Bellettre A, Couillerot J-P, Vasseur J
Laboratoire de Physiologie Cellulaire et Morphogenèse Végétales, USTL-INRA, Université des Sciences et Technologies de Lille, F-59655 Villeneuve D'Ascq cedex, France Fax: +33-3-20336044 e-mail:
Plant Cell Rep. 1999 Nov;19(1):26-31. doi: 10.1007/s002990050705.
Direct somatic embryogenesis was induced in leaf cells of a Cichorium hybrid (Cichorium intybus L var. sativum×Cichorium endivia L. var. latifolia) through a two-step procedure. Leaf tissue explants were cultured for 5 days in M17 liquid medium supplemented with 30 mM sucrose and 330 mM glycerol (M17S30Gly330 medium). Synchronised divisions of embryogenic cells occurred after transfer for 7 days onto glycerol free-medium (M17S30). By doubling the sucrose concentration (60 mM) in the presence of glycerol (M17S60Gly330) during the induction step, embryogenesis increased and the length of the induction step was reduced from 5 to 4 days. Compared to sucrose, glycerol as carbon source during the induction and the expression steps had an inhibitory effect on the embryogenic response. During culture, glycerol was not detected in M17S60 medium and was at a low level in leaf fragments incubated in this medium. Initially supplied as an osmoticum, glycerol disappeared from M17S60Gly330 medium during the 4-day induction period and penetrated into the tissues where most of was metabolised. Furthermore, glycerol modified it carbohydrate metabolism, particularly during the induction period of embryogenesis. Sucrose hydrolysis was affected in the medium and sucrose and hexose contents in tissues were higher than in glycerol-free medium. The effects of glycerol as osmoticum and as a molecule itself are discussed.
通过两步法在菊苣杂交种(菊苣var. sativum×苦苣var. latifolia)的叶片细胞中诱导直接体细胞胚胎发生。将叶片组织外植体在添加了30 mM蔗糖和330 mM甘油的M17液体培养基(M17S30Gly330培养基)中培养5天。在转移到无甘油培养基(M17S30)7天后,胚性细胞发生同步分裂。在诱导步骤中,通过在甘油存在下将蔗糖浓度加倍(60 mM)(M17S60Gly330),胚胎发生增加,诱导步骤的长度从5天减少到4天。与蔗糖相比,甘油在诱导和表达步骤中作为碳源对胚胎发生反应有抑制作用。在培养过程中,M17S60培养基中未检测到甘油,在该培养基中培养的叶片片段中甘油含量较低。最初作为渗透剂提供的甘油在4天的诱导期内从M17S60Gly330培养基中消失,并渗透到组织中,其中大部分被代谢。此外,甘油改变了其碳水化合物代谢,特别是在胚胎发生的诱导期。培养基中的蔗糖水解受到影响,组织中的蔗糖和己糖含量高于无甘油培养基。讨论了甘油作为渗透剂和作为分子本身的作用。