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1.
J Nat Prod ; 79(10): 2504-2513, 2016 10 28.
Artigo em Inglês | MEDLINE | ID: mdl-27680198

RESUMO

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.


Assuntos
Antineoplásicos/isolamento & purificação , Cianobactérias/química , Glicolipídeos/isolamento & purificação , Glicosídeos/isolamento & purificação , Resorcinóis/isolamento & purificação , Antineoplásicos/química , Antineoplásicos/farmacologia , Cianobactérias/genética , Ensaios de Seleção de Medicamentos Antitumorais , Glicolipídeos/química , Glicolipídeos/farmacologia , Glicosídeos/química , Glicosídeos/farmacologia , Humanos , Biologia Marinha , Estrutura Molecular , Família Multigênica , Ressonância Magnética Nuclear Biomolecular , Resorcinóis/química
2.
Sci Rep ; 6: 23436, 2016 Mar 21.
Artigo em Inglês | MEDLINE | ID: mdl-26996104

RESUMO

Terpenes, a large family of natural products with important applications, are commonly associated with plants and fungi. The diterpenoids dehydroabietic and abietic acids are defense metabolites abundant in resin, and are used as biomarkers for conifer plants. We report here for the first time that the two diterpenoid acids are produced by members of several genera of cyanobacteria. Dehydroabietic acid was isolated from two cyanobacterial strains and its identity was confirmed spectroscopically. One or both of the diterpenoids were detected in the cells of phylogenetically diverse cyanobacteria belonging to four cyanobacterial 'botanical orders', from marine, estuarine and inland environments. Dehydroabietic acid was additionally found in culture supernatants. We investigated the natural role of the two resin acids in cyanobacteria using ecologically-relevant bioassays and found that the compounds inhibited the growth of a small coccoid cyanobacterium. The unexpected discovery of dehydroabietic and abietic acids in a wide range of cyanobacteria has implications for their use as plant biomarkers.


Assuntos
Abietanos/biossíntese , Cianobactérias/metabolismo , Traqueófitas/metabolismo , Abietanos/química , Biomarcadores
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