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 Abstract"Intraspecific nucleotide variation at the pheromone binding protein locus in the turnip moth, Agrotis segetum"    Next AbstractAn acoustic microscopy technique reveals hidden morphological defenses in Daphnia »

Food Microbiol


Title:Hydroxycinnamic acid decarboxylase activity of Brettanomyces bruxellensis involved in volatile phenol production: relationship with cell viability
Author(s):Laforgue R; Lonvaud-Funel A;
Address:"Universite de Bordeaux, ISVV, EA 4577, Unite de recherche Oenologie, CS 50008, 210 chemin de Leysotte, 33882 Villenave d'Ornon Cedex, France. remi.laforgue@hotmail.fr"
Journal Title:Food Microbiol
Year:2012
Volume:20120628
Issue:2
Page Number:230 - 234
DOI: 10.1016/j.fm.2012.06.004
ISSN/ISBN:1095-9998 (Electronic) 0740-0020 (Linking)
Abstract:"Brettanomyces bruxellensis populations have been correlated with an increase in phenolic off-flavors in wine. The volatile phenols causing the olfactory defect result from the successive decarboxylation and reduction of hydroxycinnamic acids that are normal components of red wines. The growth of B. bruxellensis is preventable by adding sulfur dioxide (SO(2)), with variable effectiveness. Moreover, it was hypothesized that SO(2) was responsible for the entry of B. bruxellensis into a viable but non-culturable (VBNC) state. The aim of this project was to investigate the effects of SO(2) on the remaining enzyme activities of B. bruxellensis populations according to their viability and cultivability, focusing on the hydroxycinnamate decarboxylase enzyme, the first enzyme needed, rather than the metabolites produced. Enzyme activity was determined both in cell-free extracts and resting cells after various SO(2) treatments in synthetic media. After slight sulfiting (around 50 mg/L total SO(2)), the yeasts had lost part of their enzyme activity but not their cultivability. At higher doses (at least 75 mg/L total SO(2)) the majority of yeasts had lost their cultivability but still retained part of their enzyme activity. These results suggested that non culturable cells retained some enzyme activity"
Keywords:Brettanomyces/drug effects/*enzymology/growth & development/metabolism Carboxy-Lyases/*metabolism Coumaric Acids/*metabolism Fungal Proteins/metabolism Microbial Viability/drug effects Phenols/*metabolism Sulfur Dioxide/pharmacology Volatile Organic Compo;
Notes:"MedlineLaforgue, R Lonvaud-Funel, A eng Research Support, Non-U.S. Gov't England 2012/09/19 Food Microbiol. 2012 Dec; 32(2):230-4. doi: 10.1016/j.fm.2012.06.004. Epub 2012 Jun 28"

 
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 16-11-2024