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Genetic diversity of Datisca cannabina-compatible Frankia strains as determined by sequence analysis of the PCR-amplified 16S rRNA gene

The presence of Frankia strains in soil samples collected from northern areas of Pakistan was detected by inoculating Coriaria nepalensis and Datisca cannabina plants. The abundance of compatible Frankia strains in some areas was indicated by profuse nodulation of the host plants, whereas soil sampl...

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Published in:Applied and Environmental Microbiology 1994-07, Vol.60 (7), p.2371-2376
Main Authors: Mirza, M.S, Hameed, S, Akkermans, A.D.L
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description The presence of Frankia strains in soil samples collected from northern areas of Pakistan was detected by inoculating Coriaria nepalensis and Datisca cannabina plants. The abundance of compatible Frankia strains in some areas was indicated by profuse nodulation of the host plants, whereas soil samples from other localities failed to result in nodulation. An oligonucleotide probe (COR/DAT) directed against the 16S rRNA gene of the endophytes of Coriaria and Datisca spp. that did not cross-react with the RNA gene of Frankia strains isolated from other hosts was developed. Genetic diversity among Frankia strains nodulating D. cannabina was determined by sequence analysis of the partial 16S rRNA gene amplified from nodules induced by soil samples from different localities by PCR. Four types of Frankia sequences and one non-Frankia sequence were detected by hybridization with a Frankia genus probe and the COR/DAT probe as well as by sequence analysis of the cloned PCR products
doi_str_mv 10.1128/aem.60.7.2371-2376.1994
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The abundance of compatible Frankia strains in some areas was indicated by profuse nodulation of the host plants, whereas soil samples from other localities failed to result in nodulation. An oligonucleotide probe (COR/DAT) directed against the 16S rRNA gene of the endophytes of Coriaria and Datisca spp. that did not cross-react with the RNA gene of Frankia strains isolated from other hosts was developed. Genetic diversity among Frankia strains nodulating D. cannabina was determined by sequence analysis of the partial 16S rRNA gene amplified from nodules induced by soil samples from different localities by PCR. 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Soil science and plant productions ; AMPLIFICATION CHAINE POLYMERASE ; Animal, plant and microbial ecology ; ARN RIBOSOMAL ; ARN RIBOSOMIAL ; Bacteria ; Base Sequence ; Biological and medical sciences ; Cellular biology ; DATISCACEAE ; DICOTILEDONEAS ; DICOTYLEDONE ; DIFERENCIAS BIOLOGICAS ; DIFFERENCE BIOLOGIQUE ; DNA Primers - genetics ; DNA Probes - genetics ; DNA, Bacterial - genetics ; DNA, Ribosomal - genetics ; Economic plant physiology ; Flowers &amp; plants ; FRANKIA ; Fundamental and applied biological sciences. Psychology ; GENE ; GENES ; Genes, Bacterial ; Genetic Variation ; Laboratorium voor Microbiologie ; Microbial ecology ; Microbiological Laboratory ; Microbiologie ; Microbiology ; Microflora of plants ; Molecular Sequence Data ; Nitrogen Fixation ; Plants - microbiology ; Polymerase Chain Reaction ; REACCION DE CADENAS DE POLIMERASA ; Ribonucleic acid ; RIBOSOMAS ; RIBOSOME ; RNA ; RNA, Bacterial - genetics ; RNA, Ribosomal, 16S - genetics ; SECUENCIA NUCLEICA ; Sequence Homology, Nucleic Acid ; SEQUENCE NUCLEIQUE ; Soil Microbiology ; Soils ; Species Specificity ; Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</subject><ispartof>Applied and Environmental Microbiology, 1994-07, Vol.60 (7), p.2371-2376</ispartof><rights>1994 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Jul 1994</rights><rights>Wageningen University &amp; Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5085-95c466f1617f9f1a87a03739dfc6634808d82beaeed8473b0a204049a879c3da3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC201658/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC201658/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4199777$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7521157$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mirza, M.S</creatorcontrib><creatorcontrib>Hameed, S</creatorcontrib><creatorcontrib>Akkermans, A.D.L</creatorcontrib><title>Genetic diversity of Datisca cannabina-compatible Frankia strains as determined by sequence analysis of the PCR-amplified 16S rRNA gene</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>The presence of Frankia strains in soil samples collected from northern areas of Pakistan was detected by inoculating Coriaria nepalensis and Datisca cannabina plants. The abundance of compatible Frankia strains in some areas was indicated by profuse nodulation of the host plants, whereas soil samples from other localities failed to result in nodulation. An oligonucleotide probe (COR/DAT) directed against the 16S rRNA gene of the endophytes of Coriaria and Datisca spp. that did not cross-react with the RNA gene of Frankia strains isolated from other hosts was developed. Genetic diversity among Frankia strains nodulating D. cannabina was determined by sequence analysis of the partial 16S rRNA gene amplified from nodules induced by soil samples from different localities by PCR. Four types of Frankia sequences and one non-Frankia sequence were detected by hybridization with a Frankia genus probe and the COR/DAT probe as well as by sequence analysis of the cloned PCR products</description><subject>Actinomycetales - genetics</subject><subject>Actinomycetales - isolation &amp; purification</subject><subject>ADN</subject><subject>Agronomy. Soil science and plant productions</subject><subject>AMPLIFICATION CHAINE POLYMERASE</subject><subject>Animal, plant and microbial ecology</subject><subject>ARN RIBOSOMAL</subject><subject>ARN RIBOSOMIAL</subject><subject>Bacteria</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cellular biology</subject><subject>DATISCACEAE</subject><subject>DICOTILEDONEAS</subject><subject>DICOTYLEDONE</subject><subject>DIFERENCIAS BIOLOGICAS</subject><subject>DIFFERENCE BIOLOGIQUE</subject><subject>DNA Primers - genetics</subject><subject>DNA Probes - genetics</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Ribosomal - genetics</subject><subject>Economic plant physiology</subject><subject>Flowers &amp; plants</subject><subject>FRANKIA</subject><subject>Fundamental and applied biological sciences. 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Soil science and plant productions</topic><topic>AMPLIFICATION CHAINE POLYMERASE</topic><topic>Animal, plant and microbial ecology</topic><topic>ARN RIBOSOMAL</topic><topic>ARN RIBOSOMIAL</topic><topic>Bacteria</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cellular biology</topic><topic>DATISCACEAE</topic><topic>DICOTILEDONEAS</topic><topic>DICOTYLEDONE</topic><topic>DIFERENCIAS BIOLOGICAS</topic><topic>DIFFERENCE BIOLOGIQUE</topic><topic>DNA Primers - genetics</topic><topic>DNA Probes - genetics</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Ribosomal - genetics</topic><topic>Economic plant physiology</topic><topic>Flowers &amp; plants</topic><topic>FRANKIA</topic><topic>Fundamental and applied biological sciences. 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The abundance of compatible Frankia strains in some areas was indicated by profuse nodulation of the host plants, whereas soil samples from other localities failed to result in nodulation. An oligonucleotide probe (COR/DAT) directed against the 16S rRNA gene of the endophytes of Coriaria and Datisca spp. that did not cross-react with the RNA gene of Frankia strains isolated from other hosts was developed. Genetic diversity among Frankia strains nodulating D. cannabina was determined by sequence analysis of the partial 16S rRNA gene amplified from nodules induced by soil samples from different localities by PCR. Four types of Frankia sequences and one non-Frankia sequence were detected by hybridization with a Frankia genus probe and the COR/DAT probe as well as by sequence analysis of the cloned PCR products</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>7521157</pmid><doi>10.1128/aem.60.7.2371-2376.1994</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source American Society for Microbiology; PubMed Central
subjects Actinomycetales - genetics
Actinomycetales - isolation & purification
ADN
Agronomy. Soil science and plant productions
AMPLIFICATION CHAINE POLYMERASE
Animal, plant and microbial ecology
ARN RIBOSOMAL
ARN RIBOSOMIAL
Bacteria
Base Sequence
Biological and medical sciences
Cellular biology
DATISCACEAE
DICOTILEDONEAS
DICOTYLEDONE
DIFERENCIAS BIOLOGICAS
DIFFERENCE BIOLOGIQUE
DNA Primers - genetics
DNA Probes - genetics
DNA, Bacterial - genetics
DNA, Ribosomal - genetics
Economic plant physiology
Flowers & plants
FRANKIA
Fundamental and applied biological sciences. Psychology
GENE
GENES
Genes, Bacterial
Genetic Variation
Laboratorium voor Microbiologie
Microbial ecology
Microbiological Laboratory
Microbiologie
Microbiology
Microflora of plants
Molecular Sequence Data
Nitrogen Fixation
Plants - microbiology
Polymerase Chain Reaction
REACCION DE CADENAS DE POLIMERASA
Ribonucleic acid
RIBOSOMAS
RIBOSOME
RNA
RNA, Bacterial - genetics
RNA, Ribosomal, 16S - genetics
SECUENCIA NUCLEICA
Sequence Homology, Nucleic Acid
SEQUENCE NUCLEIQUE
Soil Microbiology
Soils
Species Specificity
Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)
title Genetic diversity of Datisca cannabina-compatible Frankia strains as determined by sequence analysis of the PCR-amplified 16S rRNA gene
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