2015Nauka Przyroda Technologie. Uniwersytet Przyrodniczy w PoznaniuOpen access

Optimization of chemical mutagenesis of yeast Saccharomyces cerevisiae using ethyl methanesulfonate (EMS)

Zakład Innowacyjnych Biomateriałów i Nanotechnologii, Instytut Włókien Naturalnych i Roślin Zielarskich w Poznaniu, Aleksandra Wawro, Adam Rzeszutek, Żaneta Bartkowiak, Dominika Pieprzyk-Kokocha, W. Grajek

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Abstract

This paper attempts to optimize the methods of chemical mutagenesis of distillers yeast Saccharomyces cerevisiae using an alkylating agent ethyl methanesulfonate (EMS). Several rounds of mutagenesis were carried out, mutagen concentration and duration of exposure were adopted as variables. Optimal conditions required to ensure the death of the yeast cells were achieved during the log phase of cell, at concentration of mutagen 114.5–137.4 mg/cm3 and during the mutagenesis duration exposure time 60 min. As a result, several tens of yeast mutants were obtained. Based on testing of fermentation were selected five mutants characterized by a higher volumetric ethanol productivity than the starting strain. The obtained mutants were subjected to the screening test for their resistance to acetic acid. It was found that the mutants showed two times higher resistance to acetic acid than the starting strain.

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What this paper is about

This paper attempts to optimize the methods of chemical mutagenesis of distillers yeast Saccharomyces cerevisiae using an alkylating agent ethyl methanesulfonate (EMS). Several rounds of mutagenesis were carried out, mutagen concentration and duration of exposure were adopted as variables. Optimal conditions required to ensure the death of the yeast cells were achieved during the log phase of cell, at concentration of mutagen 114.5–137.4 mg/cm3 and during the mutagenesis duration exposure time 60 min. As a result, several tens of yeast mutants were obtained. Based on testing of fermentation were selected five mutants characterized by a higher volumetric ethanol productivity than the starting strain. The obtained mutants were subjected to the screening test for their resistance to acetic acid. It was found that the mutants showed two times higher resistance to acetic acid than the starting strain.

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Available abstract

This paper attempts to optimize the methods of chemical mutagenesis of distillers yeast Saccharomyces cerevisiae using an alkylating agent ethyl methanesulfonate (EMS). Several rounds of mutagenesis were carried out, mutagen concentration and duration of exposure were adopted as variables. Optimal conditions required to ensure the death of the yeast cells were achieved during the log phase of cell, at concentration of mutagen 114.5–137.4 mg/cm3 and during the mutagenesis duration exposure time 60 min. As a result, several tens of yeast mutants were obtained. Based on testing of fermentation were selected five mutants characterized by a higher volumetric ethanol productivity than the starting strain. The obtained mutants were subjected to the screening test for their resistance to acetic acid. It was found that the mutants showed two times higher resistance to acetic acid than the starting strain.

Key concepts: Ethyl methanesulfonate, Mutagen, Mutagenesis, Yeast, Saccharomyces cerevisiae, Methyl methanesulfonate, Acetic acid, Mutant

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