Agrobacterium-mediated Genetic Transformation of Rice var. BRRI Dhan 58

M. S. A. Banu, B. Ahmed, S. Parveen, H. Rashid, K. M. K. Huda
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引用次数: 1

Abstract

Agrobacterium mediated genetic transformation of BRRI Dhan 58 was conducted by using immature embryos following indirect regeneration. High percentage of callus induction at 96.5% was obtained when seeds of BRRI dhan 58 were cultured on modified MS medium supplemented with 2.5 mg/l 2, 4-D under dark condition. The maximum regeneration response was rerecorded when MS was supplemented with 3 mg/l BAP + 0.5 mg/l NAA and 1.0 mg/l Kn. Genetic transformation was performed using A. tumefaciens strain LBA4404 harboring pCAMBIA1301 plasmid carrying the marker genes for β-glucuronidase (GUS) and hygromycin resistance (hptII). Integration of the GUS gene into the genome of the rice plants was confirmed by PCR. The leaf segments of the PCR positive transformed plants showed the expression of GUS. The results of this study would be an effective tool for crop improvement and functional studies of gene on rice plant. Plant Tissue Cult. & Biotech. 31(1): 71-80, 2021 (June)
农杆菌介导的水稻品种BRRI Dhan 58的遗传转化
通过使用间接再生后的未成熟胚胎进行农杆菌介导的BRRI Dhan 58的遗传转化。BRRI dhan 58种子在添加2.5 mg/l 2,4-D的改良MS培养基上,在黑暗条件下培养,愈伤组织诱导率高达96.5%。当MS补充3mg/l BAP+0.5mg/lNAA和1.0mg/l Kn时,再生反应最大。用携带β-葡糖苷酸酶(GUS)和潮霉素抗性(hptII)标记基因的pCAMBIA1301质粒的根癌分枝杆菌LBA4404菌株进行遗传转化。通过PCR证实GUS基因整合到水稻基因组中。PCR阳性转化植株的叶片段显示出GUS的表达。该研究结果将为作物改良和水稻基因功能研究提供有效的工具。植物组织培养生物技术。31(1):71-802021(6月)
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