2016
DOI: 10.1111/jam.13080
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Characterization of malolactic bacteria isolated from Aosta Valley wines and evidence of psychrotrophy in some strains

Abstract: The natural emergence of strains able to perform the MLF at 10°C in wine is a new finding, interesting because it confirms the ecological ability of O. oeni species to adapt itself to environmental conditions by strain phenotype variations. It can be also a starting point for more sustainable oenological practices, since it would be alternative to the conditioning systems of the tanks or of the wineries where they are costly in terms of investment and energy consumption.

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Cited by 12 publications
(8 citation statements)
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“…The results show an endemic microbiota for the Albariño variety grown in the region of Val do Salnés. Unlike what has been described for most wine regions traditionally studied [3,4,25], LAB predominant species in wines of the Albariño variety grown in this region belong to the genus Lactobacillus and not to species O. oeni, which in any of the years analyzed has not yet been found in MLF. Our data coincide with those of some wine regions recently studied for which the species of the genus Lactobacillus were also described as predominant [13,23,26].…”
Section: Isolation and Identification Of The Isolates: Ecological Discontrasting
confidence: 61%
“…The results show an endemic microbiota for the Albariño variety grown in the region of Val do Salnés. Unlike what has been described for most wine regions traditionally studied [3,4,25], LAB predominant species in wines of the Albariño variety grown in this region belong to the genus Lactobacillus and not to species O. oeni, which in any of the years analyzed has not yet been found in MLF. Our data coincide with those of some wine regions recently studied for which the species of the genus Lactobacillus were also described as predominant [13,23,26].…”
Section: Isolation and Identification Of The Isolates: Ecological Discontrasting
confidence: 61%
“…This includes pulsed-field gel electrophoresis of large DNA fragments produced by restriction enzyme digestion of the bacterial chromosome (REA-PFGE). It was first used in 1993, and often afterwards, although it is difficult and time-consuming (Kelly et al 1993 ; Tenreiro et al 1994 ; Sato et al 2001 ; Guerrini et al 2003 ; López et al 2007 ; Larisika et al 2008 ; Gonzalez-Arenzana et al 2012a , b ; Zapparoli et al 2012 ; Wang et al 2015 ; Vigentini et al 2016 ). More simple and rapid methods based on the use of PCR were later developed and applied, such as Rapid Amplification of Polymorphic DNA (RAPD) (Zavaleta et al 1997 ; Zapparoli et al 2000 ; Reguant & Bordons 2003 ; Lechiancole et al 2006 ; Canas et al 2009 ; Capozzi et al 2010 ; Solieri et al 2010 ; Marques et al 2011 ), Amplified Fragment Length Polymorphism (AFLP) (Viti et al 1996 ; Sato et al 2000 ; Cappello et al 2008 ; Cappello et al 2010 ), or more recently Multiple Loci VNTR Analysis (MLVA), which targets genomic regions conserved among all strains but with different sizes as they contain a variable number of tandem repeats (VNTR) (Claisse & Lonvaud-Funel 2012 ; Claisse & Lonvaud-Funel 2014 ; Garofalo et al 2015 ; Cruz-Pio et al 2017 ; El Khoury et al 2017 ; Franquès et al 2017 ).…”
Section: O Oeni Strains Diversity: Methods and Applicationsmentioning
confidence: 99%
“…The DNA from the LAB was extracted by using phenol/chloroform protocol according to Green and Sambrook [15]. Universal primers for bacteria named BSF8 (5 -AGAGTTTGATCCTGGCTCAG-3 ) and BSR1541 (5 -AAGGAGGTGATCCAGCCGCA-3 ) [16] were used and the relevant amplification conditions were those reported by Vigentini et al [17]. The DNA extraction from yeasts was performed according to Querol et al [14].…”
Section: Isolation and Identification Of Micro-organismsmentioning
confidence: 99%