: 9274-9279
[Abstract]
[Full Text]
-
Barrangou, R., Azcarate-Peril, M. A., Duong, T., Conners, S. B., Kelly, R. M., Klaenhammer, T. R.
(2006). Global analysis of carbohydrate utilization by Lactobacillus acidophilus using cDNA microarrays. Proc. Natl. Acad. Sci. USA
103: 3816-3821
[Abstract]
[Full Text]
-
Callanan, M. J., Beresford, T. P., Ross, R. P.
(2005). Genetic Diversity in the Lactose Operons of Lactobacillus helveticus Strains and Its Relationship to the Role of These Strains as Commercial Starter Cultures. Appl. Environ. Microbiol.
71: 1655-1658
[Abstract]
[Full Text]
-
Dellaglio, F., Felis, G. E., Castioni, A., Torriani, S., Germond, J.-E.
(2005). Lactobacillus delbrueckii subsp. indicus subsp. nov., isolated from Indian dairy products. Int. J. Syst. Evol. Microbiol.
55: 401-404
[Abstract]
[Full Text]
-
Kurogochi, M., Nishimura, S.-I., Lee, Y. C.
(2004). Mechanism-based Fluorescent Labeling of {beta}-Galactosidases: AN EFFICIENT METHOD IN PROTEOMICS FOR GLYCOSIDE HYDROLASES. J. Biol. Chem.
279: 44704-44712
[Abstract]
[Full Text]
-
Soki, J., Fodor, E., Hecht, D. W., Edwards, R., Rotimi, V. O., Kerekes, I., Urban, E., Nagy, E.
(2004). Molecular characterization of imipenem-resistant, cfiA-positive Bacteroides fragilis isolates from the USA, Hungary and Kuwait. J Med Microbiol
53: 413-419
[Abstract]
[Full Text]
-
Stroman, P., Muller, C. C., Sorensen, K. I.
(2003). Heat Shock Treatment Increases the Frequency of Loss of an Erythromycin Resistance-Encoding Transposable Element from the Chromosome of Lactobacillus crispatus CHCC3692. Appl. Environ. Microbiol.
69: 7173-7180
[Abstract]
[Full Text]
-
Bongers, R. S., Hoefnagel, M. H. N., Starrenburg, M. J. C., Siemerink, M. A. J., Arends, J. G. A., Hugenholtz, J., Kleerebezem, M.
(2003). IS981-Mediated Adaptive Evolution Recovers Lactate Production by ldhB Transcription Activation in a Lactate Dehydrogenase-Deficient Strain of Lactococcus lactis. J. Bacteriol.
185: 4499-4507
[Abstract]
[Full Text]
-
Fortina, M. G., Ricci, G., Mora, D., Guglielmetti, S., Manachini, P. L.
(2003). Unusual Organization for Lactose and Galactose Gene Clusters in Lactobacillus helveticus. Appl. Environ. Microbiol.
69: 3238-3243
[Abstract]
[Full Text]
-
Bringel, F., Hubert, J.-C.
(2003). Extent of Genetic Lesions of the Arginine and Pyrimidine Biosynthetic Pathways in Lactobacillus plantarum, L. paraplantarum, L. pentosus, and L. casei: Prevalence of CO2-Dependent Auxotrophs and Characterization of Deficient arg Genes in L. plantarum. Appl. Environ. Microbiol.
69: 2674-2683
[Abstract]
[Full Text]
-
Duncan, M. J.
(2003). GENOMICSOF ORAL BACTERIA. Crit. Rev. Oral Biol. Med.
14: 175-187
[Abstract]
[Full Text]
-
Germond, J.-E., Lapierre, L., Delley, M., Mollet, B., Felis, G. E., Dellaglio, F.
(2003). Evolution of the Bacterial Species Lactobacillus delbrueckii: A Partial Genomic Study with Reflections on Prokaryotic Species Concept. Mol Biol Evol
20: 93-104
[Abstract]
[Full Text]
Copyright © 2002 by the American Society for Microbiology. All rights reserved.