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首页> 外文期刊>Molecular biotechnology >Expression of Cry1Ac in Transgenic Tobacco Plants Under the Control of a Wound-Inducible Promoter (AoPR1) Isolated from Asparagus officinalis to Control Heliothis virescens and Manduca sexta
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Expression of Cry1Ac in Transgenic Tobacco Plants Under the Control of a Wound-Inducible Promoter (AoPR1) Isolated from Asparagus officinalis to Control Heliothis virescens and Manduca sexta

机译:Cry1Ac在从芦笋中分离的伤口诱导型启动子(AoPR1)的控制下在转基因烟草中的表达,以控制棉铃虫和六倍体

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Expression of cry1Ac gene from Bacillus thuringiensis (Bt) was evaluated under the control of a wound-inducible AoPR1 promoter from Asparagus officinalis in transgenic tobacco plants. The leaves of transgenic plants were mechanically wounded to evaluate the activity of the AoPR1 promoter in driving the expression of Cry1Ac protein at the wound site. Our results indicate that mechanical wounding of transgenic plants was effective in inducing the expression of Cry1Ac protein. As a result of this induction, the accumulated levels of Cry1Ac protein increased during 6-72 h post-wounding period. The leaves of transgenic tobacco plants were evaluated for resistance against Heliothis virescens and Manduca sexta in insect bioassays in two different ways. The detached tobacco leaves were either fed directly to the insect larvae or they were first mechanically wounded followed by a 72 h post-wounding feeding period. Complete protection of mechanically wounded leaves of transgenic plants was observed within 24 h of the bioassay. The leaves of transgenic plants fed directly (without pre-wounding) to the larvae achieved the same level of protection between 24 and 72 h of the bioassay.
机译:在转基因烟草植物中,在来自芦笋的伤口诱导型AoPR1启动子的控制下,评估了苏云金芽孢杆菌(Bt)的cry1Ac基因的表达。机械损伤转基因植物的叶子,以评估AoPR1启动子在伤口部位驱动Cry1Ac蛋白表达的活性。我们的结果表明,转基因植物的机械损伤可有效诱导Cry1Ac蛋白的表达。这种诱导的结果是,在伤后6-72小时内,Cry1Ac蛋白的累积水平增加。在昆虫生物测定法中,以两种不同的方式评估了转基因烟草植物的叶片对Heliothis virescens和Manduca sexta的抗性。将分离的烟叶直接喂食昆虫幼虫,或者先对其进行机械创伤,然后在伤后72小时喂食。在生物测定法的24小时内,观察到转基因植物的机械伤叶片得到了完全保护。直接(无需预先伤口处理)喂食幼虫的转基因植物叶片在生物测定的24至72小时内达到了相同的保护水平。

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