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BMC Genomics


Title:QTL mapping of volatile compound production in Saccharomyces cerevisiae during alcoholic fermentation
Author(s):Eder M; Sanchez I; Brice C; Camarasa C; Legras JL; Dequin S;
Address:"SPO, INRA, SupAgro, Universite de Montpellier, F-34060, Montpellier, France. MISTEA, INRA, SupAgro, F-34060, Montpellier, France. SPO, INRA, SupAgro, Universite de Montpellier, F-34060, Montpellier, France. sylvie.dequin@inra.fr"
Journal Title:BMC Genomics
Year:2018
Volume:20180301
Issue:1
Page Number:166 -
DOI: 10.1186/s12864-018-4562-8
ISSN/ISBN:1471-2164 (Electronic) 1471-2164 (Linking)
Abstract:"BACKGROUND: The volatile metabolites produced by Saccharomyces cerevisiae during alcoholic fermentation, which are mainly esters, higher alcohols and organic acids, play a vital role in the quality and perception of fermented beverages, such as wine. Although the metabolic pathways and genes behind yeast fermentative aroma formation are well described, little is known about the genetic mechanisms underlying variations between strains in the production of these aroma compounds. To increase our knowledge about the links between genetic variation and volatile production, we performed quantitative trait locus (QTL) mapping using 130 F2-meiotic segregants from two S. cerevisiae wine strains. The segregants were individually genotyped by next-generation sequencing and separately phenotyped during wine fermentation. RESULTS: Using different QTL mapping strategies, we were able to identify 65 QTLs in the genome, including 55 that influence the formation of 30 volatile secondary metabolites, 14 with an effect on sugar consumption and central carbon metabolite production, and 7 influencing fermentation parameters. For ethyl lactate, ethyl octanoate and propanol formation, we discovered 2 interacting QTLs each. Within 9 of the detected regions, we validated the contribution of 13 genes in the observed phenotypic variation by reciprocal hemizygosity analysis. These genes are involved in nitrogen uptake and metabolism (AGP1, ALP1, ILV6, LEU9), central carbon metabolism (HXT3, MAE1), fatty acid synthesis (FAS1) and regulation (AGP2, IXR1, NRG1, RGS2, RGT1, SIR2) and explain variations in the production of characteristic sensorial esters (e.g., 2-phenylethyl acetate, 2-metyhlpropyl acetate and ethyl hexanoate), higher alcohols and fatty acids. CONCLUSIONS: The detection of QTLs and their interactions emphasizes the complexity of yeast fermentative aroma formation. The validation of underlying allelic variants increases knowledge about genetic variation impacting metabolic pathways that lead to the synthesis of sensorial important compounds. As a result, this work lays the foundation for tailoring S. cerevisiae strains with optimized volatile metabolite production for fermented beverages and other biotechnological applications"
Keywords:"Alcohols/*metabolism Amino Acid Substitution Chromatography, High Pressure Liquid *Chromosome Mapping *Fermentation Gas Chromatography-Mass Spectrometry Genetic Association Studies Genome, Fungal Genomics/methods Lod Score Metabolic Networks and Pathways;"
Notes:"MedlineEder, Matthias Sanchez, Isabelle Brice, Claire Camarasa, Carole Legras, Jean-Luc Dequin, Sylvie eng 606795/FP7 People: Marie-Curie Actions/International Research Support, Non-U.S. Gov't England 2018/03/02 BMC Genomics. 2018 Mar 1; 19(1):166. doi: 10.1186/s12864-018-4562-8"

 
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