Itoh Y, Matsumoto H
Division of Applied Microbiology, National Food Research Institute, Ministry of Agriculture, Forestry and Fisheries, Ibaraki, Japan.
Mol Gen Genet. 1992 Feb;231(3):417-25. doi: 10.1007/BF00292711.
The nucleotide sequence required for a fully functional promoter and operator of the Pseudomonas aeruginosa argF gene (argFpo), the arginine-repressible gene for anabolic ornithine carbamoyltransferase, was defined within a 160 bp region. The streptomycin (Sm) resistance genes strAB of plasmid RSF1010 were fused to argFpo. This construct in P. aeruginosa strain PAO conferred resistance to Sm. Mutants of strain PAO were selected which were resistant to Sm in the presence of arginine due to constitutive expression of argFpo-strAB. These mutants were designated argR. They were unable to grow or grew poorly on arginine or ornithine as the sole carbon and nitrogen source. This growth defect (Aru-/Oru- phenotype) was correlated with a reduced level of N-succinylornithine aminotransferase, an enzyme participating in the major aerobic pathway for arginine and ornithine catabolism in this organism. The argR mutants were classified into four groups by transduction analysis and three argR mutations were mapped on the PAO chromosome. argR9901 and argR9902 were co-transducible with car-9 (at 1 min) and thus close to the oru-310 locus; argR9906 was localized in the oruI (= aru) gene cluster (67 min). Some aru mutants, which have been isolated previously and which produce very low amounts of all enzymes in the arginine succinyltransferase pathway, were unable to repress the argF gene in an arginine medium. Thus, P. aeruginosa PAO appears to have multiple genes that are involved in the regulation of both the anabolic argF and the catabolic aru genes.
铜绿假单胞菌精氨酸合成鸟氨酸氨甲酰基转移酶的精氨酸可阻遏基因(argF)的全功能启动子和操纵子所需的核苷酸序列定位于一个160bp的区域内。质粒RSF1010的链霉素(Sm)抗性基因strAB与argF启动子和操纵子融合。该构建体在铜绿假单胞菌PAO菌株中赋予对Sm的抗性。选择PAO菌株的突变体,由于argF-strAB的组成型表达,它们在精氨酸存在下对Sm具有抗性。这些突变体被命名为argR。它们在以精氨酸或鸟氨酸作为唯一碳源和氮源时无法生长或生长不良。这种生长缺陷(Aru-/Oru-表型)与N-琥珀酰鸟氨酸转氨酶水平降低相关,该酶参与该生物体中精氨酸和鸟氨酸分解代谢的主要需氧途径。通过转导分析将argR突变体分为四组,并将三个argR突变定位在PAO染色体上。argR9901和argR9902与car-9(在1分钟处)共转导,因此靠近oru-310位点;argR9906定位于oruI(=aru)基因簇(67分钟)。一些先前分离的aru突变体在精氨酸琥珀酰转移酶途径中产生的所有酶量都非常低,它们在精氨酸培养基中无法抑制argF基因。因此,铜绿假单胞菌PAO似乎有多个基因参与合成代谢的argF和分解代谢的aru基因的调控。