Becker A, Schmidt M, Jäger W, Pühler A
Lehrstuhl für Genetik, Fakultät für Biologie, Universität Bielefeld, Germany.
Gene. 1995 Aug 30;162(1):37-9. doi: 10.1016/0378-1119(95)00313-u.
A set of antibiotic-resistance and promoter-probe cassettes suitable for insertion mutagenesis and generation of transcriptional fusions was constructed. The cassettes contain the aacC1 gene of transposon Tn1696 conferring resistance to gentamicin in a large variety of Gram- and Gram+ bacteria. In addition to the antibiotic-resistance gene, a promoterless Escherichia coli lacZ gene was included in the cassettes, allowing the determination of the transcriptional activity at the insertion site. The cassettes can be excised from a plasmid mediating ampicillin resistance by many commonly used restriction enzymes. The new constructs have been successfully used for mutagenesis and studies of gene transcription in Rhizobium meliloti.
构建了一组适用于插入诱变和转录融合生成的抗生素抗性和启动子探针盒。这些盒含有转座子Tn1696的aacC1基因,该基因赋予多种革兰氏阴性和革兰氏阳性细菌对庆大霉素的抗性。除了抗生素抗性基因外,盒中还包含一个无启动子的大肠杆菌lacZ基因,可用于确定插入位点的转录活性。这些盒可以通过许多常用的限制酶从介导氨苄青霉素抗性的质粒中切除。新构建体已成功用于苜蓿根瘤菌的诱变和基因转录研究。