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机构地区:[1]云南农业大学薯类作物研究所,云南昆明650201
出 处:《西南农业学报》2006年第B09期59-62,共4页Southwest China Journal of Agricultural Sciences
基 金:本研究受云南省科技厅资助.
摘 要:以山药带芽茎段为外植体进行组织培养,试验结果表明:(1)用75%酒精消毒15s,再用2%NaOCl浸泡15~25min为最佳的外植体消毒方法;(2)MS+6-BA1.0mg/L+NAA0.2mg/L为诱导多芽体较好的培养基配方;(3)MS+NAA0.5~1.0mg/L对诱导生根较为适宜;(4)离体条件下获得的零余子在MS+6-BA0.2mg/L+NAA1.0mg/L的培养基上平均出芽数能达4.0,且芽的长势较好。The explants tissue culture of cauline tip with bud of Dioscorea oppsita was studied, The results showed that: The best sterilization method was to sterilized with 2% NaOCl for 15-20 min after being treated with 75% C2H2OH for 15 s ; The optimum medium for the induction of the multiple buds was the MS + 6-BA 1.0 mg/L + NAA 0.2 mg/L; Root could be induced in the medium of MS + NAA 0.5-1.0 mg/L ; The average number of shoot produced by bulbil from the in vitro culture was 4.0 by culturing in the medium of MS + 6-BA 0.2 mg/L + NAA 1.0 mg/L , and the buds grew well.
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