Creative Biogene is a leading biotechnology company offering the best Saccharomyces cerevisiae genome editing services. With years of experience and expertise in microbial genome editing, our talented scientists will work closely with you to provide any help in Saccharomyces cerevisiae genome editing services.
Saccharomyces cerevisiae is an important eukaryotic model organism, which is widely used as industrial host for production of fuels, chemicals and recombinant proteins. Genome editing of S. cerevisiae has profound meaning in the research and industry. Thanks to its excellent HR capability, S. cerevisiae is relatively easy to engineer genetically.
Our S. cerevisiae genome editing services based on CRISPR/Cas9 technology and homologous recombination technique. The state-of-art S. cerevisiae editing system helps you successfully achieve gene knockout, gene insertion and point mutation for either research or industrial purposes.
Saccharomyces cerevisiae Genome Editing Based on Homologous Recombination
Red/ET Recombination permits the engineering of DNA in S. cerevisiae using homologous recombination mediated by phage protein pairs, either RecE/RecT or Reda/Redb. The central step in Red/ET recombination is the crossover step between a targeting construct containing homology arms and the target which can be a gene locus on the S. cerevisiae chromosome by designing a homologous fusion fragment of the target gene, it is cloned into a suicide vector, and the suicide vector is transformed into the target S. cerevisiae. An insertion mutant is selected by antibiotic screening. Under the second round of reverse selection pressure, only the mutation that contain second homologous recombination and the loss of the suicide plasmid can survive. By PCR screening and sequencing, we can obtain the mutant of the strain.
Fig.1. Workflow of homologous recombination genome editing
• Homology arms design and suicide plasmid construction
CRISPR/Cas9-mediated S. cerevisiae Genome Editing
CRISPR technology, which derived from the immune system present in bacteria and archaea, is an efficient genome-scale editing tool that has revolutionized conventional genetic engineering methods and unprecedentedly facilitated strain engineering. It enables fast and reliable genetic manipulation in S. cerevisiae. Two components are requested to work: a guide RNA (gRNA), e.g. under an RNA polymerase III promoter, and the nuclear localization tag fused DNA endonuclease, with Cas9 being the most commonly used.
When Cas9 protein and gRNA are expressed in yeast cells, Cas9 introduces DSBs that must be repaired by the cells via non-homologous end joining (NHEJ) or homologous recombination (HR). By supplying a DNA repair template for use in HR, various DNA modifications can be obtained.
Fig.2. Workflow of homologous recombination genome editing
• sgRNA design and construction
The advantages of CRISPR based S. cerevisiae genome editing in Creative Biogene:
• Fast turnaround time
• Scarless genome editing
• Multigene editing: can knock-out up to 5 genes simultaneously
• Easy selection: no selectable marker is required
What we could help?
• Gene disruption, deletion or insertion
• Reporter gene and tag integration
• Promoter fine tuning
• Introduction of point mutations
With years of experience in genome editing field, Creative Biogene could provide the most excellent service for S. cerevisiae’ genome editing. Our talent experts are dedicated to edit your S. cerevisiae with the greatest chance to succeed. Meanwhile, based on the commitment of prompt communication and on-time reporting, our staffs will ensure a high-efficiency service to meet the strict project timelines.
If you have any special requirements in our S. cerevisiae genome editing service, please feel free to contact us at email@example.com. We are looking forward to working together with your attractive projects.
1. Yu D, et al. An efficient recombination system for chromosome engineering in Escherichia coli. Proc. Natl. Acad. Sci. U. S. A. 2000;97:5978–5983
2. Stovicek V, Holkenbrink C. Borodina I. CRISPR/Cas system for yeast genome engineering: advances and applications. FEMS Yeast Res. 2017;17:fox030.