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幼胚和花药培养诱导荔枝胚性愈伤组织 被引量:29

Induction of litchi embryogenic calli by immature embryos and anthers culture in vitro
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摘要 以福建荔枝主栽品种元红的幼胚为外植体,优化了离体培养诱导胚性愈伤组织(EC)的培养基.对EC的诱导,较高质量浓度的蔗糖(50gL-1)和2,4-D(2~4mgL-1)优于较低质量浓度的蔗糖(30gL-1)和2,4-D(0.5~1.0mgL-1).BA和活性炭(AC)对EC的诱导有抑制作用.适当的硫代硫酸银(STS)(29.4μmolL-1)可以抵消BA的抑制作用.在MS附加质量浓度为50gL-1的蔗糖和2mgL-1的2,4-D培养基上,下番枝、乌叶、元红和陈紫幼胚诱导EC的频率分别为22%、14.5%、17.2%和16.8%.在上述培养基中,元红花药产生EC的频率为0.1%~0.6%,而加入STS(29.4μmolL-1)可提高至1.2%~5.6%. Immature embryos of Yuanhong, one of major litchi (Litchi chinensis Sonn.) cultivars in Fujian, were used as explants to optimizing media for inducing embryogenic callus (EC). Sucrose at 50 g·L -1 and 2,4 D at 2 ̄4 mg·L -1 had favorable effect on inducing EC in comparison with sucrose at 30 g·L -1 and 2,4 D at 0. 5 ̄ 1.0 mg·L -1 . The presence of active carbon at 5 g·L -1 or BA 0.5 mg·L -1 decreased percentage of EC. However, supplementing STS (29.[KG-4]4 μmol·L -1 ) could counteract the prohibitory effect of BA. On MS basal medium supplemented with 2,4 D at 2 mg·L -1 and sucrose at 50 g·L -1 , ECs were induced from immature embryos of litchi cultivars Xiaofanzhi, Wuye, Chenzi and Yuanhong with a frequency of 22%, 14.5%, 17.2% and 16.8%, respectively. EC was also induced from anthers of Yuanhong on the medium above with a frequency of 0.1% ̄0.6% and the presence of STS in this medium enhenced the frequency to 1.2% ̄5.6%. Discussions were made about effect of these factors and their interactions on the induction of EC.
出处 《福建农业大学学报》 CSCD 1997年第2期168-172,共5页 Journal of Fujian Agricultural University
关键词 荔枝 胚培养 花药培养 胚胎发生 litchi embryo culture anther culture embryogenesis
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  • 1周俊颜,植物学报,1992年,34卷,889页 被引量:1
  • 2杨业正,贵州农学院学报,1988年,7卷,11页 被引量:1
  • 3余沛涛,植物生理学报,1987年,13卷,14页 被引量:1
  • 4张志良,植物生物化学技术和方法,1986年 被引量:1
  • 5应振土,李曙轩.乙烯、乙烯利和ACC对瓠瓜性别表现的影响[J]园艺学报,1987(01). 被引量:1
  • 6E. C. Sisler,M. S. Reid,S. F. Yang. Effect of antagonists of ethylene action on binding of ethylene in cut carnations[J] 1986,Plant Growth Regulation(3):213~218 被引量:1

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