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作 者:张慧英[1] 张耀华[2] 农友业[3] 薛艳霞[1]
机构地区:[1]广西大学农学院,南宁530004 [2]中北大学化工与环境学院,中北大学图书馆,太原030051 [3]广西大学支农开发中心,南宁530004
出 处:《玉米科学》2008年第6期79-82,共4页Journal of Maize Sciences
基 金:广西大学博士启动基金(XO61182)
摘 要:以不同玉米自交系幼胚为外植体,研究不同2,4-D浓度对愈伤组织诱导、6-BA浓度对愈伤组织分化和6-BA与NAA配合使用对试管苗生根的影响。结果表明:不同2,4-D浓度对愈伤组织诱导率影响差异不明显,但对胚性率诱导有明显影响,其诱导最佳培养基为MS+2,4-D 2 mg/L+水解酪蛋白500 mg/L+脯氨酸500 mg/L;愈伤组织分化的最佳培养基是MS+6-BA0.5 mg/L+水解酪蛋白500 mg/L+谷氨酰胺200 mg/L+PP333 2 mg/L;试管苗生根的最佳培养基是1/2 MS+6-BA0.5 mg/L+NAA2.0 mg/L+PP333 2.0 mg/L+活性炭0.2%。The inducement, differentiation and plantlet roots of callus were studied from immature embryos of the different maize inbred lines in vitro on different medium with the different 2,4-D concentration. The results showed that the inducement rate of callus was not significant with the different 2,4-D concentration, but the rate of inducement of EC was significant, and the medium was MS + 2,4-D 2 mg/L + CH 500 mg/L + Pro 500 mg/L. The differentiation of callus was best on the culture medium of 1/2 MS + 6-BA 0.5 mg/L + NAA 2.0 mg/L + PP333 2.0 mg/L+ active carbon MS + 6-BA 0.5 mg/L + CH 500 mg/L + GLU 200 mg/L + PP333 2 mg/L. The plantlet rooting was best on the culture medium of 1/2 MS + 6-BA 0.5 mg/L + NAA 2.0 mg/L + PP333 2.0 mg/L + active carbon 0.2%.
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