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Biosynthesis of para-Cyclophane-Containing Hirsutellone Family of Fungal Natural Products
- Source :
- Journal of the American Chemical Society, vol 143, iss 15
- Publication Year :
- 2021
- Publisher :
- eScholarship, University of California, 2021.
-
Abstract
- Hirsutellones are fungal natural products containing a macrocyclic para-cyclophane connected to a decahydrofluorene ring system. We have elucidated the biosynthetic pathway for pyrrocidine B (3) and GKK1032 A2 (4). Two small hypothetical proteins, an oxidoreductase and a lipocalin-like protein, function cooperatively in the oxidative cyclization of the cyclophane, while an additional hypothetical protein in the pyrrocidine pathway catalyzes the exo-specific cycloaddition to form the cis-fused decahydrofluorene.
- Subjects :
- Bridged-Ring Compounds
Stereochemistry
Hypothetical protein
Molecular Conformation
Pyrrocidine B
010402 general chemistry
Ring (chemistry)
01 natural sciences
Biochemistry
Catalysis
chemistry.chemical_compound
Colloid and Surface Chemistry
Biosynthesis
Oxidoreductase
Heterocyclic Compounds
chemistry.chemical_classification
Biological Products
Cycloaddition Reaction
Fungi
Stereoisomerism
General Chemistry
4 or More Rings
Cycloaddition
Pyrrolidinones
0104 chemical sciences
Acremonium
chemistry
Hypocreales
Chemical Sciences
Oxidoreductases
Oxidation-Reduction
Function (biology)
Cyclophane
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society, vol 143, iss 15
- Accession number :
- edsair.doi.dedup.....c71a0acd66833da0e423ad1bc2713e39