Please use this identifier to cite or link to this item:
https://hdl.handle.net/10216/120263
Author(s): | Afonso T.B. Costa M.S. Rezende De Castro R. Freitas S. Silva A. Schneider M.P.C. Martins R. Leão P.N. |
Title: | Bartolosides E-K from a Marine coccoid cyanobacterium |
Publisher: | American Chemical Society |
Issue Date: | 2016 |
Abstract: | The glycosylated and halogenated dialkylresorcinol (DAR) compounds bartolosides A-D (1-4) were recently discovered from marine cyanobacteria and represent a novel family of glycolipids, encoded by the brt biosynthetic gene cluster. Here, we report the isolation and NMR- and MS-based structure elucidation of monoglycosylated bartolosides E-K (5-11), obtained from Synechocystis salina LEGE 06099, a strain closely related to the cyanobacterium that produces the diglycosylated 2-4. In addition, a genome region containing orthologues of brt genes was identified in this cyanobacterium. Interestingly, the major bartoloside in S. salina LEGE 06099 was 1 (above 0.5% dry wt), originally isolated from the phylogenetically distant filamentous cyanobacterium Nodosilinea sp. LEGE 06102. Compounds 5-11 are analogues of 1, with different alkyl chain lengths or halogenation patterns. Their structures and the organization of the brt genes suggest that the DAR-forming ketosynthase BrtD can generate structural diversity by accepting fatty acyl-derived substrates of varying length. Compound 9 features a rare midchain gem-dichloro moiety, indicating that the putative halogenase BrtJ is able to act twice on the same midchain carbon. © 2016 The American Chemical Society and American Society of Pharmacognosy. |
URI: | https://hdl.handle.net/10216/120263 |
Source: | Journal of Natural Products, vol. 79(10), p. 2504-2513 |
Document Type: | Artigo em Revista Científica Internacional |
Rights: | openAccess |
Appears in Collections: | CIIMAR - Artigo em Revista Científica Internacional |
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Afonso TB_2016.pdf | 781.32 kB | Adobe PDF | View/Open |
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