Plant Tissue Culture Laboratory, Department of Botany, Institute of Biosciences, University of São Paulo, C. P. 11461-05499, São Paulo, Brasil.
Planta Med. 1988 Apr;54(2):157-60. doi: 10.1055/s-2006-962377.
A micropropagation method for STEVIA REBAUDIANA plants was established by culturing young leaves of adult plants on medium containing 6-benzyladenine (BA) (2.0 mg/l) in the light or BA (2.0 mg/l) plus 1-naphthaleneacetic acid (NAA) (2.0 mg/l) in the dark. An open-ended system was obtained by transfer of the regenerating material to medium containing BA (0.1 mg/l), with continuous subculture and isolation of suitable shoots. Auxin addition to the rooting medium (especially at 0.1 mg/l 3-indolebutyric acid - IBA) favored root formation and improved EXTRA VITRUM plant survival. Regenerated plants transferred to the soil were uniform and cytological observation in root tip cells showed normal chromosome number (2n = 22). Cultures treated with colchicine originated altered plants.
建立了甜叶菊(Stevia rebaudiana)的微繁殖方法,通过在含有 6-苄基腺嘌呤(BA)(2.0mg/L)的培养基上培养成年植株的幼叶,在光照下或在黑暗中添加萘乙酸(NAA)(2.0mg/L)和 BA(2.0mg/L)。通过将再生材料转移到含有 BA(0.1mg/L)的培养基中,进行开放式系统的获得,进行连续的继代培养和合适芽的分离。在生根培养基中添加生长素(特别是 0.1mg/L 的吲哚丁酸 - IBA)有利于根的形成,并提高了离体植物的存活率。转移到土壤中的再生植物是均匀的,根尖细胞的细胞学观察显示正常的染色体数目(2n=22)。用秋水仙碱处理的培养物产生了变异的植物。