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作 者:张继栋[1,2,3] 杨雪清[4] 乔爱民[2] 孙敏[1] 何生根[3] 雷桅[1] 尹彩霞[2]
机构地区:[1]西南大学生命科学学院,重庆400715 [2]仲恺农业工程学院农业与园林学院,广州510225 [3]仲恺农业工程学院生命科学学院,广州510225 [4]洛阳理工学院附中,河南洛阳471003
出 处:《热带亚热带植物学报》2008年第5期480-485,共6页Journal of Tropical and Subtropical Botany
摘 要:建立了木本曼陀罗(Datura arborea L.)毛状根的植株再生体系并对再生植株进行了初步检测。采用"一步法"诱导不定芽的适宜培养基为MS+6-BA2.0mgL-1+NAA0.2mgL-1;采用"两步法"诱导不定芽时,先在MS+6-BA4.0mgL-1+KT0.5mgL-1+2,4-D0.5mgL-1上诱导愈伤组织,然后在MS+6-BA4.0mgL-1+NAA0.2mgL-1上诱导愈伤组织分化不定芽。诱导不定芽的最适宜生根培养基为1/2MS+IBA0.1mgL-1。用PCR技术从再生植株叶片中得到了rolB、rolC目的基因片段。HPLC检测结果表明毛状根再生植株中莨菪烷类生物碱(Tropane alkaloids,TA)的含量较野生植株有明显的提高。Plant regeneration system derived from hairy roots ofDatura arborea L. was established. The optimum medium for inducing adventitious buds by‘ one-step method’was MS + 6-BA 2.0 mg L^-1 + NAA 0.2 mg L^-1. Using ' two-step method' ,callus was induced on MS medium supplement with 6-BA 4.0 mg L1 +KT 0.5 mg L^-1 + 2,4-D 0.5 mg L^-1at first, then adventitious buds were differentiated from the induced callus on MS medium supplemented with 6-BA 4.0 mg L^-1 + NAA 0.2 mg L^-1. The optimum rooting medium for adventitious buds was 1/2MS + IBA 0.1 mg L^-1. By using PCR technique, the gene segnents ro/B and rolC were obtained from the leaves of regeneration plant. The results of HPLC showed that the contents of tropane alkaloids (TA) in regeneration plants was much more than those in the wild plants.
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