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首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >Adventitious shoot regeneration of two dwarfing pear rootstocks and the development of a transformation protocol
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Adventitious shoot regeneration of two dwarfing pear rootstocks and the development of a transformation protocol

机译:两种矮化梨砧木的不定芽再生和转化方案的发展

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The ability to form adventitious shoots was investigated from in vitro produced leaves of the dwarfing pear rootstock BP10030 and the semi-dwarfing pear rootstock OHF333. To increase rooting ability, transformation of the rootstock BP10030 with the rolB gene was performed. For BP10030, 98% leaves gave rise to shoots on the medium containing 1 #mu#M NAA, 15 #mu#M TDZ and sucrose, and 88% from the medium with 0.1 #mu#M NAA, 5 #mu#M TDZ and sorbitol. For OHF333, the best result was obtained from the medium containing 0.1 #mu#M NAA, 1 #mu#M TDZ and sorbitol, using which 66% of leaves gave rise to shoots, whereas the regeneration percentage was generally low on the sucrose medium (0-22%). In the experiments where IBA was used as a substitute for NAA and CPPU as a substitute for TDZ on the sucrose medium, shoot regeneration of OHF333 was not improved. Scanning electron microscopy (SEM) observations on BP10030 revealed that meristem-like structures were already visible at day 8 after the beginning of the experiments and well-developed shoots appeared after one month. SEM also showed that shoots eventually formed. Transformation experiments on BP10030 using the published protocol failed. However, transformation based on the results from the regeneration tests was successful, indicating genotype differences and that a good protocol for adventitious shoot regeneration is necessary for a successful transformation. However, the transformation efficiency was low, suggesting that a good regeneration protocol cannot guarantee high transformation efficiency.
机译:从矮化梨砧木BP10030和半矮化梨砧木OHF333的体外生产叶片中研究了形成不定芽的能力。为了增加生根能力,用rolB基因转化了砧木BP10030。对于BP10030,98%的叶子在含有1#mu#M NAA,15#mu#M TDZ和蔗糖的培养基上长出芽,而88%的叶子从含有0.1#mu#M NAA,5#mu#M TDZ的培养基上长出芽。和山梨糖醇。对于OHF333,从含有0.1#mu#M NAA,1#mu#M TDZ和山梨糖醇的培养基中可获得最佳结果,使用66%的叶子可以生出芽,而在蔗糖培养基上再生百分比通常较低(0-22%)。在蔗糖培养基上使用IBA代替NAA和CPPU代替TDZ的实验中,OHF333的芽再生没有得到改善。在BP10030上进行的扫描电子显微镜(SEM)观察表明,在实验开始后的第8天已经可见分生组织样结构,一个月后出现了发育良好的芽。 SEM还显示最终形成了芽。使用已发布的协议在BP10030上进行转化实验失败。然而,基于再生测试结果的转化是成功的,表明基因型不同,并且不定芽再生的良好方案对于成功转化是必要的。但是,转化效率很低,表明良好的再生方案不能保证较高的转化效率。

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