Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract2-Tridecanone impacts surface-associated bacterial behaviours and hinders plant-bacteria interactions    Next Abstract"Effects of addition of alpha-cyclodextrin on the sensory quality, volatile compounds, and color parameters of fresh pear juice" »

Yeast


Title:Genetic improvement of Saccharomyces cerevisiae wine strains for enhancing cell viability after desiccation stress
Author(s):Lopez-Martinez G; Pietrafesa R; Romano P; Cordero-Otero R; Capece A;
Address:"Department of Biochemistry and Biotechnology, University Rovira i Virgili, Tarragona, Spain"
Journal Title:Yeast
Year:2013
Volume:20130522
Issue:8
Page Number:319 - 330
DOI: 10.1002/yea.2952
ISSN/ISBN:1097-0061 (Electronic) 0749-503X (Linking)
Abstract:"In the last few decades spontaneous grape must fermentations have been replaced by inoculated fermentation with Saccharomyces cerevisiae strains as active dry yeast (ADY). Among the essential genes previously characterized to overcome the cell-drying/rehydration process, six belong to the group of very hydrophilic proteins known as hydrophilins. Among them, only SIP18 has shown early transcriptional response during dehydration stress. In fact, the overexpression in S. cerevisiae of gene SIP18 increases cell viability after the dehydration process. The purpose of this study was to characterize dehydration stress tolerance of three wild and one commercial S. cerevisiae strains of wine origin. The four strains were submitted to transformation by insertion of the gene SIP18. Selected transformants were submitted to the cell-drying-rehydration process and yeast viability was evaluated by both viable cell count and flow cytometry. The antioxidant capacity of SIP18p was illustrated by ROS accumulation reduction after H2 O2 attack. Growth data as cellular duplication times and lag times were calculated to estimate cell vitality after the cell rehydration process. The overexpressing SIP18 strains showed significantly longer time of lag phase despite less time needed to stop the leakage of intracellular compounds during the rehydration process. Subsequently, the transformants were tested in inoculated grape must fermentation at laboratory scale in comparison to untransformed strains. Chemical analyses of the resultant wines indicated that no significant change for the content of secondary compounds was detected. The obtained data showed that the transformation enhances the viability of ADY without affecting fermentation efficiency and metabolic behaviour"
Keywords:"Desiccation Fermentation *Microbial Viability Saccharomyces cerevisiae/*chemistry/cytology/*genetics/metabolism Saccharomyces cerevisiae Proteins/genetics/metabolism Stress, Physiological Wine/*microbiology Ady Saccharomyces cerevisiae dehydration stress;"
Notes:"MedlineLopez-Martinez, Gema Pietrafesa, Rocchina Romano, Patrizia Cordero-Otero, Ricardo Capece, Angela eng Research Support, Non-U.S. Gov't England 2013/04/12 Yeast. 2013 Aug; 30(8):319-30. doi: 10.1002/yea.2952. Epub 2013 May 22"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 30-12-2024