Related Experiment Video
Updated: Jan 12, 2026

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
RECKLEEN is a lambda Red/CRISPR-Cas9 based single plasmid platform for enhanced genome editing in Klebsiella
Eslam M Elsayed1,2,3, Daniel Stukenberg1,4, Doreen Meier1,2
1Center for Synthetic Microbiology (SYNMIKRO), Philipps-Universität Marburg, Marburg, Germany.
Abstract:
Klebsiella pneumoniae (Kp) has evolved as a major public health threat due to its multidrug-resistance (MDR) and hypervirulence. Current Kp genome-editing tools are constrained by cumbersome workflows, low flexibility, and limited scalability. Here, we present the RECKLEEN system -Recombineering/CRISPR-based KLebsiella Engineering for Efficient Nucleotide editing - as a single plasmid platform designed for precise genetic manipulation of Kp. RECKLEEN combines lambda Red recombineering with powerful CRISPR-Cas9-based targeted counterselection, achieving up to 99.998% killing efficiency. By implementing the near PAM-less SpG Cas9 variant in RECKLEEN, the compatible target sequence spectrum was significantly broadened. This approach enables deletions, point mutations, and DNA integrations, with efficiencies reaching 100% of the counter-selected clones. Simultaneous multi-target deletions were accomplished with up to 72% efficiency. To streamline the process, we developed a toolbox of eleven plasmids based on a modular cloning standard, enabling time- and resource-efficient assembly of editing constructs. This allows a 5-days workflow, from plasmid construction to the generation of strains with the desired genetic modification(s). The efficacy of RECKLEEN extends to various MDR Kp strains, such as ATCC 700721, ATCC BAA-1705, and ATCC 700603, demonstrating its broad applicability. RECKLEEN significantly enhances genome-editing capabilities for Kp, advancing research into its pathology and MDR mechanisms.
Insights
A new genome-editing system, RECKLEEN, offers precise genetic manipulation for Klebsiella pneumoniae (Kp). This efficient tool streamlines the process, aiding research into Kp
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- Klebsiella pneumoniae (Kp) poses a significant public health risk due to multidrug-resistance (MDR) and hypervirulence.
- Existing genome-editing tools for Kp are inefficient, complex, and lack scalability.
Purpose of the Study:
- To develop a novel, efficient, and scalable platform for precise genetic manipulation of Klebsiella pneumoniae.
- To overcome limitations of current genome-editing technologies in Kp research.
Main Methods:
- Introduction of the RECKLEEN system, a single plasmid platform combining lambda Red recombineering with CRISPR-Cas9 counterselection.
- Utilized a near PAM-less SpG Cas9 variant to expand targetable sequences.
- Developed a modular cloning system with eleven plasmids for efficient construct assembly.
Main Results:
- RECKLEEN achieves high killing efficiency (up to 99.998%) and precise genetic modifications (deletions, point mutations, integrations) with up to 100% efficiency in counter-selected clones.
- Enabled simultaneous multi-target deletions with up to 72% efficiency.
- Established a streamlined 5-day workflow from plasmid construction to modified Kp strains.
Conclusions:
- RECKLEEN significantly enhances genome-editing capabilities for Klebsiella pneumoniae.
- The system demonstrates broad applicability across various MDR Kp strains.
- Facilitates advanced research into Kp pathology and mechanisms of multidrug resistance.
More Related Videos
11:35Selection-dependent and Independent Generation of CRISPR/Cas9-mediated Gene Knockouts in Mammalian Cells
Published on: June 16, 2017
07:46CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.
Published on: December 11, 2020
Related Concept Videos
CRISPR/Cas9 Genome Editing
Conservative Site-specific Recombination and Phase Variation
The recognition sites for Cre recombinase called LoxP...
CRISPR
CRISPR and crRNAs
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...