TY - JOUR A1 - Dashti, Yousef A1 - Grkovic, Tanja A1 - Abdelmohsen, Usama Ramadan A1 - Hentschel, Ute A1 - Quinn, Ronald J. T1 - Production of Induced Secondary Metabolites by a Co-Culture of Sponge-Associated Actinomycetes, Actinokineospora sp EG49 and Nocardiopsis sp RV163 JF - MARINE DRUGS N2 - Two sponge-derived actinomycetes, Actinokineospora sp. EG49 and Nocardiopsis sp. RV163, were grown in co-culture and the presence of induced metabolites monitored by H-1 NMR. Ten known compounds, including angucycline, diketopiperazine and beta-carboline derivatives 1-10, were isolated from the EtOAc extracts of Actinokineospora sp. EG49 and Nocardiopsis sp. RV163. Co-cultivation of Actinokineospora sp. EG49 and Nocardiopsis sp. RV163 induced the biosynthesis of three natural products that were not detected in the single culture of either microorganism, namely N-(2-hydroxyphenyl)-acetamide (11), 1,6-dihydroxyphenazine (12) and 5a, 6,11a, 12-tetrahydro-5a, 11a-dimethyl[1,4]benzoxazino[3,2-b][1,4]benzoxazine (13a). When tested for biological activity against a range of bacteria and parasites, only the phenazine 12 was active against Bacillus sp. P25, Trypanosoma brucei and interestingly, against Actinokineospora sp. EG49. These findings highlight the co-cultivation approach as an effective strategy to access the bioactive secondary metabolites hidden in the genomes of marine actinomycetes. KW - co-cultivation KW - induced metabolites KW - sponge-associated actinomyetes KW - NMR fingerprint KW - bioactivity KW - natural products KW - A-D KW - aspergillus fumigatus KW - marine KW - biosynthesis Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-116547 SN - 1660-3397 VL - 12 IS - 5 ER - TY - JOUR A1 - Kunz, Anna Lena A1 - Labes, Antje A1 - Wiese, Jutta A1 - Bruhn, Torsten A1 - Bringmann, Gerhard A1 - Imhoff, Johannes F. T1 - Nature's Lab for Derivatization: New and Revised Structures of a Variety of Streptophenazines Produced by a Sponge-Derived Streptomyces Strain JF - Marine Drugs N2 - Eight streptophenazines (A-H) have been identified so far as products of Streptomyces strain HB202, which was isolated from the sponge Halichondria panicea from the Baltic Sea. The variation of bioactivities based on small structural changes initiated further studies on new derivatives. Three new streptophenazines (I-K) were identified after fermentation in the present study. In addition, revised molecular structures of streptophenazines C, D, F and H are proposed. Streptophenazines G and K exhibited moderate antibacterial activity against the facultative pathogenic bacterium Staphylococcus epidermidis and against Bacillus subtilis. All tested compounds (streptophenazines G, I-K) also showed moderate activities against PDE 4B. KW - marine natural product KW - phenazine KW - Baltic Sea KW - streptomyces KW - halichondria panicea KW - obstructive pulmonary disease KW - phosphodiesterase-4 inhibitor KW - absolute configuration KW - biosynthesis KW - rofumilast Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-116816 SN - 1660-3397 VL - 12 IS - 4 ER -