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用Nitsch及Nitsch培养基添加吲哚乙酸,细胞激动素和1p.p.m2.4—D,在pH5.~5条件下培养GT_1无性系实生苗茎切片,所获愈伤组织生长良好。从新的绿色愈伤组织切片看出:橡胶状粒子已经形成。应用分化愈伤组织的同一培养基也形成了根。
Indoleacetic acid, cytokinin and 1p.p.m2.4-D were added into Nitsch and Nitsch medium to cultivate stems of GT1 clones at pH5. ~ 5, and the callus obtained grew well. Seen from the new green callus slices: rubbery particles have been formed. The same medium to which differentiated callus is applied also forms roots.