AI Article Synopsis

  • A plasmid containing chitinase and beta-1,3-glucanase genes was introduced into a rice hybrid (Nan29) to enhance disease resistance.
  • 93 resistant regenerants were produced, with 17 confirmed as transgenic through dot blotting and further genetic integration established via Southern blotting.
  • The resistance of six transgenic lines to rice blast was tested, showing improved resistance compared to the original line, indicating potential for use in breeding programs for rice blast resistance.

Article Abstract

Plasmid pBLGC containing chitinase gene from Phaseolus limensis and beta-1,3-glucanase gene from Nicotiana tabacum was bombarded into the restorer line "Nan29" of Dian-type hybrid rice (Oryza sativa L. ssp. japonica) from Yunnan province of South-west China. 93 regenerants were obtained from the calli that were resistant to G418 (100 to 150 mg/L) on NB medium. Using beta-1,3 glucanase gene as the probe, 17 of the regenerants were identified to be transgenic lines by dot blotting and the foreign genes construction were integrated into the genomes of T1 lines by Southern blotting hybridization. Two foreign genes were inherited stably to T4 generation according to PCR results of the lines. The resistance to rice blast of six transgenic lines were evaluated by inoculating four violent biological races of Magnaporthe grisea from Yunnan province and inducing the disease in the field. The results indicated that the resistance to rice blast of transgenic lines were enhanced to varying degrees compared with the receptor line and the transgenic lines could be used in rice blast resistant breeding.

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