Bioreduction of aryl azides during mutasynthesis of new ansamitocins

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • Lena Mancuso
  • Gerrit Jürjens
  • Jekaterina Hermane
  • Kirsten Harmrolfs
  • Simone Eichner
  • Jörg Fohrer
  • Wera Collisi
  • Florenz Sasse
  • Andreas Kirschning

Externe Organisationen

  • Helmholtz-Zentrum für Infektionsforschung GmbH (HZI)
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Details

OriginalspracheEnglisch
Seiten (von - bis)4442-4445
Seitenumfang4
FachzeitschriftOrganic Letters
Jahrgang15
Ausgabenummer17
PublikationsstatusVeröffentlicht - 27 Aug. 2013

Abstract

Supplementing a culture of a mutant strain of Actinosynnema pretiosum that is unable to biosynthesize aminohydroxy benzoic acid (AHBA), with 3-azido-5-hydroxy-benzoic acid and 3-azido-5-amino-benzoic acid, unexpectedly yielded anilino ansamitocins instead of the expected azido derivatives. This is the first example of the bioreduction of organic azides. The unique nature of these results was demonstrated when 3-azido-5-amino-benzoic acid was fed to the corresponding AHBA blocked mutant of Streptomyces hygroscopicus, the geldanamycin producer. This mutasynthetic experiment yielded the fully processed azido derivative of geldanamycin.

ASJC Scopus Sachgebiete

Zitieren

Bioreduction of aryl azides during mutasynthesis of new ansamitocins. / Mancuso, Lena; Jürjens, Gerrit; Hermane, Jekaterina et al.
in: Organic Letters, Jahrgang 15, Nr. 17, 27.08.2013, S. 4442-4445.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Mancuso, L, Jürjens, G, Hermane, J, Harmrolfs, K, Eichner, S, Fohrer, J, Collisi, W, Sasse, F & Kirschning, A 2013, 'Bioreduction of aryl azides during mutasynthesis of new ansamitocins', Organic Letters, Jg. 15, Nr. 17, S. 4442-4445. https://doi.org/10.1021/ol401989e
Mancuso, L., Jürjens, G., Hermane, J., Harmrolfs, K., Eichner, S., Fohrer, J., Collisi, W., Sasse, F., & Kirschning, A. (2013). Bioreduction of aryl azides during mutasynthesis of new ansamitocins. Organic Letters, 15(17), 4442-4445. https://doi.org/10.1021/ol401989e
Mancuso L, Jürjens G, Hermane J, Harmrolfs K, Eichner S, Fohrer J et al. Bioreduction of aryl azides during mutasynthesis of new ansamitocins. Organic Letters. 2013 Aug 27;15(17):4442-4445. doi: 10.1021/ol401989e
Mancuso, Lena ; Jürjens, Gerrit ; Hermane, Jekaterina et al. / Bioreduction of aryl azides during mutasynthesis of new ansamitocins. in: Organic Letters. 2013 ; Jahrgang 15, Nr. 17. S. 4442-4445.
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abstract = "Supplementing a culture of a mutant strain of Actinosynnema pretiosum that is unable to biosynthesize aminohydroxy benzoic acid (AHBA), with 3-azido-5-hydroxy-benzoic acid and 3-azido-5-amino-benzoic acid, unexpectedly yielded anilino ansamitocins instead of the expected azido derivatives. This is the first example of the bioreduction of organic azides. The unique nature of these results was demonstrated when 3-azido-5-amino-benzoic acid was fed to the corresponding AHBA blocked mutant of Streptomyces hygroscopicus, the geldanamycin producer. This mutasynthetic experiment yielded the fully processed azido derivative of geldanamycin.",
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AU - Mancuso, Lena

AU - Jürjens, Gerrit

AU - Hermane, Jekaterina

AU - Harmrolfs, Kirsten

AU - Eichner, Simone

AU - Fohrer, Jörg

AU - Collisi, Wera

AU - Sasse, Florenz

AU - Kirschning, Andreas

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Y1 - 2013/8/27

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