FIELD: biotechnology. SUBSTANCE: method involves using zygote embryos from yew seeds of species Taxus cuspidata as explants. Callus tissue is cultured up to formation of somatic embryos and then to embryogenic callus preparing. The latter is passaged in liquid nutrient medium and cultured on Hamburg medium mB5 containing 2-4 ppm 2,4-D (2,4-dichlorophenoxyacetic acid) for cellular mass increase. Then culturing is continued on Murasige-Skoog Ms or Hamburg mB5 medium containing 1-2 ppm NAA (α--naphthylacetic acid) that stimulates the yield of the end product. The end product is isolated by extraction from somatic embryos at stage of callus culturing or from embryogenic callus at stage of disinfected embryos culturing. The end product can be isolated from cellular suspension mass and cultural fluid. EFFECT: increased yield of taxol and taxones. 7 cl, 7 dwg, 3 tbl, 11 ex
Authors
Dates
1998-10-27—Published
1994-07-06—Filed