Roehl R A, Feary T W, Phibbs P V
J Bacteriol. 1983 Dec;156(3):1123-9. doi: 10.1128/jb.156.3.1123-1129.1983.
Mutations in carbohydrate-negative mutants of Pseudomonas aeruginosa PAO1 individually deficient in glucose 6-phosphate dehydrogenase (zwf), 6-phosphogluconate dehydratase (edd), or pyruvate carboxylase (pyc) were mapped on the chromosome by plasmid R68.45-mediated conjugation and by bacteriophage F116L-mediated transduction. Loci for all three genes were located in the 45- to 55-min region of the chromosome; both zwf-1 and edd-1 were linked by transduction to nalA, whereas pyc-2 was linked by conjugation to argF10. The zwf-1 mutation exhibited cotransduction frequencies of greater than 95% with both edd-1 and the hex-9001 marker, a mutation reported to prevent growth on hexoses. The latter mutation was shown to cause a specific deficiency in 2-keto-3-deoxy-6-phosphogluconate aldolase activity and was redesignated eda-9001. These results demonstrate tight clustering of the gene loci for glucose 6-phosphate dehydrogenase and for both enzymes unique to the Entner-Doudoroff pathway in P. aeruginosa. Our evidence suggests supraoperonic clustering of these and other inducible carbohydrate catabolic genes in the 45- to 55-min region of the chromosome.
利用质粒R68.45介导的接合作用以及噬菌体F116L介导的转导作用,对铜绿假单胞菌PAO1中分别缺乏6-磷酸葡萄糖脱氢酶(zwf)、6-磷酸葡萄糖酸脱水酶(edd)或丙酮酸羧化酶(pyc)的碳水化合物阴性突变体中的突变进行了染色体定位。所有这三个基因的位点都位于染色体的45至55分钟区域;zwf-1和edd-1通过转导与nalA相连,而pyc-2通过接合与argF10相连。zwf-1突变与edd-1以及hex-9001标记(据报道该突变可阻止在己糖上生长)的共转导频率均大于95%。后者的突变被证明导致2-酮-3-脱氧-6-磷酸葡萄糖酸醛缩酶活性出现特异性缺陷,并被重新命名为eda-9001。这些结果表明,在铜绿假单胞菌中,6-磷酸葡萄糖脱氢酶以及Entner-Doudoroff途径特有的两种酶的基因位点紧密聚集。我们的证据表明,这些以及其他可诱导的碳水化合物分解代谢基因在染色体的45至55分钟区域存在超操纵子聚集。