...
首页> 外文期刊>日本作物学会紀事 >Effect of seed preconditioning and culture under different light intensities on callus induction and regeneration in excised cotyledon cultures of mungbean (Vigna radiata (L.) Wilczek).
【24h】

Effect of seed preconditioning and culture under different light intensities on callus induction and regeneration in excised cotyledon cultures of mungbean (Vigna radiata (L.) Wilczek).

机译:种子预处理和培养对不同光强度下的疗效诱导和再生术治疗豆腐(Vigna radiata(L.)Wilczekk)中的愈伤组织诱导和再生。

获取原文
获取原文并翻译 | 示例
           

摘要

V. radiata cv. PAEC5 seeds were soaked in sterile distilled water for (a) 16 or (b) 48 h, soaked in sterile distilled water for 16 h then placed on (c) plain agar, (d) Murashige and Skoog (MS) medium or (e) MS medium + benzyladenine (BA) for 48 h, or (f) placed on plain agar for 16 h. The cultures were incubated under full light (50 鎚ol m-2 s-1) or low light (8.5 鎚ol m-2 s-1). Cotyledons of the preconditioned seeds were excised and cultured on MS basal medium, MS medium + NAA + BA or B5 basal medium + NAA + BA. After 3 weeks of culture, (a), (b) and (c) had a lower percentage of callus formation than the other treatments, except in MS medium. Treatments (d), (e) and (f) had the highest callus growth ratings, particularly in the BA-supplemented media and under low light. Plantlet regeneration in B5 basal medium + NAA + BA was relatively higher than the other regeneration media under full light, while MS basal medium and MS basal medium + NAA + BA had higher plantlet regeneration under low light.
机译:V. radiata cv。将PAEC5种子浸泡在无菌蒸馏水中(a)16或(b)48 h,浸泡在无菌蒸馏水中,以16小时,然后置于(c)普通琼脂(d)murashige和skoog(ms)培养基或(e )MS培养基+苄基苯胺(BA)48小时,或(f)放置在平原琼脂上16小时。将培养物在全光(50℃M-2 S-1)或低光(8.5℃M-2 S-1)下孵育。切除预处理种子的子叶并在MS基础培养基中,MS培养基+ NAA + BA或B5基础培养基+ NAA + Ba培养。在培养3周后,(a),(b)和(c)的愈伤组织形成百分比比其他治疗较低,除了MS培养基。治疗(D),(E)和(F)具有最高的愈伤组织生长评级,特别是在BA补充培养基和低光下。 B5基础培养基+ NAA + BA中的小植物再生比全光下的其他再生培养基相对高,而MS基础培养基和MS基础培养基+ NAA + BA在低光下具有更高的植物再生。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号