Academic Journal

Champacyclin, a New Cyclic Octapeptide from Streptomyces Strain C42 Isolated from the Baltic Sea

التفاصيل البيبلوغرافية
العنوان: Champacyclin, a New Cyclic Octapeptide from Streptomyces Strain C42 Isolated from the Baltic Sea
المؤلفون: Alexander Pesic, Heike I. Baumann, Katrin Kleinschmidt, Paul Ensle, Jutta Wiese, Roderich D. Süssmuth, Johannes F. Imhoff
المصدر: Marine Drugs, Vol 11, Iss 12, Pp 4834-4857 (2013)
بيانات النشر: MDPI AG, 2013.
سنة النشر: 2013
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: Streptomyces champavatii, antimicrobial activity, fire blight, cyclic peptides, sequence ladder analysis, chiral GC-PCI/EI-MS, ESI-Ion-Trap-MSn, solid phase peptide synthesis (SPPS), on-resin cyclization, 2D NMR, Biology (General), QH301-705.5
الوصف: New isolates of Streptomyces champavatii were isolated from marine sediments of the Gotland Deep (Baltic Sea), from the Urania Basin (Eastern Mediterranean), and from the Kiel Bight (Baltic Sea). The isolates produced several oligopeptidic secondary metabolites, including the new octapeptide champacyclin (1a) present in all three strains. Herein, we report on the isolation, structure elucidation and determination of the absolute stereochemistry of this isoleucine/leucine (Ile/Leu = Xle) rich cyclic octapeptide champacyclin (1a). As 2D nuclear magnetic resonance (NMR) spectroscopy could not fully resolve the structure of (1a), additional information on sequence and configuration of stereocenters were obtained by a combination of multi stage mass spectrometry (MSn) studies, amino acid analysis, partial hydrolysis and subsequent enantiomer analytics with gas chromatography positive chmical ionization/electron impact mass spectrometry (GC-PCI/EI-MS) supported by comparison to reference dipeptides. Proof of the head-to-tail cyclization of (1a) was accomplished by solid phase peptide synthesis (SPPS) compared to an alternatively side chain cyclized derivative (2). Champacyclin (1a) is likely synthesized by a non-ribosomal peptide synthetase (NRPS), because of its high content of (d)-amino acids. The compound (1a) showed antimicrobial activity against the phytopathogen Erwinia amylovora causing the fire blight disease of certain plants.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1660-3397
Relation: http://www.mdpi.com/1660-3397/11/12/4834; https://doaj.org/toc/1660-3397
DOI: 10.3390/md11124834
URL الوصول: https://doaj.org/article/60012e340cad410f85762c0e1995f5b6
رقم الانضمام: edsdoj.60012e340cad410f85762c0e1995f5b6
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16603397
DOI:10.3390/md11124834