Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens
We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the...
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description | We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene. |
doi_str_mv | 10.1007/s11627-013-9489-9 |
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Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.</description><identifier>ISSN: 1054-5476</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/s11627-013-9489-9</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Agrobacterium ; Agrobacterium radiobacter ; Amaranth ; Amaranthus tricolor ; Antibiotics ; Aqueous solutions ; beta-glucuronidase ; Biomedical and Life Sciences ; BIOTECHNOLOGY ; Cell Biology ; Chlorophyll ; Cultivation ; Developmental Biology ; DNA ; Drinking water ; Epicotyls ; explants ; Genes ; genetic transformation ; Genetically altered foods ; germ cells ; Infections ; kanamycin ; kanamycin kinase ; leaf protein ; Life Sciences ; Membrane filters ; Microbiology ; Plant Breeding/Biotechnology ; Plant cells ; Plant Genetics and Genomics ; Plant Sciences ; Plants ; plasmids ; polymerase chain reaction ; progeny ; Seedlings ; Seeds ; Shoots ; Southern blotting ; Transgenes ; Transgenic plants ; vegetable crops ; Vegetables</subject><ispartof>In vitro cellular & developmental biology. Plant, 2013-04, Vol.49 (2), p.114-128</ispartof><rights>2013 Society for In Vitro Biology</rights><rights>The Society for In Vitro Biology 2013</rights><rights>Copyright Society for In Vitro Biology Apr 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-a93b04c819266ce4f53cbf92829cbfdb3ed78bf1a224326fb50aa6e0b8c288a43</citedby><cites>FETCH-LOGICAL-c386t-a93b04c819266ce4f53cbf92829cbfdb3ed78bf1a224326fb50aa6e0b8c288a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/42568706$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/42568706$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,41464,42533,51294,57992,58225</link.rule.ids></links><search><creatorcontrib>Pal, Ajantaa</creatorcontrib><creatorcontrib>Swain, Swasti S</creatorcontrib><creatorcontrib>Das, Anath B</creatorcontrib><creatorcontrib>Mukherjee, Arup K</creatorcontrib><creatorcontrib>Chand, Pradeep K</creatorcontrib><title>Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens</title><title>In vitro cellular & developmental biology. Plant</title><addtitle>In Vitro Cell.Dev.Biol.-Plant</addtitle><description>We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.</description><subject>Agrobacterium</subject><subject>Agrobacterium radiobacter</subject><subject>Amaranth</subject><subject>Amaranthus tricolor</subject><subject>Antibiotics</subject><subject>Aqueous solutions</subject><subject>beta-glucuronidase</subject><subject>Biomedical and Life Sciences</subject><subject>BIOTECHNOLOGY</subject><subject>Cell Biology</subject><subject>Chlorophyll</subject><subject>Cultivation</subject><subject>Developmental Biology</subject><subject>DNA</subject><subject>Drinking water</subject><subject>Epicotyls</subject><subject>explants</subject><subject>Genes</subject><subject>genetic transformation</subject><subject>Genetically altered foods</subject><subject>germ cells</subject><subject>Infections</subject><subject>kanamycin</subject><subject>kanamycin kinase</subject><subject>leaf protein</subject><subject>Life Sciences</subject><subject>Membrane filters</subject><subject>Microbiology</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant cells</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Sciences</subject><subject>Plants</subject><subject>plasmids</subject><subject>polymerase chain reaction</subject><subject>progeny</subject><subject>Seedlings</subject><subject>Seeds</subject><subject>Shoots</subject><subject>Southern blotting</subject><subject>Transgenes</subject><subject>Transgenic plants</subject><subject>vegetable crops</subject><subject>Vegetables</subject><issn>1054-5476</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kU1r3DAQhk1poWmaH9BDqaCX9OBk9GFZOi6haQILPaQ5i5FW2nqxra0kF_bYf14Fh9JTTjOg551hHjXNBwpXFKC_zpRK1rdAeauF0q1-1ZxR0Xctk0q_rj10ou1EL98273I-AAAF2p81fx4K2tGTvU8TGYfZk5JwziGmCcsQZxIDQTJ6DCfy2-_9SrsUjwQnrGj5SS43z92Sa3pwcYyJbK--kMnvBix-R-yJbPYpWnTFp2GZSFkmH9ANfs7vmzcBx-wvnut583j79cfNXbv9_u3-ZrNtHVeytKi5BeEU1UxK50XouLNBM8V0rTvL_a5XNlBkTHAmg-0AUXqwyjGlUPDz5vM695jir8XnYg5xSXNdaagQQoLodF8pulL1xJyTD-aYhnreyVAwT6bNatpU0-bJtNE1w9ZMruxcTf43-YXQxzV0yCWmf1sE66TqQdb3T-t7wGhwn4ZsHh8YUFG_rgoR_EWCgQDB_wJtmZ6t</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Pal, Ajantaa</creator><creator>Swain, Swasti S</creator><creator>Das, Anath B</creator><creator>Mukherjee, Arup K</creator><creator>Chand, Pradeep K</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20130401</creationdate><title>Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens</title><author>Pal, Ajantaa ; Swain, Swasti S ; Das, Anath B ; Mukherjee, Arup K ; Chand, Pradeep K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-a93b04c819266ce4f53cbf92829cbfdb3ed78bf1a224326fb50aa6e0b8c288a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Agrobacterium</topic><topic>Agrobacterium radiobacter</topic><topic>Amaranth</topic><topic>Amaranthus tricolor</topic><topic>Antibiotics</topic><topic>Aqueous solutions</topic><topic>beta-glucuronidase</topic><topic>Biomedical and Life Sciences</topic><topic>BIOTECHNOLOGY</topic><topic>Cell Biology</topic><topic>Chlorophyll</topic><topic>Cultivation</topic><topic>Developmental Biology</topic><topic>DNA</topic><topic>Drinking water</topic><topic>Epicotyls</topic><topic>explants</topic><topic>Genes</topic><topic>genetic transformation</topic><topic>Genetically altered foods</topic><topic>germ cells</topic><topic>Infections</topic><topic>kanamycin</topic><topic>kanamycin kinase</topic><topic>leaf protein</topic><topic>Life Sciences</topic><topic>Membrane filters</topic><topic>Microbiology</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant cells</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Sciences</topic><topic>Plants</topic><topic>plasmids</topic><topic>polymerase chain reaction</topic><topic>progeny</topic><topic>Seedlings</topic><topic>Seeds</topic><topic>Shoots</topic><topic>Southern blotting</topic><topic>Transgenes</topic><topic>Transgenic plants</topic><topic>vegetable crops</topic><topic>Vegetables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pal, Ajantaa</creatorcontrib><creatorcontrib>Swain, Swasti S</creatorcontrib><creatorcontrib>Das, Anath B</creatorcontrib><creatorcontrib>Mukherjee, Arup K</creatorcontrib><creatorcontrib>Chand, Pradeep K</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><jtitle>In vitro cellular & developmental biology. Plant</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pal, Ajantaa</au><au>Swain, Swasti S</au><au>Das, Anath B</au><au>Mukherjee, Arup K</au><au>Chand, Pradeep K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens</atitle><jtitle>In vitro cellular & developmental biology. Plant</jtitle><stitle>In Vitro Cell.Dev.Biol.-Plant</stitle><date>2013-04-01</date><risdate>2013</risdate><volume>49</volume><issue>2</issue><spage>114</spage><epage>128</epage><pages>114-128</pages><issn>1054-5476</issn><eissn>1475-2689</eissn><abstract>We have optimized a procedure for genetic transformation of a major leafy vegetable crop, Amaranthus tricolor L., using epicotyl explant co-cultivation with Agrobacterium tumefaciens. Two disarmed A. tumefaciens strains EHA 105 and LBA 4404, both carrying the binary plasmid p35SGUSINT harboring the neomycin phosphotransferase II gene (nptII) and the β-glucuronidase gene (gus), were evaluated as vector systems. The former displayed a higher transforming efficiency. Several key factors influencing the transformation events were optimized. The highest percentage of transformed shoots (24.24%) was achieved using hand-pricked epicotyl explants, a 10-min infection period, with 100 μM acetosyringone-pretreated Agrobacterium culture corresponding to OD₆₀₀ ≅ 0.6 and diluted to 10⁹ cells ml⁻¹, followed by 4 d co-cultivation in the regeneration medium. Putative transformed explants capable of forming shoots were selected on medium supplemented with 75 μg ml⁻¹ kanamycin, and transient as well as stable glucuronidase expression was determined by histochemical analysis. From a total of 48 selected shoot lines derived from independent transformation events with epicotyl explants co-cultivated with EHA 105, 32 showed positive PCR amplification for both the nptII and gus genes. Germ line transformation and transgene stability were evident in progeny of primary transformed plants (T₀). Among T₁ seedlings of 12 selected transgenic plant lines, kanamycin-resistant and kanamycin-sensitive seedlings segregated in a ratio typical of the Mendelian monohybrid pattern (3:1) as verified by the chi-square (χ ²) test. Southern hybridization of genomic DNA from kanamycin-resistant T₁ transgenic segregants to an nptII probe substantiated stable integration of the transgene. Neomycin phosphotransferase (NPTII) activity was detected in leaf protein extracts of selected T₁ transgenic plants, thereby confirming stable expression of the nptII gene.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><doi>10.1007/s11627-013-9489-9</doi><tpages>15</tpages></addata></record> |
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subjects | Agrobacterium Agrobacterium radiobacter Amaranth Amaranthus tricolor Antibiotics Aqueous solutions beta-glucuronidase Biomedical and Life Sciences BIOTECHNOLOGY Cell Biology Chlorophyll Cultivation Developmental Biology DNA Drinking water Epicotyls explants Genes genetic transformation Genetically altered foods germ cells Infections kanamycin kanamycin kinase leaf protein Life Sciences Membrane filters Microbiology Plant Breeding/Biotechnology Plant cells Plant Genetics and Genomics Plant Sciences Plants plasmids polymerase chain reaction progeny Seedlings Seeds Shoots Southern blotting Transgenes Transgenic plants vegetable crops Vegetables |
title | Stable germ line transformation of a leafy vegetable crop amaranth (Amaranthus tricolor L.) mediated by Agrobacterium tumefaciens |
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