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Volumn 62, Issue 11, 2009, Pages 643-646

Enzymatic preparation of neomycin C from ribostamycin

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; BUTIROSIN; FRAMYCETIN; LIVIDOMYCIN; NEOMYCIN; NEOMYCIN C; OXIDOREDUCTASE; PAROMOMYCIN; RIBOSTAMYCIN; UNCLASSIFIED DRUG;

EID: 72449183148     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2009.88     Document Type: Article
Times cited : (8)

References (11)
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  • 3
    • 65249168100 scopus 로고    scopus 로고
    • In vitro biosynthesis of unnatural enterocin and wailupemycin polyketides
    • Kalaitzis, J. A., Cheng, Q., Thomas, P. M., Kelleher, N. L. & Moore, B. S. In vitro biosynthesis of unnatural enterocin and wailupemycin polyketides. J. Nat. Prod. 72, 469-472 (2009).
    • (2009) J. Nat. Prod. , vol.72 , pp. 469-472
    • Kalaitzis, J.A.1    Cheng, Q.2    Thomas, P.M.3    Kelleher, N.L.4    Moore, B.S.5
  • 4
    • 64049089984 scopus 로고    scopus 로고
    • Biosynthetic enzymes for the aminoglycosides butirosin and neomycin
    • Kudo, F. & Eguchi, T. Biosynthetic enzymes for the aminoglycosides butirosin and neomycin. Methods Enzymol. 459, 493-519 (2009).
    • (2009) Methods Enzymol. , vol.459 , pp. 493-519
    • Kudo, F.1    Eguchi, T.2
  • 5
    • 44049095529 scopus 로고    scopus 로고
    • Involvement of two distinct N-cetylglucosaminyltransferases and a dual-function deacetylase in neomycin biosynthesis
    • Yokoyama, K., Yamamoto, Y., Kudo, F. & Eguchi, T. Involvement of two distinct N-cetylglucosaminyltransferases and a dual-function deacetylase in neomycin biosynthesis. Chembiochem 9, 865-869 (2008).
    • (2008) Chembiochem , vol.9 , pp. 865-869
    • Yokoyama, K.1    Yamamoto, Y.2    Kudo, F.3    Eguchi, T.4
  • 7
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    • Biosynthetic genes for aminoglycoside antibiotics
    • Kudo, F. & Eguchi, T. Biosynthetic genes for aminoglycoside antibiotics. J. Antibiot. 62, 471-481 (2009).
    • (2009) J. Antibiot. , vol.62 , pp. 471-481
    • Kudo, F.1    Eguchi, T.2
  • 8
    • 34547562892 scopus 로고    scopus 로고
    • Elaboration of neosamine rings in the biosynthesis of neomycin and butirosin
    • Huang, F. et al. Elaboration of neosamine rings in the biosynthesis of neomycin and butirosin. Chembiochem 8, 283-288 (2007).
    • (2007) Chembiochem , vol.8 , pp. 283-288
    • Huang, F.1
  • 9
    • 0019414017 scopus 로고
    • Hydroxy derivatives, as intermediates in the biosynthesis of neomycin and paromomycin
    • Autissier, D., Barthelemy, P., Mazieres, N., Peyre, M. & Penasse, L. Hydroxy derivatives, as intermediates in the biosynthesis of neomycin and paromomycin. J. Antibiot. 34, 536-543 (1981).
    • (1981) J. Antibiot. , vol.34 , pp. 536-543
    • Autissier, D.1    Barthelemy, P.2    Mazieres, N.3    Peyre, M.4    Deamino, P.L.5
  • 10
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    • S-adenosylmethionine as an oxidant: The radical SAM superfamily
    • Wang, S. C. & Frey, P. A. S-adenosylmethionine as an oxidant: the radical SAM superfamily. Trends Biochem. Sci. 32, 101-110 (2007).
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    • Wang, S.C.1    Frey, P.A.2
  • 11
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    • A proton and carbon 13 nuclear magnetic resonance study of neomycin B and its interactions with phosphatidylinositol 4,5-bisphosphate
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.