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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 101 (2000), S. 15-20 
    ISSN: 1432-2242
    Keywords: Key words Xa21 ; IR72 ; Bacterial leaf blight ; Transformation ; Field testing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Based on the characterization of the resistance phenotype and molecular analysis, several homozygous lines carrying Xa21 against the bacterial blight (BB) pathogen were obtained from previously transformed indica rice, IR72. The homozygous line, T103-10, with the best phenotype and seed-setting, was repeatedly tested under normal field conditions to evaluate its levels of resistance to the BB pathogen in Wuhan, China, in 1998 and 1999. The isolates of Xanthomonas oryzae pv oryzae (Xoo) used in this experiments were PXO61, PXO79, PXO99 and PXO112 isolated from the Philippines, T2 isolated from Japan, and Zhe173 isolated from China. The results demonstrated that the transgenic homozygous line expressed the same resistance spectrum, but with a shorter lesion length to each inoculated isolates as the lesion length of the Xa21 donor line IRBB21. The non-transformed control IR72 carrying Xa4 was resistant to PXO61, PXO112, Zhe173 and T2, but susceptible to PXO99 and PXO79. The negative control variety IR24 was susceptible to all isolates under field conditions. The results demonstrated clearly that the Xa21 transgene led to an excellent field performance of the introduced bacterial blight resistance trait on the recipient plants. The yield performance of this transgenic homozygous line, T103-10, is comparable with that of the control under field conditions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 97 (1998), S. 31-36 
    ISSN: 1432-2242
    Keywords: Key words Indica rice ; Xa21 ; Transgenic plants ; Disease resistance ; Xanthomonas oryzae pv. oryzae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  An elite indica rice variety, ‘IR72’, was transformed with a cloned gene, Xa21, through particle bombardment. Molecular analysis of transgenic plants revealed the presence of a 3.8-kb EcoRV-digested DNA fragment corresponding to most of the Xa21 coding region and its complete intron sequence, indicating the integration of Xa21 into the genome of ‘IR72’. In the T1 generation, the transgene was inherited and segregated in a 3:1 ratio. After inoculation with the prevalent races 4 and 6 of Xanthomonas oryzae pv. oryzae (Xoo), T1 plants positive for the transgene were found to be resistant to bacterial blight (BB). We also observed that the level of resistance to race 4 of Xoo was higher due to the pyramiding of Xa21 and Xa4 present in ‘IR72’. Since the inactivation of the transgene Xa21 occurred in the two transgenic T1 plants, a larger progeny should be obtained for selecting homozygous line with a consistently higher level of resistance to the BB pathogen.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: Adenylate cyclase ; Cyclic AMP ; Diurnal variation ; Histochemistry ; Clover yellow mosaic virus ; White clover
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Diurnal changes in the concentration of cAMP in white clover were investigated biochemically and histochemically. Biochemical assays showed that a) the concentration of cAMP in healthy leaves was consistently higher than in CYMV-diseased leaves under the same light condition and b) the concentration of cAMP in clover leaves exhibited a diurnal cycle. The diurnal changes in cAMP concentration were present in both healthy and CYMV-diseased clover leaves. Histochemical localization tests indicated that the adenylate cyclase activity could be semi quantilated as more dense reaction products were present in the membrane systems of healthy than CYMV-diseased leaves. The histochemical results were consistent with the biochemical data.
    Type of Medium: Electronic Resource
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