Autor(es):
Candeias, Marta 
; Alves-Pereira, I ; Ferreira, Rui
Data: 2013
Identificador Persistente: http://hdl.handle.net/10174/9936
Origem: Repositório Científico da Universidade de Évora
Assunto(s): peptone; phenylurea; yeast; glutathione; malate dehydrogenase; alcohol dehydrogenase
Descrição
The peptone is used to provide nitrogen to Saccharomyces cerevisiae, which is an essential element for growth.
In nature and in industrial musts, essential nutrients for yeast growth are available in complex and variable flux.
Some of these compounds are herbicides, where some specific microorganisms are capable to mineralize or
degrade into more basic and less harmful compounds to the environmental. The isoproturon (IPU), a phenylurea
used as an herbicide, is a compound very difficult to degrade in soils and aquifers, reaching levels considered
toxic by European legislation, contributing to both surface and ground water pollution, and it may be also
involved in the triggering of serious illnesses. So, it’s urgent to discover biological models to contribute to
degrade or eliminate phenylureas in situations of accidental or systematic contamination.
The main target of this study was to evaluate the influence of nitrogen to extend the fermentative phase of S.
cerevisiae by IPU, using the wild-type strain UE-ME3 deposited in the collection of Enology Laboratory of
University of Évora, Portugal.
Cells at mid-exponential phase were inoculated in presence of 100μM IPU in YEPD or YED medium and
incubated during 72 h with orbital stirring, at 28 ºC. Samples from each treatment were used to obtain OD, cfu,
dry weight and to prepare post-12000 g supernatant for determination of protein [1], glutathione (GSH,GSSG)
[2] and malondialdehyde (MDA) [3] contents, and cell capacity to scavenge free radicals by the 2,2-diphenyl-1-
picryl-hidrazil (DPPH) [4] method, as well as, enzyme activities catalase T (CAT T) [5], glutathione reductase
(GR) [6], glutathione peroxidase (GPx) [7], glucose-6-phosphate dehydrogenase (G6PD) [8], alcohol
dehydrogenase (ADH) [9], malate dehydrogenase (MDH2) [10] and lactate dehydrogenase (LDH) [11] by
fluorescence and spectrophotometry. The post-12000 g pellet was also used for protein content and enzyme
activity catalase A (CAT A) determination.
The results show that yeast grown in presence of IPU in peptone starvation conditions (YED-IPU) exhibit at 72 h
a differential growth profile, with cfu, OD, dry weight and level of protein lower than cells grown in YEPD-IPU.
The same type of response was detected in terms of antioxidant power estimated by the GSH/GSSG ratio and
ability to scavenge free radicals detected by DPPH, as well as the levels of enzyme activities CAT T, CAT A,
GR and G6PD which appears much lower in yeast cells grown in YED-IPU medium. On the other hand, cells
exposed to IPU in YEPD medium exhibited fermentative activities, ADH and LDH, higher than those detected in
cells exposed to phenylurea in the restrictive nitrogen medium, YED-IPU. This set of results suggests that yeast
grown in rich medium, YEPD-IPU, remained more fermentative than those grew up in restrictive YED-IPU
medium. This interpretation maybe confirmed by higher levels of glutathione and MDA contents, as well as
enzyme activities GPx and MDH2 detected in S. cerevisiae exposed to YEPD-IPU which started early the
respiratory-fermentative transition. So, S. cerevisiae grown in the nitrogen starvation conditions may more easily
recognize isoproturon as substrate and expand its fermentative phase.
