| Literature DB >> 31728740 |
Yusuf Sürmeli1,2,3, Can Holyavkin1,2, Alican Topaloğlu1,2, Mevlüt Arslan1,2,4, Halil İbrahim Kısakesen1,2, Zeynep Petek Çakar5,6.
Abstract
Caffeine is a naturally occurring alkaloid, where its major consumption occurs with beverages such as coffee, soft drinks and tea. Despite a variety of reports on the effects of caffeine on diverse organisms including yeast, the complex molecular basis of caffeine resistance and response has yet to be understood. In this study, a caffeine-hyperresistant and genetically stable Saccharomyces cerevisiae mutant was obtained for the first time by evolutionary engineering, using batch selection in the presence of gradually increased caffeine stress levels and without any mutagenesis of the initial population prior to selection. The selected mutant could resist up to 50 mM caffeine, a level, to our knowledge, that has not been reported for S. cerevisiae so far. The mutant was also resistant to the cell wall-damaging agent lyticase, and it showed cross-resistance against various compounds such as rapamycin, antimycin, coniferyl aldehyde and cycloheximide. Comparative transcriptomic analysis results revealed that the genes involved in the energy conservation and production pathways, and pleiotropic drug resistance were overexpressed. Whole genome re-sequencing identified single nucleotide polymorphisms in only three genes of the caffeine-hyperresistant mutant; PDR1, PDR5 and RIM8, which may play a potential role in caffeine-hyperresistance.Entities:
Keywords: Adaptive laboratory evolution; Caffeine; Evolutionary engineering; Pleiotropic drug resistance (PDR); Saccharomyces cerevisiae; Stress resistance
Year: 2019 PMID: 31728740 DOI: 10.1007/s11274-019-2762-2
Source DB: PubMed Journal: World J Microbiol Biotechnol ISSN: 0959-3993 Impact factor: 3.312