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Improved designs for pET expression plasmids increase protein production yield in Escherichia coli
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
Vise andre og tillknytning
Rekke forfattare: 62020 (engelsk)Inngår i: Communications Biology, E-ISSN 2399-3642, Vol. 3, nr 1Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The pET series of expression plasmids are widely used for recombinant protein production in Escherichia coli. The genetic modules controlling transcription and translation in these plasmids were first described in the 1980s and have not changed since. Herein we report design flaws in these genetic modules. We present improved designs and demonstrate that, when incorporated into pET28a, they support increases in protein production. The improved designs are applicable to most of the 103 vectors in the pET series and can be easily implemented. Patrick Shilling et al. increase the protein production yield from the pET28a expression plasmid by modifying the genetic modules that control transcription and translation initiation. These improved designs are applicable to most vectors in the pET series and can be easily implemented.

sted, utgiver, år, opplag, sider
2020. Vol. 3, nr 1
HSV kategori
Identifikatorer
URN: urn:nbn:se:su:diva-183013DOI: 10.1038/s42003-020-0939-8ISI: 000533893600003PubMedID: 32382055OAI: oai:DiVA.org:su-183013DiVA, id: diva2:1450438
Tilgjengelig fra: 2020-07-01 Laget: 2020-07-01 Sist oppdatert: 2023-08-07bibliografisk kontrollert
Inngår i avhandling
1. Next generation tools for microbial cell factories
Åpne denne publikasjonen i ny fane eller vindu >>Next generation tools for microbial cell factories
2023 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The bacterium E. coli is a popular choice for expressing recombinant proteins. It is easy to culture and many molecular tools for are available for directing protein production. When producing recombinant proteins, high yields and good quality soluble products are desirable. Poor yields or misfolded, aggregated and insoluble products are unwanted outcomes. In this thesis, existing tools have been evolved to enable increased yields of recombinant products from microbial cell factories. New tools have also been developed that help the user avoid bacterial stress and improve the quality of the recombinant proteins. 

sted, utgiver, år, opplag, sider
Stockholm: Department of Biochemistry and Biophysics, Stockholm University, 2023. s. 64
Emneord
Microbial cell factories, Recombinant protein production, Bacteria, Plasmid, Genetic sensor, Inducible promoter, Genetic cassette
HSV kategori
Forskningsprogram
biokemi
Identifikatorer
urn:nbn:se:su:diva-219865 (URN)978-91-8014-444-5 (ISBN)978-91-8014-445-2 (ISBN)
Disputas
2023-09-20, Magnelisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 14:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2023-08-28 Laget: 2023-08-07 Sist oppdatert: 2025-02-20bibliografisk kontrollert

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