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Volumn 50, Issue 8, 1997, Pages 701-703

Biosynthesis of the shikimate-derived starter unit of the immunosuppressant ascomycin: Stereochemistry of the 1,4-conjugate elimination

Author keywords

[No Author keywords available]

Indexed keywords

ASCOMYCIN; IMMUNOSUPPRESSIVE AGENT; RAPAMYCIN; SHIKIMIC ACID; TACROLIMUS;

EID: 0030828993     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.50.701     Document Type: Short Survey
Times cited : (16)

References (10)
  • 1
    • 0028585864 scopus 로고
    • Biosynthetic studies of ascomycin (FK520): Formation of the (1R,3R,4R)-3,4-dihydroxycyclohexanecarboxylic acid-derived moiety
    • WALLACE, K. K.; K. A. REYNOLDS, K. A., KOCH, H. A. I. MCARTHUR, M. S. BROWN, R. G. WAX & B. S. MOORE: Biosynthetic studies of ascomycin (FK520): Formation of the (1R,3R,4R)-3,4-dihydroxycyclohexanecarboxylic acid-derived moiety. J. Amer. Chem. Soc. 116: 11600-11601, 1994
    • (1994) J. Amer. Chem. Soc. , vol.116 , pp. 11600-11601
    • Wallace, K.K.1    Reynolds, K.A.2    Koch, K.A.3    Mcarthur, H.A.I.4    Brown, M.S.5    Wax, R.G.6    Moore, B.S.7
  • 2
    • 0002539866 scopus 로고
    • The biosynthesis and enzymology of an immunosuppresant, immunomycin, produced by Streptomyces hygroscopicus var. ascomyceticus
    • BYRNE, K. M.; A. SHAFIEE, J. B. NIELSEN, B. ARISON, R. L. MONAGHAN & L. KAPLAN: The biosynthesis and enzymology of an immunosuppresant, immunomycin, produced by Streptomyces hygroscopicus var. ascomyceticus. Develop. Ind. Microbiol. 32: 29-44, 1993
    • (1993) Develop. Ind. Microbiol. , vol.32 , pp. 29-44
    • Byrne, K.M.1    Shafiee, A.2    Nielsen, J.B.3    Arison, B.4    Monaghan, R.L.5    Kaplan, L.6
  • 4
    • 0025973839 scopus 로고
    • Incorporation of acetate, propionate, methionine into rapamycin by Streptomyces hygroscopicus
    • PAIVA, N.; A. L. DEMAIN & M. F. ROBERTS: Incorporation of acetate, propionate, methionine into rapamycin by Streptomyces hygroscopicus. J. Nat. Prod. 54: 167-177, 1991
    • (1991) J. Nat. Prod. , vol.54 , pp. 167-177
    • Paiva, N.1    Demain, A.L.2    Roberts, M.F.3
  • 5
    • 0002455067 scopus 로고    scopus 로고
    • Biosynthesis of ω-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius: The stereochemistry of the initial 1,4-conjugate elimination
    • HANDA, S. & H. G. FLOSS: Biosynthesis of ω-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius: the stereochemistry of the initial 1,4-conjugate elimination. J. Chem. Soc., Chem. Commun. 1997: 153-154, 1997
    • (1997) J. Chem. Soc., Chem. Commun. , vol.1997 , pp. 153-154
    • Handa, S.1    Floss, H.G.2
  • 6
    • 0029872079 scopus 로고    scopus 로고
    • Organization of the biosynthetic gene cluster for rapamycin in Streptomyces hygroscopicus: Analysis of the enzymatic domains in the modular polyketide synthase
    • APARICIO, J. F.; I. MOLNAR, T. SCHWECKE, A. KÖNIG, S. F. HAYDOCK, L. H. KHAW, J. STAUNTON & P. F. LEADLAY: Organization of the biosynthetic gene cluster for rapamycin in Streptomyces hygroscopicus: analysis of the enzymatic domains in the modular polyketide synthase. Gene 169: 9-16, 1996
    • (1996) Gene , vol.169 , pp. 9-16
    • Aparicio, J.F.1    Molnar, I.2    Schwecke, T.3    König, A.4    Haydock, S.F.5    Khaw, L.H.6    Staunton, J.7    Leadlay, P.F.8
  • 8
    • 0001024921 scopus 로고
    • Biosynthesis of the cyclohexanecarboxylic acid starter unit of ω-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius
    • MOORE, B. S.; K. PORALLA & H. G. FLOSS. Biosynthesis of the cyclohexanecarboxylic acid starter unit of ω-cyclohexyl fatty acids in Alicyclobacillus acidocaldarius. J. Amer. Chem. Soc. 115: 5267-5274, 1993
    • (1993) J. Amer. Chem. Soc. , vol.115 , pp. 5267-5274
    • Moore, B.S.1    Poralla, K.2    Floss, H.G.3
  • 9
    • 0025821260 scopus 로고
    • Biosynthesis of ansatrienin: Stereochemical course of the final reduction step leading to the cyclohexanecarboxylic acid moiety
    • REYNOLDS, K. A.; K. M. FOX, Z.-M. YUAN & Y. LAM: Biosynthesis of ansatrienin: Stereochemical course of the final reduction step leading to the cyclohexanecarboxylic acid moiety. J. Amer. Chem. Soc. 113: 4339-4340, 1991
    • (1991) J. Amer. Chem. Soc. , vol.113 , pp. 4339-4340
    • Reynolds, K.A.1    Fox, K.M.2    Yuan, Z.-M.3    Lam, Y.4
  • 10
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    • Linking diversity in evolutionary origin and stereospecificity for enoyl thioester reductases: Determinaton and interpretation of the novel stereochemical course of reaction catalyzed by crotonyl CoA reductase from Streptomyces collinus
    • LIU, H.; K. K. WALLACE & K. A. REYNOLDS: Linking diversity in evolutionary origin and stereospecificity for enoyl thioester reductases: Determinaton and interpretation of the novel stereochemical course of reaction catalyzed by crotonyl CoA reductase from Streptomyces collinus. J. Amer. Chem. Soc. 119: 2973-2979, 1997
    • (1997) J. Amer. Chem. Soc. , vol.119 , pp. 2973-2979
    • Liu, H.1    Wallace, K.K.2    Reynolds, K.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.