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CRISPR/Cpf1-Mediated Multiplex and Large-Fragment Gene Editing in Staphylococcus aureus .

Zhipeng WangYu WangYujue WangWeizhong ChenQuanjiang Ji
Published in: ACS synthetic biology (2022)
Staphylococcus aureus is a major human pathogen that causes a variety of infections, including life-threatening diseases. Research on S. aureus is constrained by complex and limited genetic manipulation methods. Here, we report a CRISPR/Cpf1-mediated system, pCpfSA, for rapid and versatile genome editing in S. aureus . In direct comparison with the existing CRISPR/Cas9-mediated genome-editing system, the pCpfSA system exhibits enhanced colony-forming units (CFUs) after editing and an expanded targetable range with comparable editing efficiency. Given the precursor crRNA (pre-crRNA) processing activity of Cpf1, the pCpfSA system also allows multiplex gene editing and large-fragment DNA knockout simply by introducing two crRNAs and the corresponding donor templates, which is difficult to achieve using the CRISPR/Cas9 system, thereby greatly expanding the genome editor toolbox for S. aureus .
Keyphrases
  • genome editing
  • crispr cas
  • staphylococcus aureus
  • endothelial cells
  • high throughput
  • genome wide
  • biofilm formation
  • single molecule
  • escherichia coli
  • pseudomonas aeruginosa
  • gene expression