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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:2006-09-13

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
Affiliation: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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