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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Cloning, characterization, expression analysis and inhibition studies of a novel gene encoding Bowman-Birk type protease inhibitor from rice bean
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Cloning, characterization, expression analysis and inhibition studies of a novel gene encoding Bowman-Birk type protease inhibitor from rice bean

机译:稻豆Bowman-Birk型蛋白酶抑制剂编码新基因的克隆,鉴定,表达分析及抑制研究

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This paper presents the first study describing the isolation; cloning and characterization of a full length gene encoding Bowman-Birk protease inhibitor (RbTI) from rice bean (Vigna umbellata). A full-length protease inhibitor gene with complete open reading frame of 327 bp encoding 109 amino acids was cloned from rice bean seeds using degenerate primer set. BlastP search revealed that the RbTI encoded amino acid of approx 13.0 kDa and shared 99% homology each with BBI from Phaseolus parvulus, Vigna trilobata and Vigna vexilata. Phylogenetic tree also showed close relationship of RbTI with BBI from other members of Leguminaceae family. RbTI gene was further confirmed as intronless (GenBank accession no. KJ159908). The secondary and 3D-structural models for the RbTI were predicted with homology modeling. qRT-PCR studies revealed the highest RbTI expression in the seeds nearing maturity, whereas the low expression of the gene was noticed in young leaves. The isolated RbTI was successfully expressed in Escherichia coli and the highest expression was recorded after 5.5 h of induction. Study on the inhibitory activity of expressed protein against the gut proteases of Hessian fly larvae revealed 87% inhibition. The novel RbTI gene will further broaden the pool of plant defense genes and could be an ideal choice for developing transgenic crops resistant to insect pests with high economic value. In addition, it has the potential to be used as a probe for selection of insect- and pathogen-resistant genotypes. (C) 2014 Elsevier B.V. All rights reserved.
机译:本文提出了第一个描述隔离的研究;稻米Vigna umbellata的Bowman-Birk蛋白酶抑制剂(RbTI)全长基因的克隆和鉴定。使用简并引物组从稻豆种子中克隆了一个完整的蛋白酶抑制剂基因,其全长327bp的开放阅读框编码109个氨基酸。 BlastP搜索显示,RbTI编码的氨基酸约为13.0 kDa,与小菜豆,三叶草和三叶草的BBI均具有99%的同源性。系统发育树还显示,RbTI与豆科其他成员的BBI密切相关。 RbTI基因被进一步确认为无内含子(GenBank登录号KJ159908)。 RbTI的二级和3D结构模型已通过同源性建模进行了预测。 qRT-PCR研究表明,接近成熟的种子中RbTI的表达最高,而在幼叶中发现该基因的低表达。分离的RbTI在大肠杆菌中成功表达,诱导5.5小时后记录到最高表达。对表达的蛋白对黑森州蝇幼虫肠道蛋白酶的抑制活性的研究表明其抑制率为87%。新的RbTI基因将进一步拓宽植物防御基因库,并且可能是开发具有高经济价值的抗虫害的转基因作物的理想选择。此外,它有潜力用作选择抗昆虫和病原体的基因型的探针。 (C)2014 Elsevier B.V.保留所有权利。

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