Journal
RSC ADVANCES
Volume 5, Issue 81, Pages 66360-66366Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra13580j
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Funding
- BIOTA/BIOprospecTA FAPESP program [2010/50190-2, 2013/50228-8]
- CNPq [301289/2009-3]
- CNPq
- NSERC grant
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Degradation of the dye Remazol Brilliant Blue R (RBBR) by the marine-derived fungus Tinctoporellus sp. CBMAI 1061 led to the formation of four unprecedented anthraquinones, of which two were halogenated. Investigation of the RBBR degradation medium also led to the isolation of three new tremulene terpenes, of which two bear novel 2-hydroxy- or 2-methoxy-3,4-dihydro-2H-pyrrole N-oxide moieties. The products of RBBR degradation and of the fungus metabolism have been identified by analysis of spectroscopic data.
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