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ClosTron-mediated engineering of Clostridium
Members of the genus Clostridium are of both medical and industrial importance. The molecular tools necessary to study and exploit their wide ranging physiological diversity through directed mutational analysis have until recently been lacking. The situation was transformed in the mid-2000s with the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476875/ https://www.ncbi.nlm.nih.gov/pubmed/22750794 http://dx.doi.org/10.4161/bioe.21004 |
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author | Kuehne, Sarah A. Minton, Nigel P. |
author_facet | Kuehne, Sarah A. Minton, Nigel P. |
author_sort | Kuehne, Sarah A. |
collection | PubMed |
description | Members of the genus Clostridium are of both medical and industrial importance. The molecular tools necessary to study and exploit their wide ranging physiological diversity through directed mutational analysis have until recently been lacking. The situation was transformed in the mid-2000s with the specific adaptation of intron re-targeting technology to the genus, through the development of the ClosTron. By making a handful of nucleotide changes to the group II intron encoding region, the intron can be directed to insert into almost any region within the genome. Through the use of a retrotransposition-activated marker (RAM), based on the ermB gene, successful insertion is selected on the basis of acquisition of resistance to erythromycin. The re-targeted region is designed using an online re-targeting algorithm (www.clostron.com), and then an order is placed with DNA2.0 for both the synthesis of the re-targeted region and its custom cloning into the ClosTron vector. Re-targeted ClosTrons are delivered ready for use in 10–14 days, allowing mutants to be isolated 5–7 days after receipt. Its availability has revolutionized clostridial molecular biology. |
format | Online Article Text |
id | pubmed-3476875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-34768752013-01-03 ClosTron-mediated engineering of Clostridium Kuehne, Sarah A. Minton, Nigel P. Bioengineered Addendum Members of the genus Clostridium are of both medical and industrial importance. The molecular tools necessary to study and exploit their wide ranging physiological diversity through directed mutational analysis have until recently been lacking. The situation was transformed in the mid-2000s with the specific adaptation of intron re-targeting technology to the genus, through the development of the ClosTron. By making a handful of nucleotide changes to the group II intron encoding region, the intron can be directed to insert into almost any region within the genome. Through the use of a retrotransposition-activated marker (RAM), based on the ermB gene, successful insertion is selected on the basis of acquisition of resistance to erythromycin. The re-targeted region is designed using an online re-targeting algorithm (www.clostron.com), and then an order is placed with DNA2.0 for both the synthesis of the re-targeted region and its custom cloning into the ClosTron vector. Re-targeted ClosTrons are delivered ready for use in 10–14 days, allowing mutants to be isolated 5–7 days after receipt. Its availability has revolutionized clostridial molecular biology. Landes Bioscience 2012-07-01 /pmc/articles/PMC3476875/ /pubmed/22750794 http://dx.doi.org/10.4161/bioe.21004 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Addendum Kuehne, Sarah A. Minton, Nigel P. ClosTron-mediated engineering of Clostridium |
title | ClosTron-mediated engineering of Clostridium |
title_full | ClosTron-mediated engineering of Clostridium |
title_fullStr | ClosTron-mediated engineering of Clostridium |
title_full_unstemmed | ClosTron-mediated engineering of Clostridium |
title_short | ClosTron-mediated engineering of Clostridium |
title_sort | clostron-mediated engineering of clostridium |
topic | Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476875/ https://www.ncbi.nlm.nih.gov/pubmed/22750794 http://dx.doi.org/10.4161/bioe.21004 |
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