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Volumn 96, Issue 6, 2003, Pages 581-584

Stereoselective Biotransformation of Limonene and Limonene Oxide by Cyanobacterium, Synechococcus sp. PCC 7942

Author keywords

Cyanobacterium; Enantioselective hydroxylation; Limonene; Limonene oxide

Indexed keywords

CALCIUM; CELL IMMOBILIZATION; CELLS; CHEMICAL BONDS; ORGANIC COMPOUNDS; STEREOCHEMISTRY;

EID: 0345864013     PISSN: 13891723     EISSN: None     Source Type: Journal    
DOI: 10.1263/jbb.96.581     Document Type: Article
Times cited : (43)

References (19)
  • 2
    • 44949269802 scopus 로고
    • Biotransformation of exogenous substrates by plant cell cultures
    • Suga, T. and Hirata, T.: Biotransformation of exogenous substrates by plant cell cultures. Phytochemistry, 29, 2394-2406 (1990).
    • (1990) Phytochemistry , vol.29 , pp. 2394-2406
    • Suga, T.1    Hirata, T.2
  • 3
    • 12044253833 scopus 로고
    • Baker's yeast mediated transformations in organic chemistry
    • Cusk, R. and Glänzer, B. I.: Baker's yeast mediated transformations in organic chemistry. Chem. Rev., 91, 49-97 (1991).
    • (1991) Chem. Rev. , vol.91 , pp. 49-97
    • Cusk, R.1    Glänzer, B.I.2
  • 4
    • 0000251275 scopus 로고
    • Enzymes in synthetic organic chemistry
    • 1st ed., Pergamon, Elsevier, Amsterdam
    • Wong, C.-H. and Whitesides, G. M.: Enzymes in synthetic organic chemistry. Tetrahedron Organic Series, vol. 12, 1st ed., p. 41-194. Pergamon, Elsevier, Amsterdam (1994).
    • (1994) Tetrahedron Organic Series , vol.12 , pp. 41-194
    • Wong, C.-H.1    Whitesides, G.M.2
  • 5
    • 33748628870 scopus 로고    scopus 로고
    • Preparative biotransformations: The employment of enzymes and whole cells in synthetic organic chemistry
    • Roberts, S. M.: Preparative biotransformations: the employment of enzymes and whole cells in synthetic organic chemistry. J. Chem. Soc., Perkin 1, 157-169 (1998).
    • (1998) J. Chem. Soc., Perkin 1 , pp. 157-169
    • Roberts, S.M.1
  • 6
    • 0032807862 scopus 로고    scopus 로고
    • Application of enzyme- and microorganism-catalyzed reaction to organic synthesis
    • Sugai, T.: Application of enzyme-and microorganism-catalyzed reaction to organic synthesis. Curr. Org. Chem., 3, 373-406 (1999).
    • (1999) Curr. Org. Chem. , vol.3 , pp. 373-406
    • Sugai, T.1
  • 7
    • 0020423165 scopus 로고
    • Synthetic study of polyene macrolides, synthesis of a C29-37 fragment for amphotericin B and nystatin
    • Brooks, D. W. and Kellogg, R. P.: Synthetic study of polyene macrolides, synthesis of a C29-37 fragment for amphotericin B and nystatin. Tetrahedron Lett., 23, 4991-4994 (1982).
    • (1982) Tetrahedron Lett. , vol.23 , pp. 4991-4994
    • Brooks, D.W.1    Kellogg, R.P.2
  • 8
    • 84957327821 scopus 로고
    • Synthesis of the sex-attractant of pine sawflies
    • Kikukawa, T., Imaida, M., and Tai, A.: Synthesis of the sex-attractant of pine sawflies. Bull. Chem. Soc. Jpn., 57, 1954-1960 (1984).
    • (1984) Bull. Chem. Soc. Jpn. , vol.57 , pp. 1954-1960
    • Kikukawa, T.1    Imaida, M.2    Tai, A.3
  • 9
    • 0000397873 scopus 로고
    • Biochemical methods in enantioselective synthesis of bioactive natural products
    • Mori, K.: Biochemical methods in enantioselective synthesis of bioactive natural products. Synlett, 1097-1109 (1995).
    • (1995) Synlett , pp. 1097-1109
    • Mori, K.1
  • 10
    • 0022691540 scopus 로고
    • Application of immobilized cells of Thermoanaerobium brockii for stereoselective reductions of oxo-acid esters
    • Sonnleitner, B. and Fiechter, A.: Application of immobilized cells of Thermoanaerobium brockii for stereoselective reductions of oxo-acid esters. Appl. Microbiol. Biotechnol., 23, 424-429 (1986).
    • (1986) Appl. Microbiol. Biotechnol. , vol.23 , pp. 424-429
    • Sonnleitner, B.1    Fiechter, A.2
  • 11
    • 84907036080 scopus 로고
    • A study of the stereocontrolled reduction of aliphatic β-ketoesters by Geotrichum candidum
    • Buisson, D., Azerad, R., Sanner, C., and Larcheveque, M.: A study of the stereocontrolled reduction of aliphatic β-ketoesters by Geotrichum candidum. Biocatalysis, 5, 249-265 (1992).
    • (1992) Biocatalysis , vol.5 , pp. 249-265
    • Buisson, D.1    Azerad, R.2    Sanner, C.3    Larcheveque, M.4
  • 12
    • 0029016140 scopus 로고
    • Stereochemical control in microbial reduction. XXV. Additives controlling diastereoselectivity in a microbial reduction of ethyl 2-methyl-3-oxobutanoate
    • Nakamura, K., Takanobe, K., and Ohno, A.: Stereochemical control in microbial reduction. XXV. Additives controlling diastereoselectivity in a microbial reduction of ethyl 2-methyl-3-oxobutanoate. Bull. Chem. Soc. Jpn., 68, 285-288 (1995).
    • (1995) Bull. Chem. Soc. Jpn. , vol.68 , pp. 285-288
    • Nakamura, K.1    Takanobe, K.2    Ohno, A.3
  • 14
    • 0034684069 scopus 로고    scopus 로고
    • Stereocontrolled reduction of α-keto esters with thermophilic actinomycete, Streptomyces thermocyaneoviolaceus IFO 14271
    • Ishihara, K., Yamaguchi, H., Nakamura, K., Hamada, H., and Nakajima, N.: Stereocontrolled reduction of α-keto esters with thermophilic actinomycete, Streptomyces thermocyaneoviolaceus IFO 14271. J. Mol. Catal., B: Enzym., 10, 429-434 (2000).
    • (2000) J. Mol. Catal., B: Enzym. , vol.10 , pp. 429-434
    • Ishihara, K.1    Yamaguchi, H.2    Nakamura, K.3    Hamada, H.4    Nakajima, N.5
  • 15
    • 0030879573 scopus 로고    scopus 로고
    • Biotransformation of (+) limonene and (-) piperitone by yeasts and yeast-like fungi
    • Rensburg, E., Moleleki, N., Walt, J. P., Botes, P. J., and Dyk, M. S.: Biotransformation of (+) limonene and (-) piperitone by yeasts and yeast-like fungi. Biotechnol. Lett., 19, 779-782 (1997).
    • (1997) Biotechnol. Lett. , vol.19 , pp. 779-782
    • Rensburg, E.1    Moleleki, N.2    Walt, J.P.3    Botes, P.J.4    Dyk, M.S.5
  • 16
    • 0032955152 scopus 로고    scopus 로고
    • Biotransformation of (S)-(-)- and (R)-(+)-limonene using Solanum aviculare and Dioscorea deltoidea plant cells
    • Vanek, T., Valterova, I., and Vaisar, T.: Biotransformation of (S)-(-)-and (R)-(+)-limonene using Solanum aviculare and Dioscorea deltoidea plant cells. Phytochemistry, 50, 1347-1351 (1999).
    • (1999) Phytochemistry , vol.50 , pp. 1347-1351
    • Vanek, T.1    Valterova, I.2    Vaisar, T.3
  • 17
    • 0034718384 scopus 로고    scopus 로고
    • Cyanobacterium-catalyzed asymmetric reduction of ketones
    • Nakamura, K., Yamanaka, R., Tohi, K., and Hamada, H.: Cyanobacterium-catalyzed asymmetric reduction of ketones. Tetrahedron Lett., 41, 6799-6802 (2000).
    • (2000) Tetrahedron Lett. , vol.41 , pp. 6799-6802
    • Nakamura, K.1    Yamanaka, R.2    Tohi, K.3    Hamada, H.4
  • 18
    • 0010409202 scopus 로고
    • Enantioselective introduction of oxygen functions into alkenes - Oxidation of limonene by the cultured suspension cells of Nicotiana tabacum
    • Hirata, T., Izumi, S., Kido, T., Shimoi, Y., and Ikeda, Y.: Enantioselective introduction of oxygen functions into alkenes - oxidation of limonene by the cultured suspension cells of Nicotiana tabacum. Plant Tissue Culture Lett., 10, 89-91 (1993).
    • (1993) Plant Tissue Culture Lett. , vol.10 , pp. 89-91
    • Hirata, T.1    Izumi, S.2    Kido, T.3    Shimoi, Y.4    Ikeda, Y.5
  • 19
    • 0030682453 scopus 로고    scopus 로고
    • Preparation of optically active α-hydroxy esters: Stereoselective reduction of α-keto esters using thermophilic actinomycetes
    • Ishihara, K., Nishitani, M., Yamaguchi, H., Nakajima, N., Ohshima, T., and Nakamura, K.: Preparation of optically active α-hydroxy esters: stereoselective reduction of α-keto esters using thermophilic actinomycetes. J. Ferment. Bioeng., 84, 268-270 (1997).
    • (1997) J. Ferment. Bioeng. , vol.84 , pp. 268-270
    • Ishihara, K.1    Nishitani, M.2    Yamaguchi, H.3    Nakajima, N.4    Ohshima, T.5    Nakamura, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.