Plant Cell Biology Lab., Genetic Engineering Research Institute, KIST, P.O. Box 17, 305-606, Taedok Science Town, Taejon, Korea.
Plant Cell Rep. 1994 Mar;13(6):319-22. doi: 10.1007/BF00232629.
A system for high frequency plant regeneration from cell suspension cultures in Catharanthus roseus is described. Calli were obtained from anthers cultured on Murashige and Skoog's medium supplemented with 1 mgl(-1) α-naphthaleneacetic acid and 0.1 mgl(-1) kinetin. After the second subculture on solid medium, embryogenic callus was identified and transferred to liquid medium to initiate suspension cultures. Cells dispersed finely in the medium were subcultured at 14-day intervals. Upon plating onto the basal medium, yellowish compact colonies proliferated from the cells and more than 80% of them gave rise to somatic embryos. Subsequently, plantlets developed from the embryos. Both the plantlets and the source plants showed the normal somatic chromosome number of 2n=2x=16.
描述了一种从长春花细胞悬浮培养物中进行高频植物再生的系统。愈伤组织是从在添加了 1 mgl(-1) α-萘乙酸和 0.1 mgl(-1)激动素的 Murashige 和 Skoog 培养基上培养的花粉中获得的。在第二次固体培养基培养后,鉴定出胚性愈伤组织,并将其转移到液体培养基中以启动悬浮培养。在培养基中分散良好的细胞每 14 天进行一次继代培养。在接种到基础培养基上后,黄色致密的菌落从细胞中增殖,其中超过 80%的菌落产生体细胞胚。随后,从胚中发育出植株。植株和来源植株均显示出正常的体细胞染色体数 2n=2x=16。