Durham D R, Phibbs P V
J Bacteriol. 1982 Feb;149(2):534-41. doi: 10.1128/jb.149.2.534-541.1982.
The initial reactions involved in the catabolism of fructose in Pseudomonas aeruginosa include the participation of a phosphoenolpyruvate:fructose 1-phosphotransferase system (F-PTS). Fractionation of crude extracts of fructose-grown cells revealed that both membrane-associated and soluble components were essential for F-PTS activity. Further resolution of the soluble fraction by both size exclusion and ion-exchange chromatography revealed the presence of only one component, functionally analogous to enzyme I. Enzyme I exhibited a relative molecular weight of 72,000, catalyzed the pyruvate-stimulated hydrolysis of phosphoenolpyruvate to pyruvate, and mediated the phosphorylation of fructose when combined with a source of enzyme II (washed membranes). No evidence for the requirement of a phosphate carrier protein, such as HPr, could be demonstrated. Thus, the F-PTS requires a minimum of two components, a soluble enzyme I and a membrane-associated enzyme II complex, and both were shown to be inducible. Reconstituted F-PTS activity was specific for phosphoenolpyruvate as a phosphate donor (Km, approximately -0.6 mM) and fructose as the sugar substrate (Km, approximately 18 microM). Components of the Pseudomonas F-PTS did not restore activity to extracts of deletion mutants of Salmonella typhimurium deficient in individual proteins of the PTS or to fractionated membrane and soluble components of the F-PTS of Escherichia coli. Similarly, membrane and soluble components of E. coli and S. typhimurium would not cross-complement the F-PTS components from P. aeruginosa.
果糖1-磷酸转移酶系统(F-PTS)的参与。对果糖培养细胞的粗提物进行分级分离发现,膜相关成分和可溶性成分对于F-PTS活性都是必不可少的。通过尺寸排阻色谱和离子交换色谱对可溶性部分进行进一步分离,结果显示仅存在一种成分,其功能类似于酶I。酶I的相对分子质量为72,000,催化磷酸烯醇丙酮酸在丙酮酸刺激下水解为丙酮酸,并在与酶II来源(洗涤过的膜)结合时介导果糖的磷酸化。未发现需要诸如HPr之类的磷酸载体蛋白的证据。因此,F-PTS至少需要两种成分,一种可溶性酶I和一种膜相关酶II复合物,并且两者均显示为可诱导的。重组后的F-PTS活性对作为磷酸盐供体的磷酸烯醇丙酮酸(Km约为-0.6 mM)和作为糖底物的果糖(Km约为18 microM)具有特异性。铜绿假单胞菌F-PTS的成分不能恢复鼠伤寒沙门氏菌中PTS单个蛋白缺陷的缺失突变体提取物的活性,也不能恢复大肠杆菌F-PTS的分级分离膜成分和可溶性成分的活性。同样,大肠杆菌和鼠伤寒沙门氏菌的膜成分和可溶性成分也不能与铜绿假单胞菌的F-PTS成分进行交叉互补。