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AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies
The assembly of large DNA constructs coding for entire pathways poses a major challenge in the field of synthetic biology. Here, we present AssemblX, a novel, user-friendly and highly efficient multi-gene assembly strategy. The software-assisted AssemblX process allows even unexperienced users to ra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449548/ https://www.ncbi.nlm.nih.gov/pubmed/28130422 http://dx.doi.org/10.1093/nar/gkx034 |
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author | Hochrein, Lena Machens, Fabian Gremmels, Juergen Schulz, Karina Messerschmidt, Katrin Mueller-Roeber, Bernd |
author_facet | Hochrein, Lena Machens, Fabian Gremmels, Juergen Schulz, Karina Messerschmidt, Katrin Mueller-Roeber, Bernd |
author_sort | Hochrein, Lena |
collection | PubMed |
description | The assembly of large DNA constructs coding for entire pathways poses a major challenge in the field of synthetic biology. Here, we present AssemblX, a novel, user-friendly and highly efficient multi-gene assembly strategy. The software-assisted AssemblX process allows even unexperienced users to rapidly design, build and test DNA constructs with currently up to 25 functional units, from 75 or more subunits. At the gene level, AssemblX uses scar-free, overlap-based and sequence-independent methods, allowing the unrestricted design of transcriptional units without laborious parts domestication. The assembly into multi-gene modules is enabled via a standardized, highly efficient, polymerase chain reaction-free and virtually sequence-independent scheme, which relies on rare cutting restriction enzymes and optimized adapter sequences. Selection and marker switching strategies render the whole process reliable, rapid and very effective. The assembly product can be easily transferred to any desired expression host, making AssemblX useful for researchers from various fields. |
format | Online Article Text |
id | pubmed-5449548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54495482017-06-05 AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies Hochrein, Lena Machens, Fabian Gremmels, Juergen Schulz, Karina Messerschmidt, Katrin Mueller-Roeber, Bernd Nucleic Acids Res Methods Online The assembly of large DNA constructs coding for entire pathways poses a major challenge in the field of synthetic biology. Here, we present AssemblX, a novel, user-friendly and highly efficient multi-gene assembly strategy. The software-assisted AssemblX process allows even unexperienced users to rapidly design, build and test DNA constructs with currently up to 25 functional units, from 75 or more subunits. At the gene level, AssemblX uses scar-free, overlap-based and sequence-independent methods, allowing the unrestricted design of transcriptional units without laborious parts domestication. The assembly into multi-gene modules is enabled via a standardized, highly efficient, polymerase chain reaction-free and virtually sequence-independent scheme, which relies on rare cutting restriction enzymes and optimized adapter sequences. Selection and marker switching strategies render the whole process reliable, rapid and very effective. The assembly product can be easily transferred to any desired expression host, making AssemblX useful for researchers from various fields. Oxford University Press 2017-06-02 2017-01-27 /pmc/articles/PMC5449548/ /pubmed/28130422 http://dx.doi.org/10.1093/nar/gkx034 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Hochrein, Lena Machens, Fabian Gremmels, Juergen Schulz, Karina Messerschmidt, Katrin Mueller-Roeber, Bernd AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title | AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title_full | AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title_fullStr | AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title_full_unstemmed | AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title_short | AssemblX: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
title_sort | assemblx: a user-friendly toolkit for rapid and reliable multi-gene assemblies |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449548/ https://www.ncbi.nlm.nih.gov/pubmed/28130422 http://dx.doi.org/10.1093/nar/gkx034 |
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