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1.
Yeast ; 34(9): 359-370, 2017 09.
Article in English | MEDLINE | ID: mdl-28556381

ABSTRACT

Zygosaccharomyces bailii is a non-Saccharomyces budding yeast known as one of the most aggressive food spoilage microorganisms, often isolated as a contaminant during wine fermentation, as well as from many acidic, high-sugar and canned foods. The spoilage ability relies on the yeast's unique feature of tolerating the most common preservatives such as sulphite, dimethyl dicarbonate, acetic acid and sorbic acid. Therefore, many studies have focused on the description of this peculiar tolerance with the aim of developing preventative measures against Z. bailii food spoilage. These studies demonstrated the involvement of diverse molecular and physiological mechanisms in the yeast resistance, comprising detoxification of preservatives, adaptation of the cytoplasmic pH and modulation of the cell wall/membrane composition. At the same time, the described traits unveiled Z. bailii as a novel potential workhorse for industrial bioprocesses. Here we present the yeast Z. bailii starting from important aspects of its robustness and concluding with the exploitation of its potential in biotechnology. Overall, the article describes Z. bailii from different perspectives, converging in presenting it as one of the most interesting species of the Saccharomycotina subphylum. Copyright © 2017 John Wiley & Sons, Ltd.


Subject(s)
Drug Resistance, Fungal , Food Contamination/prevention & control , Food Preservatives/pharmacology , Zygosaccharomyces/drug effects , Acetic Acid/pharmacology , Adaptation, Physiological , Diethyl Pyrocarbonate/analogs & derivatives , Diethyl Pyrocarbonate/pharmacology , Fermentation , Food, Preserved/microbiology , Hydrogen-Ion Concentration , Sorbic Acid/pharmacology , Sulfites/pharmacology , Wine/microbiology , Zygosaccharomyces/genetics , Zygosaccharomyces/metabolism
2.
Microbiology (Reading) ; 158(Pt 9): 2325-2335, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22790396

ABSTRACT

In living organisms, copper (Cu) contributes to essential functions but at high concentrations it may elicit toxic effects. Cu-tolerant yeast strains are of relevance for both biotechnological applications and studying physiological and molecular mechanisms involved in stress resistance. One way to obtain tolerant strains is to exploit experimental methods that rely on the principles of natural evolution (evolutionary engineering) and allow for the development of complex phenotypic traits. However, in most cases, the molecular and physiological basis of the phenotypic changes produced have not yet been unravelled. We investigated the determinants of Cu resistance in a Saccharomyces cerevisiae strain that was evolved to tolerate up to 2.5 g CuSO(4) l(-1) in the culture medium. We found that the content of intracellular Cu and the expression levels of several genes encoding proteins involved in Cu metabolism and oxidative stress response were similar in the Cu-tolerant (evolved) and the Cu-sensitive (non-evolved) strain. The major difference detected in the two strains was the copy number of the gene CUP1, which encodes a metallothionein. In evolved cells, a sevenfold amplification of CUP1 was observed, accounting for its strongly and steadily increased expression. Our results implicate CUP1 in protection of the evolved S. cerevisiae cells against Cu toxicity. In these cells, robustness towards Cu is stably inheritable and can be reproducibly selected by controlling environmental conditions. This finding corroborates the effectiveness of laboratory evolution of whole cells as a tool to develop microbial strains for biotechnological applications.


Subject(s)
Antifungal Agents/toxicity , Copper/toxicity , Drug Tolerance , Gene Amplification , Metallothionein/genetics , Saccharomyces cerevisiae/drug effects , Saccharomyces cerevisiae/genetics , Metallothionein/metabolism , Selection, Genetic , Serial Passage
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