首页> 外文期刊>Journal of biochemical and molecular toxicology >Determining the involvement of two aminopeptidase Ns in the resistance of Plutella xylostella to the Bt toxin Cry1Ac: cloning and study of in vitro function.
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Determining the involvement of two aminopeptidase Ns in the resistance of Plutella xylostella to the Bt toxin Cry1Ac: cloning and study of in vitro function.

机译:确定两个氨基肽酶Ns在小菜蛾对Bt毒素Cry1Ac的抗性中的参与:克隆和体外功能研究。

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摘要

The cloning, expression in vitro, and characterization of two aminopeptidase Ns (APN5s and APN2s) isolated from the midgut of Cry1Ac-resistant (R) and susceptible (S) strains of Plutella xylostella larvae are presented in this paper. The deduced amino acid sequences of APN5s included C-terminal GPI-modification sites, the gluzincin aminopeptidase motif GATEN, and three N-glycosylated sites; those of APN2s had no GPI-modification sites, had gluzincin aminopeptidase motif GAMEN, and had four N-glycosylated sites. O-glycosylated sites were not predicted for either APN. Because APN2R and APN2S cDNAs contained the same nucleotides, only full-length cDNAs encoding APN5R and APN5S were expressed in Trichoplusia ni cells. Far-Western blotting showed that the expressed receptor APN5 bound to the Cry1Ac toxin. An enzyme-specific activity experiment also showed that APN5 genes were expressed in T. ni cells. ELISA revealed no differences in the binding of expression proteins from the resistant and susceptible strain with Cry1Ac.
机译:本文介绍了从小菜蛾小虫的Cry1Ac抗性和易感性菌株中肠分离的两个氨基肽酶Ns(APN5和APN2s)的克隆,体外表达和鉴定。推导的APN5s的氨基酸序列包括C端GPI修饰位点,葡聚糖锌肽酶基序GATEN和三个N-糖基化位点。 APN2的那些没有GPI修饰位点,有gluzincin氨基肽酶基序GAMEN,并且有四个N-糖基化位点。 APN均未预测O-糖基化位点。由于APN2R和APN2S cDNA包含相同的核苷酸,因此在Trichoplusia ni细胞中仅表达了编码APN5R和APN5S的全长cDNA。远西印迹显示,表达的受体APN5与Cry1Ac毒素结合。酶特异性活性实验还显示APN5基因在T.ni细胞中表达。 ELISA显示抗性和易感菌株与Cry1Ac的表达蛋白结合没有差异。

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