메뉴 건너뛰기




Volumn 96, Issue 2, 2003, Pages 199-202

Selective α-glucosylation of eugenol by α-glucosyl transfer enzyme of Xanthomonas campestris WU-9701

Author keywords

Eugenol; Pro drug; Selective glucosylation; Transglucosylation; Xanthomonas campestris

Indexed keywords

BIOSYNTHESIS; NUCLEAR MAGNETIC RESONANCE; PH;

EID: 0042377114     PISSN: 13891723     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1389-1723(03)90127-7     Document Type: Article
Times cited : (16)

References (13)
  • 1
    • 0041460469 scopus 로고    scopus 로고
    • Effects of clove bud oil related eugenyl glucoside on hair growth
    • in Japanese
    • Hamada, K. and Ikemoto, T.: Effects of clove bud oil related eugenyl glucoside on hair growth. Fragrance J., 29, 47-52 (2001). (in Japanese)
    • (2001) Fragrance J. , vol.29 , pp. 47-52
    • Hamada, K.1    Ikemoto, T.2
  • 2
    • 0030470193 scopus 로고    scopus 로고
    • Anomer selective formation of l-menthyl α-D-glucopyranoside by α-glucosidase-catalyzed reaction
    • Nakagawa, H., Yoshiyama, M., Shimura, S., Kirimura, K., and Usami, S.: Anomer selective formation of l-menthyl α-D-glucopyranoside by α-glucosidase-catalyzed reaction. Biosci. Biotech. Biochem., 60, 1914-1915 (1996).
    • (1996) Biosci. Biotech. Biochem. , vol.60 , pp. 1914-1915
    • Nakagawa, H.1    Yoshiyama, M.2    Shimura, S.3    Kirimura, K.4    Usami, S.5
  • 4
    • 0031925792 scopus 로고    scopus 로고
    • Anomer-selective glucosylation of l-menthol using lyophilized cells of Saccharomyces cerevisiae
    • Noguchi, K., Nakagawa, H., Yoshiyama, M., Shimura, S., Kirimura, K., and Usami, S.: Anomer-selective glucosylation of l-menthol using lyophilized cells of Saccharomyces cerevisiae. J. Ferment. Bioeng., 85, 436-438 (1998).
    • (1998) J. Ferment. Bioeng. , vol.85 , pp. 436-438
    • Noguchi, K.1    Nakagawa, H.2    Yoshiyama, M.3    Shimura, S.4    Kirimura, K.5    Usami, S.6
  • 5
    • 0034037964 scopus 로고    scopus 로고
    • α-Anomer-selective glucosylation of menthol with high yield through a crystal accumulation reaction using lyophilized cells of Xanthomonas campestris WU-9701
    • Nakagawa, H., Dobashi, Y., Sato, T., Yoshida, K., Tsugane, T., Shimura, S., Kirimura, K., Kino, K., and Usami, S.: α-Anomer-selective glucosylation of menthol with high yield through a crystal accumulation reaction using lyophilized cells of Xanthomonas campestris WU-9701. J. Biosci. Bioeng., 89, 138-144 (2000).
    • (2000) J. Biosci. Bioeng. , vol.89 , pp. 138-144
    • Nakagawa, H.1    Dobashi, Y.2    Sato, T.3    Yoshida, K.4    Tsugane, T.5    Shimura, S.6    Kirimura, K.7    Kino, K.8    Usami, S.9
  • 6
    • 0034511884 scopus 로고    scopus 로고
    • α-Anomer-selective glucosylation of (+)-catechin by the crude enzyme, showing glucosyl transfer activity, of Xanthomonas campestris WU-9701
    • Sato, T., Nakagawa, H., Kurosu, J., Yoshida, K., Tsugane, T., Shimura, S., Kirimura, K., Kino, K., and Usami, S.: α-Anomer-selective glucosylation of (+)-catechin by the crude enzyme, showing glucosyl transfer activity, of Xanthomonas campestris WU-9701. J. Biosci. Bioeng., 90, 625-630 (2000).
    • (2000) J. Biosci. Bioeng. , vol.90 , pp. 625-630
    • Sato, T.1    Nakagawa, H.2    Kurosu, J.3    Yoshida, K.4    Tsugane, T.5    Shimura, S.6    Kirimura, K.7    Kino, K.8    Usami, S.9
  • 7
    • 0036098664 scopus 로고    scopus 로고
    • Enzymatic synthesis of α-arbutin by α-anomer-selective glucosylation of hydroquinone using lyophilized cells of Xanthomonas campestris WU-9701
    • Kurosu, J., Sato, T., Yoshida, K., Tsugane, T., Shimura, S., Kirimura, K., Kino, K., and Usami, S.: Enzymatic synthesis of α-arbutin by α-anomer-selective glucosylation of hydroquinone using lyophilized cells of Xanthomonas campestris WU-9701. J. Biosci. Bioeng., 93, 328-330 (2002).
    • (2002) J. Biosci. Bioeng. , vol.93 , pp. 328-330
    • Kurosu, J.1    Sato, T.2    Yoshida, K.3    Tsugane, T.4    Shimura, S.5    Kirimura, K.6    Kino, K.7    Usami, S.8
  • 8
    • 0036379776 scopus 로고    scopus 로고
    • Enzymatic synthesis of l-menthyl α-maltoside and l-menthyl α-maltooligosides from l-menthyl α-glucoside by cyclodextrin glucanotransferase
    • Do, H., Sato, T., Kirimura, K., Kino, K., and Usami, S.: Enzymatic synthesis of l-menthyl α-maltoside and l-menthyl α-maltooligosides from l-menthyl α-glucoside by cyclodextrin glucanotransferase. J. Biosci. Bioeng., 94, 119-123 (2002).
    • (2002) J. Biosci. Bioeng. , vol.94 , pp. 119-123
    • Do, H.1    Sato, T.2    Kirimura, K.3    Kino, K.4    Usami, S.5
  • 9
    • 0026824443 scopus 로고
    • Biotransformation of isoeugenol and eugenol by cultured cells of Eucalyptus perriniana
    • Orihara, Y., Furuya, T., Hashimoto, N., Deguchi, Y., Tokoro, K., and Kanisawa, T.: Biotransformation of isoeugenol and eugenol by cultured cells of Eucalyptus perriniana. Phytochemistry, 31, 827-831 (1992).
    • (1992) Phytochemistry , vol.31 , pp. 827-831
    • Orihara, Y.1    Furuya, T.2    Hashimoto, N.3    Deguchi, Y.4    Tokoro, K.5    Kanisawa, T.6
  • 10
    • 0036009873 scopus 로고    scopus 로고
    • Arbutin synthase, a novel member of the NRD1β glycosyltransferase family, is a unique multifunctional enzyme converting various natural products and xenobiotics
    • Hefner, T., Arend, J., Warzecha, H., Siems, K., and Stöckigt, J.: Arbutin synthase, a novel member of the NRD1β glycosyltransferase family, is a unique multifunctional enzyme converting various natural products and xenobiotics. Bioorg. Med. Chem., 10, 1731-1741 (2002).
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 1731-1741
    • Hefner, T.1    Arend, J.2    Warzecha, H.3    Siems, K.4    Stöckigt, J.5
  • 11
    • 0028095950 scopus 로고
    • α-D-Glucosyl transfer to phenolic compounds by sucrose phosphorylase from Leuconostoc mesenteroides and production of α-arbutin
    • Kitao, K. and Sekine, H.: α-D-Glucosyl transfer to phenolic compounds by sucrose phosphorylase from Leuconostoc mesenteroides and production of α-arbutin. Biosci. Biotech. Biochem., 58, 38-42 (1994).
    • (1994) Biosci. Biotech. Biochem. , vol.58 , pp. 38-42
    • Kitao, K.1    Sekine, H.2
  • 12
    • 0031673648 scopus 로고    scopus 로고
    • Conversion of cyclodextrin into high-amylose starch of low molecular mass by means of cyclodextrin glucanotransferase
    • Rendleman, J. A. and Knutson, C. A.: Conversion of cyclodextrin into high-amylose starch of low molecular mass by means of cyclodextrin glucanotransferase. Biotechnol. Appl. Biochem., 28, 219-228 (1998).
    • (1998) Biotechnol. Appl. Biochem. , vol.28 , pp. 219-228
    • Rendleman, J.A.1    Knutson, C.A.2
  • 13
    • 0026926218 scopus 로고
    • Accepter specificity of cyclodextrin glucanotransferase from Bacillus stearothermophilus and synthesis of α-D-glucosyl O-β -galactosyl-(1→4)-β-D-glucoside
    • Kitahata, S., Hara, K., Nakano, H., Kuwahara, N., and Koizumi, K.: Accepter specificity of cyclodextrin glucanotransferase from Bacillus stearothermophilus and synthesis of α-D-glucosyl O-β -galactosyl-(1→4)-β-D-glucoside. Biosci. Biotech. Biochem., 56, 1386-1391 (1992).
    • (1992) Biosci. Biotech. Biochem. , vol.56 , pp. 1386-1391
    • Kitahata, S.1    Hara, K.2    Nakano, H.3    Kuwahara, N.4    Koizumi, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.