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Volumn 70, Issue 6, 2006, Pages 663-669

Microbial production of optically active β-phenylalanine ethyl ester through stereoselective hydrolysis of racemic β-phenylalanine ethyl ester

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; ENZYME KINETICS; HYDROLYSIS; MICROBIOLOGY; MICROORGANISMS; STEREOCHEMISTRY;

EID: 33646776055     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00253-005-0141-4     Document Type: Article
Times cited : (7)

References (11)
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    • β-lactam derivatives as enzyme inhibitors: 1-peptidyl derivatives of 4-phenylazetidin-2-one as inhibitors of elastase and papain
    • Achilles K, Schirmeister T, Otto HH (2000) β-lactam derivatives as enzyme inhibitors: 1-peptidyl derivatives of 4-phenylazetidin-2-one as inhibitors of elastase and papain. Arch Pharm Pharm Med Chem 333:243-253
    • (2000) Arch Pharm Pharm Med Chem , vol.333 , pp. 243-253
    • Achilles, K.1    Schirmeister, T.2    Otto, H.H.3
  • 3
    • 0017184389 scopus 로고
    • A rapid sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford M (1972) A rapid sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254
    • (1972) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.1
  • 4
    • 0000218708 scopus 로고
    • Hydrolysis of D(-)-ethyl β-phenyl-β-hydroxypropionate and D(-)-ethyl β-phenyl-β-acetamidepropionate by α-chymotrypsin
    • Cohen SG, Weinstein SY (1964) Hydrolysis of D(-)-ethyl β-phenyl-β-hydroxypropionate and D(-)-ethyl β-phenyl-β- acetamidepropionate by α-chymotrypsin. J Am Chem Soc 86:725-728
    • (1964) J Am Chem Soc , vol.86 , pp. 725-728
    • Cohen, S.G.1    Weinstein, S.Y.2
  • 6
    • 0015243885 scopus 로고
    • Polypeptides of the tail fibres of bacteriophage T4
    • King J, Laemmli U (1971) Polypeptides of the tail fibres of bacteriophage T4. J Mol Biol 62:465-477
    • (1971) J Mol Biol , vol.62 , pp. 465-477
    • King, J.1    Laemmli, U.2
  • 7
    • 0347735411 scopus 로고
    • Reversed-phase high-performance liquid chromatographic resolution of non-esterified enantiomeric amino acids by derivatization with 2,3,4, 6-tetra-o-acetyl-β-D-glucopyranosyl isothiocyanate and 2,3,4-tri-o-acetyl- α-D-arabinopyranosyl isothiocyanate
    • Kinoshita T, Kasahara Y, Nimura N (1981) Reversed-phase high-performance liquid chromatographic resolution of non-esterified enantiomeric amino acids by derivatization with 2,3,4, 6-tetra-o-acetyl-β-D-glucopyranosyl isothiocyanate and 2,3,4-tri-o-acetyl-α-D-arabinopyranosyl isothiocyanate. J Chromatogr 210:77-81
    • (1981) J Chromatogr , vol.210 , pp. 77-81
    • Kinoshita, T.1    Kasahara, Y.2    Nimura, N.3
  • 9
    • 0019125070 scopus 로고
    • Reversed-phase liquid chromatographic resolution of amino acid enantiomers by derivatization with 2,3,4,6-tetra-o-acetyl-β-D- glucopyranosyl isothiocyanate
    • Nimura N, Ogura H, Kinoshita T (1980) Reversed-phase liquid chromatographic resolution of amino acid enantiomers by derivatization with 2,3,4,6-tetra-o-acetyl-β-D-glucopyranosyl isothiocyanate. J Chromatogr 202:375-379
    • (1980) J Chromatogr , vol.202 , pp. 375-379
    • Nimura, N.1    Ogura, H.2    Kinoshita, T.3
  • 10
    • 0000444905 scopus 로고
    • Optical resolution of amino acid enantiomers by high-performance liquid chromatography
    • Nimura N, Toyama A, Kinoshita T (1984) Optical resolution of amino acid enantiomers by high-performance liquid chromatography. J Chromatogr 316:547-552
    • (1984) J Chromatogr , vol.316 , pp. 547-552
    • Nimura, N.1    Toyama, A.2    Kinoshita, T.3
  • 11
    • 0033531990 scopus 로고    scopus 로고
    • Enantioselective acylation of β-aminoesters using penicillin G acylase in organic solvents
    • Roche D, Prasad K, Repic O (1999) Enantioselective acylation of β-aminoesters using penicillin G acylase in organic solvents. Tetrahedron Lett 40:3665-3668
    • (1999) Tetrahedron Lett , vol.40 , pp. 3665-3668
    • Roche, D.1    Prasad, K.2    Repic, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.