Highlander S K, Wickersham E A, Garza O, Weinstock G M
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, Texas 77030.
Infect Immun. 1993 Sep;61(9):3942-51. doi: 10.1128/iai.61.9.3942-3951.1993.
Multicopy and single-copy chromosomal fusions between the Pasteurella haemolytica leukotoxin regulatory region and the Escherichia coli beta-galactosidase gene have been constructed. These fusions were used as reporters to identify and isolate regulators of leukotoxin expression from a P. haemolytica cosmid library. A cosmid clone, which inhibited leukotoxin expression from multicopy and single-copy protein fusions, was isolated and found to contain the complete leukotoxin gene cluster plus additional upstream sequences. The locus responsible for inhibition of expression from leukotoxin-beta-galactosidase fusions was mapped within these upstream sequences, by transposon mutagenesis with Tn5, and its DNA sequence was determined. The inhibitory activity was found to be associated with a predicted 440-amino-acid reading frame (lapA) that lies within a four-gene arginine transport locus. LapA is predicted to be the nucleotide-binding component of this transport system and shares homology with the Clp family of proteases.
已构建了溶血巴斯德氏菌白细胞毒素调节区与大肠杆菌β-半乳糖苷酶基因之间的多拷贝和单拷贝染色体融合体。这些融合体用作报告基因,以从溶血巴斯德氏菌粘粒文库中鉴定和分离白细胞毒素表达的调节因子。分离出一个抑制多拷贝和单拷贝蛋白融合体中白细胞毒素表达的粘粒克隆,发现其包含完整的白细胞毒素基因簇以及额外的上游序列。通过用Tn5进行转座子诱变,将负责抑制白细胞毒素-β-半乳糖苷酶融合体表达的位点定位在这些上游序列内,并测定了其DNA序列。发现抑制活性与位于四基因精氨酸转运位点内的一个预测的440个氨基酸的可读框(lapA)相关。LapA预计是该转运系统的核苷酸结合成分,与蛋白酶的Clp家族具有同源性。