Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers
The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from dif...
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Gespeichert in:
| Autor*in: |
SERRANO, MYRNA G. [verfasserIn] CAMARGO, ERNEY P. [verfasserIn] TEIXEIRA, MARTA M. G. [verfasserIn] |
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E-Artikel |
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| Erschienen: |
Oxford, UK: Blackwell Publishing Ltd ; 1999 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2007 ; Blackwell Publishing Journal Backfiles 1879-2005 |
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In: The journal of eukaryotic microbiology - Oxford [u.a.] : Wiley-Blackwell, 1954, 46(1999), 6, Seite 0 |
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volume:46 ; year:1999 ; number:6 ; pages:0 |
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10.1111/j.1550-7408.1999.tb05138.x |
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10.1111/j.1550-7408.1999.tb05138.x doi (DE-627)NLEJ243276834 DE-627 ger DE-627 rakwb SERRANO, MYRNA G. verfasserin aut Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers Oxford, UK Blackwell Publishing Ltd 1999 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Arbitrary primers CAMARGO, ERNEY P. verfasserin aut TEIXEIRA, MARTA M. G. verfasserin aut In The journal of eukaryotic microbiology Oxford [u.a.] : Wiley-Blackwell, 1954 46(1999), 6, Seite 0 Online-Ressource (DE-627)NLEJ243927622 (DE-600)2126326-7 1550-7408 nnns volume:46 year:1999 number:6 pages:0 http://dx.doi.org/10.1111/j.1550-7408.1999.tb05138.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 46 1999 6 0 |
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10.1111/j.1550-7408.1999.tb05138.x doi (DE-627)NLEJ243276834 DE-627 ger DE-627 rakwb SERRANO, MYRNA G. verfasserin aut Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers Oxford, UK Blackwell Publishing Ltd 1999 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Arbitrary primers CAMARGO, ERNEY P. verfasserin aut TEIXEIRA, MARTA M. G. verfasserin aut In The journal of eukaryotic microbiology Oxford [u.a.] : Wiley-Blackwell, 1954 46(1999), 6, Seite 0 Online-Ressource (DE-627)NLEJ243927622 (DE-600)2126326-7 1550-7408 nnns volume:46 year:1999 number:6 pages:0 http://dx.doi.org/10.1111/j.1550-7408.1999.tb05138.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 46 1999 6 0 |
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10.1111/j.1550-7408.1999.tb05138.x doi (DE-627)NLEJ243276834 DE-627 ger DE-627 rakwb SERRANO, MYRNA G. verfasserin aut Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers Oxford, UK Blackwell Publishing Ltd 1999 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Arbitrary primers CAMARGO, ERNEY P. verfasserin aut TEIXEIRA, MARTA M. G. verfasserin aut In The journal of eukaryotic microbiology Oxford [u.a.] : Wiley-Blackwell, 1954 46(1999), 6, Seite 0 Online-Ressource (DE-627)NLEJ243927622 (DE-600)2126326-7 1550-7408 nnns volume:46 year:1999 number:6 pages:0 http://dx.doi.org/10.1111/j.1550-7408.1999.tb05138.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 46 1999 6 0 |
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10.1111/j.1550-7408.1999.tb05138.x doi (DE-627)NLEJ243276834 DE-627 ger DE-627 rakwb SERRANO, MYRNA G. verfasserin aut Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers Oxford, UK Blackwell Publishing Ltd 1999 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Arbitrary primers CAMARGO, ERNEY P. verfasserin aut TEIXEIRA, MARTA M. G. verfasserin aut In The journal of eukaryotic microbiology Oxford [u.a.] : Wiley-Blackwell, 1954 46(1999), 6, Seite 0 Online-Ressource (DE-627)NLEJ243927622 (DE-600)2126326-7 1550-7408 nnns volume:46 year:1999 number:6 pages:0 http://dx.doi.org/10.1111/j.1550-7408.1999.tb05138.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 46 1999 6 0 |
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10.1111/j.1550-7408.1999.tb05138.x doi (DE-627)NLEJ243276834 DE-627 ger DE-627 rakwb SERRANO, MYRNA G. verfasserin aut Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers Oxford, UK Blackwell Publishing Ltd 1999 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Arbitrary primers CAMARGO, ERNEY P. verfasserin aut TEIXEIRA, MARTA M. G. verfasserin aut In The journal of eukaryotic microbiology Oxford [u.a.] : Wiley-Blackwell, 1954 46(1999), 6, Seite 0 Online-Ressource (DE-627)NLEJ243927622 (DE-600)2126326-7 1550-7408 nnns volume:46 year:1999 number:6 pages:0 http://dx.doi.org/10.1111/j.1550-7408.1999.tb05138.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 46 1999 6 0 |
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The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. |
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The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. |
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The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. Moreover, Phytomonas spp. from plants and insects were grouped according to geographic origin, thus revealing a complex structure of this taxon comprising several clusters of very closely related organisms. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ243276834</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707174931.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">120427s1999 xx |||||o 00| ||und c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1111/j.1550-7408.1999.tb05138.x</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ243276834</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">SERRANO, MYRNA G.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Phytomonas: Analysis of Polymorphism and Genetic Relatedness Between Isolates From Plants and Phytophagous Insects From Different Geographic Regions By Rapd Fingerprints and Synapomorphic Markers</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Oxford, UK</subfield><subfield code="b">Blackwell Publishing Ltd</subfield><subfield code="c">1999</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The random amplification of polymorphic DNA was used for easy, quick and sensitive assessment of genetic polymorphism within Phytomonas to discriminate isolates and determine genetic relationships within the genus. We examined 48 Phytomonas spp., 31 isolates from plants and 17 from insects, from different geographic regions. Topology of the dendrogram based on randomly amplified polymorphic DNA fingerprints segregated the Phytomonas spp. into 5 main clusters, despite the high genetic variability within this genus. Similar clustering could also be obtained by both visual and cross-hybridization analysis of randomly amplified synapomorphic DNA fragments. There was some concordance between the genetic relationship of isolates and their plant tissue tropism. 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7.4010077 |