Balbás P, Alexeyev M, Shokolenko I, Bolivar F, Valle F
Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, Mexico.
Gene. 1996 Jun 12;172(1):65-9. doi: 10.1016/0378-1119(96)00028-5.
Plasmid pBRINT is an efficient vector for chromosomal integration of cloned DNA into the lacZ gene of Escherichia coli [Balbás et al., Gene 136(1993) 211-213]. A family of related plasmids containing different antibiotic-resistance markers (CmR or GmR or KmR) and a larger multiple cloning site (MCS) has been constructed. This set of plasmids, whose integration efficiencies are as good as those obtained with the prototype plasmid pBRINT, constitutes a collection of tools that allow rapid and easy integration of cloned DNA, at the chromosomal level. Their functionality as integration vectors has been ascertained by integrating the Vitreoscilla sp. hemoglobin-encoding gene and the Photobacterium leiognathi lux genes. To evaluate the level of expression obtained after chromosomal integration, we constructed strains carrying one or two copies of the cat gene integrated in the chromosome, and compared their enzymatic activities with those obtained from a strain carrying cat on a multicopy plasmid.
质粒pBRINT是一种高效载体,可将克隆的DNA整合到大肠杆菌的lacZ基因中[巴尔巴斯等人,《基因》136(1993) 211 - 213]。现已构建了一系列相关质粒,它们含有不同的抗生素抗性标记(CmR或GmR或KmR)以及更大的多克隆位点(MCS)。这组质粒的整合效率与原型质粒pBRINT相当,构成了一套工具,可在染色体水平上快速简便地整合克隆的DNA。通过整合维氏固氮菌血红蛋白编码基因和鱼发光杆菌lux基因,已确定了它们作为整合载体的功能。为了评估染色体整合后获得的表达水平,我们构建了携带一个或两个整合到染色体中的cat基因拷贝的菌株,并将它们的酶活性与从携带多拷贝质粒上的cat基因的菌株获得的酶活性进行比较。