WebAn efficient one-step transformation method for the dimorphic yeast Yarrowia lipolytica is described. Using cells grown overnight on agar plates, the whole process is carried out within 1 h. The transformant clones could be recovered on selective plates as early as 36–48 h after plating. WebWe present a teaching protocol suitable for demonstrating the use of EasyClone and CRISPR/Cas9 for metabolic engineering of industrially relevant yeasts Saccharomyces cerevisiae and Yarrowia lipolytica, using β-carotene production as a case study.
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WebFirstly, the thesis describes EasyCloneYALI, a genetic engineering toolbox, which allows for simple and rapid engineering of Y. lipolytica using either the traditional selection marker-based integration system or a marker-free Cas9-based system. Secondly, a method book chapter based on the EasyCloneYALI method is presented. WebAddgene in the status bar pictured above
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WebFeb 1, 2024 · The EasyCloneYALI genetic toolbox, which allows streamlined strain construction with high genome editing efficiencies in Y. lipolytica via the CRISPR/Cas9 technology is presented, and includes a set of integrative gene expression vectors with prototrophic markers conferring resistance to hygromycin and nourseothricin. Expand WebAug 18, 2024 · Plasmid assembly and cloning was performed according to EasyCloneYALI instructions (Holkenbrink et al., 2024). For gene deletions, DNA fragments consisting of 400–600 bp up- and downstream of the target gene were used as repair template (800–1200 bp total). All constructed plasmids were verified by Sanger sequencing … WebPurpose (Empty Backbone) EasyCloneYALI system-based yeast episomal vector carrying a nourseothricin-resistance marker for Yarrowia lipolytica, can be used for gRNA expression, amp resistance Depositing Lab Irina Borodina Publication Holkenbrink et al Biotechnol J. 2024 Jan 29. doi: 10.1002/biot.202400543. ( How to cite ) Sequence Information newitt and co ltd