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BglBricks: A flexible standard for biological part assembly

BACKGROUND: Standard biological parts, such as BioBricks™ parts, provide the foundation for a new engineering discipline that enables the design and construction of synthetic biological systems with a variety of applications in bioenergy, new materials, therapeutics, and environmental remediation. A...

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Autores principales: Anderson, J Christopher, Dueber, John E, Leguia, Mariana, Wu, Gabriel C, Goler, Jonathan A, Arkin, Adam P, Keasling, Jay D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822740/
https://www.ncbi.nlm.nih.gov/pubmed/20205762
http://dx.doi.org/10.1186/1754-1611-4-1
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author Anderson, J Christopher
Dueber, John E
Leguia, Mariana
Wu, Gabriel C
Goler, Jonathan A
Arkin, Adam P
Keasling, Jay D
author_facet Anderson, J Christopher
Dueber, John E
Leguia, Mariana
Wu, Gabriel C
Goler, Jonathan A
Arkin, Adam P
Keasling, Jay D
author_sort Anderson, J Christopher
collection PubMed
description BACKGROUND: Standard biological parts, such as BioBricks™ parts, provide the foundation for a new engineering discipline that enables the design and construction of synthetic biological systems with a variety of applications in bioenergy, new materials, therapeutics, and environmental remediation. Although the original BioBricks™ assembly standard has found widespread use, it has several shortcomings that limit its range of potential applications. In particular, the system is not suitable for the construction of protein fusions due to an unfavorable scar sequence that encodes an in-frame stop codon. RESULTS: Here, we present a similar but new composition standard, called BglBricks, that addresses the scar translation issue associated with the original standard. The new system employs BglII and BamHI restriction enzymes, robust cutters with an extensive history of use, and results in a 6-nucleotide scar sequence encoding glycine-serine, an innocuous peptide linker in most protein fusion applications. We demonstrate the utility of the new standard in three distinct applications, including the construction of constitutively active gene expression devices with a wide range of expression profiles, the construction of chimeric, multi-domain protein fusions, and the targeted integration of functional DNA sequences into specific loci of the E. coli genome. CONCLUSIONS: The BglBrick standard provides a new, more flexible platform from which to generate standard biological parts and automate DNA assembly. Work on BglBrick assembly reactions, as well as on the development of automation and bioinformatics tools, is currently underway. These tools will provide a foundation from which to transform genetic engineering from a technically intensive art into a purely design-based discipline.
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spelling pubmed-28227402010-02-17 BglBricks: A flexible standard for biological part assembly Anderson, J Christopher Dueber, John E Leguia, Mariana Wu, Gabriel C Goler, Jonathan A Arkin, Adam P Keasling, Jay D J Biol Eng Methodology BACKGROUND: Standard biological parts, such as BioBricks™ parts, provide the foundation for a new engineering discipline that enables the design and construction of synthetic biological systems with a variety of applications in bioenergy, new materials, therapeutics, and environmental remediation. Although the original BioBricks™ assembly standard has found widespread use, it has several shortcomings that limit its range of potential applications. In particular, the system is not suitable for the construction of protein fusions due to an unfavorable scar sequence that encodes an in-frame stop codon. RESULTS: Here, we present a similar but new composition standard, called BglBricks, that addresses the scar translation issue associated with the original standard. The new system employs BglII and BamHI restriction enzymes, robust cutters with an extensive history of use, and results in a 6-nucleotide scar sequence encoding glycine-serine, an innocuous peptide linker in most protein fusion applications. We demonstrate the utility of the new standard in three distinct applications, including the construction of constitutively active gene expression devices with a wide range of expression profiles, the construction of chimeric, multi-domain protein fusions, and the targeted integration of functional DNA sequences into specific loci of the E. coli genome. CONCLUSIONS: The BglBrick standard provides a new, more flexible platform from which to generate standard biological parts and automate DNA assembly. Work on BglBrick assembly reactions, as well as on the development of automation and bioinformatics tools, is currently underway. These tools will provide a foundation from which to transform genetic engineering from a technically intensive art into a purely design-based discipline. BioMed Central 2010-01-20 /pmc/articles/PMC2822740/ /pubmed/20205762 http://dx.doi.org/10.1186/1754-1611-4-1 Text en Copyright ©2010 Anderson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Anderson, J Christopher
Dueber, John E
Leguia, Mariana
Wu, Gabriel C
Goler, Jonathan A
Arkin, Adam P
Keasling, Jay D
BglBricks: A flexible standard for biological part assembly
title BglBricks: A flexible standard for biological part assembly
title_full BglBricks: A flexible standard for biological part assembly
title_fullStr BglBricks: A flexible standard for biological part assembly
title_full_unstemmed BglBricks: A flexible standard for biological part assembly
title_short BglBricks: A flexible standard for biological part assembly
title_sort bglbricks: a flexible standard for biological part assembly
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822740/
https://www.ncbi.nlm.nih.gov/pubmed/20205762
http://dx.doi.org/10.1186/1754-1611-4-1
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