Gh. Duca et al./Chem.J. Mold.. 2008, 3 (1), 22-30References[1] Sychev A., Duca, Gh. Fundamental and Applied Aspects <strong>of</strong> Homogeneous Catalysis with Metal Complexes.Chisinau, Moldova State University Publ., 2002.[2] Isac V., Onu A., Tudoreanu C., Nemtoi G., Physical <strong>chemistry</strong>, Chisinau, Stiinta Publ., 1995, Robert J. Kee,Chemically reacting flow. Theory and practice, New Jersey: John Wiley & Sons, 2003.[3] Robert J. Kee, Chemically reacting flow. Theory and practice, New Jersey: John Wiley & Sons, 2003.[4] Pure & Appl. Chem., Vol.66, No 12, 1994, pp. 2493-2500.[5] “U.S.A. Stopped-Flow: Block Diagrams”. Retrieved from http://olisweb.com.[6] Dunn B. C, Meagher N. E., Rorabacher D. (1996) J. Phys. Chem., 100, 16925-16933.[7] Berjis M, Sharma VS, Double mixing stopped-flow method for the study <strong>of</strong> equilibria and kinetics <strong>of</strong> dimertetramerassociation <strong>of</strong> hemoglobins: studies on Hb Carp, Hb A, and Hb Rothschild, Anal Biochem. 1991 Aug1;196(2):223-8.[8] Rui-Yong WANG, Xiang GAO and Ying-Tang LU, Anal. Sci., Vol. 22, 2006, p.299.[9] D. Perez-Bendito, A. Gomez-Hens, M.C. Gutierrez and S. Anton, Nonenzymatic stopped-flow fluorimetricmethod for direct determination <strong>of</strong> uric acid in serum and urine, Clinical Chemistry 35: 1989, p. 230-233.[10] Yiping Jia, Amarendra Kumar and Smita S. Patel, Equilibrium and Stopped-flow Kinetic Studies <strong>of</strong> Interactionbetween T7 RNA Polymerase and Its Promoters Measured by Protein and 2-Aminopurine Fluorescence Changes,J. Biol. Chem., vol.271, No. 48, 1996, pp. 30451-30458.[11] Oyama Munetaka, Spectroscopic Detection and Kinetic Analysis <strong>of</strong> Aromatic Amine Cation Radicals Using anElectron Transfer Stopped-Flow Method, Erekutoro Oganikku Kemisutori Toronkai Koen Yoshishu, V.25, 2001,pp.71-72.[12] Gert Verheyden, Janka Matrai, Guido Volckaert and Yves Engelborghs, A fluorescence stopped-flow kineticstudy <strong>of</strong> the conformational activation <strong>of</strong> -chymotrypsin and several mutants, Protein Science, 2004, vol 13, p.2533-2540.[13] Duca, Gh., Scutaru, Yu., Sychev A. Kinetics <strong>of</strong> Interaction <strong>of</strong> Iodine with Dihydroxyfumaric Acid, J. <strong>of</strong> PhysicalChem., vol.61, 1987, no 8, p.2266-2268.[14] Duca, Gh., Travin, S., Purmali, A. Catalytic Condensation <strong>of</strong> Epycatechol in the Presence <strong>of</strong> Iron Ion, J. <strong>of</strong>Physical Chem., 1989, vol.63, no 12, p.3214-3220.[15] Duca, Gh., Scurlatov, Yu., Sychev, A. Redox Catalysis and Ecological Chemistry. – Chisinau, Moldova: CEUSM,2002, p. 316.[16] Sychev A., Duca Gh., Scurlatov Yu., Travin S, The investigation <strong>of</strong> the process <strong>of</strong> DFH oxidation by the stoppedflowmethod, Phys. and mathem. methods in coord. chem. Abstracts <strong>of</strong> the 7 th congress, Chisinau, 1980, p.432-33.[17] Heinz Fabian and Dieter Naumann, Methods to study protein folding by stopped-flow FT-IR, Methods, 2004,Vol.34, issue 1, p. 28-40.[18] Dieckmann H., Kreuzig R., Bahadir M., Significance <strong>of</strong> keto-enol-tautomery in the analysis <strong>of</strong> 1,2,4-triazinonemetabolites, Fresenius’ j. anal. chem., vol. 348, n o 11, pp. 749-753 , 1994.[19] Philip J. Bailey et al., Barriers to Racemization in C -Symmetric Complexes Containing the Hydrotris(2-3mercapto-1-ethylimidazolyl)borate (Tm Et ) Ligand, Inorg. Chem., 44 (24), 8884 -8898, 2005.[20] Georgii E. Salnikov, Alexander M. Genaev and Victor I. Mamatyuk, Unusually strong temperature dependence<strong>of</strong> 13 C chemical shifts and degenerate conformational exchange in cyclobutenyl carbocations, MendeleevCommun., 2003, 13, 48 – 49.[21] von Ahsen B, Bach C, Balzer G, Bley B, Bodenbinder M, Hägele G, Willner H, Aubke F., Dynamic 13C NMRstudies <strong>of</strong> ligand exchange in linear (d10) silver(I) and gold(I) and square-planar (d8) rhodium(I) homolepticmetal carbonyl cations in superacidic media, Magn Reson Chem. 2005 Jul;43(7):520-7.[22] Gh. Duca, Free radicals in natural water, in Free radicals in biology and Environment, edited by F. Minisci,Vol.27, p. 475.[23] Andrew J. White, Kevin Drabble and Christopher W. Wharton, A stopped-flow apparatus for infrared spectroscopy<strong>of</strong> aqueous solutions, Biochem. J., 1995, vol. 306, p. 843-849.[24] Gerwert, K. (1993) Curr. Opin. Struct. Biol. 3, 769-773.[25] Klaus Gerwert, Molecular Reaction Mechanisms <strong>of</strong> Proteins Monitored by Time-resolved FT-IR DifferenceSpectroscopy, John Wiley & Sons Ltd, Chichester, 2002.[26] Andrew J. White, Kevin Drabble and Christopher W. Wharton, A stopped-flow apparatus for infrared spectroscopy<strong>of</strong> aqueous solutions, Biochem. J., 1995, vol. 306, p. 843-849.[27] Doig, S. J., Reid, P. J. and Mathies, R. A. (1991) J. Phys. Chem. 95, 6372-6379.[28] G. Hammes, Investigation <strong>of</strong> rates and mechanisms <strong>of</strong> reactions, “Mir”, Moscow, 1977.[29] J. E. Garland, C. M. Pettit and D. Roy, Analysis <strong>of</strong> experimental constraints and variables for time resolveddetection <strong>of</strong> Fourier transform electrochemical impedance spectra, Electrochimica Acta 49 (2004) 2623-2635.29
Gh. Duca et al./Chem.J. Mold.. 2008, 3 (1), 22-30[30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48][49][50][51][52][53]J.E. Garland, K. A. Assiongbon, C.M. Pettit, S.B. Emery and D. Roy, “Kinetic analysis <strong>of</strong> Electrosorption usingFast Fourier Transform Electrochemical Impedance spectroscopy: Underpotential Deposition <strong>of</strong> Bi 3+ In The-Presence <strong>of</strong> Coadsorbing ClO 4on Gold”, Electrochimica Acta 47 (2002) 4113-4124.Halliwell, B. & Gutteridge, J.M.C. (1999) Free Radical in Biology and Medicine. Oxford Science Publications,New York, NY.Henry J. Thompson, DNA Oxidation Products, Antioxidant Status, and Cancer Prevention, J. Nutr. 134:3186S–3187S, 2004.Fridovich,I. (1989) Oxygen radicals from acetaldehyde. Free Radic. Biol. Med., 7, 557–558.Singh,N.P., Lai,H. and Khan,A. (1995) Ethanol-induced single strand DNA breaks in rat brain cells. Mutat. Res.,345, 191–196.Rajasinghe,H., Jayatilleke,E. and Shaw,S. (1990) DNA cleavage during ethanol metabolism: role <strong>of</strong> superoxideradicals and catalytic iron. Life Sci., 47, 807–814.Ewald,S.J. and Shao, H. (1993) Ethanol increases apoptotic cell death <strong>of</strong> thymocytes in vitro. Alcohol. Clin. Exp.Res., 17, 359–365.Moore,D.R., Reinke,L.A. and McCay,P.B. (1995) Metabolism <strong>of</strong> ethanol to 1-hydroxyethyl radicals in vivo:detection with intravenous administration <strong>of</strong> -(4-pyridyl-1-oxide)-N-t-butylnitrone. Mol. Pharmacol., 47,1224–1230.Gajewski, E., Rao, G., Nackerdien, Z., Dizdaroglu, M. (1990) Modification <strong>of</strong> DNA bases in mammalianchromatin by radiation-generated free radicals Bio<strong>chemistry</strong>, 29, 7876–7882.Shibutani, S., Bodepudi, V., Johnson, F., Grollman, A.P. (1993) Translesional synthesis on DNA templatescontaining 8-oxo-7, 8-dihydrodeoxyadenosine Bio<strong>chemistry</strong>, 32, 4615–4621.Wiederholt, C.J. and Greenberg, M.M. (2002) Fapy dG instructs Klenow exo(–) to misincorporate deoxyadenosineJ. Am. Chem. Soc., 124, 7278–7279.Delaney, M.O., Wiederholt, C.J., Greenberg, M.M. (2002) Fapy•dA induces nucleotide misincorporationtranslesionally by a DNA polymerase Angew. Chem. Int. Ed. Engl., 41, 771–773.Nikita A. Kuznetsov, Vladimir V. Koval, Dmitry O. Zharkov, Georgy A. Nevinsky, Kenneth T. Douglas, andOlga S. Fedorova, Kinetics <strong>of</strong> substrate recognition and cleavage by human 8-oxoguanine-DNA glycosylase,Nucleic Acids Res., Jul 2005; 33: 3919 – 3931.Lindahl, T. (1974) An N-glycosidase from Escherichia coli that releases free uracil from DNA containingdeaminated cytosine residues Proc. Natl. Acad. Sci. U.S.A, 71, 3649–3653.Stuart R.W. Bellamy, Kuakarun Krusong, and Ge<strong>of</strong>f S. Baldwin, A rapid reaction analysis <strong>of</strong> uracil DNAglycosylase indicates an active mechanism <strong>of</strong> base flipping, Nucleic Acids Res., March 2007; 35: 1478 – 1487.Sandau, K., J. Pfeilschifter, and B. Brune. 1997. The balance between nitric oxide and superoxide determinesapoptotic and necrotic death <strong>of</strong> rat mesangial cells. J. Immunol. 158:4938-4946.Yoshie, Y., and H. Ohshima. 1997. Nitric oxide synergistically enhances DNA strand breakage induced bypolyhydroxyaromatic compounds, but inhibits that induced by the Fenton reaction. Arch. Biochem. Biophys.342:13-21.Ken-ichiro Matsumoto and Hideo Utsumi, Development <strong>of</strong> Separable Electron Spin Resonance-ComputedTomography Imaging for Multiple Radical Species: An Application to ·OH and ·NO, Biophys J, December 2000,p. 3341-3349, Vol. 79, No. 6.Takeshita, K., H. Utsumi, and A. Hamada. 1993. Whole mouse measurement <strong>of</strong> paramagnetism-loss <strong>of</strong> nitroxidefree radical in lung with an L-band ESR spectrometer. Biochem. Mol. Biol. Int. 29:17-24.Takeshita, K., A. Hamada, and H. Utsumi. 1999. Mechanisms related to reduction <strong>of</strong> radical in mouse lung usingan L-band ESR spectrometer. Free Radic. Biol. Med. 26:951-960.Miura, Y., A. Hamada, and H. Utsumi. 1995. In vivo ESR studies <strong>of</strong> antioxidant activity on free radical reactionin living mice under oxidative stress. Free Radic. Res. 22:209-214.Phumala, N., T. Ide, and H. Utsumi. 1999. Noninvasive evaluation <strong>of</strong> in vivo free radical reactions catalyzed byiron using in vivo ESR spectroscopy. Free Radic. Biol. Med. 26:1209-1217.Matsumoto, K., K. Endo, and H. Utsumi. 2000. In vivo electron spin resonance assessment <strong>of</strong> decay constant <strong>of</strong>nitroxyl radical in selenium-deficient rat. Biol. Pharm. Bull. 23:641-644.Sano, H., M. Naruse, K. Matsumoto, T. Oi, and H. Utsumi. 2000. A new nitroxyl-probe with high retentivity inbrain and its application to brain imaging. Free Radic. Biol. Med. 28:959-969.30
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