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Volumn 36, Issue 12, 1983, Pages 1735-1742

The biosynthesis of brominated pyrrolnitrin derivatives by pseudomonas aureofaciens

Author keywords

[No Author keywords available]

Indexed keywords

DRUG ACCUMULATION; DRUG ANALYSIS; DRUG IDENTIFICATION; DRUG ISOLATION; DRUG STRUCTURE; IN VITRO STUDY; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PSEUDOMONAS AERUGINOSA; PYRROLNITRIN DERIVATIVE; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 0021018442     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.7164/antibiotics.36.1735     Document Type: Article
Times cited : (37)

References (14)
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  • 6
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    • Biosynthese von Pyrrolnitrin - Nachweis von 4-(2′-Amino-3′-chIorphenyl)pyrrol-2-carbonsäure.
    • Salcher O. Lingens F. & P. Fischer: Biosynthese von Pyrrolnitrin - Nachweis von 4-(2′-Amino-3′-chIorphenyl)pyrrol-2-carbonsäure. Tetrahedron Lett. 1978: 3097–3100, 1978
    • (1978) Tetrahedron Lett. , pp. 3097-3100
    • Salcher, O.1    Lingens, F.2    Fischer, P.3
  • 7
    • 0018951781 scopus 로고
    • Isolation and characterisation of a mutant of Pseudomonas aureofaciens ATCC 15926 with an increased capacity for synthesis of pyrrolnitrin.
    • Salcher O. & F. Lingens: Isolation and characterisation of a mutant of Pseudomonas aureofaciens ATCC 15926 with an increased capacity for synthesis of pyrrolnitrin. J. Gen. Microbiol. 118: 509–513, 1980
    • (1980) J. Gen. Microbiol. , vol.118 , pp. 509-513
    • Salcher, O.1    Lingens, F.2
  • 9
    • 84942499416 scopus 로고
    • Spurenanalyse physiologisch aktiver, einfacher Indolderivate.
    • Stahl E. & H. Kaldewey: Spurenanalyse physiologisch aktiver, einfacher Indolderivate. Hoppe-Seyler's Z. Physiol. Chem. 323: 182–191, 1961
    • (1961) Hoppe-Seyler's Z. Physiol. Chem. , vol.323 , pp. 182-191
    • Stahl, E.1    Kaldewey, H.2
  • 10
    • 84985581059 scopus 로고
    • Formation of pyrrolnitrin and 3-(2-amino-3-chIorophenyl)-pyrrole from 7-chlorotryptophan.
    • van Pée, K.-H.; O. Salcher & F. Lingens: Formation of pyrrolnitrin and 3-(2-amino-3-chIorophenyl)-pyrrole from 7-chlorotryptophan. Angew. Chemie, Int. Ed. Engl. 19: 828–829, 1980
    • (1980) Angew. Chemie, Int. Ed. Engl , vol.19 , pp. 828-829
    • van Pée, K.-H.1    Salcher, O.2    Lingens, F.3
  • 11
    • 0003515609 scopus 로고
    • Applications of Nuclear Magnetic Resonance Spectroscopy in Organic Chemistry.
    • Pergamon Press, New York
    • Jackman L.M. & S. Sternhell: Applications of Nuclear Magnetic Resonance Spectroscopy in Organic Chemistry. 2nd ed. pp. 202–215, Pergamon Press, New York, 1969
    • (1969) , pp. 202-215
    • Jackman, L.M.1    Sternhell, S.2
  • 12
    • 85010157811 scopus 로고
    • NMR Spectra of Simple Heterocycles.
    • Batterham T.J.: NMR Spectra of Simple Heterocycles. Wiley, New York, 1973
    • (1973) Wiley, New York
    • Batterham, T.J.1
  • 13
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    • Analyse kernmagnetischer Resonanzspektren vom Typ A2B2 mit Ergebnissen von para-disubstituierten Benzolen, Äthylengruppen und Pyrrol.
    • Dischler B.: Analyse kernmagnetischer Resonanzspektren vom Typ A2B2 mit Ergebnissen von para-disubstituierten Benzolen, Äthylengruppen und Pyrrol. Z. Naturforsch. 20 a: S88–901, 1965
    • (1965) Z. Naturforsch. , vol.20 , pp. S88-901
    • Dischler, B.1
  • 14
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    • Isolation of the bromo analogue of caldariomycin from Caldariomyces fumago
    • Patterson E.L. Andres W.W. & Mitcher L.A.: Isolation of the bromo analogue of caldariomycin from Caldariomyces fumago. Appl. Microbiol. 15: 528–530, 1967
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.