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榨菜嫩叶高效分化愈伤组织的诱导及无性系的建立
引用本文:朱婷,陈晓露,师伟,姜长阳.榨菜嫩叶高效分化愈伤组织的诱导及无性系的建立[J].哈尔滨师范大学自然科学学报,2007,23(1):100-104.
作者姓名:朱婷  陈晓露  师伟  姜长阳
作者单位:辽宁师范大学
基金项目:辽宁师范大学教学改革项目(20050101123)
摘    要:本实验研究了榨菜嫩叶的愈伤组织的诱导,愈伤组织的分化,分化苗生根、移栽、扦插所需要的条件,建立起榨菜嫩叶的无性系及快速繁殖技术.结果证明:榨菜嫩叶愈伤组织诱导的理想培养基是MS BA 1.2 mg/L 2,4-D 0.5 mg/L;愈伤组织分化的理想培养基是MS BA0.5 mg/L;生根的理想培养基是I/2MS 0.4~0.8 mg/L;以炉灰渣为试管苗的移栽扦插机制,移栽成活率为85%,扦插成活率为80%.

关 键 词:榨菜  无性系  快速繁殖
修稿时间:2006年9月13日

A HIGH EFFICIENT CALLUS INDUCTION AND ESTABLISHMENT OF REGENERATION CLONE OF BRASSICA JUNEAS VAR.TSATSAI
Zhu Ting,Chen Xiaolu,Shi Wei,Jiang Changyang.A HIGH EFFICIENT CALLUS INDUCTION AND ESTABLISHMENT OF REGENERATION CLONE OF BRASSICA JUNEAS VAR.TSATSAI[J].Natural Science Journal of Harbin Normal University,2007,23(1):100-104.
Authors:Zhu Ting  Chen Xiaolu  Shi Wei  Jiang Changyang
Institution:Liaoning Normal University
Abstract:The conditions were studied forinduction, differentation, radication, transplatation, and graftage of the callus of Brassica juneas var. tsatsai and its regenerative clone was established. MS BA 0. 5 mg/L is suitable for differentiation. 1/2MS IAA 0.4 mg/L is suitable for radication with cinder as medium. Survival ration of 85% for transplatation,of 80% for graftage were observed.
Keywords:Brassica juneas var  tsatsai  Clone  Rapid propagation
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