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Genetic organization and expression of citrate permease in lactic acid bacteria
Djamel Drider1, Sadjia Bekal2 and Hervé Prévost1
1Laboratoire de Microbiologie Alimentaire et Industrielle (QM2A), ENITIAA,
rue de la Géraudière BP 82225, 44322 Nantes cedex 3, France
2Laboratoire de Santé Publique du Québec, 20045 Chemin Saint-Marie,
Sainte Anne de Bellevue Québec H9X355, Canada
Corresponding author: H. Prévost
E-mail: prevost@enitiaa-nantes.fr
Genet. Mol. Res. 3 (2): 273-281 (2004)
Received December 22, 2003
Accepted May 3, 2004
Published June 9, 2004

This study is dedicated to the memory of Prof. Charles Diviès deceased on January 5, 2003.

ABSTRACT. Citrate is present in many natural substrates, such as milk, vegetables and fruits, and its metabolism by lactic acid bacteria (LAB) plays an important role in food fermentation. The industrial importance of LAB stems mainly from their ability to convert carbohydrates into lactic acid and, in some species, like Lactococcus lactis and Leuconostoc mesenteroides, to produce C4 flavor compounds (diacetyl, acetoin) through citrate metabolism. Three types of genetic organization and gene locations, involving citrate metabolism, have been found in LAB. Citrate uptake is mediated by a citrate permease, which leads to a membrane potential upon electrogenic exchange of divalent citrate and monovalent lactate. The internal citrate is cleaved into acetate and oxaloacetate by a citrate lyase, and oxaloacetate is decarboxylated into pyruvate by an oxaloacetate decarboxylase, yielding a pH gradient through the consumption of scalar protons.

Key words: Lactic acid bacteria, Citrate permease, Citrate lyase, Citrate lyase ligase, Proton motive force, Open reading frame

 

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