A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae

Research output: Contribution to journalJournal article – Annual report year: 2019Researchpeer-review

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  • Author: Zhang, Yueping

    Beijing University of Chemical Technology, China

  • Author: Wang, Juan

    Beijing University of Chemical Technology, China

  • Author: Wang, Zibai

    Beijing University of Chemical Technology, China

  • Author: Zhang, Yiming

    Beijing University of Chemical Technology, China

  • Author: Shi, Shuobo

    Beijing University of Chemical Technology, China

  • Author: Nielsen, Jens

    Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet, 2800, Kgs. Lyngby, Denmark

  • Author: Liu, Zihe

    Beijing University of Chemical Technology, China

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With rapid progress in DNA synthesis and sequencing, strain engineering starts to be the rate-limiting step in synthetic biology. Here, we report a gRNA-tRNA array for CRISPR-Cas9 (GTR-CRISPR) for multiplexed engineering of Saccharomyces cerevisiae. Using reported gRNAs shown to be effective, this system enables simultaneous disruption of 8 genes with 87% efficiency. We further report an accelerated Lightning GTR-CRISPR that avoids the cloning step in Escherichia coli by directly transforming the Golden Gate reaction mix to yeast. This approach enables disruption of 6 genes in 3 days with 60% efficiency using reported gRNAs and 23% using un-optimized gRNAs. Moreover, we applied the Lightning GTR-CRISPR to simplify yeast lipid networks, resulting in a 30-fold increase in free fatty acid production in 10 days using just two-round deletions of eight previously identified genes. The GTR-CRISPR should be an invaluable addition to the toolbox of synthetic biology and automation.
Original languageEnglish
Article number1053
JournalNature Communications
Volume10
Number of pages10
ISSN2041-1723
DOIs
Publication statusPublished - 2019
CitationsWeb of Science® Times Cited: No match on DOI

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