Microbial Cell Factories · 2022 · 13 citations · 32 references
Life SciencesGeneticsMolecular BiologyGenome EditingGenome EngineeringGenomicsCell CryopreservationCrispr-cas SystemsGenome Editing For Stress ToleranceLow-temperature PreservationYeast GeneticsBaker's YeastBakingCrispr Multiplex EditingCrispr-cas Genome EditingFreezingSmall Heat Shock ProteinsYeast Adaptation To StressYeast Strain Engineering
BACKGROUND: The intracellular molecule trehalose in Saccharomyces cerevisiae may have a major protective function under extreme environmental conditions. NTH1 is one gene which expresses trehalase to degrade trehalose. Small heat shock protein 12 (HSP12 expressed) plays a role in protecting membranes and enhancing freezing stress tolerance. RESULTS: An optimized S. cerevisiae CRISPR-Cpf1 genome-editing system was constructed. Multiplex genome editing using a single crRNA array was shown to be functional. NTH1 or/and HSP12 knockout in S. cerevisiae enhanced the freezing stress tolerance and improved the leavening ability after freezing and thawing. CONCLUSIONS: Deleting NTH1 in the combination with deleting HSP12 would strengthen the freezing tolerance and protect the cell viability from high rates of death in longer-term freezing. It provides valuable insights for breeding novel S. cerevisiae strains for the baking industry through a more precise, speedy, and economic genome-editing system.
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Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System
Bernd Zetsche, Jonathan S. Gootenberg, Omar O. Abudayyeh et al. · Cell · 2015 · 4.9K citations · Full text
In vivo high-throughput profiling of CRISPR–Cpf1 activity
Hui Kwon Kim · Nature Methods · 2016 · 402 citations · Full text