naphthoquinones has been researched along with bostrycoidin* in 5 studies
5 other study(ies) available for naphthoquinones and bostrycoidin
Article | Year |
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Production and Selectivity of Key Fusarubins from
Natural products display a large structural variation and different uses within a broad spectrum of industries. In this study, we investigate the influence of carbohydrates and nitrogen sources on the production and selectivity of production of four different polyketides produced by Topics: Culture Media; Fusarium; Isoquinolines; Naphthoquinones; Nitrogen; Polyketides; Sucrose | 2021 |
Heterologous Expression of the Core Genes in the Complex Fusarubin Gene Cluster of
Topics: Cloning, Molecular; Fungal Proteins; Fusarium; Isoquinolines; Multigene Family; Naphthoquinones; Polyketide Synthases; Promoter Regions, Genetic; Saccharomyces cerevisiae | 2020 |
Bioactive compounds from the endophytic fungus Fusarium proliferatum.
The crude extract of an endophytic fungus isolated from Syzygium cordatum and identified as Fusarium proliferatum showed 100% cytotoxicity against the brine shrimp Artemia salina at 100 μg/mL. Seven coloured, biologically active metabolites - including ergosta-5,7,22-trien-3β-ol, nectriafurone-8-methyl ether, 9-O-methyl fusarubin, bostrycoidin, bostrycoidin-9-methyl ether and 8-hydroxy-5,6-dimethoxy-2-methyl-3-(2-oxo-propyl)-1,4-naphthoquinone- were isolated from the extract. Topics: Animals; Artemia; Color; Fusarium; Isoquinolines; Liquid-Liquid Extraction; Naphthoquinones; Toxicological Phenomena | 2016 |
A heptaketide naphthaldehyde produced by a polyketide synthase from Nectria haematococca.
Bostrycoidin and fusarubin are biologically active fungal polyketides produced by Nectria haematococca. This azaanthraquinone and naphthoquinone are thought to be biosynthesized via formation of a C(14) heptaketide aldehyde as a common key intermediate. A BLAST search against the genome of N. haematococca revealed one candidate gene (NECHADRAFT_101778, NhPKS1), which encodes a multi-domain polyketide synthase (PKS) with a thiol reductase (TR) domain that would facilitate the reductive release of the intermediate to produce a free aldehyde. To investigate the possible involvement of NhPKS1 in the biosynthesis of bostrycoidin and fusarubin, NhPKS1 was heterologously expressed in Aspergillus oryzae, and shown to produce a heptaketide 3-acetonyl-1,6,8-trihydroxy-2-naphthaldehyde as a single product. Thus, NhPKS1 catalyzes a C-2/C-11 and C-4/C-9 aldol-type cyclization of a linear intermediate followed by a subsequent reductive product release to yield the naphthaldehyde. The results indicate NhPKS1 is the enzyme involved in the biosynthesis of bostrycoidin and fusarubin. Topics: Aldehydes; Aspergillus oryzae; Cyclization; Isoquinolines; Magnetic Resonance Spectroscopy; Molecular Conformation; Multienzyme Complexes; Naphthalenes; Naphthoquinones; Nectria; Polyketide Synthases; Recombinant Proteins | 2012 |
Synthesis of two naphthoquinone antibiotics, dehydroherbarin and 6-deoxybostrycoidin.
The synthesis of two naphthoquinone antibiotics, dehydroherbarin (7) and 6-deoxybostrycoidin (5), was accomplished by reaction of 3-acetonyl-2-bromomethyl-6,8-dimethoxy-1,4-naphthoquinone (23) with either triethylamine or ammonia, respectively. This is the first report on their synthesis. Topics: Anti-Bacterial Agents; Isoquinolines; Molecular Structure; Naphthoquinones; Spectrum Analysis | 2000 |