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Genetic transformation and mutant isolation in Ganoderma lucidum by restriction enzyme-mediated integration
Abstract A white-rot basidiomycete Ganoderma lucidum has long been used as a medicinal mushroom in Asia, and it has an array of enzymes important for wood degrading activity. There have been many reports about the ingredients which show health aiding effects. In order to analyze gene functions and i...
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Published in: | FEMS microbiology letters 2004-04, Vol.233 (2), p.201-204 |
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creator | Kim, Sunkyung Song, Jaemahn Choi, Hyoung T. |
description | Abstract
A white-rot basidiomycete Ganoderma lucidum has long been used as a medicinal mushroom in Asia, and it has an array of enzymes important for wood degrading activity. There have been many reports about the ingredients which show health aiding effects. In order to analyze gene functions and introduce foreign genes into this fungus, genetic transformation is required. We have successfully transformed G. lucidum to geneticin resistance using pJS205-1 which has the antibiotic resistance genes against geneticin and phosphinothricin. Many different mutants have been generated during the transformation by restriction enzyme mediated integration, and the transformation yield was 4–17 transformants (μg plasmid DNA)−1. The plasmid was integrated stably into the recipient chromosome, which was confirmed by PCR with the plasmid-specific primers. |
doi_str_mv | 10.1111/j.1574-6968.2004.tb09483.x |
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A white-rot basidiomycete Ganoderma lucidum has long been used as a medicinal mushroom in Asia, and it has an array of enzymes important for wood degrading activity. There have been many reports about the ingredients which show health aiding effects. In order to analyze gene functions and introduce foreign genes into this fungus, genetic transformation is required. We have successfully transformed G. lucidum to geneticin resistance using pJS205-1 which has the antibiotic resistance genes against geneticin and phosphinothricin. Many different mutants have been generated during the transformation by restriction enzyme mediated integration, and the transformation yield was 4–17 transformants (μg plasmid DNA)−1. The plasmid was integrated stably into the recipient chromosome, which was confirmed by PCR with the plasmid-specific primers.</description><identifier>ISSN: 0378-1097</identifier><identifier>EISSN: 1574-6968</identifier><identifier>DOI: 10.1111/j.1574-6968.2004.tb09483.x</identifier><identifier>PMID: 15063487</identifier><identifier>CODEN: FMLED7</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Antibiotic resistance ; Antibiotics ; Basidiocarps ; Biological and medical sciences ; Chromosomes ; Cloning, Molecular ; Deoxyribonuclease EcoRI - genetics ; Deoxyribonucleases, Type II Site-Specific - genetics ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Fungal transformation ; Fungi ; Ganoderma lucidum ; Genes ; Genetic Testing - methods ; Genetic transformation ; Geneticin ; Growth, nutrition, metabolism, transports, enzymes. Molecular biology ; Integration ; Microbiology ; Miscellaneous ; Mushrooms ; Mutation ; Mycology ; Phosphinothricin ; Plasmids ; Reishi - genetics ; Rot ; Transformation, Genetic</subject><ispartof>FEMS microbiology letters, 2004-04, Vol.233 (2), p.201-204</ispartof><rights>2004 Federation of European Microbiological Societies 2004</rights><rights>2004 INIST-CNRS</rights><rights>2004 Federation of European Microbiological Societies</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3211-ccb76286aabb438ad98e4d7bf30df8cbfe2a54dc7396cc208ceabc0306e175c43</citedby><cites>FETCH-LOGICAL-c3211-ccb76286aabb438ad98e4d7bf30df8cbfe2a54dc7396cc208ceabc0306e175c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15638433$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15063487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Sunkyung</creatorcontrib><creatorcontrib>Song, Jaemahn</creatorcontrib><creatorcontrib>Choi, Hyoung T.</creatorcontrib><title>Genetic transformation and mutant isolation in Ganoderma lucidum by restriction enzyme-mediated integration</title><title>FEMS microbiology letters</title><addtitle>FEMS Microbiol Lett</addtitle><description>Abstract
A white-rot basidiomycete Ganoderma lucidum has long been used as a medicinal mushroom in Asia, and it has an array of enzymes important for wood degrading activity. There have been many reports about the ingredients which show health aiding effects. In order to analyze gene functions and introduce foreign genes into this fungus, genetic transformation is required. We have successfully transformed G. lucidum to geneticin resistance using pJS205-1 which has the antibiotic resistance genes against geneticin and phosphinothricin. Many different mutants have been generated during the transformation by restriction enzyme mediated integration, and the transformation yield was 4–17 transformants (μg plasmid DNA)−1. The plasmid was integrated stably into the recipient chromosome, which was confirmed by PCR with the plasmid-specific primers.</description><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Basidiocarps</subject><subject>Biological and medical sciences</subject><subject>Chromosomes</subject><subject>Cloning, Molecular</subject><subject>Deoxyribonuclease EcoRI - genetics</subject><subject>Deoxyribonucleases, Type II Site-Specific - genetics</subject><subject>Enzymes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal transformation</subject><subject>Fungi</subject><subject>Ganoderma lucidum</subject><subject>Genes</subject><subject>Genetic Testing - methods</subject><subject>Genetic transformation</subject><subject>Geneticin</subject><subject>Growth, nutrition, metabolism, transports, enzymes. Molecular biology</subject><subject>Integration</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Mushrooms</subject><subject>Mutation</subject><subject>Mycology</subject><subject>Phosphinothricin</subject><subject>Plasmids</subject><subject>Reishi - genetics</subject><subject>Rot</subject><subject>Transformation, Genetic</subject><issn>0378-1097</issn><issn>1574-6968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqVkc-P1CAcxYnRuOPqv2Aajd5aoVCgHkzMxh1NxnjRM-FXDWMLI9C4418v3TZqjB7kQgKf9-XxHgBPEGxQWS-ODeoYqWlPedNCSJqsYE84bm7ugN3Pq7tgBzHjNYI9uwAPUjrCwraQ3gcXqIMUE8524MveepudrnKUPg0hTjK74CvpTTXNWfpcuRTG9dD5ai99MLZQ1ThrZ-apUucq2pSj07eM9d_Pk60na5zM1hRNtp_jrf4huDfIMdlH234JPl2_-Xj1tj582L-7en2oNW4RqrVWjLacSqkUwVyanltimBowNAPXarCt7IjRDPdU6xZybaXSEENqEes0wZfg-Tr3FMPXuXgTk0vajqP0NsxJMMQhpGwBn_4BHsMcffEmWgwZoowSWqiXK6VjSCnaQZyim2Q8CwTFUog4iiV1saQulkLEVoi4KeLH2xOzKpn8km4NFODZBsik5TiUGrRLv3EUc4Jx4V6t3Dc32vN_WBDX7w8tRGVAtw4I8-kf8vpvP_gBW9K6rw</recordid><startdate>200404</startdate><enddate>200404</enddate><creator>Kim, Sunkyung</creator><creator>Song, Jaemahn</creator><creator>Choi, Hyoung T.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200404</creationdate><title>Genetic transformation and mutant isolation in Ganoderma lucidum by restriction enzyme-mediated integration</title><author>Kim, Sunkyung ; Song, Jaemahn ; Choi, Hyoung T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3211-ccb76286aabb438ad98e4d7bf30df8cbfe2a54dc7396cc208ceabc0306e175c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Basidiocarps</topic><topic>Biological and medical sciences</topic><topic>Chromosomes</topic><topic>Cloning, Molecular</topic><topic>Deoxyribonuclease EcoRI - genetics</topic><topic>Deoxyribonucleases, Type II Site-Specific - genetics</topic><topic>Enzymes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal transformation</topic><topic>Fungi</topic><topic>Ganoderma lucidum</topic><topic>Genes</topic><topic>Genetic Testing - methods</topic><topic>Genetic transformation</topic><topic>Geneticin</topic><topic>Growth, nutrition, metabolism, transports, enzymes. Molecular biology</topic><topic>Integration</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mushrooms</topic><topic>Mutation</topic><topic>Mycology</topic><topic>Phosphinothricin</topic><topic>Plasmids</topic><topic>Reishi - genetics</topic><topic>Rot</topic><topic>Transformation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Sunkyung</creatorcontrib><creatorcontrib>Song, Jaemahn</creatorcontrib><creatorcontrib>Choi, Hyoung T.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Sunkyung</au><au>Song, Jaemahn</au><au>Choi, Hyoung T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic transformation and mutant isolation in Ganoderma lucidum by restriction enzyme-mediated integration</atitle><jtitle>FEMS microbiology letters</jtitle><addtitle>FEMS Microbiol Lett</addtitle><date>2004-04</date><risdate>2004</risdate><volume>233</volume><issue>2</issue><spage>201</spage><epage>204</epage><pages>201-204</pages><issn>0378-1097</issn><eissn>1574-6968</eissn><coden>FMLED7</coden><abstract>Abstract
A white-rot basidiomycete Ganoderma lucidum has long been used as a medicinal mushroom in Asia, and it has an array of enzymes important for wood degrading activity. There have been many reports about the ingredients which show health aiding effects. In order to analyze gene functions and introduce foreign genes into this fungus, genetic transformation is required. We have successfully transformed G. lucidum to geneticin resistance using pJS205-1 which has the antibiotic resistance genes against geneticin and phosphinothricin. Many different mutants have been generated during the transformation by restriction enzyme mediated integration, and the transformation yield was 4–17 transformants (μg plasmid DNA)−1. The plasmid was integrated stably into the recipient chromosome, which was confirmed by PCR with the plasmid-specific primers.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>15063487</pmid><doi>10.1111/j.1574-6968.2004.tb09483.x</doi><tpages>4</tpages></addata></record> |
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subjects | Antibiotic resistance Antibiotics Basidiocarps Biological and medical sciences Chromosomes Cloning, Molecular Deoxyribonuclease EcoRI - genetics Deoxyribonucleases, Type II Site-Specific - genetics Enzymes Fundamental and applied biological sciences. Psychology Fungal transformation Fungi Ganoderma lucidum Genes Genetic Testing - methods Genetic transformation Geneticin Growth, nutrition, metabolism, transports, enzymes. Molecular biology Integration Microbiology Miscellaneous Mushrooms Mutation Mycology Phosphinothricin Plasmids Reishi - genetics Rot Transformation, Genetic |
title | Genetic transformation and mutant isolation in Ganoderma lucidum by restriction enzyme-mediated integration |
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