首页> 外文期刊>农业科学与技术(英文版) >野桑蚕中肠组织cDNA文库的构建及丝氨酸蛋白酶基因片段的克隆与序列分析
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野桑蚕中肠组织cDNA文库的构建及丝氨酸蛋白酶基因片段的克隆与序列分析

机译:Construction of Midgut Tissue-Specific cDNA Library of Bombyx mandarina M. and Isolation and Sequence Analysis of Serine Protease Gene Fragment野桑蚕中肠组织cDNA文库的构建及丝氨酸蛋白酶基因片段的克隆与序列分析

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[Objective] The aim of the study is to construct cDNA library of midgut tissue of wild silkworm and isolate the serine protease gene. [Method] The midgut tissue-specific cDNA library of wild silkworm was constructed via cDNA Library Construction Kit (TaKaRa), then the serine protease gene was cloned via sequencing of the yielded cDNA library. [Result] The titer of cDNA library reached 6.2×105 pfu/ml, average insert size was about 1.2 kb. The serine protease gene cDNA fragment was obtained from colony sequencing (Accession No: EU672968). The nucleotide sequence of the cloned 854 bp fragment encodes 284 amino acid residues. Homology analyses showed some homology between putative amino acid sequence of the cloned fragment and amino acid sequences of serine proteases from other ten insects. [Conclusion] The results may avail to reveal the resistance of silkworm and wild silkworm to exotic intrusion.
机译:[目的]构建野生蚕中肠组织的cDNA文库,并分离丝氨酸蛋白酶基因。 [方法]通过cDNA文库构建试剂盒(Takara)构建野生蚕的中肠组织特异性cDNA文库,然后通过产量cDNA文库测序克隆丝氨酸蛋白酶基因。 [结果] cDNA文库滴度达到6.2×105 pfu / ml,平均嵌件尺寸约为1.2 kB。丝氨酸蛋白酶基因cDNA片段由菌落测序获得(加入NO:EU672968)。克隆的854bp片段的核苷酸序列编码284个氨基酸残基。同源性分析显示了来自其他十种昆虫的克隆片段和丝氨酸蛋白酶氨基酸序列的推定氨基酸序列之间的一些同源性。 [结论]结果可能有利于揭示蚕和野生蚕的抗性对异国侵扰。

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