HENG Jing,HAN Chunye,WANG Mingshan,et al.Induction of Callus of Stem Segments of Lonicera japonica Thunb.var.chinensis (Wats.) Bak[J].Northern Horticulture,2018,42(19):94-99.[doi:10.11937/bfyy.20174342]
红金银花茎段愈伤组织的诱导
- Title:
- Induction of Callus of Stem Segments of Lonicera japonica Thunb.var.chinensis (Wats.) Bak
- 文献标志码:
- A
- 摘要:
- 以红金银花当年生幼嫩茎段为试材,采用正交实验设计,研究了红金银花愈伤组织诱导和增殖培养的影响因素。结果表明:6-BA、KT促进了愈伤组织的诱导,提高了出愈率;当NAA、KT分别为0.4、1.0 mg·L-1时最有利于愈伤组织的增殖培养。不同季节外植体愈伤组织诱导效果不同,春季采集的当年生的幼嫩茎段更有利于愈伤组织的诱导;MS培养基中添加6.5 mg·L-1 琼脂比较适宜;红金银花愈伤组织诱导最适宜的培养基为MS+KT 1.0 mg·L-1+NAA 0.2 mg·L-1+6-BA 1.5 mg·L-1;愈伤组织增殖培养最适宜的培养基为MS+6-BA 1.5 mg·L-1+NAA 0.4 mg·L-1+KT 0.1 mg·L-1。
- Abstract:
- The stem of Lonicera japonica Thunb.var.chinensis (Wats.) Bak was taken as experimental materials,the factors affecting the callus induction and proliferation of Lonicera japonica Thunb.var.chinensis (Wats.) Bak were studied by orthogonal design.The results showed that 6-BA and KT had obviously promoted callus induction and increased the rate of callus induction.It was the most beneficial to the proliferation of callus when the concentration NAA and KT were 0.4 mg·L-1 and 1.0 mg·L-1,respectively.The effect of callus induction was different in different seasons,and the stem segments collected in spring were more favorable for callus induction,and it was better to use 6.5 mg·L-1 agar.The callus induction medium was suitable for MS+KT 1.0 mg·L-1+NAA 0.2 mg·L-1+6-BA 1.5 mg·L-1.The optimum medium for callus proliferation was MS+6-BA 1.5 mg·L-1+NAA 0.4 mg·L-1+KT 0.1 mg·L-1.
相似文献/References:
[1]陈丽文,荣薏,何贵整.金钻蔓绿绒组培再生体系的建立[J].北方园艺,2012,36(01):120.
CHEN Li-wen,RONG Yi,HE Gui-zheng.Establishment of Tissue Culture Regeneration System for Philodendron con-go[J].Northern Horticulture,2012,36(19):120.
[2]关丽霞.牡丹沙培嫩茎段离体培养的初步研究[J].北方园艺,2012,36(04):74.
GUAN Li-xia.Preliminary Study on in Vitro Culture of Sand-cultured Tender Stem Segments of Paeonia suffruticosa[J].Northern Horticulture,2012,36(19):74.
[3]王文静,李维强,王鹏.多效唑预处理对红金银花直接培养成壮苗的影响[J].北方园艺,2012,36(09):184.
WANG-Wen-jing,LI Wei-qiang,WANG Peng.Effect of Pretreatment with PP333on Culture Directly into Seedling to Lonicera japonica var.chinensis[J].Northern Horticulture,2012,36(19):184.
[4]孙骏威,方晓峰,陈珍.不同植物生长调节剂对黄秋葵组织培养的影响[J].北方园艺,2012,36(07):139.
SUN Jun-wei,FANG Xiao-feng,CHEN Zhen.Effects of Plant Growth Regulator on Tissue Culture of Abelmoschus esculentus (L.) Moench [Hibiscus esculentus L.[J].Northern Horticulture,2012,36(19):139.
[5]王文静,王鹏,李伟强.红金银花组培快繁技术研究[J].北方园艺,2013,37(18):100.
WANG Wen-jing,WANG Peng,LI Wei-qiang.Study on the Tissue Culture and Rapid Propagation of Lonicera japonica var.chinensis[J].Northern Horticulture,2013,37(19):100.
[6]董敬超.沙棘品种“实优1号”的组织培养技术[J].北方园艺,2012,36(19):127.
DONG Jing-chao.Study on Tissue Culture of Hippophae rhamnoides ‘Real gifted one’[J].Northern Horticulture,2012,36(19):127.
[7]叶飞,建德锋.“维多利亚”葡萄茎段离体培养技术研究[J].北方园艺,2012,36(19):149.
YE Fei,JIAN De-feng.Study on the Technology of Stem Segments Culture of ‘Victoria’ Grape in vitro[J].Northern Horticulture,2012,36(19):149.
[8]张洪岩,陈秀玲,李景富,等.番茄材料“0946”和“0949”再生体系的研究[J].北方园艺,2012,36(12):125.
ZHANGHong-yan,CHENXiu-ling,LIJing-fu,et al.StudyonRegenererationSystemofTomatoAccessions‘0946’and‘0949’[J].Northern Horticulture,2012,36(19):125.
[9]管艳,梁国平,李玲,等.星点木愈伤组织诱导及植株再生研究[J].北方园艺,2013,37(24):109.
GUAN Yan,LIANG Guo-ping,LI Ling,et al.Study on Callus Induction and Plantlet Regeneration of Dracaena godseffiana[J].Northern Horticulture,2013,37(19):109.
[10]周佳红,邢才华,曹慧,等.秋子梨茎段薄层细胞培养再生初探[J].北方园艺,2015,39(06):95.[doi:10.11937/bfyy.201506026]
ZHOU Jia-hong,XING Cai-hua,CAO Hui,et al.Study on Regeneration of Thin Cell Layer of Pyrus ussuriensis[J].Northern Horticulture,2015,39(19):95.[doi:10.11937/bfyy.201506026]
备注/Memo
第一作者简介:衡静(1984-),女,硕士,讲师,研究方向为园林植物栽培及养护。E-mail:hnacwms@126.com.责任作者:马丽(1982-),女,博士,副教授,研究方向为园艺植物抗性生理。E-mail:ndmali@163.com.基金项目:河南省科技攻关资助项目(162102110092);国家自然科学基金资助项目(31401918)。收稿日期:2018-02-07