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pUdOs: Concise Plasmids for Bacterial and Mammalian Cells.
Manigat, France O; Connell, Louise B; Stewart, Brittany N; LePabic, Abdel-Rahman; Tessier, Christian J G; Emlaw, Johnathon R; Calvert, Nicholas D; Rössl, Anthony; Shuhendler, Adam J; daCosta, Corrie J B; Campbell-Valois, François-Xavier.
  • Manigat FO; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Connell LB; bioGARAGE, Faculty of Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Stewart BN; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • LePabic AR; bioGARAGE, Faculty of Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Tessier CJG; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Emlaw JR; bioGARAGE, Faculty of Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Calvert ND; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Rössl A; bioGARAGE, Faculty of Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Shuhendler AJ; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • daCosta CJB; bioGARAGE, Faculty of Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
  • Campbell-Valois FX; Center for Chemical and Synthetic Biology, Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
ACS Synth Biol ; 13(2): 485-497, 2024 02 16.
Article en En | MEDLINE | ID: mdl-38235654
ABSTRACT
The plasmids from the Université d'Ottawa (pUdOs) are 28 small plasmids each comprising one of four origins of replication and one of seven selection markers, which together afford flexible use in Escherichia coli and several related gram-negative bacteria. The promoterless multicloning site is insulated from upstream spurious promoters by strong transcription terminators and contains type IIP or IIS restriction sites for conventional or Golden Gate cloning. pUdOs can be converted into efficient expression vectors through the insertion of a promoter at the user's discretion. For example, we demonstrate the utility of pUdOs as the backbone for an improved version of a Type III Secretion System reporter in Shigella. In addition, we derive a series of pUdO-based mammalian expression vectors, affording distinct levels of expression and transfection efficiency comparable to commonly used mammalian expression plasmids. Thus, pUdOs could advantageously replace traditional plasmids in a wide variety of cell types and applications.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vectores Genéticos / Bacterias Gramnegativas Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vectores Genéticos / Bacterias Gramnegativas Idioma: En Año: 2024 Tipo del documento: Article