Efficient integrative transformation of Cephalosporium acremonium
A hybrid gene, IPNSp/HPTorf, was constructed by placing an 850 bp sequence of Cephalosporium acremonium DNA next to the 5' end of a bacterial open reading frame, HPTorf. The sequence was obtained as an 850 bp NcoI restriction fragment from the 5' non-coding region of the C. acremonium isop...
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Veröffentlicht in: | Current genetics 1987-01, Vol.12 (5), p.337-348 |
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description | A hybrid gene, IPNSp/HPTorf, was constructed by placing an 850 bp sequence of Cephalosporium acremonium DNA next to the 5' end of a bacterial open reading frame, HPTorf. The sequence was obtained as an 850 bp NcoI restriction fragment from the 5' non-coding region of the C. acremonium isopenicillin N synthetase (IPNS) gene. The HPTorf was obtained from a bacterial gene that coded for a hygromycin B phosphotransferase (HPT). Plasmids that contained IPNSp/HPTorf transformed C. acremonium to a stably maintained hygromycin B resistant phenotype. Southern analysis of total DNA from transformants demonstrated multiple integrations of the transforming DNA in the high molecular weight DNA of most transformants, but single integrations were observed in a few transformants. The number of transformants per microgram of DNA was about 100 times greater than for plasmids that contained the HPTorf without any juxtaposed eucaryotic promoter sequence. Plasmids with the promoterless HPTorf and plasmids with a truncated S. cerevisiae phosphoglycerate kinase promoter juxtaposed to the HPTorf transformed C. acremonium at equivalent low frequencies. Transformation of C. acremonium with linearized plasmid DNA produced at least 2-3 fold more transformants than the corresponding circular molecule. Several observations were made concerning protoplast formation and handling which made the transformation procedure more efficient and allowed a greater proportion of protoplasts to regenerate to viable walled cells. Plasmids were constructed that contained both the IPNSp/HPTorf and additional elements: fragments of C. acremonium ribosomal DNA (rDNA), or a fragment of C. acremonium mitochondrial DNA possessing activity as an autonomous replication sequence (ARS) in S. cerevisiae, or putative transcriptional termination/polyadenylation signals from the IPNS gene. These plasmids transformed C. acremonium at frequencies experimentally equivalent to those containing IPNSp/HPTorf without any of these additional elements. |
doi_str_mv | 10.1007/bf00405756 |
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The sequence was obtained as an 850 bp NcoI restriction fragment from the 5' non-coding region of the C. acremonium isopenicillin N synthetase (IPNS) gene. The HPTorf was obtained from a bacterial gene that coded for a hygromycin B phosphotransferase (HPT). Plasmids that contained IPNSp/HPTorf transformed C. acremonium to a stably maintained hygromycin B resistant phenotype. Southern analysis of total DNA from transformants demonstrated multiple integrations of the transforming DNA in the high molecular weight DNA of most transformants, but single integrations were observed in a few transformants. The number of transformants per microgram of DNA was about 100 times greater than for plasmids that contained the HPTorf without any juxtaposed eucaryotic promoter sequence. Plasmids with the promoterless HPTorf and plasmids with a truncated S. cerevisiae phosphoglycerate kinase promoter juxtaposed to the HPTorf transformed C. acremonium at equivalent low frequencies. Transformation of C. acremonium with linearized plasmid DNA produced at least 2-3 fold more transformants than the corresponding circular molecule. Several observations were made concerning protoplast formation and handling which made the transformation procedure more efficient and allowed a greater proportion of protoplasts to regenerate to viable walled cells. Plasmids were constructed that contained both the IPNSp/HPTorf and additional elements: fragments of C. acremonium ribosomal DNA (rDNA), or a fragment of C. acremonium mitochondrial DNA possessing activity as an autonomous replication sequence (ARS) in S. cerevisiae, or putative transcriptional termination/polyadenylation signals from the IPNS gene. These plasmids transformed C. acremonium at frequencies experimentally equivalent to those containing IPNSp/HPTorf without any of these additional elements.</description><identifier>ISSN: 0172-8083</identifier><identifier>EISSN: 1432-0983</identifier><identifier>DOI: 10.1007/bf00405756</identifier><identifier>PMID: 2833362</identifier><identifier>CODEN: CUGED5</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Acremonium - genetics ; Acremonium strictum ; Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents ; Applied microbiology ; Biological and medical sciences ; Biotechnology ; Cephalosporium acremonium ; DNA Restriction Enzymes ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; General aspects ; Genes ; Genes, Bacterial ; Genes, Fungal ; Genetic engineering ; Genetic technics ; genetic transformation ; hygromycin B phosphotransferase ; Kanamycin Kinase ; Methods. Procedures. Technologies ; Microbiology ; Nucleic Acid Hybridization ; Phosphotransferases - genetics ; Plasmids ; transformation ; Transformation, Genetic ; Vectors (cloning, transfer, expression). Insertion sequences and transposons</subject><ispartof>Current genetics, 1987-01, Vol.12 (5), p.337-348</ispartof><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-9265a44bfeb754c88992690474b8ecd9041e9565733cf5abbec2de4bb67c69643</citedby><cites>FETCH-LOGICAL-c468t-9265a44bfeb754c88992690474b8ecd9041e9565733cf5abbec2de4bb67c69643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7602549$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2833362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skatrud, P.L</creatorcontrib><creatorcontrib>Queener, S.W</creatorcontrib><creatorcontrib>Carr, L.G</creatorcontrib><creatorcontrib>Fisher, D.L</creatorcontrib><title>Efficient integrative transformation of Cephalosporium acremonium</title><title>Current genetics</title><addtitle>Curr Genet</addtitle><description>A hybrid gene, IPNSp/HPTorf, was constructed by placing an 850 bp sequence of Cephalosporium acremonium DNA next to the 5' end of a bacterial open reading frame, HPTorf. The sequence was obtained as an 850 bp NcoI restriction fragment from the 5' non-coding region of the C. acremonium isopenicillin N synthetase (IPNS) gene. The HPTorf was obtained from a bacterial gene that coded for a hygromycin B phosphotransferase (HPT). Plasmids that contained IPNSp/HPTorf transformed C. acremonium to a stably maintained hygromycin B resistant phenotype. Southern analysis of total DNA from transformants demonstrated multiple integrations of the transforming DNA in the high molecular weight DNA of most transformants, but single integrations were observed in a few transformants. The number of transformants per microgram of DNA was about 100 times greater than for plasmids that contained the HPTorf without any juxtaposed eucaryotic promoter sequence. Plasmids with the promoterless HPTorf and plasmids with a truncated S. cerevisiae phosphoglycerate kinase promoter juxtaposed to the HPTorf transformed C. acremonium at equivalent low frequencies. Transformation of C. acremonium with linearized plasmid DNA produced at least 2-3 fold more transformants than the corresponding circular molecule. Several observations were made concerning protoplast formation and handling which made the transformation procedure more efficient and allowed a greater proportion of protoplasts to regenerate to viable walled cells. Plasmids were constructed that contained both the IPNSp/HPTorf and additional elements: fragments of C. acremonium ribosomal DNA (rDNA), or a fragment of C. acremonium mitochondrial DNA possessing activity as an autonomous replication sequence (ARS) in S. cerevisiae, or putative transcriptional termination/polyadenylation signals from the IPNS gene. These plasmids transformed C. acremonium at frequencies experimentally equivalent to those containing IPNSp/HPTorf without any of these additional elements.</description><subject>Acremonium - genetics</subject><subject>Acremonium strictum</subject><subject>Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents</subject><subject>Applied microbiology</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cephalosporium acremonium</subject><subject>DNA Restriction Enzymes</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genes, Fungal</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>genetic transformation</subject><subject>hygromycin B phosphotransferase</subject><subject>Kanamycin Kinase</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbiology</subject><subject>Nucleic Acid Hybridization</subject><subject>Phosphotransferases - genetics</subject><subject>Plasmids</subject><subject>transformation</subject><subject>Transformation, Genetic</subject><subject>Vectors (cloning, transfer, expression). Insertion sequences and transposons</subject><issn>0172-8083</issn><issn>1432-0983</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0TtLBDEQB_Agip6Pxl7cQiyE1ck7KfU4H3BgodZLkkt0ZXdzJnuC397InbYWITOZH1P8g9AxhksMIK9sAGDAJRdbaIIZJTVoRbfRBLAktQJF99B-zu8AmCgtd9EuUZRSQSboehZC61o_jFU7jP41mbH99NWYzJBDTH1p41DFUE398s10MS9jald9ZVzyfRxKeYh2gumyP9rcB-jldvY8va_nj3cP0-t57ZhQY62J4IYxG7yVnDmldHnRwCSzyrtFqbDXXHBJqQvcWOsdWXhmrZBOaMHoATpf712m-LHyeWz6NjvfdWbwcZUbKbXWEuS_EDOpyxEFXqyhSzHn5EOzTG1v0leDofkJtrm5_Q224JPN1pXt_eKPbpIs87PN3GRnulACdG3-Y1IA4UwXdrpmwcTGvKZCXp4IYArl3wQHTb8BkJqIkw</recordid><startdate>19870101</startdate><enddate>19870101</enddate><creator>Skatrud, P.L</creator><creator>Queener, S.W</creator><creator>Carr, L.G</creator><creator>Fisher, D.L</creator><general>Springer</general><scope>FBQ</scope><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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19870101</creationdate><title>Efficient integrative transformation of Cephalosporium acremonium</title><author>Skatrud, P.L ; Queener, S.W ; Carr, L.G ; Fisher, D.L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-9265a44bfeb754c88992690474b8ecd9041e9565733cf5abbec2de4bb67c69643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Acremonium - genetics</topic><topic>Acremonium strictum</topic><topic>Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents</topic><topic>Applied microbiology</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cephalosporium acremonium</topic><topic>DNA Restriction Enzymes</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Genes</topic><topic>Genes, Bacterial</topic><topic>Genes, Fungal</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>genetic transformation</topic><topic>hygromycin B phosphotransferase</topic><topic>Kanamycin Kinase</topic><topic>Methods. Procedures. Technologies</topic><topic>Microbiology</topic><topic>Nucleic Acid Hybridization</topic><topic>Phosphotransferases - genetics</topic><topic>Plasmids</topic><topic>transformation</topic><topic>Transformation, Genetic</topic><topic>Vectors (cloning, transfer, expression). Insertion sequences and transposons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skatrud, P.L</creatorcontrib><creatorcontrib>Queener, S.W</creatorcontrib><creatorcontrib>Carr, L.G</creatorcontrib><creatorcontrib>Fisher, D.L</creatorcontrib><collection>AGRIS</collection><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>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Current genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skatrud, P.L</au><au>Queener, S.W</au><au>Carr, L.G</au><au>Fisher, D.L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient integrative transformation of Cephalosporium acremonium</atitle><jtitle>Current genetics</jtitle><addtitle>Curr Genet</addtitle><date>1987-01-01</date><risdate>1987</risdate><volume>12</volume><issue>5</issue><spage>337</spage><epage>348</epage><pages>337-348</pages><issn>0172-8083</issn><eissn>1432-0983</eissn><coden>CUGED5</coden><abstract>A hybrid gene, IPNSp/HPTorf, was constructed by placing an 850 bp sequence of Cephalosporium acremonium DNA next to the 5' end of a bacterial open reading frame, HPTorf. The sequence was obtained as an 850 bp NcoI restriction fragment from the 5' non-coding region of the C. acremonium isopenicillin N synthetase (IPNS) gene. The HPTorf was obtained from a bacterial gene that coded for a hygromycin B phosphotransferase (HPT). Plasmids that contained IPNSp/HPTorf transformed C. acremonium to a stably maintained hygromycin B resistant phenotype. Southern analysis of total DNA from transformants demonstrated multiple integrations of the transforming DNA in the high molecular weight DNA of most transformants, but single integrations were observed in a few transformants. The number of transformants per microgram of DNA was about 100 times greater than for plasmids that contained the HPTorf without any juxtaposed eucaryotic promoter sequence. Plasmids with the promoterless HPTorf and plasmids with a truncated S. cerevisiae phosphoglycerate kinase promoter juxtaposed to the HPTorf transformed C. acremonium at equivalent low frequencies. Transformation of C. acremonium with linearized plasmid DNA produced at least 2-3 fold more transformants than the corresponding circular molecule. Several observations were made concerning protoplast formation and handling which made the transformation procedure more efficient and allowed a greater proportion of protoplasts to regenerate to viable walled cells. Plasmids were constructed that contained both the IPNSp/HPTorf and additional elements: fragments of C. acremonium ribosomal DNA (rDNA), or a fragment of C. acremonium mitochondrial DNA possessing activity as an autonomous replication sequence (ARS) in S. cerevisiae, or putative transcriptional termination/polyadenylation signals from the IPNS gene. These plasmids transformed C. acremonium at frequencies experimentally equivalent to those containing IPNSp/HPTorf without any of these additional elements.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><pmid>2833362</pmid><doi>10.1007/bf00405756</doi><tpages>12</tpages></addata></record> |
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subjects | Acremonium - genetics Acremonium strictum Antibiotics, microbial producers, chemotherapic agents, antiseptics, disinfecting agents Applied microbiology Biological and medical sciences Biotechnology Cephalosporium acremonium DNA Restriction Enzymes Escherichia coli - genetics Fundamental and applied biological sciences. Psychology General aspects Genes Genes, Bacterial Genes, Fungal Genetic engineering Genetic technics genetic transformation hygromycin B phosphotransferase Kanamycin Kinase Methods. Procedures. Technologies Microbiology Nucleic Acid Hybridization Phosphotransferases - genetics Plasmids transformation Transformation, Genetic Vectors (cloning, transfer, expression). Insertion sequences and transposons |
title | Efficient integrative transformation of Cephalosporium acremonium |
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