Whitehead T R, Rabinowitz J C
J Bacteriol. 1986 Jul;167(1):205-9. doi: 10.1128/jb.167.1.205-209.1986.
The gene for 10-formyltetrahydrofolate synthetase (EC 6.3.4.3) from the purinolytic anaerobic bacterium Clostridium acidiurici ("Clostridium acidi-urici") was cloned into Escherichia coli JM83 with plasmid pUC8. A C. acidiurici genomic library was prepared in E. coli from a partial Sau3A digest and screened with antibody against the synthetase. Of 10 antibody-positive clones, 1 expressed a high level of synthetase activity. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblot analysis demonstrated that the protein synthesized in E. coli had the same subunit molecular weight as the C. acidiurici enzyme. The gene was located on an 8.3-kilobase genomic insert and appeared to be transcribed from its own promoter. Analysis of genomic digests with a fragment of the synthetase gene indicated that one copy of the gene was present in the C. acidiurici chromosome.
将来自嘌呤分解厌氧细菌尿酸梭菌(“尿酸梭菌”)的10-甲酰四氢叶酸合成酶(EC 6.3.4.3)基因,用质粒pUC8克隆到大肠杆菌JM83中。用Sau3A部分酶切法从尿酸梭菌制备基因组文库,并在大肠杆菌中进行构建,然后用抗该合成酶的抗体进行筛选。在10个抗体阳性克隆中,有1个克隆表达了高水平的合成酶活性。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和免疫印迹分析表明,在大肠杆菌中合成的蛋白质与尿酸梭菌的酶具有相同的亚基分子量。该基因位于一个8.3千碱基的基因组插入片段上,并且似乎是从其自身的启动子转录而来。用合成酶基因片段分析基因组酶切产物表明,尿酸梭菌染色体中存在该基因的一个拷贝。