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Method for micropropagation monocot based on continuous totipotent cell cultures

机译:基于连续全能细胞培养物的单子叶植物微繁方法

摘要

Method for increasing the growth rate of an embryogenic embryogenic cultivocelular totipotent family monocot grass or plant reed in operacionesa industrial scale, comprising cell mass: (a) culturing an explant of tissue shoot apex of monocotyledonous plant on a primary medium in queel explant had been previously treated with a cold temperature and the primary medium comprises auxin oauxina and cytokinin to produce a totipotent embryogenic cell culture; (b) treating the cell culture embryonic totipotent cold temperature to increase the speed decrease of the mass of totipotent embryonic cell culture compared to control elque treatment with a cold temperature is to last 30 days to 325 days which aTemperature in a range of 4 to 10 ° C ; and (c) maintaining totipotent embryogenic cell culture by further cultivation on primary medium and / or enun secondary medium, whereby a culture of a monocotyledonous plant having unamayor growth rate of the embryogenic cell mass with a velocity occurs multiplication of 5x to 8xen 2x to 3x compared to a control without cold treatment.
机译:在操作规模的工业规模上增加胚发生的胚性全能单子叶植物单子叶植物或植物芦苇的生长速率的方法,其包括细胞团:(a)将单子叶植物的组织芽顶的外植体培养在同质外植体的主要培养基上用低温处理,并且主要培养基包含生长素oauxina和细胞分裂素以产生全能胚胎发生细胞培养物; (b)处理细胞培养物的胚胎全能低温以增加全能胚胎细胞培养物的速度下降,与对照Elque处理相比,用寒冷温度持续30天至325天,温度范围为4至10 °C; (c)通过在原代培养基和/或enun次生培养基上进一步培养来维持全能胚发生细胞的培养,从而以不超过胚发生细胞团生长速度的速度进行单子叶植物的培养发生5x至8xen 2x至3x的倍增与未进行冷处理的对照组相比。

著录项

  • 公开/公告号ES2388353T3

    专利类型

  • 公开/公告日2012-10-11

    原文格式PDF

  • 申请/专利权人 UNIVERSITY OF SOUTH CAROLINA;

    申请/专利号ES20070794611T

  • 发明设计人 MARTON LAZLO;CZAKO MIHALY;

    申请日2007-05-07

  • 分类号A01H4/00;A01H17/00;C12N15/82;

  • 国家 ES

  • 入库时间 2022-08-21 17:21:01

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