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Typification of Oenococcus oeni strains by multiplex RAPD‐PCR and study of population dynamics during malolactic fermentation
Author(s) -
Reguant C.,
Bordons A.
Publication year - 2003
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1046/j.1365-2672.2003.01985.x
Subject(s) - oenococcus oeni , malolactic fermentation , rapd , biology , wine , population , multiplex polymerase chain reaction , typification , multiplex , fermentation , microbiology and biotechnology , genetics , botany , polymerase chain reaction , food science , taxonomy (biology) , bacteria , gene , genetic diversity , lactic acid , sociology , nomenclature , demography
Abstract Aims: The goal of this study was to develop a reproducible method for molecular typing strains of Oenococcus oeni , and also to apply it in the study of population dynamics of these strains during malolactic fermentation of wine. Methods and Results: A new method of multiplex randomly amplified polymorphic DNA (RAPD)‐PCR has been developed, based on the combination of one random 10‐mer and one specific 23‐mer oligonucleotide in a single PCR. This method generates unique and discriminant DNA profiles for strains of O. oeni . The strains of this species were also clearly distinguished from other species of lactic acid bacteria. The method was applied to study the dynamics of O. oeni strains during malolactic fermentation, in three vintages in the same cellar. Conclusions: A fast and reliable method for typing strains of O. oeni has been designed and optimized. It improves the reproducibility and rapidity of conventional RAPD‐PCR, and it has been validated monitoring the population dynamics during malolactic fermentation. Significance and Impact of the Study: This method will be a good tool to study the population dynamics of bacteria during malolactic fermentation and to evaluate the performance of new malolactic starter cultures and their dominance over the native microbiota.