Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715

The objective of this work is to clone flanking DNA derived from Tn-5 mutagenesis of wild type strain Xanthomonas axonopodis pv. glycines as first step to clone and to identify the gene involved in pathogenicity mechanism. We have localized the flanking DNA fragment from a nonpathogenic mutant of Xa...

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Main Authors: ALINA AKHDIYA RUSMANA, ANTONIUS SUWANTO, BUDI TJAHJONO
Format: Article
Language:English
Published: Bogor Agricultural University 2005-06-01
Series:Hayati Journal of Biosciences
Subjects:
Online Access:http://journal.ipb.ac.id/index.php/hayati/article/viewFile/173/40
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spelling doaj-270589d576b342f6b0805637e6cf886a2020-11-24T23:46:19ZengBogor Agricultural UniversityHayati Journal of Biosciences1978-30192086-40942005-06-011225760Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715ALINA AKHDIYA RUSMANAANTONIUS SUWANTOBUDI TJAHJONOThe objective of this work is to clone flanking DNA derived from Tn-5 mutagenesis of wild type strain Xanthomonas axonopodis pv. glycines as first step to clone and to identify the gene involved in pathogenicity mechanism. We have localized the flanking DNA fragment from a nonpathogenic mutant of Xag M715. Southern hybridization analysis using 2.8 kb EcoRI from pYR103 as a probe showed that the fragment is located within 2.0 kb PstI fragment. A 0.7 kb flanking DNA was amplified using inverse PCR technique, and inserted into pGEM-T Easy vector generating a 3.7 kb recombinant plasmid (pAA01). Southern hybridization analysis of the wild type (YR32) with pAA01 as a probe indicated a hybridization signal located at approximately 3.0 kb PstI fragment. DNA sequence analysis revealed that the DNA fragment has a 64% identity to a vir gene of Bacillus anthracis.http://journal.ipb.ac.id/index.php/hayati/article/viewFile/173/40CloningDNA Flanking TransposonXanthomonas axonopodispv. glycines
collection DOAJ
language English
format Article
sources DOAJ
author ALINA AKHDIYA RUSMANA
ANTONIUS SUWANTO
BUDI TJAHJONO
spellingShingle ALINA AKHDIYA RUSMANA
ANTONIUS SUWANTO
BUDI TJAHJONO
Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
Hayati Journal of Biosciences
Cloning
DNA Flanking Transposon
Xanthomonas axonopodis
pv. glycines
author_facet ALINA AKHDIYA RUSMANA
ANTONIUS SUWANTO
BUDI TJAHJONO
author_sort ALINA AKHDIYA RUSMANA
title Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
title_short Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
title_full Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
title_fullStr Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
title_full_unstemmed Cloning of Genomic DNA Flanking Transposon in the Nonpathogenic Mutant of Xanthomonas axonopodis pv. glycines M715
title_sort cloning of genomic dna flanking transposon in the nonpathogenic mutant of xanthomonas axonopodis pv. glycines m715
publisher Bogor Agricultural University
series Hayati Journal of Biosciences
issn 1978-3019
2086-4094
publishDate 2005-06-01
description The objective of this work is to clone flanking DNA derived from Tn-5 mutagenesis of wild type strain Xanthomonas axonopodis pv. glycines as first step to clone and to identify the gene involved in pathogenicity mechanism. We have localized the flanking DNA fragment from a nonpathogenic mutant of Xag M715. Southern hybridization analysis using 2.8 kb EcoRI from pYR103 as a probe showed that the fragment is located within 2.0 kb PstI fragment. A 0.7 kb flanking DNA was amplified using inverse PCR technique, and inserted into pGEM-T Easy vector generating a 3.7 kb recombinant plasmid (pAA01). Southern hybridization analysis of the wild type (YR32) with pAA01 as a probe indicated a hybridization signal located at approximately 3.0 kb PstI fragment. DNA sequence analysis revealed that the DNA fragment has a 64% identity to a vir gene of Bacillus anthracis.
topic Cloning
DNA Flanking Transposon
Xanthomonas axonopodis
pv. glycines
url http://journal.ipb.ac.id/index.php/hayati/article/viewFile/173/40
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AT antoniussuwanto cloningofgenomicdnaflankingtransposoninthenonpathogenicmutantofxanthomonasaxonopodispvglycinesm715
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