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甜(辣)椒花药培养胚状体诱导与植株再生
引用本文:孙少霞,戈伟,王述彬,刘金兵,潘宝贵,刁卫平. 甜(辣)椒花药培养胚状体诱导与植株再生[J]. 江苏农业学报, 2009, 25(6)
作者姓名:孙少霞  戈伟  王述彬  刘金兵  潘宝贵  刁卫平
作者单位:1. 南京农业大学园艺学院,江苏,南京,210095;江苏省农业科学院蔬菜研究所,江苏,南京,210014
2. 江苏省农业科学院蔬菜研究所,江苏,南京,210014
基金项目:国家"863"计划项目,国家科技支撑计划项目,江苏省科技支撑计划项目,江苏省农业科技自主创新资金项目,江苏省科技基础设施建设计划项目,江苏省农业科学院基金项目 
摘    要:以10份不同基因型甜(辣)椒为试材进行花药培养,通过对基因型、取蕾时期、低温预处理、热激处理、碳源及外源激素浓度配比等因素的研究,建立有效的甜(辣)椒花药培养胚状体发生体系.结果表明:基因型是限制甜(辣)椒花药培养胚状体诱导的关键因素,不同品种间出胚率差异显著,其中品种003出胚率最高,为10.8%;处于盛花期的花蕾最适于甜(辣)椒花药培养;4℃低温预处理1-3 d有利于胚状体的诱导,以处理2 d的胚状体产率最高;以2%的麦芽糖代替3%的蔗糖能显著提高出胚率和子叶形胚的比率,筛选出适于甜(辣)椒花药培养胚状体诱导的最佳培养基为Ms+0.5 mg/L NAA+1.0 mg/L KT+2%麦芽糖,能有效地提高出胚率并促进植株冉牛;获得了6个基因型的子叶形胚和再生植株.

关 键 词:甜(辣)椒  花药培养  胚状体  植株再生

Embryoid Induction and Plant Regeneration of Capsicum annuum L. through Anther Culture
SUN Shao-xia,GE Wei,WANG Shu-bin,LIU Jin-bing,PAN Bao-gui,DIAO Wei-ping. Embryoid Induction and Plant Regeneration of Capsicum annuum L. through Anther Culture[J]. Jiangsu Journal of Agricultural Sciences, 2009, 25(6)
Authors:SUN Shao-xia  GE Wei  WANG Shu-bin  LIU Jin-bing  PAN Bao-gui  DIAO Wei-ping
Abstract:Ten varieties of pepper were used to study the effects of genotype,flower buds harvest time,cold-pretreat-ment,hot-shock treatment,carbon source and combination of hormones on the anther culture in Capsicum annuum L.Through these tests,an effective system of embryoid production was established.Cotyledonary embryoids and plantlets were obtained from six genotypes.The results showed that genotype was the key factor in embryoid induction.The embryoid for-mation frequency Was different significantly among different genotypes.The variety 003 had the highest embryoid formation frequency which was 10.8%.The flower buds at full-bloom stage were found to optimum for anther culture in pepper.Cold-pretreatment (4℃)for 1-3 d also promoted embryoid induction,while the highest embryoid formation frequency was ob-mined from anther pretreated at 4℃ for 2 d.Embryoid and cotyledonary embryoid formation frequency could be more re-markably improved by 2% maltose than 3% sucrose.The optimal culture medium which could effectively improve embryoid and regenerated plantlets formation Was MS+0.5 mg/L NAA+1.0 mg/L KT+2% maltose.
Keywords:pepper(Capsicum annuum L.)  an-ther culture  embryoid  plant regeneration
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