Poupart P, Coene M, Van Heuverswyn H, Cocito C
Microbiology & Genetics Unit, University of Louvain, Medical School, Brussels, Belgium.
J Clin Microbiol. 1993 Jun;31(6):1601-5. doi: 10.1128/jcm.31.6.1601-1605.1993.
A species-specific recombinant clone (F57) was obtained from a genomic library of Mycobacterium paratuberculosis in the transcription vector pGem 3Z. This clone proved to be specific for all mycobacteria tested, including M. avium, and was able to recognize all of the tested M. paratuberculosis strains isolated from animals and humans (patients with Crohn's disease). The F57 insert was sequenced and a segment of 620 bp with a G + C content of 58.9% was identified. Comparison of the sequence with sequences in the EMBL and UGEN data banks revealed the uniqueness of the F57 sequence, which had no resemblance to other known genes.
从副结核分枝杆菌基因组文库中,在转录载体pGem 3Z中获得了一个物种特异性重组克隆(F57)。该克隆被证明对所有测试的分枝杆菌具有特异性,包括鸟分枝杆菌,并且能够识别从动物和人类(克罗恩病患者)分离出的所有测试副结核分枝杆菌菌株。对F57插入片段进行了测序,鉴定出一段620 bp的片段,其G + C含量为58.9%。将该序列与EMBL和UGEN数据库中的序列进行比较,发现F57序列具有独特性,与其他已知基因没有相似之处。