Flynn J L, Ohman D E
Department of Microbiology and Immunology, University of California, Berkeley 94720.
J Bacteriol. 1988 Jul;170(7):3228-36. doi: 10.1128/jb.170.7.3228-3236.1988.
Pseudomonas aeruginosa can convert to a mucoid colony morphology by a genetic mechanism called alginate conversion; this results in the production of copious amounts of the exopolysaccharide alginate. The mucoid phenotype of P. aeruginosa is commonly associated with its ability to cause chronic pulmonary tract infections in patients with cystic fibrosis. In this study we isolated the cis-acting locus involved in alginate conversion, called algS, from both mucoid and nonmucoid isogenic strains. We then examined the role of algS in the control of algT, a trans-active gene required for alginate production in P. aeruginosa. We used a new cosmid cloning vector, called pEMR2, that permitted both the cloning of large DNA fragments and their subsequent gene replacement in P. aeruginosa. To verify the predicted properties of this vector, we isolated and tested a pEMR2 hisI+ clone. Using cloned algS-containing DNA and a method for gene replacement, we constructed isogenic strains of P. aeruginosa that had Tn501 adjacent to algS on the chromosome. Two pEMR2 clone banks containing genomic fragments from isogenic algS(On) (exhibiting the alginate production phenotype) and algS(Off) (exhibiting the non-alginate production phenotype) strains were constructed, and Tn501 served as an adjacent marker to select for clones containing the respective algS allele. The pEMR2 algS(On) and pEMR2 algS(Off) clones were shown to contain the indicated algS allele by gene replacement with the chromosome of strains that carried the opposite allele. To test whether algS controls the expression of the adjacent algT gene, we constructed a pLAFR1 algS(Off)T clone and showed it to be unable to complement an algT::Tn501 mutation in trans. In contrast, a pLAFR1 algS(On)T clone did complement algT::Tn501 in trans. Thus, algS appears to control the activation of algT expression, bringing about alginate conversion.
铜绿假单胞菌可通过一种称为藻酸盐转化的遗传机制转变为黏液样菌落形态;这会导致产生大量胞外多糖藻酸盐。铜绿假单胞菌的黏液样表型通常与其在囊性纤维化患者中引起慢性呼吸道感染的能力相关。在本研究中,我们从黏液样和非黏液样同基因菌株中分离出参与藻酸盐转化的顺式作用位点,称为algS。然后我们研究了algS在控制algT中的作用,algT是铜绿假单胞菌产生藻酸盐所需的反式作用基因。我们使用了一种新的黏粒克隆载体,称为pEMR2,它既允许克隆大的DNA片段,又能在铜绿假单胞菌中进行后续的基因替换。为了验证该载体的预测特性,我们分离并测试了一个pEMR2 hisI+克隆。使用克隆的含algS的DNA和一种基因替换方法,我们构建了铜绿假单胞菌的同基因菌株,这些菌株在染色体上algS附近有Tn501。构建了两个包含来自同基因algS(On)(表现出藻酸盐产生表型)和algS(Off)(表现出非藻酸盐产生表型)菌株基因组片段的pEMR2克隆文库,Tn501作为相邻标记来选择含有各自algS等位基因的克隆。通过用携带相反等位基因的菌株染色体进行基因替换,表明pEMR2 algS(On)和pEMR2 algS(Off)克隆含有所示的algS等位基因。为了测试algS是否控制相邻algT基因的表达,我们构建了一个pLAFR1 algS(Off)T克隆,并表明它不能反式互补algT::Tn501突变。相反,一个pLAFR1 algS(On)T克隆确实能反式互补algT::Tn501。因此,algS似乎控制algT表达的激活,从而导致藻酸盐转化。