TY - JOUR
T1 - Five naturally bioactive molecules including two rhamnopyranoside derivatives isolated from the Streptomyces sp. strain TN58
AU - Ben Ameur Mehdi, Raoudha
AU - Shaaban, Khaled A.
AU - Rebai, Ines Karray
AU - Smaoui, Slim
AU - Bejar, Samir
AU - Mellouli, Lotfi
PY - 2009/1
Y1 - 2009/1
N2 - Extraction of 25 L fermentation broth of the newly isolated Streptomyces sp. strain TN58 and various separation and purification steps led to the isolation of five bioactive metabolites, namely brevianamide F (C1), reported from a streptomycete for the first time, N-acetyltryptamine (C2), thiazolidomycin (C3), and two rhamnopyranosides (C4 and C5). These two rhamnopyranosides were produced directly, without precursor addition. The chemical structure of these five active compounds was established on the basis of 1H, 13C/APT and 2D NMR spectra, ESI and EI-MS data, and by comparison with data from the literature. According to the biological studies, we show in this work that the compounds C1, C2, C4 and C5 possess antimicrobial activities.
AB - Extraction of 25 L fermentation broth of the newly isolated Streptomyces sp. strain TN58 and various separation and purification steps led to the isolation of five bioactive metabolites, namely brevianamide F (C1), reported from a streptomycete for the first time, N-acetyltryptamine (C2), thiazolidomycin (C3), and two rhamnopyranosides (C4 and C5). These two rhamnopyranosides were produced directly, without precursor addition. The chemical structure of these five active compounds was established on the basis of 1H, 13C/APT and 2D NMR spectra, ESI and EI-MS data, and by comparison with data from the literature. According to the biological studies, we show in this work that the compounds C1, C2, C4 and C5 possess antimicrobial activities.
KW - Antimicrobial activities
KW - Chemical structure
KW - Purification
KW - Rhamnopyranoside derivatives
KW - Streptomyces sp. TN58
UR - http://www.scopus.com/inward/record.url?scp=70349487949&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70349487949&partnerID=8YFLogxK
U2 - 10.1080/14786410802362352
DO - 10.1080/14786410802362352
M3 - Article
C2 - 19662574
AN - SCOPUS:70349487949
SN - 1478-6419
VL - 23
SP - 1095
EP - 1107
JO - Natural Product Research
JF - Natural Product Research
IS - 12
ER -