首页> 外文期刊>Physiology and Molecular Biology of Plants >Development of an efficient in vitro plant regeneration sys amenable to Agrobacterium- mediated transformation of a recalcitrant grain legume blackgram (Vigna mungo L. Hepper)
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Development of an efficient in vitro plant regeneration sys amenable to Agrobacterium- mediated transformation of a recalcitrant grain legume blackgram (Vigna mungo L. Hepper)

机译:开发一种适合农杆菌介导的顽固性豆科植物豆科黑麦草的高效体外植物再生系统(Vigna mungo L. Hepper)

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摘要

An efficient, rapid and direct multiple shoot regeneration system amenable to^gro^ac/en'wm-mediated transformation from primary leaf with intact petiole of blackgram {Vigna mungo) is established for the first time. The effect of the explant type and its age, type and concentration of cytoki-nin and auxin either alone or in combination and genotype on multiple shoot regeneration efficiency and frequency was optimized. The primary leaf explants with petiole excised from 4-day-old seedlings directly developed multiple shoots (an average of 10 shoots/ explant) from the cut ends of the petiole in 95 % of the cultures on MSB (MS salts and B5 vitamins) medium containing 1.0 uM 6-benzylaminopurine. Elongated (2-3 cm) shoots were rooted on MSB medium with 2.5 uM indole-butyric acid and resulted plantlets were hardened and established in soil, where they resumed growth and reached maturity with normal seed set. The regenerated plants were morphologically similar to seed-raised plants and required 8 weeks time from initiation of culture to establish them in soil. The regeneration competent cells present at the cut ends of petiole are fully exposed and are, thus, easily accessible to Agrobacterium, making this plant regeneration protocol amenable for the production of transgenic plants. The protocol was further successfully used to develop fertile transgenic plants of blackgram using Agrobacterium tumefaciens strain EHA 105 carrying a binary vector pCAMBIA2301 that contains a neomycin phosphotransferase gene(nptU) and a |3-glucuronidase (GUS) gene (uidA) interrupted with an intron.The presence and integration of transgenes in putative T0 plants were confirmed by polymerase chain reaction (PCR) and Southern blot hybridization, respectively. The transgenes were inherited in Mendelian fashion in T! progeny and a transformation frequency of 1.3 % was obtained. This protocol can be effectively used for transferring new traits in blackgram and other legumes for their quantitative and qualitative improvements.
机译:首次建立了一种有效,快速,直接的多芽再生系统,该系统应能从具有完整的黑穗病叶柄(Vigna mungo)的初生叶片进行gro / ac / en'wm介导的转化。优化了外植体类型及其年龄,单独或组合的细胞分裂素和生长素的类型和浓度以及基因型对多枝再生效率和频率的影响。在95%的MSB(MS盐和B5维生素)培养基上,从4天大的幼苗上切下的叶柄的初生叶外植体直接从叶柄的切端发育出多芽(平均10枝/外植体)。含有1.0μM的6-苄基氨基嘌呤。将伸长的(2-3 cm)芽根植于含2.5 uM吲哚丁酸的MSB培养基上,使所得的小植株变硬并在土壤中定植,恢复正常生长并恢复正常种子的成熟状态。再生的植物在形态上与种子培养的植物相似,并且从培养开始需要8周的时间才能在土壤中建立它们。存在于叶柄切端的再生感受态细胞被充分暴露,因此土壤杆菌很容易接近,从而使该植物再生方案适合生产转基因植物。该协议进一步成功地用于携带根癌农杆菌菌株EHA 105的黑麦草可育转基因植物的发育,该菌株携带二元载体pCAMBIA2301,该载体包含新霉素磷酸转移酶基因(nptU)和被内含子中断的| 3-葡萄糖醛酸苷酶(GUS)基因(uidA)推定的T0植物中转基因的存在和整合分别通过聚合酶链反应(PCR)和Southern印迹杂交来证实。转基因以孟德尔方式在T!中继承!后代,转化频率为1.3%。该协议可以有效地用于在黑豆科动物和其他豆类中转移新的性状,以改善其数量和质量。

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