Plate flooding as an alternative Agrobacterium-mediated transformation method for American chestnut somatic embryos
In an attempt to improve Agrobacterium-mediated transformation frequency of American chestnut somatic embryos, a novel method of inoculation/co-cultivation was developed. Plate flooding is a simple method where the Agrobacterium inoculum is poured onto the embryos while they remain on multiplication...
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Veröffentlicht in: | Plant cell, tissue and organ culture tissue and organ culture, 2007-01, Vol.88 (1), p.93-99 |
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creator | Rothrock, Ronald E Polin-McGuigan, Linda D Newhouse, Andrew E Powell, William A Maynard, Charles A |
description | In an attempt to improve Agrobacterium-mediated transformation frequency of American chestnut somatic embryos, a novel method of inoculation/co-cultivation was developed. Plate flooding is a simple method where the Agrobacterium inoculum is poured onto the embryos while they remain on multiplication medium. This method tested the hypothesis that wounding tissues prior to co-cultivation was unnecessary or counterproductive. Two clones, WB296 and P1-1, were tested for differences in transformation efficiency as measured by the number of transformed embryogenic cell lines per Petri dish, the total number of transformed cell lines (embryos plus callus) and percentage of transformants that remained embryogenic. Plate flooding using clone WB296 produced significantly more transformed embryo cell lines and had a higher percentage of transformants remain embryogenic. The number of total transformed cell lines (embryos plus callus) was the same as obtained by other methods (desiccation, blot dry, sand abrasion, sonication and vacuum infiltration). With clone P1-1 there were no significant differences among the inoculation/co-cultivation treatments tested. Polymerase chain reaction and Southern hybridizations confirmed that the transgene of interest had been stably integrated into both American chestnut clones. Whole plants were regenerated from clone P1-1. |
doi_str_mv | 10.1007/s11240-006-9170-7 |
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Plate flooding is a simple method where the Agrobacterium inoculum is poured onto the embryos while they remain on multiplication medium. This method tested the hypothesis that wounding tissues prior to co-cultivation was unnecessary or counterproductive. Two clones, WB296 and P1-1, were tested for differences in transformation efficiency as measured by the number of transformed embryogenic cell lines per Petri dish, the total number of transformed cell lines (embryos plus callus) and percentage of transformants that remained embryogenic. Plate flooding using clone WB296 produced significantly more transformed embryo cell lines and had a higher percentage of transformants remain embryogenic. The number of total transformed cell lines (embryos plus callus) was the same as obtained by other methods (desiccation, blot dry, sand abrasion, sonication and vacuum infiltration). With clone P1-1 there were no significant differences among the inoculation/co-cultivation treatments tested. Polymerase chain reaction and Southern hybridizations confirmed that the transgene of interest had been stably integrated into both American chestnut clones. Whole plants were regenerated from clone P1-1.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1007/s11240-006-9170-7</identifier><identifier>CODEN: PTCEDJ</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : Springer Netherlands</publisher><subject>Agrobacterium ; Biological and medical sciences ; Biotechnology ; callus culture ; Castanea dentata ; cell lines ; clones ; culture media ; endangered species ; Eukaryotic cell cultures ; forest trees ; Fundamental and applied biological sciences. Psychology ; genetic transformation ; genetic vectors ; Methods. Procedures. Technologies ; Miscellaneous ; new methods ; nucleic acid hybridization ; Plant cells and fungal cells ; polymerase chain reaction ; somatic embryogenesis ; temperate forests ; transgenic plants</subject><ispartof>Plant cell, tissue and organ culture, 2007-01, Vol.88 (1), p.93-99</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c330t-1312e369a4c2b4664815657ee69b8de913c6fd4410efce2044328c99315e90623</citedby><cites>FETCH-LOGICAL-c330t-1312e369a4c2b4664815657ee69b8de913c6fd4410efce2044328c99315e90623</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=18522623$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Rothrock, Ronald E</creatorcontrib><creatorcontrib>Polin-McGuigan, Linda D</creatorcontrib><creatorcontrib>Newhouse, Andrew E</creatorcontrib><creatorcontrib>Powell, William A</creatorcontrib><creatorcontrib>Maynard, Charles A</creatorcontrib><title>Plate flooding as an alternative Agrobacterium-mediated transformation method for American chestnut somatic embryos</title><title>Plant cell, tissue and organ culture</title><description>In an attempt to improve Agrobacterium-mediated transformation frequency of American chestnut somatic embryos, a novel method of inoculation/co-cultivation was developed. Plate flooding is a simple method where the Agrobacterium inoculum is poured onto the embryos while they remain on multiplication medium. This method tested the hypothesis that wounding tissues prior to co-cultivation was unnecessary or counterproductive. Two clones, WB296 and P1-1, were tested for differences in transformation efficiency as measured by the number of transformed embryogenic cell lines per Petri dish, the total number of transformed cell lines (embryos plus callus) and percentage of transformants that remained embryogenic. Plate flooding using clone WB296 produced significantly more transformed embryo cell lines and had a higher percentage of transformants remain embryogenic. The number of total transformed cell lines (embryos plus callus) was the same as obtained by other methods (desiccation, blot dry, sand abrasion, sonication and vacuum infiltration). With clone P1-1 there were no significant differences among the inoculation/co-cultivation treatments tested. Polymerase chain reaction and Southern hybridizations confirmed that the transgene of interest had been stably integrated into both American chestnut clones. Whole plants were regenerated from clone P1-1.</description><subject>Agrobacterium</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>callus culture</subject><subject>Castanea dentata</subject><subject>cell lines</subject><subject>clones</subject><subject>culture media</subject><subject>endangered species</subject><subject>Eukaryotic cell cultures</subject><subject>forest trees</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genetic transformation</subject><subject>genetic vectors</subject><subject>Methods. Procedures. Technologies</subject><subject>Miscellaneous</subject><subject>new methods</subject><subject>nucleic acid hybridization</subject><subject>Plant cells and fungal cells</subject><subject>polymerase chain reaction</subject><subject>somatic embryogenesis</subject><subject>temperate forests</subject><subject>transgenic plants</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LJDEQhoO44OjuD9iTuegtWpWk053jIH4sDCjseg6ZdPVMS3dnTHoE_70ZRthTQfG8L1UPY78RbhCgvs2IUoMAMMJiDaI-YQusaiUq0PqULQBNLUxT1WfsPOc3KKDSuGD5ZfAz8W6Ise2nDfeZ-4n7YaY0-bn_IL7cpLj2oSz6_ShGavsSaPmc_JS7mMZCxYmPNG9jy8uCL8eChtIStpTnaT_zHA9U4DSu02fMP9mPzg-Zfn3PC_b6cP_v7kmsnh__3C1XIigFs0CFkpSxXge51sboBitT1UTGrpuWLKpgulZrBOoCyfKnkk2wVmFFFoxUF-z62LtL8X1fbnFjnwMNg58o7rOTYLREZQuIRzCkmHOizu1SP_r06RDcQa876nXFmjvodXXJXH2X-xz80BUdoc__g00lZbmhcJdHrvPR-U0qzOtfCagAGjRgtfoCFNmE8g</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Rothrock, Ronald E</creator><creator>Polin-McGuigan, Linda D</creator><creator>Newhouse, Andrew E</creator><creator>Powell, William A</creator><creator>Maynard, Charles A</creator><general>Dordrecht : Springer Netherlands</general><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20070101</creationdate><title>Plate flooding as an alternative Agrobacterium-mediated transformation method for American chestnut somatic embryos</title><author>Rothrock, Ronald E ; Polin-McGuigan, Linda D ; Newhouse, Andrew E ; Powell, William A ; Maynard, Charles A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-1312e369a4c2b4664815657ee69b8de913c6fd4410efce2044328c99315e90623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Agrobacterium</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>callus culture</topic><topic>Castanea dentata</topic><topic>cell lines</topic><topic>clones</topic><topic>culture media</topic><topic>endangered species</topic><topic>Eukaryotic cell cultures</topic><topic>forest trees</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genetic transformation</topic><topic>genetic vectors</topic><topic>Methods. Procedures. Technologies</topic><topic>Miscellaneous</topic><topic>new methods</topic><topic>nucleic acid hybridization</topic><topic>Plant cells and fungal cells</topic><topic>polymerase chain reaction</topic><topic>somatic embryogenesis</topic><topic>temperate forests</topic><topic>transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rothrock, Ronald E</creatorcontrib><creatorcontrib>Polin-McGuigan, Linda D</creatorcontrib><creatorcontrib>Newhouse, Andrew E</creatorcontrib><creatorcontrib>Powell, William A</creatorcontrib><creatorcontrib>Maynard, Charles A</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Plant cell, tissue and organ culture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rothrock, Ronald E</au><au>Polin-McGuigan, Linda D</au><au>Newhouse, Andrew E</au><au>Powell, William A</au><au>Maynard, Charles A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plate flooding as an alternative Agrobacterium-mediated transformation method for American chestnut somatic embryos</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><date>2007-01-01</date><risdate>2007</risdate><volume>88</volume><issue>1</issue><spage>93</spage><epage>99</epage><pages>93-99</pages><issn>0167-6857</issn><eissn>1573-5044</eissn><coden>PTCEDJ</coden><abstract>In an attempt to improve Agrobacterium-mediated transformation frequency of American chestnut somatic embryos, a novel method of inoculation/co-cultivation was developed. Plate flooding is a simple method where the Agrobacterium inoculum is poured onto the embryos while they remain on multiplication medium. This method tested the hypothesis that wounding tissues prior to co-cultivation was unnecessary or counterproductive. Two clones, WB296 and P1-1, were tested for differences in transformation efficiency as measured by the number of transformed embryogenic cell lines per Petri dish, the total number of transformed cell lines (embryos plus callus) and percentage of transformants that remained embryogenic. Plate flooding using clone WB296 produced significantly more transformed embryo cell lines and had a higher percentage of transformants remain embryogenic. The number of total transformed cell lines (embryos plus callus) was the same as obtained by other methods (desiccation, blot dry, sand abrasion, sonication and vacuum infiltration). With clone P1-1 there were no significant differences among the inoculation/co-cultivation treatments tested. Polymerase chain reaction and Southern hybridizations confirmed that the transgene of interest had been stably integrated into both American chestnut clones. Whole plants were regenerated from clone P1-1.</abstract><cop>Dordrecht</cop><pub>Dordrecht : Springer Netherlands</pub><doi>10.1007/s11240-006-9170-7</doi><tpages>7</tpages></addata></record> |
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subjects | Agrobacterium Biological and medical sciences Biotechnology callus culture Castanea dentata cell lines clones culture media endangered species Eukaryotic cell cultures forest trees Fundamental and applied biological sciences. Psychology genetic transformation genetic vectors Methods. Procedures. Technologies Miscellaneous new methods nucleic acid hybridization Plant cells and fungal cells polymerase chain reaction somatic embryogenesis temperate forests transgenic plants |
title | Plate flooding as an alternative Agrobacterium-mediated transformation method for American chestnut somatic embryos |
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