首页> 美国卫生研究院文献>Journal of Bacteriology >Use of a gene replacement cosmid vector for cloning alginate conversion genes from mucoid and nonmucoid Pseudomonas aeruginosa strains: algS controls expression of algT.
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Use of a gene replacement cosmid vector for cloning alginate conversion genes from mucoid and nonmucoid Pseudomonas aeruginosa strains: algS controls expression of algT.

机译:基因替代粘粒载体用于从粘液样和非粘液型铜绿假单胞菌菌株克隆藻酸盐转化基因的用途:algS控制algT的表达。

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摘要

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.
机译:铜绿假单胞菌可通过一种称为藻酸盐转化的遗传机制转化为粘液样菌落形态。这导致产生大量的胞外藻酸盐藻酸盐。铜绿假单胞菌的粘液表型通常与其在囊性纤维化患者中引起慢性肺道感染的能力有关。在这项研究中,我们从粘液和非粘液同基因菌株中分离了参与藻酸盐转化的顺式作用基因座,称为algS。然后,我们检查了algS在algT(铜绿假单胞菌生产藻酸盐所需的反式基因)控制中的作用。我们使用了一种新的粘粒克隆载体,称为pEMR2,该载体既可以克隆大的DNA片段,也可以随后在铜绿假单胞菌中进行基因替换。为了验证该载体的预测特性,我们分离并测试了pEMR2 hisI +克隆。使用克隆的含algS的DNA和基因置换的方法,我们构建了铜绿假单胞菌的同基因菌株,其Tn501在染色体上与algS相邻。构建了两个pEMR2克隆库,它们包含来自同基因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)菌株的基因组片段,并且Tn501作为相邻标记选择包含各自的algS等位基因。 pEMR2 algS(On)和pEMR2 algS(Off)克隆通过基因替换携带相反等位基因的菌株的染色体显示出包含所示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,并证明它不能与反义algT :: Tn501突变互补。相反,pLAFR1 algS(On)T克隆确实反型互补了algT :: Tn501。因此,algS似乎可以控制algT表达的激活,从而导致藻酸盐转化。

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