Monsanto Agricultural Company, 700 Chesterfield Village Parkway, 63198, St. Louis, MO, USA.
Plant Cell Rep. 1986 Apr;5(2):150-4. doi: 10.1007/BF00269257.
A procedure for the regeneration of fertile plants by organogenesis from tissue cultures of soybeans, Glycine max is described. Seeds were germinated on reduced inorganic salt MS medium containing 5μM BA. Cotyledonary nodes were excised and cultured on the same medium. Presence of BA in the medium during seed germination and culture of nodal explants was required for multiple shoot and shoot-bud formation. Histological analyses established the de novo nature of shoot regeneration. Separate reduction of the concentration of inorganic salts or substitution of sucrose for fructose during culture had minimal effects on the regeneration response. Conversely, if the BA was reduced, the inhibition response could not be overcome by increased salt concentration or altered carbon source.
描述了一种通过大豆(Glycine max)组织培养的器官发生来再生可育植物的方法。种子在含有 5μM BA 的低无机盐 MS 培养基上发芽。切取子叶节并在相同的培养基上培养。在种子发芽和节点外植体培养过程中,培养基中存在 BA 是产生多个芽和芽的必需条件。组织学分析确立了芽再生的从头开始性质。在培养过程中,单独降低无机盐的浓度或用果糖代替蔗糖对再生反应的影响最小。相反,如果降低 BA 的浓度,则增加盐浓度或改变碳源都无法克服抑制反应。