Bespalhok J C F, Hattori K
School of Agriculture, Nagoya University, Chikusa ku, Nagoya, Japan 464-01, , , , , , JP.
Plant Cell Rep. 1998 Aug;17(11):870-875. doi: 10.1007/s002990050500.
Embryogenic callus and somatic embryos were induced from cotyledonary explants of African marigold (Tagetes erecta L.). Cotyledons were first cultured on MS medium supplemented with 2.0 mg l 2,4-D and 0.2 mg l kinetin. After 5 weeks, calli were transferred to MS medium supplemented with 0.02 mg l thidiazuron where compact embryogenic callus developed. Friable embryogenic callus developed when the compact embryogenic callus was transferred to medium containing 2,4-D and subcultured every 2 weeks. Friable embryogenic callus has been maintained for more than 2 years without losing the capacity to generate embryos. Embryo development was obtained when friable embryogenic callus was transferred to MS medium supplemented with 3 mg l ABA and 60 g l sucrose. The addition of 10-30 mM L-glutamine improved embryo development.
从非洲万寿菊(孔雀草)的子叶外植体诱导出胚性愈伤组织和体细胞胚。子叶首先在添加了2.0毫克/升2,4 - D和0.2毫克/升激动素的MS培养基上培养。5周后,将愈伤组织转移到添加了0.02毫克/升噻苯隆的MS培养基上,在此培养基上形成了致密胚性愈伤组织。当致密胚性愈伤组织转移到含有2,4 - D的培养基上并每2周继代培养一次时,形成了易碎胚性愈伤组织。易碎胚性愈伤组织已保持了2年多,仍具有产生胚的能力。当易碎胚性愈伤组织转移到添加了3毫克/升脱落酸和60克/升蔗糖的MS培养基上时,获得了胚的发育。添加10 - 30毫摩尔L - 谷氨酰胺可改善胚的发育。