Abstract
R6K plasmids are commonly used for a wide range of genome engineering applications due to their ability to support transient delivery of genetic cargos in many hosts. The maintenance of R6K plasmids requires specific strains. Unfortunately, many of these have obscure backgrounds, limited availability and were not built for efficient cloning. To address this issue, we present the construction and characterization of a series of Pir E. coli strains called SHARK that are built from the DH10B derivative, Marionette-Clo. All SHARK strains have a genome encoded pir gene for stable R6K plasmid maintenance and a λCI gene for tight unconditional repression of specific genes on plasmids. We show that SHARK strains are >100-fold more efficient than a commercial Pir strain when transformed with large and complex cloning reactions. SHARK is intended to help facilitate the cloning of R6K plasmids for challenging genome engineering projects, with all strains and genetic tools for their assembly being made publicly available.
| Original language | English |
|---|---|
| Pages (from-to) | 867-875 |
| Number of pages | 9 |
| Journal | ACS Synthetic Biology |
| Volume | 15 |
| Issue number | 2 |
| Early online date | 13 Jan 2026 |
| DOIs | |
| Publication status | Published - 20 Feb 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Authors.
Keywords
- genome integration
- lambda-RED
- R6K plasmids
- conditional replication
- Pir strains
- cloning
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