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Volumn 39, Issue 1, 2000, Pages 224-227

Genetic engineering of Streptomyces coelicolor A3(2) for the enantioselective reduction of unnatural β-keto-ester substrates

Author keywords

Biosynthesis; Enzyme catalysis; Genetic engineering; Polyketides; Reductions

Indexed keywords

ACTINORHODINE;

EID: 0034598535     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(20000103)39:1<224::AID-ANIE224>3.0.CO;2-R     Document Type: Article
Times cited : (21)

References (17)
  • 9
    • 0030875774 scopus 로고    scopus 로고
    • Khosla et al. have previously described the conversion of NAC thioesters into erythromycin analogues using an engineered DEBS KS1 null mutant: J. R. Jacobsen, C. R. Hutchinson, D. E. Cane, C. Khosla, Science 1997, 277, 367.
    • (1997) Science , vol.277 , pp. 367
    • Jacobsen, J.R.1    Hutchinson, C.R.2    Cane, D.E.3    Khosla, C.4
  • 15
    • 4544303707 scopus 로고
    • D. W. Brooks, L. D. L. Lu, S. Masamune, Angew. Chem. 1979, 91, 76; Angew. Chem. Int. Ed. Engl. 1979, 18, 72.
    • (1979) Angew. Chem. Int. Ed. Engl. , vol.18 , pp. 72
  • 16
    • 0027745960 scopus 로고
    • D value of (3S)-4-phenylbutanoic acid obtained from the feeding study (+2.6, c = 1) with that of the known (3R)-enantiomer (-5.3, c = 1): G. Capozzi, S. Roelens, S. Talami, J. Org. Chem. 1993, 58, 7932.
    • (1993) J. Org. Chem. , vol.58 , pp. 7932
    • Capozzi, G.1    Roelens, S.2    Talami, S.3
  • 17
    • 0342511024 scopus 로고    scopus 로고
    • note
    • 3. Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as Supplementary Publication no. CCDC-127928. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: (+ 44) 1223-336-033; e-mail: deposit@ccdc.cam.uk.ac).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.