【目的】 分析预测申克孢子丝菌cDNA中编号为Locus_168_Contig_1序列编码的基因及蛋白质结构、功能特征,并进行分子克隆。 【方法】 利用NCBI及Expasy网站提供的BLASTx、SignalIP、InterPro Scan等生物信息学软件分析其序列,判断其是否为全长编码序列、同源序列名称,并分析其结构、定位及功能等;将其中的全长编码区利用PCR方法进行扩增后克隆到pET-30a(+)载体,测序验证。 【结果】 该序列是亚精胺合成酶(SPDS)的同源基因,全长序列为1062 bp ...
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