RESUMEN
AIMS: Oenococcus oeni is the lactic acid bacteria species which is the most adapted to wine. Recently, two groups of strains that form two genetic lineages were described in red and white Burgundy wines. The aim of this study was to analyse the phenotypes of these strains in order to determine how they have adapted specifically to either red or white wine. METHODS AND RESULTS: Four strains from each group were tested in grape must and in wines to evaluate their tolerance to pH and to phenolic compound content. White wine strains proved to be the most tolerant to low pH, both in grape must and in wine, whereas they were inhibited by the presence of grape tannins in wine. Red wine strains were more sensitive to acidity, but very resistant to phenolic compounds. CONCLUSIONS: The results suggest that pH and phenolic compounds drive strain selection at several stages of wine production. SIGNIFICANCE AND IMPACT OF THE STUDY: Although it is well known that O. oeni is well adapted to wine, this study shows that strains of some genetic lineages within this species have evolved to adapt better than others to specific types of wines.
Asunto(s)
Ácidos/metabolismo , Oenococcus/metabolismo , Fenoles/química , Vitis/microbiología , Vino/microbiología , Ácidos/análisis , Fermentación , Concentración de Iones de Hidrógeno , Oenococcus/genética , Fenotipo , Taninos/análisis , Taninos/metabolismo , Vitis/química , Vino/análisisRESUMEN
The effects of sulphur dioxide and a commercial starter inoculum on yeast population dynamics have been analysed by a molecular approach. Yeast identification from fermenting Carinyena grape musts was performed by RFLP's of mtDNA and rRNA-coding DNA. As expected, the use of a commercial inoculum speeded up the start of fermentation, while SO2 addition limited the development of non-Saccharomyces species. However, this effect was also observed with yeast inoculation. Further analysis of population dynamics could lead to a recommendation for the reduction of the dosage of SO2 by the addition of appropriate inoculum of yeasts in the must. Furthermore, the timing of inoculum addition could be modified to allow a proper contribution of non-Saccharomyces species. Molecular biology analysis of population dynamics could provide a tool to efficiently reduce the dosage of SO2 and adjust the timing of inoculum addition.
Asunto(s)
Fermentación/efectos de los fármacos , Rosales/metabolismo , Dióxido de Azufre/farmacología , Levaduras/genética , Levaduras/metabolismo , ADN Mitocondrial/genética , ADN Ribosómico/genética , Excipientes Farmacéuticos/farmacología , Polimorfismo de Longitud del Fragmento de Restricción , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismo , Factores de TiempoRESUMEN
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.
Asunto(s)
Técnicas de Tipificación Bacteriana/métodos , Cocos Grampositivos/clasificación , Malatos/metabolismo , Vino/microbiología , Dermatoglifia del ADN/métodos , ADN Bacteriano/genética , Fermentación , Microbiología de Alimentos , Cocos Grampositivos/genética , Cocos Grampositivos/metabolismo , Leuconostoc/clasificación , Leuconostoc/genética , Leuconostoc/metabolismo , Dinámica Poblacional , Técnica del ADN Polimorfo Amplificado Aleatorio/métodos , Reproducibilidad de los ResultadosRESUMEN
This study shows that the growth of Oenococcus oeni CECT 4100 in a synthetic medium is affected by phenolic compounds in different ways, depending on their type and concentration. Generally they have no effects at low concentrations, but hydroxycinnamic acids are inhibitory at high concentrations. Malolactic fermentation was stimulated in the presence of catechin and quercetin, but increasingly delayed with increasing amounts of p-coumaric acid. Gallic acid appeared to delay or inhibit the formation of acetic acid from citric acid. This could lead to a better control of malolactic fermentation and suppress the increase in volatile acidity, which is undesirable in the wine-making process.
Asunto(s)
Ácidos Cumáricos/farmacología , Microbiología de Alimentos , Ácido Gálico/farmacología , Cocos Grampositivos/efectos de los fármacos , Vino/microbiología , Ácido Acético/análisis , Catequina/farmacología , Ácido Cítrico/análisis , Ácido Cítrico/metabolismo , Etanol , Industria de Alimentos , Cocos Grampositivos/crecimiento & desarrollo , Cocos Grampositivos/metabolismo , Leuconostoc/efectos de los fármacos , Leuconostoc/crecimiento & desarrollo , Leuconostoc/metabolismo , Malatos/metabolismo , Propionatos , Quercetina/farmacologíaRESUMEN
Genetic diversity of 60 Oenococcus oeni strains from different wines was evaluated by numerical analysis of (i) pulsed-field gel electrophoresis (PFGE) patterns with endonuclease ApaI and (ii) randomly amplified polymorphic DNA (RAPD)-PCR fingerprints with four oligonucleotide primers. Sixty-two percent of the strains could be distinguished by PFGE, whereas most strains were identified by distinct RAPD-PCR profiles and associated according to the geographical origin. Because of its rapidity and reliability, RAPD-PCR appeared to be a suitable method for typing and monitoring O. oeni strains in winemaking.