首页> 外国专利> A METHOD FOR NORMAL EMBRYO PRODUCTION THROUGH MICROSPORE CULTURE IN CAPSICUM ANNUUM L

A METHOD FOR NORMAL EMBRYO PRODUCTION THROUGH MICROSPORE CULTURE IN CAPSICUM ANNUUM L

机译:通过辣椒核中的微孔培养正常产胚的方法

摘要

A method for production of normal embryo of red pepper(Capsicum annuum L.) through microspore culture is provided to improve production yield of normal embryo of red pepper(Capsicum annuum L.) in the microspore culture by using the microspore as a pretreating material and performing double layer culture. The method for production of normal embryo of red pepper(Capsicum annuum L.) through microspore culture comprises the steps of: blending and vortexing the anther collected from the flower bud of red pepper(Capsicum annuum L.) to obtain microspores; removing somatic cell tissue fragments from the obtained microspores, and centrifuging them to obtain microspores; pretreating the microspores in a pretreatment medium and culturing at 32 deg.C for 3 days; culturing the pretreated microspores on NLN medium in a density of 80,000-100,000 microspores/ml for 1 day, adding fresh NLN medium into the microspores, and culturing them at 27 deg.C under dark condition for 3-4 weeks, wherein the pretreatment medium is NLN(sucrose excluded) medium containing 0.37M mannitol.
机译:本发明提供了一种通过小孢子培养生产红辣椒正常胚的方法,通过以小孢子为预处理材料,提高了小孢子培养中红辣椒正常胚的产量。进行双层培养。通过小孢子培养生产红辣椒(Capsicum annuum L.)的正常胚的方法包括以下步骤:将从红辣椒(Capsicum annuum L.)的花芽中收集的花药混合并涡旋以获得小孢子。从获得的小孢子中去除体细胞组织碎片,并将其离心以获得小孢子;在预处理介质中预处理小孢子,并在32℃下培养3天;在密度为80,000-100,000微孢子/ ml的NLN培养基上培养1天,将新鲜的NLN培养基添加到微孢子中,在黑暗条件下于27℃培养3-4周,其中是含有0.37M甘露醇的NLN(不含蔗糖)培养基。

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