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Volumn 27, Issue 16, 2005, Pages 1199-1203

α-Chymotrypsin-catalyzed peptide synthesis using N-protected D-amino acid carbamoylmethyl esters as acyl donors

Author keywords

chymotrypsin; Carbamoylmethyl ester; D amino acid; Peptide synthesis

Indexed keywords

CATALYSIS; ENZYMES; ESTERS; PH EFFECTS; SYNTHESIS (CHEMICAL);

EID: 24744470922     PISSN: 01415492     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10529-005-0018-8     Document Type: Article
Times cited : (12)

References (12)
  • 1
    • 0036882398 scopus 로고    scopus 로고
    • Proteases in organic synthesis
    • F Bordusa 2002 Proteases in organic synthesis Chem. Rev 102 4817 4867
    • (2002) Chem. Rev , vol.102 , pp. 4817-4867
    • Bordusa, F.1
  • 4
    • 9644293945 scopus 로고    scopus 로고
    • Temperature effects on protease catalyzed acyl transfer reactions in organic media
    • A Joensson E Wehtje P Adlercreutz B Mattiasson 1996 Temperature effects on protease catalyzed acyl transfer reactions in organic media J. Mol. Catal. B 2 43 51
    • (1996) J. Mol. Catal. B , vol.2 , pp. 43-51
    • Joensson, A.1    Wehtje, E.2    Adlercreutz, P.3    Mattiasson, B.4
  • 5
    • 0027208174 scopus 로고
    • Lipase-catalyzed peptide synthesis using Z-amino acid esters as acyl donors in aqueous water miscible organic solvents
    • K Kawashiro K Kaiso D Minato S Sugiyama H Hayashi 1993 Lipase-catalyzed peptide synthesis using Z-amino acid esters as acyl donors in aqueous water miscible organic solvents Tetrahedron 49 4541 4548
    • (1993) Tetrahedron , vol.49 , pp. 4541-4548
    • Kawashiro, K.1    Kaiso, K.2    Minato, D.3    Sugiyama, S.4    Hayashi, H.5
  • 6
    • 0030444898 scopus 로고    scopus 로고
    • Effect of ester moiety of substrates on enantioselectivity of protease catalysis in organic media
    • K Kawashiro H Sugahara T Tsukioka S Sugiyama H Hayashi 1996 Effect of ester moiety of substrates on enantioselectivity of protease catalysis in organic media Biotechnol. Lett 18 1381 1386
    • (1996) Biotechnol. Lett , vol.18 , pp. 1381-1386
    • Kawashiro, K.1    Sugahara, H.2    Tsukioka, T.3    Sugiyama, S.4    Hayashi, H.5
  • 7
    • 24744457269 scopus 로고    scopus 로고
    • Influence of leaving group of an acyl donor on enzymatic peptide synthesis
    • (ORGN 1689) December 14-19, Honolulu. ISBN 0-8412-3775-1
    • Kawashiro K, Sakai S (2000) Influence of leaving group of an acyl donor on enzymatic peptide synthesis. In: 2000 International Chemical Congress of Pacific Basin Societies (ORGN 1689), December 14-19, Honolulu. ISBN 0-8412-3775-1
    • (2000) 2000 International Chemical Congress of Pacific Basin Societies
    • Kawashiro, K.1    Sakai, S.2
  • 8
    • 0033516433 scopus 로고    scopus 로고
    • Expanded structural and stereospecificity in peptide synthesis with chemically modified mutants of subtilisin
    • K Khumtaveeporn G DeSantis JB Jones 1999 Expanded structural and stereospecificity in peptide synthesis with chemically modified mutants of subtilisin Tetrahedron: Asymmetry 10 2563 2572
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2563-2572
    • Khumtaveeporn, K.1    Desantis, G.2    Jones, J.B.3
  • 9
    • 0001323502 scopus 로고
    • Incorporation of D-amino acids into peptides via enzymatic condensation in organic solvents
    • AL Margolin D-F Tai AM Klibanov 1987 Incorporation of D-amino acids into peptides via enzymatic condensation in organic solvents J. Am. Chem. Soc 109 7885 7887
    • (1987) J. Am. Chem. Soc , vol.109 , pp. 7885-7887
    • Margolin, A.L.1    Tai, D.-F.2    Klibanov, A.M.3
  • 10
    • 0035926735 scopus 로고    scopus 로고
    • Glycosylation of the primary binding pocket of a subtilisin protease causes a remarkable broadening in stereospecificity in peptide synthesis
    • Matsumoto K, Davis BG, Jones JB (2001) Glycosylation of the primary binding pocket of a subtilisin protease causes a remarkable broadening in stereospecificity in peptide synthesis. J. Chem. Soc., Chem. Commun.: 903-904
    • (2001) J. Chem. Soc., Chem. Commun. , pp. 903-904
    • Matsumoto, K.1    Davis, B.G.2    Jones, J.B.3
  • 11
    • 0035819452 scopus 로고    scopus 로고
    • Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis
    • T Miyazawa K Tanaka E Ensatsu R Yanagihara T Yamada 2001 Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis J. Chem. Soc., Perkin Trans 1 87 93
    • (2001) J. Chem. Soc., Perkin Trans , vol.1 , pp. 87-93
    • Miyazawa, T.1    Tanaka, K.2    Ensatsu, E.3    Yanagihara, R.4    Yamada, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.