首页 | 本学科首页   官方微博 | 高级检索  
   检索      


In vitro shoot tip multiplication of bambara groundnut [<Emphasis Type="Italic">Vigna subterranea</Emphasis> (L.) Verdc.]
Authors:Nakpalo Silué  Tchoa Koné  André Brahima Soumahoro  Mongomaké Koné
Institution:1.Laboratoire de Physiologie Végétale,UFR Biosciences, Université Félix Houphou?t Boigny,Abidjan 22,C?te d’Ivoire;2.Laboratoire de Biologie et Amélioration des Productions Végétales,UFR Sciences de la Nature, Université Nangui Abrogoua,Abidjan 02,C?te d’Ivoire
Abstract:A rapid, simple and efficient protocol for direct in vitro multiple shoot induction and plantlet recovery was achieved from shoot tip explants of Bambara groundnut Vigna subterranea (L.) Verdc.]. Shoot tips, were isolated from in vitro-grown seedlings and cultured on Murashige and Skoog basal medium (MS) containing Gamborg’ vitamins (B5) and supplemented with different concentrations of the plant growth regulators Thidiazuron (TDZ), N6-benzylaminopurine (BAP), Kinetin (KIN) and Adenine sulfate (ADS). TDZ 0.45 μM was found to be best for shoot multiplication with a mean of 11shoots per explant. Among the carbon sources tested, the best response in terms of mean number of shoots per explant was obtained with sucrose (11). The mean number of shoots per explant induced among the studied landraces of Bambara groundnut varied from 9 to 13. Individual shoots, aseptically excised, produced normal roots within 2 weeks on the basal MS medium supplemented with Indole Butyric Acid (IBA) or Naphthalene acetic acid (NAA). The highest number of roots per shoot and the longest roots were obtained on MS medium with 2 mg/L IBA. Rooted plantlets were successfully hardened under greenhouse conditions and subsequently established in the field conditions, with a recorded survival rate of 70 and 80?%, respectively. The transferred plants in the field were morphologically normal and fertile. This protocol can be efficiently used for mass propagation, germplasm preservation and probably also for gene transfer of Vigna subterranea (L.).
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号