REGENERATION AND TRANSFORMATION SYSTEM IN EGYPTIAN SWEET POTATO (Ipomoea batatas Lam.) CULTIVARS

N. Ali, M. Rashed, A. Abdel-Azeem, T. N. El-Din, E. Metry
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引用次数: 1

Abstract

Genetic transformation is considered as one of the most favorable options for improvement of crop traits. In this study the regeneration frequency and transformation system were established on the Egyptian sweet potato (Ipomoea batatas (L.) Lam.) cv. Abees and Mabruka. The effect of different hormone combinations and type of explant on shoot regeneration was evaluated. The regeneration percentages from Abees and Mabruka cv. 26.3 and 13.3%, respectively were obtained on Murashige and Skoog MS basal salt mixture + 1.0 mg/l BA + 30.0 g/l sucrose + 2.2 g/l Phytagel with Abees cv. and the same media was used for cv. Mabruka with only cytokinin type different as 5.0 Kin and shoots were rooted on MS medium + 30 g/l sucrose and 2.2 g/l Phytagel. The Agrobacterium-mediated and microprojectile bombardement transformation system were successfully introducing the reporter gus and selectable bar marker genes in the sweet potato explants under pressure of 900 and 1100 psi and microcarrier travel distance (6 and 9 cm). Incorporation and expression of the gus and bar genes into sweet potato plants were confirmed using polymerase chain reaction (PCR) and GUS histochemical assay. Several factors were found to be important for regeneration and transformation in sweet potato. The most effective factors were plant genotype and the type of explants. Co-cultivation time and optical density of the Agrobacterium suspension were also critical for sweet potato transformation. This work is an attempt to open the door for further genetic improvement of sweet potato using important agronomic traits.
埃及甘薯的再生转化体系品种
遗传转化被认为是作物性状改良的最有利选择之一。本研究建立了埃及甘薯(Ipomoea batatas, L.)的再生频率和转化体系。Lam)简历。蜜蜂和马布鲁卡。评价了不同激素组合和外植体类型对芽再生的影响。蜜蜂和马布鲁卡的再生率。在Murashige和Skoog MS基础盐+ 1.0 mg/l BA + 30.0 g/l蔗糖+ 2.2 g/l植酸酯的培养基上,Abees cv分别为26.3%和13.3%。同样的培养基也用于cv。在MS + 30 g/l蔗糖和2.2 g/l Phytagel的培养基上,细胞分裂素类型为5.0 Kin的Mabruka幼苗生根。农杆菌介导和微弹轰击转化系统在900和1100 psi压力和微载体移动距离(6和9 cm)条件下成功地将报告基因和选择棒标记基因导入甘薯外植体。采用聚合酶链反应(PCR)和gus组织化学方法证实了gus和bar基因在甘薯植株中的表达。研究发现了影响甘薯再生转化的几个重要因素。植物基因型和外植体类型是最有效的影响因素。农杆菌悬浮液的共培养时间和光密度也对红薯的转化至关重要。本研究为进一步利用甘薯重要农艺性状进行遗传改良打开了大门。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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