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用于特异性和灵敏检测葡萄根癌土壤杆菌菌株的新型SCAR引物。

Novel SCAR primers for specific and sensitive detection of Agrobacterium vitis strains.

作者信息

Lim Seon Hwa, Kim Jong Gun, Kang Hee Wan

机构信息

Graduate School of Biotechnology and Information Technology, College of Agriculture, Hankyong National University, Ansung 456-749, Republic of Korea.

出版信息

Microbiol Res. 2009;164(4):451-60. doi: 10.1016/j.micres.2007.02.006. Epub 2007 Apr 30.

Abstract

An Agrobacterium vitis-specific DNA fragment (pAVS3) was generated from PCR polymorphic bands amplified by primer URP 2R. A. vitis specificity of this fragment was confirmed by Southern hybridization with genomic DNA from different Agrobacterium species. Sequence-characterized amplified region (SCAR) markers were developed for A. vitis specific detection, using 24-mer oligonucleotide primers designed from the flanking ends of the 670bp insert in pAVS3. The SCAR primers amplified target sequences only from A. vitis strains and not from other Agrobacterium species or other bacterial genera. First round PCR detected bacterial cells between 5x10(2) and 1x10(3)cfu/ml and the detection sensitivity was increased to as few as 2cfu/ml by nested PCR. This PCR protocol can be used to confirm the potential presence of infectious A. vitis strains in soil and furthermore, can identify A. vitis strains from naturally infected crown galls.

摘要

利用引物URP 2R扩增出的PCR多态性条带构建了一个葡萄土壤杆菌特异性DNA片段(pAVS3)。通过与不同土壤杆菌属的基因组DNA进行Southern杂交,证实了该片段对葡萄土壤杆菌的特异性。利用从pAVS3中670bp插入片段侧翼设计的24碱基寡核苷酸引物,开发了用于葡萄土壤杆菌特异性检测的序列特征性扩增区域(SCAR)标记。SCAR引物仅能从葡萄土壤杆菌菌株中扩增出目标序列,而不能从其他土壤杆菌属或其他细菌属中扩增出来。第一轮PCR能检测出浓度在5×10²至1×10³ cfu/ml之间的细菌细胞,通过巢式PCR,检测灵敏度可提高至低至2 cfu/ml。该PCR方案可用于确认土壤中感染性葡萄土壤杆菌菌株的潜在存在,此外,还可从自然感染的冠瘿中鉴定出葡萄土壤杆菌菌株。

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