Expansion of EasyClone-MarkerFree toolkit for Saccharomyces cerevisiae genome with new integration sites

Mahsa Babaei, Luisa Sartori, Alexey Karpukhin, Dmitrii Abashkin, Elena Matrosova, Irina Borodina*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

99 Downloads (Pure)

Abstract

Biotechnological production requires genetically stable recombinant strains. To ensure genomic stability, recombinant DNA is commonly integrated into the genome of the host strain. Multiple genetic tools have been developed for genomic integration into baker's yeast Saccharomyces cerevisiae. Previously, we had developed a vector toolkit EasyClone-MarkerFree for stable integration into eleven sites on chromosomes X, XI, and XII of S. cerevisiae. The markerless integration was enabled by CRISPR-Cas9 system. In this study, we have expanded the kit with eight additional intergenic integration sites located on different chromosomes. The integration efficiency into the new sites was above 80%. The expression level of green fluorescence protein (gfp) for all eight sites was similar or above XI-2 site from the original EasyClone-MarkerFree toolkit. The cellular growth was not affected by the integration into any of the new eight locations. The eight-vector expansion kit is available from AddGene.
Original languageEnglish
Article numberfoab027
JournalFEMS Yeast Research
Volume21
Issue number4
ISSN1567-1356
DOIs
Publication statusPublished - 2021

Keywords

  • Chromosomal integration
  • CRISPR-Cas9
  • Genome editing
  • Metabolic engineering

Fingerprint

Dive into the research topics of 'Expansion of EasyClone-MarkerFree toolkit for Saccharomyces cerevisiae genome with new integration sites'. Together they form a unique fingerprint.

Cite this