Skip to the main content

Food Technology and Biotechnology, Vol. 51 No. 4, 2013.

Original scientific paper

Comparison of Intraplasmid Rearrangements in Agrobacterium tumefaciens and Escherichia coli

Luka Bočkor orcid id orcid.org/0000-0002-2096-0944 ; ICGEB, AREA Science Park, Padriciano 99, IT-34149 Trieste, Italy
Srećko Jelenić† ; University of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, Croatia
Nenad Malenica ; University of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, Croatia
Jelena Mlinarec orcid id orcid.org/0000-0002-2627-5374 ; University of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, Croatia
Višnja Besendorfer ; University of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, Croatia
Ivana Ivančić-Baće orcid id orcid.org/0000-0003-2018-3150 ; University of Zagreb, Faculty of Science, Department of Molecular Biology, Horvatovac 102a, HR-10000 Zagreb, Croatia

Full text: english pdf 193 Kb

page 441-445

downloads: 689

cite

Abstract

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.

Keywords

RecA; intramolecular recombination; Agrobacterium tumefaciens; Escherichia coli

Hrčak ID:

114446

URI

https://hrcak.srce.hr/114446

Publication date:

26.12.2013.

Article data in other languages: croatian

Visits: 1.595 *