Triagem de cepas de Saccharomyces cerevisiae sensíveis ao metilglioxal

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Pavin, Sandra Sartoretto
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Brasil
Bioquímica
UFSM
Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
DNA
Link de acesso: http://repositorio.ufsm.br/handle/1/28321
Resumo: Methylglyoxal is a very reactive α-dicarbonilic compound, that can can be formed in high concentrations in hyperglycemic conditions. It is produced mainly via non-enzymatic ways from glycolytic intermediates, like glyceraldehyde-3-phophate and di-hydroxyketone phosphate. This compound is known for reacting with macromolecules such as proteins, DNA, and RNA, altering their funtions. However, the toxic mechanisms involved in MG toxicity on the biological systems are not fully elucidated. Thus, the present study aimed to perform a screening to identify Saccharomyces cerevisiae mutant strains sensitive to MG, using mainly strains with oxidative stress and DNA damage related mutations. Ninety-six mutant strains were placed in YPD-galactose medium containing different MG concentrations (5-12 mM). The MG sensitivity was evaluated through growth and cellular viability parameters. The different tests showed that the MG toxicity was more pronounced in strains with deletions in genes involved with DNA repair events: Rad23 and Rad50. The MG exposure also decreased markedly the growth and cellular viability in the mutant strains with deletions in genes for the enzymes glyoxalase 1 (Glo1) and glutathione (Gsh1). The results obtained highlight the importance of the glyoxalase 1 system in MG detoxification and point the DNA as a target for the toxicity of the compound in S. cerevisae.