In vitro shoot grafting on rootstock : an effective tool for Agrobacterium-mediated transformation of pigeonpea (Cajanus cajan (L.) Millsp.)
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DOI[10.5511/plantbiotechnology.14.0805a]to the data of the same series
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- Material Type
- 記事
- Author/Editor
- Gourab GhoshArnab PurohitShreeparna Ganguly
- Publication, Distribution, etc.
- Publication Date
- 2014
- Publication Date (W3CDTF)
- 2014
- Periodical title
- Plant biotechnology
- No. or year of volume/issue
- 31(4)
- Volume
- 31(4)
- ISSN (Periodical Title)
- 1347-6114
- ISSN-L (Periodical Title)
- 1342-4580
- Text Language Code
- eng
- DOI
- 10.5511/plantbiotechnology.14.0805a
- Persistent ID (NDL)
- info:ndljp/pid/11000376
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- Acquisition Basis
- インターネット資料収集保存事業(WARP)
- Date Accepted (W3CDTF)
- 2017-12-08T10:56:38+09:00
- Date Captured (W3CDTF)
- 2015-08-15
- Format (IMT)
- application/pdf
- Access Restrictions
- インターネット公開
- Availability of remote photoduplication service
- 不可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11000374
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- Access Restrictions
- インターネット公開
- Availability of remote photoduplication service
- 不可
- Holding library
- 国立国会図書館
- Call No.
- Z54-J126
- Related Material (URI)
- Related Material (Persistent ID (NDL))
- info:ndljp/pid/11000376
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館雑誌記事索引
- Bibliographic ID (NDL)
- 026003741
- Bibliographic Record Category (NDL)
- 632
- Summary, etc.
- Lack of reproducible in vitro transformation method in pigeonpea limits the application of biotechnological breeding approaches for its genetic improvement. The present study describes a transformation method using novel in vitro shoot grafting technique for two cultivars ICPL87 and ICPL87119. Modified Murashige and Skoog (MS) medium with 1 mg l<sup>−1</sup> 6-benzylaminopurine and 0.2 mg l<sup>−1</sup> α-naphthaleneacetic acid induced an average of 25 shoots from decapitated embryonic axis explants after six weeks of culture. These shoots were further elongated in a modified MS medium containing 0.5 mg l<sup>−1</sup> 6-benzylaminopurine along with 0.5 mg l<sup>−1</sup> gibberellic acid for another four weeks. Grafting of pigeonpea shoots to seedling rootstock allowed 95% recovery of shoots. The whole regeneration process, starting from explant preparation to complete plant development, took 12–13 weeks. Further, the explants were infected with <i>Agrobacterium tumefaciens</i> harboring a binary vector pBI121. Transient and constitutive β-glucuronidase expressions were obtained in putative transgenic shoots selected at 100 mg l<sup>−1</sup> kanamycin. The selected shoots were grafted on non-transgenic root stock to establish putative transformants. T<sub>0</sub> and T<sub>1</sub> transformants were confirmed through polymerase chain reaction for presence of <i>neomycin phosphotransferase</i> gene. An overall 9% of transformation efficiency was recorded in both cultivars.
- DOI
- 10.5511/plantbiotechnology.14.0805a
- Access Restrictions
- インターネット公開
- Data Provider (Database)
- 科学技術振興機構 : J-STAGE
- Summary, etc.
- Lack of reproducible in vitro transformation method in pigeonpea limits the application of biotechnological breeding approaches for its genetic improvement. The present study describes a transformation method using novel in vitro shoot grafting technique for two cultivars ICPL87 and ICPL87119. Modified Murashige and Skoog (MS) medium with 1 mg l<sup>−1</sup> 6-benzylaminopurine and 0.2 mg l<sup>−1</sup> α-naphthaleneacetic acid induced an average of 25 shoots from decapitated embryonic axis explants after six weeks of culture. These shoots were further elongated in a modified MS medium containing 0.5 mg l<sup>−1</sup> 6-benzylaminopurine along with 0.5 mg l<sup>−1</sup> gibberellic acid for another four weeks. Grafting of pigeonpea shoots to seedling rootstock allowed 95% recovery of shoots. The whole regeneration process, starting from explant preparation to complete plant development, took 12–13 weeks. Further, the explants were infected with <i>Agrobacterium tumefaciens</i> harboring a binary vector pBI121. Transient and constitutive β-glucuronidase expressions were obtained in putative transgenic shoots selected at 100 mg l<sup>−1</sup> kanamycin. The selected shoots were grafted on non-transgenic root stock to establish putative transformants. T<sub>0</sub> and T<sub>1</sub> transformants were confirmed through polymerase chain reaction for presence of <i>neomycin phosphotransferase</i> gene. An overall 9% of transformation efficiency was recorded in both cultivars.
- DOI
- 10.5511/plantbiotechnology.14.0805a
- Related Material (URI)
- References
- A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue CulturesSomatic embryogenesis in cell suspension cultures of pigeonpea (Cajanus cajan)Agrobacterium-mediated production of transgenic pigeonpea (Cajanus cajan L. Millsp.) expressing the synthetic BT cry1Ab geneFactors affecting regeneration of pigeonpea (Cajanus cajan L. Millsp) from mature embryonal axesSomatic Embryogenesis and Plant Regeneration in PigeonpeaHigh-Resolution Whole-Mount Imaging of Three-Dimensional Tissue Organization and Gene Expression Enables the Study of Phloem Development and Structure in <i>Arabidopsis</i>Differential Response of Cajanus cajan Varieties to Transformation with Different Strains of AgrobacteriumFactors affecting high frequency differentiation of shoots and roots from cotyledon explants of Brassica juncea (L.) czernIn vitro shoot-tip grafting improves recovery of cotton plants from cultureOrganogenesis and embryogenesis from diverse explants in pigeonpea (Cajanus cajan L.)In vitro regeneration and transformation of pigeonpea [Cajanus cajan (L.) Millsp]Regeneration of pigeonpea (Cajanus cajan) from cotyledonary node via multiple shoot formationPlant regeneration via somatic embryogenesis in pigeonpea ( Cajanus cajan L. Millsp)Expression of a synthetic <i>cry</i>1AcF gene in transgenic Pigeon pea confers resistance to <i>Helicoverpa armigera</i>Thidiazuron-induced shoot regeneration in pigeonpea (Cajanus cajan L.)Multiple shoot induction by benzyladenine and complete plant regeneration from seed explants of chickpea (Cicer arietinum L.)Agrobacterium-mediated genetic transformation of pigeon pea (Cajanus cajan (L.) Millsp.) using embryonal segments and development of transgenic plants for resistance against SpodopteraAn efficient protocol for shoot regeneration and genetic transformation of pigeonpea [Cajanus cajan (L.) Millsp.] using leaf explantsExpression of biologically active Hemagglutinin-neuraminidase protein of Peste des petits ruminants virus in transgenic pigeonpea [Cajanus cajan (L) Millsp.]Nutrient requirements of suspension cultures of soybean root cellsGenetic transformation of pigeonpea with rice chitinase geneProgress of tissue culture and genetic transformation research in pigeon pea [Cajanus cajan (L.) Millsp.]The effect of TDZ on organogenesis and somatic embryogenesis in pigeonpea (Cajanus cajan L. Millsp)Plant regeneration from leaf discs of peanut and pigeonpea: Influence of benzyladenine, indoleacetic acid and indoleacetic acid-amino acid conjugatesPlant Regeneration from Decapitated Mature Embryo Axis and Agrobacterium Mediated Genetic Transformation of PigeonpeaEfficient and rapid in vitro plant regeneration system for Indian cultivars of chickpea (Cicer arietinum L.)
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- Japan Link Center雑誌記事索引データベース雑誌記事索引データベースCrossrefCiNii ArticlesCiNii Articles
- Bibliographic ID (NDL)
- 02600374111000376
- NAID
- 13000469090540020313497