Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli
In this work we have constructed a plasmid to compare intraplasmid recombination efficiency in Agrobacterium tumefaciens and Escherichia coli. The plasmid contains two directly repeated copies of spectinomycin resistance gene, one lacking 5’ and the other lacking 3’ end. These two copies share a 570...
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doaj-76496911f7f643179d026fbaa7e55d042020-11-25T03:31:17ZengUniversity of ZagrebFood Technology and Biotechnology1330-98621334-26062013-01-01514441445Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coliLuka Bočkor0Srećko Jelenić†1Nenad Malenica2Jelena Mlinarec3Višnja Besendorfer4Ivana Ivančić-Baće5ICGEB, AREA Science Park, Padriciano 99, IT-34149 Trieste, ItalyUniversity of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, CroatiaUniversity of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, CroatiaUniversity of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, CroatiaUniversity of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, CroatiaUniversity of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, CroatiaIn this work we have constructed a plasmid to compare intraplasmid recombination efficiency in Agrobacterium tumefaciens and Escherichia coli. The plasmid contains two directly repeated copies of spectinomycin resistance gene, one lacking 5’ and the other lacking 3’ end. These two copies share a 570-bp region of homology and are separated by the ampicillin resistance gene. Homologous recombination between repeated copies of incomplete spectinomycin resistance genes results in the restoration of spectinomycin resistance. During this process, ampicillin resistance gene is either deleted or incomplete spectinomycin genes are amplified along with the ampicillin resistance gene. This experimental system enabled us to follow for the first time the generation of deletions and amplifications during intraplasmid recombination in A. tumefaciens. We show here that predominantly RecA-independent mechanism contributes to the formation of deletion and amplification products in both, A. tumefaciens and E. coli. Additionally, deletion and amplification products were detected at similar frequencies, suggesting that amplifications and deletions probably occur by a similar mechanism.http://hrcak.srce.hr/file/169393RecAintramolecular recombinationAgrobacterium tumefaciensEscherichia coli |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Luka Bočkor Srećko Jelenić† Nenad Malenica Jelena Mlinarec Višnja Besendorfer Ivana Ivančić-Baće |
spellingShingle |
Luka Bočkor Srećko Jelenić† Nenad Malenica Jelena Mlinarec Višnja Besendorfer Ivana Ivančić-Baće Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli Food Technology and Biotechnology RecA intramolecular recombination Agrobacterium tumefaciens Escherichia coli |
author_facet |
Luka Bočkor Srećko Jelenić† Nenad Malenica Jelena Mlinarec Višnja Besendorfer Ivana Ivančić-Baće |
author_sort |
Luka Bočkor |
title |
Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli |
title_short |
Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli |
title_full |
Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli |
title_fullStr |
Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli |
title_full_unstemmed |
Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli |
title_sort |
comparison of intraplasmid rearrangements in agrobacterium tumefaciens and escherichia coli |
publisher |
University of Zagreb |
series |
Food Technology and Biotechnology |
issn |
1330-9862 1334-2606 |
publishDate |
2013-01-01 |
description |
In this work we have constructed a plasmid to compare intraplasmid recombination efficiency in Agrobacterium tumefaciens and Escherichia coli. The plasmid contains two directly repeated copies of spectinomycin resistance gene, one lacking 5’ and the other lacking 3’ end. These two copies share a 570-bp region of homology and are separated by the ampicillin resistance gene. Homologous recombination between repeated copies of incomplete spectinomycin resistance genes results in the restoration of spectinomycin resistance. During this process, ampicillin resistance gene is either deleted or incomplete spectinomycin genes are amplified along with the ampicillin resistance gene. This experimental system enabled us to follow for the first time the generation of deletions and amplifications during intraplasmid recombination in A. tumefaciens. We show here that predominantly RecA-independent mechanism contributes to the formation of deletion and amplification products in both, A. tumefaciens and E. coli. Additionally, deletion and amplification products were detected at similar frequencies, suggesting that amplifications and deletions probably occur by a similar mechanism. |
topic |
RecA intramolecular recombination Agrobacterium tumefaciens Escherichia coli |
url |
http://hrcak.srce.hr/file/169393 |
work_keys_str_mv |
AT lukabockor comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli AT sreckojelenic comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli AT nenadmalenica comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli AT jelenamlinarec comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli AT visnjabesendorfer comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli AT ivanaivancicbace comparisonofintraplasmidrearrangementsinagrobacteriumtumefaciensandescherichiacoli |
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