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四棱豆茎段离体培养的研究
引用本文:刘国民,王立军.四棱豆茎段离体培养的研究[J].海南大学学报(自然科学版),1998,16(3):233-238.
作者姓名:刘国民  王立军
作者单位:海南大学农学院
摘    要:通过茎段离体培养,实现了四棱豆的快速无性繁殖.结果表明:(1)用浓H2SO4将其种子处理8min后再消毒接种可获得最高的发芽率;(2)在附加1.0mg/L6-BA的H培养基上,每粒种子平均可形成13个丛芽;(3)在增殖培养阶段,IBA浓度为1.0~2.0mg/L时对促进四棱豆离体茎段生根成苗的效果最为理想;(4)增殖培养阶段以采用H培养基的效果最为理想;(5)单独使用IBA时,即使其浓度高达4.0mg/L也只诱导离体茎段生根,绝大多数外植体不会产生愈伤组织,只有极少数外植体产生少量愈伤组织;低浓度的6-BA(0.5mg/L)或高浓度的6-BA(2.0mg/L)配以低浓度的IBA(0.25mg/L)反而会引起大多数离体茎段的基部产生大量愈伤组织.

关 键 词:四棱豆  快速繁殖  组织培养

Study on the Stem Segment Culture of Indies Goabean ( Psophocarpus tetragonolobus DC.) in Vitro
Liu Guomin,Wang Lijun,Qiu Yinghao.Study on the Stem Segment Culture of Indies Goabean ( Psophocarpus tetragonolobus DC.) in Vitro[J].Natural Science Journal of Hainan University,1998,16(3):233-238.
Authors:Liu Guomin  Wang Lijun  Qiu Yinghao
Abstract:This paper deals with the in vitro culture of the stem segment of Indies Goabean( Psophocarpus tetragonolobus DC.). The experimental results are as follows: (1)The highest germination rate could be obtained in the treatment that the seed was treated for 8 min with 98% sulfuric acid before sterilization and inoculation; (2) 13 clustered shoots per seed were formed on the H medium complemented with 1.0 mg/L 6-BA,averagely; (3) The effect on the rootage and germination of the axillary buds of the in vitro stem segements was the most ideal if the concentration of IBA ranges from 1.0 mg/L to 2.0 mg/L; (4) Among the four basic media tested in the multiplation culture, H medium was the most ideal; (5) If IBA is merely complemented, the rootage of the in vitro stem segments could only be induced, the callus could not be formed in the most explants, and only a few calli were formed in a few explants even the concentration of IBA was as high as 4.0 mg/L. Contrarily, a low concentration of 6-BA(0.5 mg/L), or a high concentration of 6-BA(2.0 mg/L) matching with a low concentration of IBA(0.25 mg/L) could result in the formation of lots calli in the most of the in vitro stem segments.
Keywords:Indies Goabean(  Psophocarpus tetragonolobus  DC  )  rapid propagation  tissue culture
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