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  The Marburg collection: A Golden Gate DNA assembly framework for synthetic biology applications in Vibrio natriegens

Stukenberg, D., Hensel, T., Hoff, J., Daniel, B., Inckemann, R., Tedeschi, J. N., et al. (2021). The Marburg collection: A Golden Gate DNA assembly framework for synthetic biology applications in Vibrio natriegens. ACS Synthetic Biology, 10(8), 1904-1919. doi:10.1021/acssynbio.1c00126.

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Locator:
https://doi.org/10.1021/acssynbio.1c00126 (Publisher version)
Description:
Verlagsversion
OA-Status:
Hybrid

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 Creators:
Stukenberg, Daniel1, Author           
Hensel, Tobias, Author
Hoff, Josef2, Author
Daniel, Benjamin, Author
Inckemann, René3, Author           
Tedeschi, Jamie N., Author
Nousch, Franziska, Author
Fritz, Georg, Author
Affiliations:
1IMPRS-Mic, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266296              
2Max Planck Research Group Bacterial Epitranscriptomics, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266299              
3Max Planck Institute for Terrestrial Microbiology, Max Planck Society, Karl-von-Frisch-Strasse 10, D-35043 Marburg, DE, ou_3135468              

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Free keywords: *Cloning, Molecular DNA, Bacterial/*genetics Escherichia coli/genetics *Gene Library *Synthetic Biology Vibrio/*genetics *Golden Gate Assembly *Vibrio natriegens *chassis organism *de novo assembly *genetic parts
 Abstract: Vibrio natriegens is known as the world's fastest growing organism with a doubling time of less than 10 min. This incredible growth speed empowers V. natriegens as a chassis for synthetic and molecular biology, potentially replacing E. coli in many applications. While first genetic parts have been built and tested for V. natriegens, a comprehensive toolkit containing well-characterized and standardized parts did not exist. To close this gap, we created the Marburg Collection-a highly flexible Golden Gate cloning toolbox optimized for the emerging chassis organism V. natriegens, containing 191 genetic parts. The Marburg Collection overcomes the paradigm of plasmid construction-integrating inserts into a backbone-by enabling the de novo assembly of plasmids from basic genetic parts. This allows users to select the plasmid replication origin and resistance part independently, which is highly advantageous when limited knowledge about the behavior of those parts in the target organism is available. Additional design highlights of the Marburg Collection are novel connector parts, which facilitate modular circuit assembly and, optionally, the inversion of individual transcription units to reduce transcriptional crosstalk in multigene constructs. To quantitatively characterize the genetic parts contained in the Marburg Collection in V. natriegens, we developed a reliable microplate reader measurement workflow for reporter experiments and overcame organism-specific challenges. We think the Marburg Collection with its thoroughly characterized parts will provide a valuable resource for the growing V. natriegens community.

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Language(s): eng - English
 Dates: 2021-07-14
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: Other: 34255476
DOI: 10.1021/acssynbio.1c00126
ISSN: 2161-5063
 Degree: -

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Title: ACS Synthetic Biology
  Abbreviation : ACS Synth. Biol.
Source Genre: Journal
 Creator(s):
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Publ. Info: Washington, D.C. : American Chemical Society
Pages: - Volume / Issue: 10 (8) Sequence Number: - Start / End Page: 1904 - 1919 Identifier: ISSN: 2161-5063
CoNE: https://pure.mpg.de/cone/journals/resource/2161-5063