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Volumn 18, Issue 11, 2003, Pages 1407-1417

Potential of enzyme mimics in biomimetic sensors: A modified-cyclodextrin as a dehydrogenase enzyme mimic

Author keywords

Biosensor; Cyclodextrins; Enzyme mimics; NAD; NADH

Indexed keywords

CATALYSIS; ELECTROCHEMISTRY; ENZYMES; FLUORESCENCE; HYDROPHOBICITY; SOL-GELS;

EID: 0041704855     PISSN: 09565663     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0956-5663(03)00077-0     Document Type: Article
Times cited : (58)

References (68)
  • 2
    • 0024792371 scopus 로고
    • Proton inventory of a bifunctional ribonuclease model
    • Anslyn E., Breslow R. Proton inventory of a bifunctional ribonuclease model. J. Am. Chem. Soc. 111:1989;8931-8932.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 8931-8932
    • Anslyn, E.1    Breslow, R.2
  • 3
    • 0035804804 scopus 로고    scopus 로고
    • Chronoamperometric determination of D-lactate using screen-printed enzyme electrodes
    • Avamescu A., Naguer T., Mageara V., Marty J.L. Chronoamperometric determination of D-lactate using screen-printed enzyme electrodes. Anal. Chim. Acta. 433:2001;81-88.
    • (2001) Anal. Chim. Acta , vol.433 , pp. 81-88
    • Avamescu, A.1    Naguer, T.2    Mageara, V.3    Marty, J.L.4
  • 4
    • 0016530770 scopus 로고
    • Electrochemical oxidation of reduced nicotinamide adenine dinucleotide
    • Baedel W.J., Jenkins R.A. Electrochemical oxidation of reduced nicotinamide adenine dinucleotide. Anal. Chem. 147:1975;1337-1343.
    • (1975) Anal. Chem. , vol.147 , pp. 1337-1343
    • Baedel, W.J.1    Jenkins, R.A.2
  • 5
    • 37049068320 scopus 로고
    • A chiral sensor based on a peroctylated alpha cyclodextrins
    • Bates, P.S., Kataky, R., Parker, D., 1992. A chiral sensor based on a peroctylated alpha cyclodextrins. J. Chem. Soc. Chem. Commun. 2, 153-154.
    • (1992) J. Chem. Soc. Chem. Commun. , vol.2 , pp. 153-154
    • Bates, P.S.1    Kataky, R.2    Parker, D.3
  • 6
    • 37049088538 scopus 로고
    • Chiral sensors based on lipophilic cyclodextrins: Interrogation of enantioselectivity by combined NMR, structural correlation and electrode studies
    • Bates P.S., Kataky R., Parker D. Chiral sensors based on lipophilic cyclodextrins: interrogation of enantioselectivity by combined NMR, structural correlation and electrode studies. J. Chem. Soc. Perkin Trans. 2:1994;669-677.
    • (1994) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 669-677
    • Bates, P.S.1    Kataky, R.2    Parker, D.3
  • 7
    • 12444260047 scopus 로고
    • Cyclodextrins as enzyme models
    • Page, M.I. (Ed.). Elsevier
    • Bender, M.L., Koiyama, M., 1984. Cyclodextrins as enzyme models. In: Page, M.I. (Ed.), The Chemistry of Enzyme Action. Elsevier, pp. 505-527 (1974).
    • (1974) The Chemistry of Enzyme Action , pp. 505-527
    • Bender, M.L.1    Koiyama, M.2
  • 8
    • 0027466338 scopus 로고
    • Kinetics and mechanism in RNA cleavage
    • Breslow R. Kinetics and mechanism in RNA cleavage. Proton Proc. Natl. Acad. Sci. USA. 90:1993;1208-1211.
    • (1993) Proton Proc. Natl. Acad. Sci. USA , vol.90 , pp. 1208-1211
    • Breslow, R.1
  • 9
    • 0028464112 scopus 로고
    • Bifunctional acid base catalysis by imidazole groups in enzyme mimics
    • Breslow R. Bifunctional acid base catalysis by imidazole groups in enzyme mimics. J. Mol. Catal. 91:1994;114-161.
    • (1994) J. Mol. Catal. , vol.91 , pp. 114-161
    • Breslow, R.1
  • 10
    • 0000817683 scopus 로고
    • Selective aromatic substitutions within a cyclodextrin mixed complex
    • Breslow R., Cambell P. Selective aromatic substitutions within a cyclodextrin mixed complex. J. Am. Chem. Soc. 91:1969;3085-3087.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 3085-3087
    • Breslow, R.1    Cambell, P.2
  • 11
    • 0000061186 scopus 로고
    • Selective aromatic substitution by hydrophobic binding of a substrate to a simple cyclodextrin catalyst
    • Breslow R., Cambell P. Selective aromatic substitution by hydrophobic binding of a substrate to a simple cyclodextrin catalyst. Bioorg. Chem. 1:1971;140.
    • (1971) Bioorg. Chem. , vol.1 , pp. 140
    • Breslow, R.1    Cambell, P.2
  • 12
    • 1842582944 scopus 로고    scopus 로고
    • Biomimetic reactions catalysed by cyclodextrins and their derivatives
    • Breslow R., Dong S.D. Biomimetic reactions catalysed by cyclodextrins and their derivatives. Chem. Rev. 98:1998;1997-2011.
    • (1998) Chem. Rev. , vol.98 , pp. 1997-2011
    • Breslow, R.1    Dong, S.D.2
  • 13
    • 0029883733 scopus 로고    scopus 로고
    • A Selective intramolecular aldol condensation directed by a bifunctional enzyme mimic
    • Breslow R.D.J., Huang Y. A Selective intramolecular aldol condensation directed by a bifunctional enzyme mimic. Tetrahedron Lett. 37:1996;2541-2544.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2541-2544
    • Breslow, R.D.J.1    Huang, Y.2
  • 14
    • 0000831276 scopus 로고
    • A γ-cycodextrin thiazolium salt holoenzyme mimic for the benzoin condensation
    • Breslow R., Kool E. A γ-cycodextrin thiazolium salt holoenzyme mimic for the benzoin condensation. Tetrahedron Lett. 29:(14):1988;1635-1638.
    • (1988) Tetrahedron Lett. , vol.29 , Issue.14 , pp. 1635-1638
    • Breslow, R.1    Kool, E.2
  • 15
    • 0014961423 scopus 로고
    • Artificial enzyme combining a metal catalytic group and a hydrophobic binding cavity
    • Breslow R., Overman L.E. Artificial enzyme combining a metal catalytic group and a hydrophobic binding cavity. J. Am. Chem. Soc. 92:1970;1075-1077.
    • (1970) J. Am. Chem. Soc. , vol.92 , pp. 1075-1077
    • Breslow, R.1    Overman, L.E.2
  • 16
    • 0000200521 scopus 로고
    • Mediated cyclodextrin and a cyclodextrin polymer as catalysts in selective anisole chlorination
    • Breslow R., Kohn H., Siegel B. Mediated cyclodextrin and a cyclodextrin polymer as catalysts in selective anisole chlorination. Tetrahedron Lett. 17:1976;1645-1646.
    • (1976) Tetrahedron Lett. , vol.17 , pp. 1645-1646
    • Breslow, R.1    Kohn, H.2    Siegel, B.3
  • 17
    • 33847085035 scopus 로고
    • Selective transamination and optical induction by a beta cyclodextrin pyridoxamine artificial enzyme
    • Breslow R., Hammond M., Lauer M. Selective transamination and optical induction by a beta cyclodextrin pyridoxamine artificial enzyme. J. Am. Chem. Soc. 102:1980;421-422.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 421-422
    • Breslow, R.1    Hammond, M.2    Lauer, M.3
  • 18
    • 33845552493 scopus 로고
    • Optimization of metallocene substrates for β-cyclodextrin reactions
    • Breslow R., Trainor G., Ueno A. Optimization of metallocene substrates for β-cyclodextrin reactions. J. Am. Chem. Soc. 105:1983;2739-2747.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 2739-2747
    • Breslow, R.1    Trainor, G.2    Ueno, A.3
  • 20
    • 0025075212 scopus 로고
    • Artificial transaminases linking pyridoxamine to binding cavities; Controlling the geometry
    • Breslow R., Canary J.W., Varney M., Wadell S.T., Yang D. Artificial transaminases linking pyridoxamine to binding cavities; controlling the geometry. J. Am. Chem. Soc. 112:1990;5212-5219.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5212-5219
    • Breslow, R.1    Canary, J.W.2    Varney, M.3    Wadell, S.T.4    Yang, D.5
  • 21
    • 84955654689 scopus 로고
    • Cyclodextrin-B12, a potential enzyme-coenzyme mimic
    • Breslow R., Duggan P.J., Light J.P. Cyclodextrin-B12, a potential enzyme-coenzyme mimic. J. Am. Chem. Soc. 114:1992;3982-3983.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 3982-3983
    • Breslow, R.1    Duggan, P.J.2    Light, J.P.3
  • 22
    • 0034620353 scopus 로고    scopus 로고
    • Electrostatically induced inclusion of anions in cyclodextrin monolayers on electrodes
    • Chamberlain R.V., Slowinska K., Majda M., Buhlmann P., Aoki H., Umezawa Y. Electrostatically induced inclusion of anions in cyclodextrin monolayers on electrodes. Langmuir. 16:2000;1388-1396.
    • (2000) Langmuir , vol.16 , pp. 1388-1396
    • Chamberlain, R.V.1    Slowinska, K.2    Majda, M.3    Buhlmann, P.4    Aoki, H.5    Umezawa, Y.6
  • 23
    • 0029021677 scopus 로고
    • Control of regioselectivity in the Diels-Alder reactions of alloys substituted 1,4 benzoquinones by β-cyclodextrin and its derivatives
    • Chung, W.S., Wang, J.Y., 1995. Control of regioselectivity in the Diels-Alder reactions of alloys substituted 1,4 benzoquinones by β-cyclodextrin and its derivatives. J. Chem. Soc. Chem. Commun. 9, 971.
    • (1995) J. Chem. Soc. Chem. Commun. , vol.9 , pp. 971
    • Chung, W.S.1    Wang, J.Y.2
  • 24
    • 37049087006 scopus 로고
    • Photo cycloaddition of fumaronitrile to adamantan-2-ones and modification of face selectivity by inclusion in a β-cyclodextrin and its derivatives
    • Chung W.S., Wang N.J., Liu Y.D., Leu Y.-J., Chiang M.Y. Photo cycloaddition of fumaronitrile to adamantan-2-ones and modification of face selectivity by inclusion in a β-cyclodextrin and its derivatives. J. Chem. Soc., Perkin Trans. 2:1995;307-313.
    • (1995) J. Chem. Soc., Perkin Trans. , vol.2 , pp. 307-313
    • Chung, W.S.1    Wang, N.J.2    Liu, Y.D.3    Leu, Y.-J.4    Chiang, M.Y.5
  • 28
    • 0036177936 scopus 로고    scopus 로고
    • Electrocatalytic oxidation of NAD (P) H at mediator modified electrodes
    • Gorton L., Dominguez E. Electrocatalytic oxidation of NAD (P) H at mediator modified electrodes. Rev. Mol. Biotech. 82:2002;371-392.
    • (2002) Rev. Mol. Biotech. , vol.82 , pp. 371-392
    • Gorton, L.1    Dominguez, E.2
  • 29
    • 58149363832 scopus 로고
    • Mediator modified electrodes for electrocatalytic oxidation of NADH
    • Grundig B., Wittstock G., Rudel U., Strehlitz B. Mediator modified electrodes for electrocatalytic oxidation of NADH. J. Electroanal. Chem. 395:1995;143-157.
    • (1995) J. Electroanal. Chem. , vol.395 , pp. 143-157
    • Grundig, B.1    Wittstock, G.2    Rudel, U.3    Strehlitz, B.4
  • 30
    • 11944266450 scopus 로고
    • Inclusion of azulene and alcohol by beta-cyclodextrin in aqueous solution
    • Hamai S., Ikeda T., Nakamura A., Ikeda H., Ueno A., Toda F. Inclusion of azulene and alcohol by beta-cyclodextrin in aqueous solution. J. Am. Chem. Soc. 114:1992;6012-6016.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 6012-6016
    • Hamai, S.1    Ikeda, T.2    Nakamura, A.3    Ikeda, H.4    Ueno, A.5    Toda, F.6
  • 31
    • 37049071525 scopus 로고
    • Flavocyclodextrins as artificial redox enzymes: Part 4. Catalytic reactions of alcohols, aldehydes and thiols
    • Hongping Y., Tongg W., D'Souza V.T. Flavocyclodextrins as artificial redox enzymes: part 4. Catalytic reactions of alcohols, aldehydes and thiols. J. Chem. Soc. Perkin Trans. 2:1994;2431-2437.
    • (1994) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 2431-2437
    • Hongping, Y.1    Tongg, W.2    D'Souza, V.T.3
  • 32
    • 0034679096 scopus 로고    scopus 로고
    • A compact chemical miniature of a holenzyme, coenzyme NADH linked dehydrogenase. Design and synthesis of bridged NADH models and their highly enantioselective reduction
    • Kanomata N., Nakata T. A compact chemical miniature of a holenzyme, coenzyme NADH linked dehydrogenase. Design and synthesis of bridged NADH models and their highly enantioselective reduction. J. Am. Chem. Soc. 122:2000;4563-4568.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 4563-4568
    • Kanomata, N.1    Nakata, T.2
  • 33
    • 0002770531 scopus 로고    scopus 로고
    • Catalytic electroxidation of NADH for dehydrogenase amperometric biosensors
    • Katakis I., Dominguez E. Catalytic electroxidation of NADH for dehydrogenase amperometric biosensors. Mikrochim. Acta. 126:1997;11-32.
    • (1997) Mikrochim. Acta , vol.126 , pp. 11-32
    • Katakis, I.1    Dominguez, E.2
  • 34
    • 0030461135 scopus 로고    scopus 로고
    • Sensitive and selective electrochemical sensors for charge diffuse cations use of a lipophilic cyclodextrin and an enzyme relay for the determination of acetylcholine
    • Kataky R., Parker D. Sensitive and selective electrochemical sensors for charge diffuse cations use of a lipophilic cyclodextrin and an enzyme relay for the determination of acetylcholine. Analyst. 121:1996;1829-1834.
    • (1996) Analyst , vol.121 , pp. 1829-1834
    • Kataky, R.1    Parker, D.2
  • 35
    • 0001197264 scopus 로고    scopus 로고
    • Selective complexation and sensitive analysis of charge diffuse cationic species using lipophilic cyclodextrins
    • Kataky R., Parker D. Selective complexation and sensitive analysis of charge diffuse cationic species using lipophilic cyclodextrins. Chem. Commun. (Feature article). 2:1997;141-145.
    • (1997) Chem. Commun. (Feature Article) , vol.2 , pp. 141-145
    • Kataky, R.1    Parker, D.2
  • 36
    • 0000529273 scopus 로고
    • Functionalised alpha cyclodextrins as potentiometric chiral sensors
    • Kataky R., Bates P.S., Parker D. Functionalised alpha cyclodextrins as potentiometric chiral sensors. Analyst. 117:1992;1313-1317.
    • (1992) Analyst , vol.117 , pp. 1313-1317
    • Kataky, R.1    Bates, P.S.2    Parker, D.3
  • 37
    • 37049075192 scopus 로고
    • Functionalised cyclodextrins as potentiometric sensors for onium ions
    • Kataky R., Bates P.S., Parker D. Functionalised cyclodextrins as potentiometric sensors for onium ions. Analyst. 119:1994;181-186.
    • (1994) Analyst , vol.119 , pp. 181-186
    • Kataky, R.1    Bates, P.S.2    Parker, D.3
  • 38
    • 0035191455 scopus 로고    scopus 로고
    • Cyclodextrin-modified biosensors: Comparision of cyclodextrin-linked ferrocenes as mediators in sol-gel and screen-printed formats for sensing acetylcholine
    • Kataky R., Dell R., Senanayake P.K. Cyclodextrin-modified biosensors: comparision of cyclodextrin-linked ferrocenes as mediators in sol-gel and screen-printed formats for sensing acetylcholine. Analyst. 126:2001;2015-2019.
    • (2001) Analyst , vol.126 , pp. 2015-2019
    • Kataky, R.1    Dell, R.2    Senanayake, P.K.3
  • 40
    • 0042991777 scopus 로고
    • The cyclodextrin-nicotinamide compound as a dehydrogenase model simulating apoenzyme-coenzyme-substrate ternary complex system
    • Kojlma M., Toda F., Hattori K. The cyclodextrin-nicotinamide compound as a dehydrogenase model simulating apoenzyme-coenzyme-substrate ternary complex system. Tetrahedron Lett. 21:(28):1980;2721-2724.
    • (1980) Tetrahedron Lett. , vol.21 , Issue.28 , pp. 2721-2724
    • Kojlma, M.1    Toda, F.2    Hattori, K.3
  • 41
    • 37049108213 scopus 로고
    • β-Cyclodextrin-nicotinamide as a model for NADH dependent enzymes
    • Kojima M., Toda F., Hattori K. β-Cyclodextrin-nicotinamide as a model for NADH dependent enzymes. J. Chem. Soc. Perkin Trans. 1:1981;1647-1651.
    • (1981) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1647-1651
    • Kojima, M.1    Toda, F.2    Hattori, K.3
  • 42
    • 0006308404 scopus 로고
    • On the mechanism of hydrogen transfer by nicotinamide co-enzymes and some dehydrogenases
    • Laurie D., Lucas E., Nonhebel D.C., Suckling C.J., Walton J.C. On the mechanism of hydrogen transfer by nicotinamide co-enzymes and some dehydrogenases. Tetrahedron. 42:(4):1986;1035-1045.
    • (1986) Tetrahedron , vol.42 , Issue.4 , pp. 1035-1045
    • Laurie, D.1    Lucas, E.2    Nonhebel, D.C.3    Suckling, C.J.4    Walton, J.C.5
  • 43
    • 37049104876 scopus 로고
    • Cyclopropyl methyl compounds as probes of the mechanism of hydrogen transfer by NAD(H) and alcohol dehydrogenase
    • MacInnes I., Nonhebel D.C., Orszulik S.T., Suckling C.J. Cyclopropyl methyl compounds as probes of the mechanism of hydrogen transfer by NAD(H) and alcohol dehydrogenase. J. Chem. Soc. Chem. Commun. 2:1982;121-122.
    • (1982) J. Chem. Soc. Chem. Commun. , vol.2 , pp. 121-122
    • MacInnes, I.1    Nonhebel, D.C.2    Orszulik, S.T.3    Suckling, C.J.4
  • 44
    • 0033341064 scopus 로고    scopus 로고
    • Immobilized nitro-fluorenone derivatives as electrocatalysts for NADH oxidation
    • Mano N., Kuhn A. Immobilized nitro-fluorenone derivatives as electrocatalysts for NADH oxidation. J. Electroanal. Chem. 477:1999;79-88.
    • (1999) J. Electroanal. Chem. , vol.477 , pp. 79-88
    • Mano, N.1    Kuhn, A.2
  • 45
    • 33947092082 scopus 로고
    • Effects of adsorption, electrode material, and operational variables on the oxidation of dihydronicotinamide adenine dinucleotide at carbon electrodes
    • Moiroux J., Elving P.J. Effects of adsorption, electrode material, and operational variables on the oxidation of dihydronicotinamide adenine dinucleotide at carbon electrodes. Anal. Chem. 50:1978;1056-1062.
    • (1978) Anal. Chem. , vol.50 , pp. 1056-1062
    • Moiroux, J.1    Elving, P.J.2
  • 46
    • 33847085840 scopus 로고
    • Mechanistic aspects of the electrochemical oxidation of dihydronicotinamide adenine dinucleotide (NADH)
    • Moiroux J., Elving P.J. Mechanistic aspects of the electrochemical oxidation of dihydronicotinamide adenine dinucleotide (NADH). J. Am. Chem. Soc. 102:1980;6533-6538.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 6533-6538
    • Moiroux, J.1    Elving, P.J.2
  • 48
    • 85031132803 scopus 로고
    • In 24, Eur. Patent Appl. EP 400918
    • Namba, A., Masahiro, F., 1990. In 24, Eur. Patent Appl. EP 400918.
    • (1990)
    • Namba, A.1    Masahiro, F.2
  • 49
    • 0000671595 scopus 로고
    • Electrochemical oxidation in aqueous and non-aqueous media of dihydropyridine nucleotides NMNH, NADH, and NADPH
    • Ohno S., Kimura T., Oka O. Electrochemical oxidation in aqueous and non-aqueous media of dihydropyridine nucleotides NMNH, NADH, and NADPH. J. Am. Chem. Soc. 101:1979;7036-7040.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 7036-7040
    • Ohno, S.1    Kimura, T.2    Oka, O.3
  • 50
    • 58149365208 scopus 로고
    • Sol-gel derived renewable surface biosensors
    • Pankrakov I., Lev O. Sol-gel derived renewable surface biosensors. J. Electroanal. Chem. 393:1995;35-41.
    • (1995) J. Electroanal. Chem. , vol.393 , pp. 35-41
    • Pankrakov, I.1    Lev, O.2
  • 51
    • 37049090497 scopus 로고
    • Complexation of NADH analogs with α-cyclodextrins: Inhibitory effects of α-cyclodextrins against hydration and cupric and ferricyanide oxidation of 1,4 dihydro-nicotinamides
    • Park J.W., Cha S.Y., Park K.K. Complexation of NADH analogs with α-cyclodextrins: inhibitory effects of α-cyclodextrins against hydration and cupric and ferricyanide oxidation of 1,4 dihydro-nicotinamides. J. Chem. Soc. Perkin Trans. 2. 10:1991;1613-1617.
    • (1991) J. Chem. Soc. Perkin Trans. 2 , vol.10 , pp. 1613-1617
    • Park, J.W.1    Cha, S.Y.2    Park, K.K.3
  • 52
    • 0023925312 scopus 로고
    • Investigation of ternary cyclodextrin complexes by fluorescence spectroscopy
    • Patonay G., Fowler K., Nelson G., Warner I.M. Investigation of ternary cyclodextrin complexes by fluorescence spectroscopy. Anal. Chim. Acta. 207:1988;251-258.
    • (1988) Anal. Chim. Acta , vol.207 , pp. 251-258
    • Patonay, G.1    Fowler, K.2    Nelson, G.3    Warner, I.M.4
  • 53
    • 0000161131 scopus 로고
    • Hydride vs. electron transfer in the reduction of flavin and flavin radical by 1,4-dihydropyridines
    • Powell M.F., Bruice T.C. Hydride vs. electron transfer in the reduction of flavin and flavin radical by 1,4-dihydropyridines. J. Am. Chem. Soc. 105:1983;1014-1021.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 1014-1021
    • Powell, M.F.1    Bruice, T.C.2
  • 54
    • 0030794535 scopus 로고    scopus 로고
    • A mutase mimic with cobalamin linked to cyclodextrin
    • Rezac M., Breslow R. A mutase mimic with cobalamin linked to cyclodextrin. Tetrahedron Lett. 38:1997;5763-5766.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5763-5766
    • Rezac, M.1    Breslow, R.2
  • 55
    • 0032050423 scopus 로고    scopus 로고
    • Electrochemical oxidation of NADH on sol-gel derived, surface renewable, non-modified and mediator modified composite-carbon electrodes
    • Sampath S., Lev O. Electrochemical oxidation of NADH on sol-gel derived, surface renewable, non-modified and mediator modified composite-carbon electrodes. J. Electroanal. Chem. 446:1998;57-65.
    • (1998) J. Electroanal. Chem. , vol.446 , pp. 57-65
    • Sampath, S.1    Lev, O.2
  • 57
    • 12444329136 scopus 로고
    • Structure of dihydrodiphosphopyridine nucleotide
    • Shifrini N., Kaplan O. Structure of dihydrodiphosphopyridine nucleotide. Nature. 183:1959;1529.
    • (1959) Nature , vol.183 , pp. 1529
    • Shifrini, N.1    Kaplan, O.2
  • 58
    • 0003461218 scopus 로고    scopus 로고
    • J. Szejtli, Osa T. first ed. Oxford, New York, Tokyo: Elsevier
    • Cyclodextrin derivatives. Cyclodextrins. Szejtli J., Osa T. first ed. Comprehensive Supramolecular Chemistry. 3:1996;Elsevier, Oxford, New York, Tokyo.
    • (1996) Comprehensive Supramolecular Chemistry , vol.3
  • 59
    • 0005205759 scopus 로고
    • Flavocyclodextrin as a promising flavoprotein model. Efficient electron transfer catalysis by flavocyclodextrin
    • Tabushi I., Kodera M.J. Flavocyclodextrin as a promising flavoprotein model. Efficient electron transfer catalysis by flavocyclodextrin. J. Am. Chem. Soc. 109:1987;4734-4735.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 4734-4735
    • Tabushi, I.1    Kodera, M.J.2
  • 60
    • 0001533216 scopus 로고
    • A (modified B6)-R-[omega-amino(ethylamino)]-beta cyclodextrin as an artificial B6 enzyme for chiral aminotransfer reaction
    • Tabushi I., Kuroda Y., Yamada M., Higashimura H., Breslow R. A (modified B6)-R-[omega-amino(ethylamino)]-beta cyclodextrin as an artificial B6 enzyme for chiral aminotransfer reaction. J. Am. Chem. Soc. 107:1985;5545-5546.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 5545-5546
    • Tabushi, I.1    Kuroda, Y.2    Yamada, M.3    Higashimura, H.4    Breslow, R.5
  • 61
    • 0001184955 scopus 로고    scopus 로고
    • The effect of alcohols on the basic cleavage of m-nitrophenyl hexanoate by β-cyclodextrin: Allosteric reaction mode switching
    • Tee O.S., Giorgi J.B. The effect of alcohols on the basic cleavage of m-nitrophenyl hexanoate by β-cyclodextrin: allosteric reaction mode switching. J. Chem. Soc. Perkin Trans. 2:1997;1013-1018.
    • (1997) J. Chem. Soc. Perkin Trans , vol.2 , pp. 1013-1018
    • Tee, O.S.1    Giorgi, J.B.2
  • 62
    • 0040341956 scopus 로고
    • Molecular modeling calculations on the acylation of β-cyclodextrin by ferrocenylacrylate esters
    • Theim H.J., Brandl M., Breslow R. Molecular modeling calculations on the acylation of β-cyclodextrin by ferrocenylacrylate esters. J. Am. Chem. Soc. 110:1988;8612-8616.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8612-8616
    • Theim, H.J.1    Brandl, M.2    Breslow, R.3
  • 63
    • 0001594225 scopus 로고
    • Mimics of tryptophan synthetase and of biochemical dehydroalanine formation
    • Weiner W.W.J., Zlmmerman S.C., Czarnik A.W., Breslow R. Mimics of tryptophan synthetase and of biochemical dehydroalanine formation. J. Am. Chem. Soc. 107:1985;4093-4094.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 4093-4094
    • Weiner, W.W.J.1    Zlmmerman, S.C.2    Czarnik, A.W.3    Breslow, R.4
  • 65
    • 0011300090 scopus 로고
    • Reduction by a model of NADPH 36. First and direct evidence for multistep mechanism
    • Yasui S., Nakamura Y., Ohno A., Oka O. Reduction by a model of NADPH 36. First and direct evidence for multistep mechanism. Bull. Chem. Soc. Jpn. 55:1982;196.
    • (1982) Bull. Chem. Soc. Jpn. , vol.55 , pp. 196
    • Yasui, S.1    Nakamura, Y.2    Ohno, A.3    Oka, O.4
  • 66
    • 0000912216 scopus 로고
    • Efficient catalysis of a redox reaction by an artificial enzyme
    • Ye H.T.W., D'Souza V.T. Efficient catalysis of a redox reaction by an artificial enzyme. J. Am. Chem. Soc. 114:1992;5470-5472.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5470-5472
    • Ye, H.T.W.1    D'Souza, V.T.2
  • 67
    • 37049070347 scopus 로고
    • Reduction of ninhydrin with cyclodextrin-1,4 dihydronicotinamides as NADH models
    • Yoon C.J., Ikeda H., Kojin R., Ikeda T., Toda F. Reduction of ninhydrin with cyclodextrin-1,4 dihydronicotinamides as NADH models. J. Chem. Soc. Chem. Commun. 14:1986;1080-1081.
    • (1986) J. Chem. Soc. Chem. Commun. , vol.14 , pp. 1080-1081
    • Yoon, C.J.1    Ikeda, H.2    Kojin, R.3    Ikeda, T.4    Toda, F.5
  • 68
    • 0030010163 scopus 로고    scopus 로고
    • The first complete set of authentic functional β-cyclodextrins with one imidazolyl group specifically attached to C-2 or C-3
    • Yuan, D., Ohta, K., Fujita, K., 1996. The first complete set of authentic functional β-cyclodextrins with one imidazolyl group specifically attached to C-2 or C-3. J. Chem. Soc. Chem. Commun. 7, 821-822.
    • (1996) J. Chem. Soc. Chem. Commun. , vol.7 , pp. 821-822
    • Yuan, D.1    Ohta, K.2    Fujita, K.3


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