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  • 2000-2004  (2)
  • Chitinase  (1)
  • Sheath blight  (1)
  • chrysanthemum  (1)
Materialart
Erscheinungszeitraum
  • 2000-2004  (2)
Jahr
  • 1
    ISSN: 1432-2242
    Schlagwort(e): Key words Agrobacterium ; Chitinase ; T-DNA ; Sheath blight ; Rice
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract  A concise T-DNA element was engineered containing the rice class-I chitinase gene expressed under the control of CaMV35S and the hygromycin phosphotransferase gene (hph) as a selectable marker. The binary plasmid vector pNO1 with the T-DNA element containing these genes of interest was mobilized to Agrobacterium tumefaciens strain LBA4404 to act as an efficient donor of T-DNA in the transformation of three different indica rice cultivars from different ecosystems. Many morphologically normal, fertile transgenic plants from these rice cultivars were generated after Agrobacterium-mediated transformation using 3-week-old scutella calli as initial explants. Stable integration, inheritance and expression of the chimeric chitinase gene were demonstrated by Southern blot and Western blot analysis of the transformants. Bioassay data showed that transgenic plants can restrict the growth of the sheath blight pathogen Rhizoctonia solani. Bioassay results were correlated with the molecular analysis. Although we obtained similar results upon DNA-mediated transformation, this report shows the potential of the cost-effective, simple Agrobacterium system for genetic manipulation of rice cultivars with a pathogenesis-related (PR) gene.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1573-5060
    Schlagwort(e): chimera ; chrysanthemum ; mutation breeding ; regeneration
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Abstract Rooted cuttings of white flowered cv. `Purnima' and red flowered cv. `Colchi Bahar' of Chrysanthemum morifolium were treated with gamma rays. Sectorial somatic mutations in flower colour were detected in both the cvs. Mutated ray florets (yellow colour for both the cvs) were cultured on agar-solidified Murashige & Skoog basal medium supplemented with sucrose and different combinations of BAP/kinetin and NAA. Direct shoot organogenesis was noticed within 2 weeks of culture initiation. SEM studies confirmed this direct shoot differentiation. The best regeneration was obtained on medium supplemented with 0.2 mg/l NAA and 0.5 mg/lBAP. Shoots regenerated from mutated ray florets were rooted in vitro and transferred to the field. These plants flowered true-to-explant floret colour and shape. These isolated yellow mutants were maintained vegetatively have proved to be true-to-type in two successive generations.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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