利用水稻通用引物(urp)对不同菌株基因组进行PCR指纹图谱分析

Hee-Wan Kang
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引用次数: 2

摘要

从水稻基因组重复序列中开发了20个引物,其中20个引物为水稻通用引物(URP)。URP-PCR方案采用严格的PCR,在整个热循环反应中采用高退火温度,重现性高。在PCR条件下,每个URP引物都能产生不同细菌基因组的特征指纹图谱。将rp - pcr应用于24株胡萝卜乳杆菌亚种,验证了该方法的普遍适用性。胡萝卜菌、葡萄农杆菌41株、黄单胞菌3株、假单胞菌5株、根瘤菌等植物致病菌、人、动物致病菌包括大肠杆菌6株、沙门氏菌4株、分枝杆菌7株、流产蓝杆菌3株。另外,从高温堆肥中随机分离出嗜热细菌,并对其URP-PCR多态性进行遗传亲缘性分析。利用URP引物的PCR方法将有助于研究不同原核生物基因组的DNA多样性,特别是在种间和种内水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PCR FINGERPRINTING OF DIVERSE GENOMES FROM BACTERIAL STRAINS USING UNIVERSAL RICE PRIMER (URP)
Twenty primers of 20 mer referred to universal rice primer (URP) were developed from a repetitive sequence of rice genome. URP-PCR protocol employed stringent PCR with high annealing temperature throughout the thermo-cycling reaction, giving high reproducibility. Under the PCR condition, each single URP primer produced characteristic fingerprints from diverse genomes of bacterial species. The universal application of URP-PCR was demonstrated by applying it to 24 strains from Pectobacterium carotovoum subsp. carotovorum, 41 Agrobacterium vitis strains, 3 Xanthomonas spp. 5 Pseudomonas spp, Rhizobium sp. plant pathogenic bacteria, human and animal pathogenic bacterial strains including 6 Escherichia coli, 4 Salmonella spp., 7 Mycobacterium spp and 3 Blucella abortus strains. In addition, thermophilic bacteria were randomly isolated form high temperature compost and their URP-PCR polymorphisms were characterized with genetic relatedness.  PCR approach using URP primers will be useful for studying DNA diversity of diverse prokaryotic genomes, especially at inter- and intra species levels.
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