Back to Search
Start Over
Shaping the Polypropionate Biosynthesis in the Solar-Powered MolluscElysia viridis
- Source :
- ChemBioChem, info:cnr-pdr/source/autori:Cutignano A.; Cimino G.; Villani G.; Fontana A./titolo:Shaping the Polypropionate Biosynthesis in the Solar-Powered Mollusc Elysia viridis/doi:10.1002%2Fcbic.200800531/rivista:ChemBioChem (Print)/anno:2009/pagina_da:315/pagina_a:322/intervallo_pagine:315–322/volume:10
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- Polypropionates that incorporate pyrones are a family of polyketides featuring the chemistry of a few marine molluscs capable of phototrophic CO2 fixation as a result of storing viable symbiotic chloroplasts in their bodies. The role and origin of these molecules is poorly investigated, although the unusual biological ACHTUNGTRENUNGactivities and chemistry of these natural products have recently received renewed interest. Here, we report the results of in vivo studies on production of g-pyrone-containing polypropionates in the Mediterranean mollusc Elysia viridis. Biosynthesis of the metabolites in the sacoglossan is shown to proceed through condensation of eight intact C3 units by polyketide synthase assembly. LC–MS and NMR spectroscopic studies demonstrate that the process involves a pyrone tetraene (10) as key intermediate, whereas the levels of the final polypropionates (6, 7 and 9) are related to each other and show a significant dependence upon light conditions.
- Subjects :
- Magnetic Resonance Spectroscopy
natural products
Polymers
Elysia viridis
Gastropoda
Biosynthesi
labelling studie
Biochemistry
chemistry.chemical_compound
Biosynthesis
Polyketide synthase
Solar Energy
Animals
marine organism
Molecular Biology
Carbon Isotopes
photochemistry
Photolysis
Staining and Labeling
biology
Phototroph
structure elucidation
Organic Chemistry
biology.organism_classification
Pyrone
Chloroplast
chemistry
Food
Sunlight
biology.protein
Molecular Medicine
biosynthesis
Propionates
Solar powered
polyketides
Subjects
Details
- ISSN :
- 14397633 and 14394227
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- ChemBioChem
- Accession number :
- edsair.doi.dedup.....e64577090740b3fd394fb6bf45cdd034
- Full Text :
- https://doi.org/10.1002/cbic.200800531