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Molecular networking assisted discovery and biosynthesis elucidation of the antimicrobial spiroketals epicospirocins
- Source :
- Chemical Communications. 56:10171-10174
- Publication Year :
- 2020
- Publisher :
- Royal Society of Chemistry (RSC), 2020.
-
Abstract
- Two pairs of dibenzospiroketal racemates, (±)-epicospirocin A (1a/1b) and (±)-1-epi-epicospirocin A (2a/2b), and two (+)-enantiomers of aspermicrones, ent-aspermicrone B (3b) and ent-aspermicrone C (4b), together with two hemiacetal epimeric mixtures, epicospirocin B/1-epi-epicospirocin B (5/6) and epicospirocin C/1-epi-epicospirocin C (7/8), were investigated from the phytopathogenic fungus Epicoccum nigrum 09116 via MS/MS molecular networking guided isolation and chiral separation for the first time. A plausible epicospirocin biosynthetic pathway was elucidated through in silico gene function annotation together with knock-out experiments. This is the first report that has applied MS/MS molecular networking to identify intermediates correlated with a biosynthetic pathway.
- Subjects :
- Stereochemistry
In silico
Stereoisomerism
01 natural sciences
Catalysis
03 medical and health sciences
chemistry.chemical_compound
Ascomycota
Biosynthesis
Materials Chemistry
Computer Simulation
Spiro Compounds
Furans
Gene
030304 developmental biology
0303 health sciences
biology
010405 organic chemistry
Metals and Alloys
General Chemistry
biology.organism_classification
Antimicrobial
3. Good health
0104 chemical sciences
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
chemistry
Ceramics and Composites
Hemiacetal
Epicoccum nigrum
Function (biology)
Subjects
Details
- ISSN :
- 1364548X and 13597345
- Volume :
- 56
- Database :
- OpenAIRE
- Journal :
- Chemical Communications
- Accession number :
- edsair.doi.dedup.....f4c28d4d6bdad6b47163ab09b62f1618
- Full Text :
- https://doi.org/10.1039/d0cc03990j