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Development of a PCR-based method for identification of Tilletia indica, causal agent of Karnal bunt of wheat

机译:基于PCR的方法识别小麦identification虫病的病原体T虫

摘要

The polymerase chain reaction (PCR) was used to identify Tilletia indica, the causal agent of Karnal bunt of wheat. The method uses two sets of oligonucleotide primers developed by sequence analysis of cloned Dra I fragments of mitochondrial DNA of T. indica. The primer pair TI17M1 (5'-TCCCCTTGGATCAGAACGTA-3') and TI17M2 (5'- AGAAGTCTAACTCCCCCCTCT- 3'), derived from clone pTI-MD17, amplified a single 825-bp product from all isolates of T. indica and no products for other Tilletia species. In addition, the primer pair TI57M1 (5'- TTTTCCCTCTCTC-CTTTTTTCA-3') and TI57M2 (5'-AGCAAAGACAAAGTAGGCTTCC-3'), derived from clone pTI-MD57, produced a product of 118 bp which was unique to T. indica.
机译:聚合酶链反应(PCR)用于鉴定印度小麦的Karnal bunt的病原体Tilletia indica。该方法使用了通过对印度线粒体线粒体DNA的Dra I克隆片段进行序列分析而开发的两组寡核苷酸引物。源自克隆pTI-MD17的引物对TI17M1(5'-TCCCCTTGGATCAGAACGCG-3')和TI17M2(5'- AGAAGTCTAACTCCCCCCTCT-3')从印度T虫的所有分离株扩增了825 bp的单个产物,没有用于其他Tilletia物种。另外,衍生自克隆pTI-MD57的引物对TI57M1(5'- TTTTCCCTCTCTCTC-CTTTTTTCA-3')和TI57M2(5'-AGCAAAGACAAAGTAGGCTTCC-3')产生了118 bp的产物,这是印度T独有的。 。

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