Department of Botany, University of Rajasthan, 302 004, Jaipur, India.
Plant Cell Rep. 1995 Dec;15(3-4):227-31. doi: 10.1007/BF00193725.
Whole immature inflorescences at 4 different developmental stages (0.5, 1.0, 1.5, 2.0 cm in size) of different genotypes of Triticum aestivum and T. durum were cultured to see the morphogenetic responses on Murashige and Skoog's (MS) medium supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D) (2.5 mg/l). Very young inflorescences 0.5 and 1.0cm long formed embryogenic callus from their entire surface while 1.5 and 2.0 cm long inflorescences formed embryogenic callus from the basal spikelets and rachis only. This embryogenic callus was maintained by regular subcultures on MS medium with 2,4-D (2.5 mg/l) for more than a year. Plantlets were regenerated by transferring the embryogenic callus on hormone-free MS medium. Inflorescences (0.5 and 1.0 cm long) responded best in forming callus as well as plantlets at a very high frequency. Variation in response was observed amongst the genotypes but the qualitative response of formation of embryogenic callus and later regeneration of plantlets was observed from all the genotypes. Immature young inflorescence explants could provide a suitable material for particle gun mediated genetic transformation in wheat.
不同基因型的小麦(Triticum aestivum 和 T. durum)在四个不同发育阶段(0.5、1.0、1.5、2.0cm 大小)的未成熟花序整体在添加 2,4-二氯苯氧乙酸(2,4-D)(2.5mg/l)的 Murashige 和 Skoog (MS)培养基上进行培养,以观察其形态发生反应。非常年轻的花序 0.5 和 1.0cm 长的花序从整个表面形成胚胎发生愈伤组织,而 1.5 和 2.0cm 长的花序仅从基部小穗和穗轴形成胚胎发生愈伤组织。这种胚胎发生愈伤组织通过定期在含有 2,4-D(2.5mg/l)的 MS 培养基上进行继代培养来维持,时间超过一年。通过将胚胎发生愈伤组织转移到无激素的 MS 培养基上再生植株。花序(0.5 和 1.0cm 长)在形成愈伤组织和植株方面的反应最佳,频率非常高。不同基因型之间观察到反应的变化,但所有基因型都观察到形成胚胎发生愈伤组织和随后再生植株的定性反应。未成熟的幼嫩花序外植体可为小麦的粒子枪介导遗传转化提供合适的材料。