Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142. |
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Authors: | Avril R M Chen Paul B Reese |
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Affiliation: | Department of Chemistry, University of the West Indies, Mona, 7, Kingston, Jamaica. |
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Abstract: | Incubation of stemodin (1) in cultures of Aspergillus niger ATCC 9142 resulted in the production of 2alpha,3beta,13-trihydroxystemodane (2), 2alpha,7beta,13-trihydroxystemodane (3) and 2alpha,13,16beta-trihydroxystemodane (4), while stemodinone (5) afforded 13,18-dihydroxystemodan-2-one (6) and 13,16beta-dihydroxystemodan-2-one (7). Four novel metabolites were obtained from the bioconversion of stemarin (8) by the fungus, namely 18-hydroxystemaran-19-oic acid (9), 7beta,18-dihydroxystemaran-19-oic acid (10), 7alpha,18,19-trihydroxystemarane (11) and 1beta-hydroxystemaran-19-oic acid (12). 19-N,N-Dimethylcarbamoxy-13-hydroxystemarane (13) was also transformed to afford 19-N,N-dimethylcarbamoxy-13,17xi,18-trihydroxystemarane (14). |
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Keywords: | Aspergillus niger ATCC 9142 Biotransformation Stemodane Stemarane Diterpene Stemodia maritima Hydroxylation |
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