Gopi C, Ponmurugan P
Department of Biotechnology, KS Rangasamy College of Technology, Tiruchengode 637 209, Namakkal District, Tamilnadu, India.
J Biotechnol. 2006 Nov 1;126(2):260-4. doi: 10.1016/j.jbiotec.2006.04.033. Epub 2006 Jun 8.
A effective protocol for complete plant regeneration via somatic embryogenesis has been developed for Ocimum basilicum L. Callus was initiated from leaf explant of young plant on supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D) 1.0 mg l(-1), 3% sucrose and 0.9% agar. The calli showed differentiation of globular structure embryos when transferred to MS medium containing 2,4-D 0.5 mg l(-1) and BAP 1.0 mg l(-1). The maximum globular structure embryos were further enlarged and produced somatic embryos in MS basal medium supplemented with BAP 1.0 mg l(-1)+NAA 1.0 mg l(-1) + KN 0.5 mg l(-1). Continued formation of globular embryo and germination of embryos occurred in this medium. Complete plantlets were transferred onto specially made plastic cup containing soilrite followed by their transfer to the garden soil. Survival rate of the plantlets under ex vitro condition was 80%.
已开发出一种通过体细胞胚胎发生实现罗勒完全植株再生的有效方案。愈伤组织从幼嫩植株的叶片外植体开始诱导,培养基中添加1.0毫克/升的2,4 - 二氯苯氧乙酸(2,4 - D)、3%蔗糖和0.9%琼脂。当将愈伤组织转移到含有0.5毫克/升2,4 - D和1.0毫克/升苄氨基嘌呤(BAP)的MS培养基上时,愈伤组织表现出球形结构胚的分化。最大数量的球形结构胚在添加了1.0毫克/升BAP + 1.0毫克/升萘乙酸(NAA)+ 0.5毫克/升激动素(KN)的MS基本培养基中进一步扩大并产生体细胞胚。在该培养基中持续形成球形胚并发生胚的萌发。完整的小植株被转移到装有园艺蛭石的特制塑料杯中,随后再转移到园土中。小植株在离体条件下的成活率为80%。