本研究在探討蝴蝶蘭根組織培養明確之配方。結果摘錄如下:1.蝴蝶蘭根經B5無機鹽及有機鹽,100mg/l myo-inositol,30g/l蔗糖,5mg/l Naphthaleneacetic acid(NAA),10mg/l 6-furfurylaminopurine(Kinetin)的培養基(pH5.5)誘導,得癒合組織及芽球相似物突起。2.芽球相似物繼代培養於相同配方的固態培養基6個月後形成蝴蝶蘭幼植株。3.芽球相似物僅能在根尖部位形成。4.照光與未照光處理對芽球相似物之誘導均未有顯著之影響。
This paper describes an efficient method of clonal propagation through Phal aenopsis root cultued in vitro. The result as summaried as follows: Calli and protocorm like bodies (PLB) were induced from root tip by using Gam borg's B5 basal medium with 100mg/l myo-inositol, 30,000mg/l sucrose, 5mg/l NAA and 10mg/l kinetin. The pH was adjusted to 5.5. In similar solid medium, the PLB were then developed into baby phalaenopsis plants in 6 months. The formation ability of PLB was only on root tip. There is no significant variation between light and dark treatment.