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A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation

BACKGROUND: With the rapid development of synthetic biology, the demand for assembling multiple DNA (genes) fragments into a large circular DNA structure in one step has dramatically increased. However, for constructions of most circular DNA, there are two contradictions in the ligation/assembly and...

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Autores principales: Guo, Ying-Ying, Shi, Zhen-Yu, Fu, Xiao-Zhi, Chen, Jin-Chun, Wu, Qiong, Chen, Guo-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455692/
https://www.ncbi.nlm.nih.gov/pubmed/25896825
http://dx.doi.org/10.1186/s12934-015-0204-x
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author Guo, Ying-Ying
Shi, Zhen-Yu
Fu, Xiao-Zhi
Chen, Jin-Chun
Wu, Qiong
Chen, Guo-Qiang
author_facet Guo, Ying-Ying
Shi, Zhen-Yu
Fu, Xiao-Zhi
Chen, Jin-Chun
Wu, Qiong
Chen, Guo-Qiang
author_sort Guo, Ying-Ying
collection PubMed
description BACKGROUND: With the rapid development of synthetic biology, the demand for assembling multiple DNA (genes) fragments into a large circular DNA structure in one step has dramatically increased. However, for constructions of most circular DNA, there are two contradictions in the ligation/assembly and transformation steps. The ligation/assembly consists of two different reactions: 1) the ligation/assembly between any two pieces of a linear form DNA; 2) the cyclization (or self-ligation) of a single linear form DNA. The first contradiction is that the bimolecular ligation/assembly requires a higher DNA concentration while the cyclization favors a lower one; the second contradiction is that a successful transformation of a ligation/assembly product requires a relatively high DNA concentration again. This study is the first attempt to use linear plasmid and Cyclization After Transformation (CAT) strategy to neutralize those contradictions systematically. RESULTS: The linear assembly combined with CAT method was demonstrated to increase the overall construction efficiency by 3–4 times for both the traditional ligation and for the new in vitro recombination-based assembly methods including recombinant DNA, Golden Gate, SLIC (Sequence and Ligation Independent Cloning) and Gibson Isothermal Assembly. Finally, the linear assembly combined with CAT method was successfully applied to assemble a pathway of 7 gene fragments responsible for synthesizing precorrin 3A which is an important intermediate in VB12 production. CONCLUSION: The linear assembly combined with CAT strategy method can be regarded as a general strategy to enhance the efficiency of most existing circular DNA construction technologies and could be used in construction of a metabolic pathway consisting of multiple genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0204-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-44556922015-06-05 A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation Guo, Ying-Ying Shi, Zhen-Yu Fu, Xiao-Zhi Chen, Jin-Chun Wu, Qiong Chen, Guo-Qiang Microb Cell Fact Research BACKGROUND: With the rapid development of synthetic biology, the demand for assembling multiple DNA (genes) fragments into a large circular DNA structure in one step has dramatically increased. However, for constructions of most circular DNA, there are two contradictions in the ligation/assembly and transformation steps. The ligation/assembly consists of two different reactions: 1) the ligation/assembly between any two pieces of a linear form DNA; 2) the cyclization (or self-ligation) of a single linear form DNA. The first contradiction is that the bimolecular ligation/assembly requires a higher DNA concentration while the cyclization favors a lower one; the second contradiction is that a successful transformation of a ligation/assembly product requires a relatively high DNA concentration again. This study is the first attempt to use linear plasmid and Cyclization After Transformation (CAT) strategy to neutralize those contradictions systematically. RESULTS: The linear assembly combined with CAT method was demonstrated to increase the overall construction efficiency by 3–4 times for both the traditional ligation and for the new in vitro recombination-based assembly methods including recombinant DNA, Golden Gate, SLIC (Sequence and Ligation Independent Cloning) and Gibson Isothermal Assembly. Finally, the linear assembly combined with CAT method was successfully applied to assemble a pathway of 7 gene fragments responsible for synthesizing precorrin 3A which is an important intermediate in VB12 production. CONCLUSION: The linear assembly combined with CAT strategy method can be regarded as a general strategy to enhance the efficiency of most existing circular DNA construction technologies and could be used in construction of a metabolic pathway consisting of multiple genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0204-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-12 /pmc/articles/PMC4455692/ /pubmed/25896825 http://dx.doi.org/10.1186/s12934-015-0204-x Text en © Guo et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Guo, Ying-Ying
Shi, Zhen-Yu
Fu, Xiao-Zhi
Chen, Jin-Chun
Wu, Qiong
Chen, Guo-Qiang
A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title_full A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title_fullStr A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title_full_unstemmed A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title_short A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation
title_sort strategy for enhanced circular dna construction efficiency based on dna cyclization after microbial transformation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455692/
https://www.ncbi.nlm.nih.gov/pubmed/25896825
http://dx.doi.org/10.1186/s12934-015-0204-x
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