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番木瓜优质组培苗生产体系的建立
引用本文:周鹏,黎小瑛,沈文涛,阮孟斌.番木瓜优质组培苗生产体系的建立[J].热带作物学报,2005,26(1):43-46.
作者姓名:周鹏  黎小瑛  沈文涛  阮孟斌
作者单位:中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海南,海口,571101;中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海南,海口,571101;中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海南,海口,571101;中国热带农业科学院热带生物技术研究所,热带作物生物技术国家重点实验室,海南,海口,571101
基金项目:本研究获得国家十五“863计划”项目(2002AA241141)、海南省自然科学基金项目(30203)的资助.本技术生产体系申请国家专利.
摘    要:用含有100mg/LVc+1mg/LAgNO;+20mg/LPVP液体处理成龄番木瓜(CricappayaL)侧芽,再用70%酒精浸泡50s、0.15%升汞消毒5min,经消毒的外植体接种于MS+KT0.5mg/L+NAA0.2mg/L+GA31.0mg/L+30g/L蔗糖+7g/L琼脂(pH=5.7),26~28℃,每日光照培养12h,光照强度为15001x,连续培养20d;外植体经初始培养后,继代接种于MS+BA0.5mg/L+NAA0.1 mg/L+GA,1.0mg/L+蔗糖30gL+琼脂7g/L(pH=5.7),26~28℃,每日光照培养16h,光照强度为2000Ix,连续培养40d,繁殖系数达3~5倍;继代芽接种MS+BA0.2mg/L+KT0.3mg/L+NAA0.Img/L+NAA0.1 mg/L+GA;1.0 mg/L+ADS40mg/L+蔗糖30g/L+琼脂7g/L(pH=5.7),26~28℃,每日光照培养16h,光照强度为20001x,连续培养20d进行壮苗培养,经壮苗培养芽接种于MS+KT0.1~0.2mg/L+ NAA0.05~0.1mg/L+ IBA0.2-0.3mg/L+蔗糖20~30gL+琼脂6.5g/L(pH=5.6),26~28℃,每日光照培养12h,光照强度为1500kx,连续培养 15~20d 进行催根培养,生根率达85%以上。生根苗经2~3d的自然光炼苗后,移栽于沙土∶椰糠∶菜园土质量比为1∶1∶1 混和的基质中,移苗后1周内,每天喷施浓度为200~400mg/L的IBA,移栽成活率达80%以上。笔者就目前番木瓜组培快繁中的问题作了系统的研究,建立了一套适合番木瓜优质种苗生产的技术体系。

关 键 词:番木瓜  成龄侧芽  快繁  种苗  生产体系
收稿时间:2004-10-20
修稿时间:2004年10月20

Establishment of a Tissue Culture System for Papaya
Zhou Peng,Li Xiaoying,Shen Wentao,Ruan Mengbin.Establishment of a Tissue Culture System for Papaya[J].Chinese Journal of Tropical Crops,2005,26(1):43-46.
Authors:Zhou Peng  Li Xiaoying  Shen Wentao  Ruan Mengbin
Institution:State Key Biotechnology Laboratory for Tropical Crops/Institute of Bio-Science and Bio-Technology, CATAS Haikou Hainan 571101 China
Abstract:Papaya is a giant herbaceous plant and has an important value for food industry. It has been grown in tropical and subtropical regions of the world for a long time.An attempt was made to establish a tisue culture sys-tem for rapid propagation of papaya.Mature buds were treated with a solution of 100mg/L.PVP+1 mg/LVc+20mg/L. AgNO,then dipped in 70%(V/)of ethanol for 15S, treated with 0.15%(V/V) of mercury(Hg)chloride for5min. These buds were then culured on MS medium(pH=5.7) supplemented with KT0.5mg/L,NAA0.2 mg/L,GA41.0, sucrose 30g/L and agar7g/L under the condition of 26~28Cand 1 500k,20h per day for 20d.The explants, when initally cultured, were subeultured on the MS medium(pH=5.7) including BA0.5 mg/L,NAA0.I mg/L, GA,1.0 mg/L,sucrose30 g/L.and agar7g/Lunder the condition of 26~28Cand2000k,16h perday for40 d. Shoots were grown on the MS medium containing BA0.2 mg/L,KT0.3mg/L,NAA0.I mg/L,NAA0.1 mg/L, GA31.0mg/L.ADS40 mg/L,sucrose30 g/L+agar7 g/L(pH=5.7)uder the condition of26~-28Cand 2000k, 16 h per day for20d. The rols of propagated buds were induced on the MS medium(pH=5.7)induding KT 0.1-0.2 mg/L,NAA0.05~0.I mg/L,IBA0.2-0.3 m/L,sucrose20~30 g/L and agar7 g/L underthe condition of 26~28°C and 1500k,12 h per day for 15~20 d.The inducedroing rate was up to 85%.Then roted planlets were hardened of fr2-3days, transfered into pots containing mixture of humusich soil, coir dust and sandy soil(w:w:w=1:1:1) and then over 80% of the plantlets survived with 200~400 mg/L of IBA being spraied with being sprained 200~400mg/L of IBA.A tisue culure system for rapid propagation of papaya young plants was established.
Keywords:Carica papaya L  lateral buds micropropagation shoots tissue culture  
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