Klaasen P, Woodward M J, van Zijderveld F G, de Graaf F K
Department of Molecular Microbiology, Faculty of Biology, Free University, Amsterdam, The Netherlands.
Infect Immun. 1990 Mar;58(3):801-7. doi: 10.1128/iai.58.3.801-807.1990.
The genetic determinant for the production of 987P fimbriae has been cloned into pBR322. Analysis of frequently occurring deletions in the resultant recombinant plasmid, pPK180, revealed that the 987P gene cluster contains a transposon that encodes the synthesis of heat-stable enterotoxin STpa and is flanked by inverted repeats of IS1. Hybridization experiments with STpa- and 987P-specific probes demonstrated that a variety of STpa+ 987P+ wild-type Escherichia coli strains contained contiguous STpa-987P DNA, most likely on their chromosome. Transcription of the 987P gene cluster appeared to be activated by the adjacent IS1 element.
编码987P菌毛产生的遗传决定因子已被克隆到pBR322中。对所得重组质粒pPK180中频繁出现的缺失进行分析后发现,987P基因簇包含一个转座子,该转座子编码热稳定肠毒素STpa的合成,并且两侧是IS1的反向重复序列。用STpa特异性探针和987P特异性探针进行的杂交实验表明,多种STpa+987P+野生型大肠杆菌菌株含有相邻的STpa-987P DNA,很可能位于它们的染色体上。987P基因簇的转录似乎被相邻的IS1元件激活。