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PCR Based Detection of Phellinus linteus using Specific Primers Generated from Universal Rice Primer (URP) Derived PCR Polymorphic Band

机译:使用从通用水稻引物(URP)衍生的PCR多态性条带产生的特异性引物进行基于PCR的桑黄检测

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This study was carried out to develop specific primers for PCR detection of Phellinus linteus . Diverse genomes of 15 Phellinus spp. including five Phellinus linteus isolates were fingerprinted by Primer Universal rice primer (URP)1F. The URP-PCR pattern differentiated P. linteus isolates from other phellinus spp. A polymorphic band (2.8 kb), which is unique for P. linteus isolates, was isolated and sequenced. Twenty four-oligonucleotide primer pairs were designed based on information of DNA sequence. The primer set (PLSPF2/PLSPR1) amplified single band (2.2 kb) of expected size with genomic DNA from seven Phellinus linteus , but not with that of other Phellinus species tested. The primers could be used identically in both DNA samples from mycelium and fruit bodies. This specific primers could offer a useful tool for detecting and identifying P. linteus rapidly.
机译:进行这项研究以开发特异性引物,用于PCR检测桑黄。 15个桑黄属物种的不同基因组。 Primer Universal水稻引物(URP)1F对包括五个桑黄分离株的指纹图谱进行了指纹分析。 URP-PCR模式区分了亚麻假单胞菌与其他百日草属的菌种。分离和测序了多形性条带(2.8 kb),这对于亚麻状假单胞菌分离物是唯一的。根据DNA序列信息设计了二十四个寡核苷酸引物对。引物组(PLSPF2 / PLSPR1)用来自七个桑黄的基因组DNA扩增了预期大小的单条带(2.2 kb),但未检测到其他桑黄种的扩增。这些引物可用于菌丝体和子实体的DNA样品中。这种特异的引物可以为快速检测和鉴定亚麻假单胞菌提供有用的工具。

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