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Volumn 99, Issue 7, 2008, Pages 2116-2120

Corrigendum to "Transesterification of primary and secondary alcohols using Pseudomonas aeruginosa lipase" Bioresource Technology 99 (2008) 2116-2120 (DOI:10.1016/j.biortech.2007.05.041);Transesterification of primary and secondary alcohols using Pseudomonas aeruginosa lipase

Author keywords

Benzyl acetate; Lipase; Pseudomonas aeruginosa; Transesterification

Indexed keywords

BIOCATALYSTS; DIMETHYL SULFOXIDE; HEPTANE; LIPASES; SOLVENTS; TRANSESTERIFICATION;

EID: 38849137395     PISSN: 09608524     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biortech.2008.09.038     Document Type: Erratum
Times cited : (34)

References (18)
  • 1
    • 45249126845 scopus 로고
    • Enzymatic ester hydrolysis and synthesis-two approaches to cycloalkane derivatives of high enantiomeric purity
    • Alder U., Breitgoff D., Klein P., Laumen K., and Schneirder P. Enzymatic ester hydrolysis and synthesis-two approaches to cycloalkane derivatives of high enantiomeric purity. Tetrahedron Lett. 30 (1989) 1793-1796
    • (1989) Tetrahedron Lett. , vol.30 , pp. 1793-1796
    • Alder, U.1    Breitgoff, D.2    Klein, P.3    Laumen, K.4    Schneirder, P.5
  • 3
    • 0000404890 scopus 로고
    • Enzymatic reactions in organic synthesis: 2-ester interchange of vinyl esters
    • Castaing M.D., Jeso B.D., Drouillard S., and Maillard B. Enzymatic reactions in organic synthesis: 2-ester interchange of vinyl esters. Tetrahedron Lett. 28 (1987) 953-954
    • (1987) Tetrahedron Lett. , vol.28 , pp. 953-954
    • Castaing, M.D.1    Jeso, B.D.2    Drouillard, S.3    Maillard, B.4
  • 6
    • 0032717591 scopus 로고    scopus 로고
    • Bacterial biocatalysts: molecular biology, three dimensional structures and biotechnological applications of lipases
    • Jaeger K.E., Dijkstra B.W., and Reetz M.T. Bacterial biocatalysts: molecular biology, three dimensional structures and biotechnological applications of lipases. Ann. Rev. Microbiol. 53 (1999) 315-351
    • (1999) Ann. Rev. Microbiol. , vol.53 , pp. 315-351
    • Jaeger, K.E.1    Dijkstra, B.W.2    Reetz, M.T.3
  • 7
    • 0028878079 scopus 로고
    • Enzymatic resolution of alcohols via lipases immobilized in microemulsion-based gels
    • Jesus P.C., Rezende M.C., and Nascimento M.G. Enzymatic resolution of alcohols via lipases immobilized in microemulsion-based gels. Tetrahedron Asymm. 6 (1995) 63-66
    • (1995) Tetrahedron Asymm. , vol.6 , pp. 63-66
    • Jesus, P.C.1    Rezende, M.C.2    Nascimento, M.G.3
  • 8
    • 0030574039 scopus 로고    scopus 로고
    • 1-Ethoxyvinyl acetate as a novel, highly reactive, and reliable acyl donor for enzymatic resolution of alcohols
    • Kita Y., Takede Y., Murata K., Naka T., and Akai N. 1-Ethoxyvinyl acetate as a novel, highly reactive, and reliable acyl donor for enzymatic resolution of alcohols. Tetrahedron Lett. 37 (1996) 7369-7372
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7369-7372
    • Kita, Y.1    Takede, Y.2    Murata, K.3    Naka, T.4    Akai, N.5
  • 9
    • 0029132275 scopus 로고
    • Kinetics of acyl transfer in organic media catalyzed by Candida antarctica lipase B
    • Martinelle M., and Hult K. Kinetics of acyl transfer in organic media catalyzed by Candida antarctica lipase B. Biochim. Biophys. Acta. 1251 (1995) 191-197
    • (1995) Biochim. Biophys. Acta. , vol.1251 , pp. 191-197
    • Martinelle, M.1    Hult, K.2
  • 10
    • 0026927093 scopus 로고
    • A kinetic study of immobilized lipase catalysing the synthesis of isoamyl acetate by transesterification in n-hexane
    • Rizzi M., Stylos P., Riek A., and Reuss M. A kinetic study of immobilized lipase catalysing the synthesis of isoamyl acetate by transesterification in n-hexane. Enzme Microb. Technol. 14 (1992) 709-714
    • (1992) Enzme Microb. Technol. , vol.14 , pp. 709-714
    • Rizzi, M.1    Stylos, P.2    Riek, A.3    Reuss, M.4
  • 11
    • 0035725911 scopus 로고    scopus 로고
    • Production, purification, characterization, and applications of lipases
    • Sharma R., Chisti Y., and Banerjee U.C. Production, purification, characterization, and applications of lipases. Biotechnol Adv. 19 (2001) 627-662
    • (2001) Biotechnol Adv. , vol.19 , pp. 627-662
    • Sharma, R.1    Chisti, Y.2    Banerjee, U.C.3
  • 12
    • 38849158658 scopus 로고    scopus 로고
    • Sharma, R., Singh, S., Roy, A., Chawla, H.P.S., Kaul, C.L., Banerjee, U.C., 2003. An improved process for enantioselective hydrolysis of trans-(-)-MPGM using a novel microbial lipase. Indian Patent Application No. 1358/DEL/2003.
    • Sharma, R., Singh, S., Roy, A., Chawla, H.P.S., Kaul, C.L., Banerjee, U.C., 2003. An improved process for enantioselective hydrolysis of trans-(-)-MPGM using a novel microbial lipase. Indian Patent Application No. 1358/DEL/2003.
  • 13
    • 26244442519 scopus 로고    scopus 로고
    • Enantioselective hydrolysis of methoxyphenyl glycidic acid methyl ester [(±)-MPGM] by a thermostable and alkalostable lipase from Pseudomonas aeruginosa
    • Singh S., and Banerjee U.C. Enantioselective hydrolysis of methoxyphenyl glycidic acid methyl ester [(±)-MPGM] by a thermostable and alkalostable lipase from Pseudomonas aeruginosa. J. Mol. Catal. B: Enz. 36 (2005) 30-35
    • (2005) J. Mol. Catal. B: Enz. , vol.36 , pp. 30-35
    • Singh, S.1    Banerjee, U.C.2
  • 14
    • 34347266596 scopus 로고    scopus 로고
    • Studies on the production of lipase by a newly isolated strain of Pseudomonas aeruginosa for the enantioselective hydrolysis of (±)methyl trans-3(4-methoxyphenyl)glycidate (MPGM)
    • Singh S., Kaur G., Chakraborti A.K., Jain R.K., and Banerjee U.C. Studies on the production of lipase by a newly isolated strain of Pseudomonas aeruginosa for the enantioselective hydrolysis of (±)methyl trans-3(4-methoxyphenyl)glycidate (MPGM). Bioproc. Biosyst. Eng. 13 (2006) 1-8
    • (2006) Bioproc. Biosyst. Eng. , vol.13 , pp. 1-8
    • Singh, S.1    Kaur, G.2    Chakraborti, A.K.3    Jain, R.K.4    Banerjee, U.C.5
  • 15
    • 33845279035 scopus 로고
    • Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallics
    • Wang Y.F., Lalonade J.J., Momongan M., Bergbretter D.E., and Wong C.H. Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallics. J. Am. Chem. Soc. 110 (1988) 7200-7205
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 7200-7205
    • Wang, Y.F.1    Lalonade, J.J.2    Momongan, M.3    Bergbretter, D.E.4    Wong, C.H.5
  • 16
    • 0018399632 scopus 로고
    • Glycogen, hyaluronate, and some other polysaccharides greatly enhance the formation of exolipase by Serratia marcescens
    • Winkler U.K., and Stuckmann M. Glycogen, hyaluronate, and some other polysaccharides greatly enhance the formation of exolipase by Serratia marcescens. J. Bacteriol. 138 (1979) 663-670
    • (1979) J. Bacteriol. , vol.138 , pp. 663-670
    • Winkler, U.K.1    Stuckmann, M.2
  • 17
    • 0038735357 scopus 로고    scopus 로고
    • Kinetic modeling of immobilized-lipase catalyzed transesterification of n-octanol with vinyl acetate in non-aqueous media
    • Yadav G.D., and Trivedi A.H. Kinetic modeling of immobilized-lipase catalyzed transesterification of n-octanol with vinyl acetate in non-aqueous media. Enzyme Microb. Technol. 32 (2003) 783-789
    • (2003) Enzyme Microb. Technol. , vol.32 , pp. 783-789
    • Yadav, G.D.1    Trivedi, A.H.2
  • 18
    • 0000836283 scopus 로고
    • Substrate specificity of enzyme in organic solvent vs water is reversed
    • Zaks A., and Klibanov A.M. Substrate specificity of enzyme in organic solvent vs water is reversed. J. Am. Chem. Soc. 108 (1986) 2767-2768
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2767-2768
    • Zaks, A.1    Klibanov, A.M.2


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