An artifact of recombinatorial cloning challenges established beliefs of plasmid cotransformation, selection, and maintenance

Gateway cloning is an easy, efficient, accurate, and versatile cloning strategy. During Expression clone validation, we sometimes see an additional band co-migrating with the pDONR (Entry) backbone. We show that this "mystery" band is not an artifact of aberrant recombination but instead originates from a cotransformation event, where more than one different plasmid is transformed into a single <i>Escherichia coli</i> cell simultaneously and in the absence of antibiotic selection. We find that the unselected pDONR Entry plasmid is cotransformed into <i>E. coli</i> with the desired Expression vector in 9%-29% of colonies and is maintained without antibiotic selection, despite plasmid incompatibility. We propose an easy strategy to screen for and eliminate cotransformants. Our results challenge accepted beliefs of bacterial plasmid transformation, selection, and maintenance and comprise the first documented occurrence of cotransformation in Gateway cloning.

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Publication Details

Journal
Biochemistry and Cell Biology
Published
2025-01-01
DOI
https://doi.org/10.1139/bcb-2025-0096
Citations
1
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
1.82
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article

An artifact of recombinatorial cloning challenges established beliefs of plasmid cotransformation, selection, and maintenance

Michael Charette, Courtney L. Geer
1 citations
Biochemistry and Cell Biology
Bacterial Genetics and Biotechnology
1.82
article

An artifact of recombinatorial cloning challenges established beliefs of plasmid cotransformation, selection, and maintenance

Michael Charette, Courtney L. Geer
article en
1 citations

Abstract

Gateway cloning is an easy, efficient, accurate, and versatile cloning strategy. During Expression clone validation, we sometimes see an additional band co-migrating with the pDONR (Entry) backbone. We show that this "mystery" band is not an artifact of aberrant recombination but instead originates from a cotransformation event, where more than one different plasmid is transformed into a single <i>Escherichia coli</i> cell simultaneously and in the absence of antibiotic selection. We find that the unselected pDONR Entry plasmid is cotransformed into <i>E. coli</i> with the desired Expression vector in 9%-29% of colonies and is maintained without antibiotic selection, despite plasmid incompatibility. We propose an easy strategy to screen for and eliminate cotransformants. Our results challenge accepted beliefs of bacterial plasmid transformation, selection, and maintenance and comprise the first documented occurrence of cotransformation in Gateway cloning.

Biochemistry and Cell BiologyVol. 103
Paul Scherrer Institute (CH), CancerCare Manitoba (CA), Children's Hospital Research Institute of Manitoba (CA), Research Institute in Oncology and Hematology (CA), University of Manitoba (CA), Brandon University (CA)
Openalex Percentile: Top 16%
Bacterial Genetics and Biotechnology
1.82
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An artifact of recombinatorial cloning challenges established beliefs of plasmid cotransformation, selection, and maintenance — Michael Charette, Courtney L. Geer · Biochemistry and Cell Biology (2025) | TGRS Research Map | TGRS