메뉴 건너뛰기




Volumn 48, Issue 8, 2013, Pages 1208-1211

Influence of substituent groups in regioselective acylation of nucleosides by Novozym 435 lipase

Author keywords

Novozym 435; Nucleosides; Regioselective acylation; Substituent; Substrate specificity

Indexed keywords

NOVOZYM435; NUCLEOSIDES; REGIOSELECTIVE ACYLATION; SUBSTITUENT; SUBSTRATE SPECIFICITY;

EID: 84881173790     PISSN: 13595113     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2013.06.022     Document Type: Article
Times cited : (20)

References (23)
  • 1
    • 80055007420 scopus 로고    scopus 로고
    • Regioselective enzymatic acylation of complex natural products: Expanding molecular diversity
    • J. González-Sabín, R. Morán-Ramallal, and F. Rebolledo Regioselective enzymatic acylation of complex natural products: expanding molecular diversity Chem Soc Rev 40 2011 5321 5335
    • (2011) Chem Soc Rev , vol.40 , pp. 5321-5335
    • González-Sabín, J.1    Morán-Ramallal, R.2    Rebolledo, F.3
  • 3
    • 79953305092 scopus 로고    scopus 로고
    • Recent progress in industrial biocatalysis
    • B.M. Nestl, B.A. Nebel, and B. Hauer Recent progress in industrial biocatalysis Curr Opin Chem Biol 15 2011 187 193
    • (2011) Curr Opin Chem Biol , vol.15 , pp. 187-193
    • Nestl, B.M.1    Nebel, B.A.2    Hauer, B.3
  • 4
    • 0034681499 scopus 로고    scopus 로고
    • Substrate specificity of lipase B from Candida antarctica in the synthesis of arylaliphatic glycolipids
    • R.T. Otto, H. Scheib, U.T. Bornscheuer, J. Pleiss, C. Syldatk, and R.D. Schmid Substrate specificity of lipase B from Candida antarctica in the synthesis of arylaliphatic glycolipids J Mol Catal B: Enzym 8 2000 201 211
    • (2000) J Mol Catal B: Enzym , vol.8 , pp. 201-211
    • Otto, R.T.1    Scheib, H.2    Bornscheuer, U.T.3    Pleiss, J.4    Syldatk, C.5    Schmid, R.D.6
  • 5
    • 73249129394 scopus 로고    scopus 로고
    • The pronounced effect of water activity on the positional selectivity of Novozym 435 during 1,3-diolein synthesis by esterification
    • Z.Q. Duan, W. Du, and D.H. Liu The pronounced effect of water activity on the positional selectivity of Novozym 435 during 1,3-diolein synthesis by esterification Catal Commun 11 2010 356 358
    • (2010) Catal Commun , vol.11 , pp. 356-358
    • Duan, Z.Q.1    Du, W.2    Liu, D.H.3
  • 6
    • 79951968104 scopus 로고    scopus 로고
    • A 40-year journey in the antiviral drug field
    • E. de Clercq A 40-year journey in the antiviral drug field Annu Rev Pharmacol Toxicol 51 2011 1 24
    • (2011) Annu Rev Pharmacol Toxicol , vol.51 , pp. 1-24
    • De Clercq, E.1
  • 7
    • 1242286151 scopus 로고    scopus 로고
    • Antiproliferative activity and mechanism of action of fatty acid derivatives of arabinofuranosylcytosine in leukemia and solid tumor cell lines
    • A.M. Bergman, C.M. Kuiper, D.A. Voorn, E.M. Comijn, F. Myhren, M.L. Sandvold, H.R. Hendriks, and G.J. Peters Antiproliferative activity and mechanism of action of fatty acid derivatives of arabinofuranosylcytosine in leukemia and solid tumor cell lines Biochem Pharmacol 67 2004 503 511
    • (2004) Biochem Pharmacol , vol.67 , pp. 503-511
    • Bergman, A.M.1    Kuiper, C.M.2    Voorn, D.A.3    Comijn, E.M.4    Myhren, F.5    Sandvold, M.L.6    Hendriks, H.R.7    Peters, G.J.8
  • 8
    • 0034500277 scopus 로고    scopus 로고
    • Biocatalytic selective modifications of conventional nucleosides, carbocyclic nucleosides, and C-nucleosides
    • M. Ferrero, and V. Gotor Biocatalytic selective modifications of conventional nucleosides, carbocyclic nucleosides, and C-nucleosides Chem Rev 100 2000 4319 4348
    • (2000) Chem Rev , vol.100 , pp. 4319-4348
    • Ferrero, M.1    Gotor, V.2
  • 9
    • 77955783895 scopus 로고    scopus 로고
    • Structural modifications of nucleosides in ionic liquids
    • V. Kumar, V.S. Parmar, and S.V. Malhotra Structural modifications of nucleosides in ionic liquids Biochimie 92 2010 1260 1265
    • (2010) Biochimie , vol.92 , pp. 1260-1265
    • Kumar, V.1    Parmar, V.S.2    Malhotra, S.V.3
  • 10
    • 81955160797 scopus 로고    scopus 로고
    • Highly regioselective synthesis of 3′-O-acyl-trifluridines catalyzed by Pseudomonas cepacia lipase
    • Z.Y. Wang, Y.H. Bi, and M.H. Zong Highly regioselective synthesis of 3′-O-acyl-trifluridines catalyzed by Pseudomonas cepacia lipase Appl Biochem Biotechnol 165 2011 1161 1168
    • (2011) Appl Biochem Biotechnol , vol.165 , pp. 1161-1168
    • Wang, Z.Y.1    Bi, Y.H.2    Zong, M.H.3
  • 11
    • 67651087017 scopus 로고    scopus 로고
    • Recognition of acyl donors by lipase CAL-B in the acylation of 6-azauridine
    • Z.Y. Wang, and M.H. Zong Recognition of acyl donors by lipase CAL-B in the acylation of 6-azauridine Biotechnol Prog 25 2009 784 791
    • (2009) Biotechnol Prog , vol.25 , pp. 784-791
    • Wang, Z.Y.1    Zong, M.H.2
  • 12
    • 80053462912 scopus 로고    scopus 로고
    • Substrate recognition of the PS im in regioselective synthesis of nucleoside analogs 3′-O-esters
    • Z.Y. Wang, and M.H. Zong Substrate recognition of the PS IM in regioselective synthesis of nucleoside analogs 3′-O-esters Chin J Org Chem 31 2011 1032 1042
    • (2011) Chin J Org Chem , vol.31 , pp. 1032-1042
    • Wang, Z.Y.1    Zong, M.H.2
  • 13
    • 79955086397 scopus 로고    scopus 로고
    • Influence of 2′-substituent in the nucleosides on Burkholderia cepacia lipase-catalyzed regioselective acylation
    • Z.Y. Wang, and M.H. Zong Influence of 2′-substituent in the nucleosides on Burkholderia cepacia lipase-catalyzed regioselective acylation Chin J Catal 32 2011 357 361
    • (2011) Chin J Catal , vol.32 , pp. 357-361
    • Wang, Z.Y.1    Zong, M.H.2
  • 14
    • 77949570525 scopus 로고    scopus 로고
    • Biocatalytic transformation of nucleoside derivatives
    • N. Li, T.J. Smith, and M.H. Zong Biocatalytic transformation of nucleoside derivatives Biotechnol Adv 28 2010 348 366
    • (2010) Biotechnol Adv , vol.28 , pp. 348-366
    • Li, N.1    Smith, T.J.2    Zong, M.H.3
  • 15
    • 83055188144 scopus 로고    scopus 로고
    • Regioselectivity-reversal in acylation of 6-azauridine catalyzed by Burkholderia cepacia lipase
    • Z.Y. Wang, Y.H. Bi, and M.H. Zong Regioselectivity-reversal in acylation of 6-azauridine catalyzed by Burkholderia cepacia lipase Biotechnol Lett 34 2012 55 59
    • (2012) Biotechnol Lett , vol.34 , pp. 55-59
    • Wang, Z.Y.1    Bi, Y.H.2    Zong, M.H.3
  • 16
    • 4143127620 scopus 로고    scopus 로고
    • Hydration of enzyme in nonaqueous media is consistent with solvent dependence of its activity
    • L. Yang, J.S. Dordick, and S. Garde Hydration of enzyme in nonaqueous media is consistent with solvent dependence of its activity Biophys J 87 2004 812 821
    • (2004) Biophys J , vol.87 , pp. 812-821
    • Yang, L.1    Dordick, J.S.2    Garde, S.3
  • 17
    • 0029417196 scopus 로고
    • Crystallographic and molecular-modeling studies of lipase B from Candida antarctica reveal a stereospecificity pocket for secondary alcohols
    • J. Uppenberg, N. Oehrner, M. Norin, K. Hult, G.J. Kleywegt, S. Patkar, V. Waagen, T. Anthonsen, and T.A. Jones Crystallographic and molecular-modeling studies of lipase B from Candida antarctica reveal a stereospecificity pocket for secondary alcohols Biochemistry 34 1995 16838 16851
    • (1995) Biochemistry , vol.34 , pp. 16838-16851
    • Uppenberg, J.1    Oehrner, N.2    Norin, M.3    Hult, K.4    Kleywegt, G.J.5    Patkar, S.6    Waagen, V.7    Anthonsen, T.8    Jones, T.A.9
  • 18
    • 23644447557 scopus 로고    scopus 로고
    • An inverse substrate orientation for the regioselective acylation of 3′,5′-diaminonucleosides catalyzed by Candida antarctica lipase B
    • I. Lavandera, S. Fernandez, J. Magdalena, M. Ferrero, R.J. Kazlauskas, and V. Gotor An inverse substrate orientation for the regioselective acylation of 3′,5′-diaminonucleosides catalyzed by Candida antarctica lipase B ChemBioChem 6 2005 1381 1390
    • (2005) ChemBioChem , vol.6 , pp. 1381-1390
    • Lavandera, I.1    Fernandez, S.2    Magdalena, J.3    Ferrero, M.4    Kazlauskas, R.J.5    Gotor, V.6
  • 19
    • 0032103791 scopus 로고    scopus 로고
    • Anatomy of lipase binding sites: The scissile fatty acid binding site
    • J. Pleiss, M. Fischer, and R.D. Schmid Anatomy of lipase binding sites: the scissile fatty acid binding site Chem Phys Lipids 93 1998 67 80
    • (1998) Chem Phys Lipids , vol.93 , pp. 67-80
    • Pleiss, J.1    Fischer, M.2    Schmid, R.D.3
  • 20
    • 57349091377 scopus 로고    scopus 로고
    • Regioselective acylation of nucleosides catalyzed by Candida antarctica lipase B: Enzyme substrate recognition
    • N. Li, M.H. Zong, and D. Ma Regioselective acylation of nucleosides catalyzed by Candida antarctica lipase B: enzyme substrate recognition Eur J Org Chem 2008 2008 5375 5378
    • (2008) Eur J Org Chem , vol.2008 , pp. 5375-5378
    • Li, N.1    Zong, M.H.2    Ma, D.3
  • 22
    • 68649084001 scopus 로고    scopus 로고
    • Novozym 435 displays very different selectivity compared to lipase from Candida antarctica B adsorbed on other hydrophobic supports
    • Z. Cabrera, G. Fernandez-Lorente, R. Fernandez-Lafuente, J.M. Palomo, and J.M. Guisan Novozym 435 displays very different selectivity compared to lipase from Candida antarctica B adsorbed on other hydrophobic supports J Mol Catal B: Enzym 57 2009 171 176
    • (2009) J Mol Catal B: Enzym , vol.57 , pp. 171-176
    • Cabrera, Z.1    Fernandez-Lorente, G.2    Fernandez-Lafuente, R.3    Palomo, J.M.4    Guisan, J.M.5
  • 23
    • 80051787511 scopus 로고    scopus 로고
    • Coupling chemical modification and immobilization to improve the catalytic performance of enzymes
    • R.C. Rodrigues, Á. Berenguer-Murcia, and R. Fernandez-Lafuente Coupling chemical modification and immobilization to improve the catalytic performance of enzymes Adv Synth Catal 353 2011 2216 2238
    • (2011) Adv Synth Catal , vol.353 , pp. 2216-2238
    • Rodrigues, R.C.1    Berenguer-Murcia, Á.2    Fernandez-Lafuente, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.