Urease activity and l-ascorbic acid

References

• Krajewska B, Ureases I. Functional, kinetic and catalytic properties: a review. J Mol Catal B: Enzym 2009; 59:9–21.
   Web of Science ®Google Scholar
• Follmer C. Ureases as a target for the treatment of gastric and urinary infections. J Clin Pathol 2010; 63:424–430.
   PubMed Web of Science ®Google Scholar
• Riddles PW, Andrews RK, Blakeley RL, Zerner B. Jack bean urease. VI. Determination of thiol and disulfide content: Reversible inactivation of the enzyme by the blocking of the unique cysteine residue. Biochim Biophys Acta 1983; 743:115–120.
   Web of Science ®Google Scholar
• Todd MJ, Hausinger RP. Reactivity of the essential thiol of Klebsiella aerogenes urease. Effect of pH and ligands on thiol modification. J Biol Chem 1991; 266:10260–10267.
   PubMed Web of Science ®Google Scholar
• Benini S, Rypniewski WR, Wilson KS, Ciurli S, Mangani S. The complex of Bacillus pasteurii urease with β-marcaptoethanol from X-ray data at 1.65-Å resolution. J Biol Inorg Chem 1998; 3:268–273.
   Web of Science ®Google Scholar
• Zhang L, Mulrooney SB, Leung AF, Zeng Y, Ko BBC, Hausinger RP, Sun H. Inhibition of urease by bismuth(III): implications for the mechanism of action of bismuth drugs. BioMetals 2006; 19:503–511.
   PubMed Web of Science ®Google Scholar
• Zaborska W, Krajewska B, Kot M, Karcz W. Quinone-induced inhibition of urease: elucidation of its mechanisms by probing thiol groups of the enzyme. Bioorg Chem 2007; 35:233–242.
   PubMed Web of Science ®Google Scholar
• Krajewska B. Mono- (Ag, Hg) and di- (Cu, Hg) valent metal ions effects on the activity of jack bean urease. Probing the modes of metal binding to the enzyme. J Enzyme Inhib Med Chem 2008; 23:535–542.
   PubMed Web of Science ®Google Scholar
• Odake S, Morikawa T, Tsuchiya M, Imamura L, Kobashi K. Inhibition of Helicobacter pylori urease activity by hydroxamic acid derivatives. Biol Pharm Bull 1994; 17:1329–1332.
   PubMed Web of Science ®Google Scholar
• Benini S, Rypniewski WR, Wilson KS, Miletti S, Ciurli S, Mangani S. A new proposal for urease mechanism based on the crystal structures of the native and inhibited enzyme from Bacillus pasteurii: why urea hydrolysis costs two nickels. Structure 1999; 7:205–216.
   PubMed Web of Science ®Google Scholar
• Vassiliou S, Grabowiecka A, Kosikowska P, Yiotakis A, Kafarski P, Berlicki L. Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases. J Med Chem 2008; 51:5736–5744.
   PubMedGoogle Scholar
• Krajewska B, Zaborska W, Leszko M. Inhibition of chitosan-immobilized urease by boric acid as determined by integration methods. J Mol Catal B: Enzym 1997; 3:231–238.
   Google Scholar
• Reddy KR, Kayastha AM. Boric acid and boronic acids inhibition of pigeonpea urease. J Enzyme Inhib Med Chem 2006; 21:467–470.
   PubMed Web of Science ®Google Scholar
• Krajewska B, Ciurli S. Jack bean (Canavalia ensiformis) urease. Probing acid-base groups of the active site by pH variation. Plant Physiol Biochem 2005; 43:651–658.
   PubMedGoogle Scholar
• Marshall BJ, Warren JR. Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration. Lancet 1984; 1:1311–1315.
   PubMed Web of Science ®Google Scholar
• Mobley HLT. (2001) Urease. In: Mobley HLT, Mendz GL, Hazell SL, editors, Helicobacter pylori: Physiology and Genetics, ASM Press, Washington, p. 179, Chapter 16.
   Google Scholar
• Crespo A, Suh B. Helicobacter pylori infection: epidemiology, pathophysiology, and therapy. Arch Pharm Res 2001; 24:485–498.
   PubMed Web of Science ®Google Scholar
• Zhang ZW, Abdullahi M, Farthing MJG. Effect of physiological concentrations of vitamin C on gastric cancer cells and Helicobacter pylori. Gut 2002; 50:165–169.
   Google Scholar
• Drake IM, Davies MJ, Mapstone NP, Dixon MF, Schorah CJ, White KLM, Chalmers DM, Axon ATR. Ascorbic acid may protect against human gastric cancer by scavenging mucosal oxygen radicals. Carcinogenesis 1996; 17:559–562.
   PubMed Web of Science ®Google Scholar
• Correa P, Malcom G, Schmidt B, Fontham E, Ruiz B, Bravo JC, Bravo LE, Zarama G, Realpe JL. Antioxidant micronutrients and gastric cancer. Aliment Pharmacol Ther 1998; 12 Suppl 1:73–82.
   Google Scholar
• Zhang HM, Wakisaka N, Maeda O, Yamamoto T. Vitamin C inhibits the growth of a bacterial risk factor for gastric carcinoma: Helicobacter pylori. Cancer 1997; 80:1897–1903.
   PubMed Web of Science ®Google Scholar
• Jarosz M, Dzieniszewski J, Dabrowska-Ufniarz E, Wartanowicz M, Ziemlanski S, Reed PI. Effects of high dose vitamin C treatment on Helicobacter pylori infection and total vitamin C concentration in gastric juice. Eur J Cancer Prev 1998; 7:449–454.
   PubMed Web of Science ®Google Scholar
• Goldie J, Jalali S, Van Zanten S, Stowe C, Hunt RH. Ascorbic acid inhibits the growth and urease activity of Campylobacter pylori. Gut 1989; 30:A1484.
   Google Scholar
• Nilius M, Bode G, Lehnhardt G, Malfertheiner P. In vitro inhibition of Helicobacter pylori urease: biochemical and ultrastructural analysis. Eur J Clin Invest 1991; 21:551–557.
   PubMed Web of Science ®Google Scholar
• Agha A, Opekun AR, Abudayyeh S, Graham DY. Effect of different organic acids (citric, malic and ascorbic) on intragastric urease activity. Aliment Pharmacol Ther 2005; 21:1145–1148.
   Google Scholar
• Ogata Y, Kosugi Y. Ultraviolet spectra of L-ascorbic acid and cupric ascorbate complex. Tetrahedron 1970; 26:4711–4716.
   PubMed Web of Science ®Google Scholar
• Stadtman ER. Ascorbic acid and oxidative inactivation of proteins. Am J Clin Nutr 1991; 54:1125S–1128S.
   Web of Science ®Google Scholar
• Halliwell B. Vitamin C: poison, prophylactic or panacea? Trends Biochem Sci 1999; 24:255–259.
   PubMed Web of Science ®Google Scholar
• Deutsch JC, Santhosh-Kumar CR. Dehydroascorbic acid undergoes hydrolysis on solubilization which can be reversed with mercaptoethanol J Chromatogr 1996; A724:271–278.
   Google Scholar
• Khan MMT, Martell AE. Metal ion and metal chelate catalyzed oxidation of ascorbic acid by molecular oxygen. I. Cupric and ferric ion catalyzed oxidation. J Am Chem Soc 1967; 89:4176–4185.
   PubMed Web of Science ®Google Scholar
• Samuni A, Aronovitch J, Godinger D, Chevion M, Czapski G. On the cytotoxicity of vitamin C and metal ions. A site-specific Fenton mechanism. Eur J Biochem 1983; 137:119–124.
   PubMedGoogle Scholar
• Elson LA. Inhibition of urease activity by ascorbic acid. Nature 1943; 152:149.
   Google Scholar
• Quastel JH. Urease activity and ascorbic acid. Nature 1943; 152:215.
   Google Scholar
• Giri KV, Seshagiri R. Urease activity and ascorbic acid. Nature 1946; 153:253–254.
   Google Scholar
• Mapson LW. Inhibition of urease by copper salts in the presence of ascorbic acid and related substances. Biochem J 1946; 40:240–247.
   Google Scholar
• Chiyoda T, Iida K, Takatori K, Kajiwara M. Screening system for urease inhibitors using 13C-NMR. Chem Pharm Bull 1998; 46:718–720.
   Google Scholar
• Krajewska B. Urease immobilized on chitosan membrane. Inactivation by heavy metal ions. J Chem Tech Biotechnol 1991; 52:157–162.
   Web of Science ®Google Scholar
• Weatherburn MW. Phenol-hypochlorite reaction for determination of ammonia. Anal Chem 1967; 39:971–974.
   Web of Science ®Google Scholar
• Todd MJ, Hausinger RP. Purification and characterization of the nickel-containing multicomponent urease from Klebsiella aerogenes. J Biol Chem 1987; 262:5963–5967.
   PubMed Web of Science ®Google Scholar
• Srivastava PK, Kayastha AM. Significance of sulfhydryl groups in the activity of urease from pigeonpea (Cajanus cajan L.) seeds. Plant Sci 2000; 159:149–158.
   PubMed Web of Science ®Google Scholar
• Krajewska B, Zaborska W. Double mode of inhibition-inducing interactions of 1,4-naphthoquinone with urease: arylation versus oxidation of enzyme thiols. Bioorg Med Chem 2007; 15:4144–4151.
   PubMed Web of Science ®Google Scholar
• Srivastava PK, Kayastha AM, Reddy RC, Grant DF. Molecular asymmetry in pigeonpea urease: pH inactivation studies. J Plant Biochem Biotechnol 2003; 12:49–51.
   Google Scholar
• Dixon NE, Gazzola C, Asher CJ, Lee DSW, Blakeley RL, Zerner B. Jack been urease (EC 3.5.1.5). II. The relationship between nickel, enzymatic activity, and the “abnormal” ultraviolet spectrum. The nickel content of jack beans. Can J Biochem 1980; 58:474–480.
   Google Scholar
• Bauerfeind P, Garner R, Dunn BE, Mobley HLT. Synthesis and activity of Helicobacter pylori urease and catalase at low pH. Gut 1997; 40:25–30.
   Google Scholar
• Goto Y, Takahashi N, Fink AL. Mechanism of acid-induced folding of proteins. Biochemistry 1990; 29:3480–3488.
   PubMed Web of Science ®Google Scholar
• Bhowmick R, Jagannadham MV. Multiple intermediate conformations of jack bean urease at low pH: anion-induced refolding. Protein J 2006; 25:399–410.
   Google Scholar
• Jung CH, Wells WW. Spontaneous conversion of L-dehydroascorbic acid to L-ascorbic acid and L-erythroascorbic acid. Arch Biochem Biophys 1998; 355:9–14.
   PubMedGoogle Scholar
• Deutsch JC. Dehydroascorbic acid. J Chromatogr A 2000; 881:299–307.
   PubMed Web of Science ®Google Scholar
• Hancock J, Desikan R, Harrison J, Bright J, Hooley R, Neill S. Doing the unexpected: proteins involved in hydrogen peroxide perception. J Exp Bot 2006; 57:1711–1718.
   PubMed Web of Science ®Google Scholar