首页> 外国专利> METHOD FOR CARRYING OUT IN VITRO CULTURES OF ARNICA MONTANA L. SPECIES USED FOR EVALUATING THE BIOSYNTHESIS OF SOME BIOLOGICALLY ACTIVE COMPOUNDS

METHOD FOR CARRYING OUT IN VITRO CULTURES OF ARNICA MONTANA L. SPECIES USED FOR EVALUATING THE BIOSYNTHESIS OF SOME BIOLOGICALLY ACTIVE COMPOUNDS

机译:进行山茱AR体外培养的方法,用于评估某些生物活性化合物的生物合成

摘要

The present invention relates to a method for carrying out in vitro culture of Arnica montana L. species by developing the following processes: cultures of differentiated tissues (meristematic tissues) and undifferentiated tissues (callus and cell clusters), in order to carry out an integrated evaluation of the biosynthesis of biologically active compounds. These consist of micropropagation cultures (explant - stem apices obtained by the germination of seeds under aseptic conditions) by using a Murashige and Skoog (1962) (MS) culture medium with 25 g/l saccharose, solidified with 8...8.5% agar and supplemented with 1.0 mg/l BAP, callus cultures (explant - foliar and root fragments sampled from in vitro regenerated plants, immature inflorescences) by using a culture medium MS with 30g/l saccharose solidified with 7.5% agar, in three hormonal balances variants (0.5 mg/l BAP and 1.5 mg/l 2.4D, 0.5mg/l kinetine and 1.5 mg/l2.4D, 1.0 mg/l kinetine and 1.0 mg/l NAA), submerged cultures (inoculum - callus obtained under the above-mentioned conditions), by using a culture medium MS (liquid) with 30 g/l saccharose, without growth regulators.
机译:本发明涉及通过开发以下过程进行山金车种的体外培养的方法:分化的组织(分生组织)和未分化的组织(愈伤组织和细胞团)的培养,以便进行整合评估生物活性化合物的生物合成。这些由微繁殖培养物(通过在无菌条件下使种子萌发而获得的外植体-茎尖)组成,使用的是Murashige and Skoog(1962)(MS)培养基,其中含25 g / l蔗糖,并用8 ... 8.5%琼脂固化并通过使用含有30g / l蔗糖和7.5%琼脂固化的MS培养基在三种荷尔蒙平衡变量中添加1.0 mg / l BAP,愈伤组织培养物(外植体-从体外再生植物中提取的叶和根碎片,未成熟的花序) (0.5 mg / l BAP和1.5 mg / l 2.4D,0.5mg / l kinetine和1.5 mg / l2.4D,1.0 mg / l kinetine和1.0 mg / l NAA),浸没培养物(接种物-根据上述方法获得的愈伤组织所述条件),通过使用具有30 g / l蔗糖的培养基MS(液体),无生长调节剂。

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