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Published on: April 23, 2012
Polycyclic aromatic hydrocarbons storage by Fusarium solani in intracellular lipid vesicles
Anthony Verdin1, Anissa Lounès-Hadj Sahraoui, Ray Newsam
1Laboratoire de Mycologie/Phytopathologie/Environnement, Université du Littoral-Côte d'Opale, 17 avenue Blériot, BP 699, 62228 Calais Cedex, France.
Abstract:
Accumulation and elimination of polycyclic aromatic hydrocarbons (PAHs) were studied in the fungus Fusarium solani. When the fungus was grown on a synthetic medium containing benzo[a]pyrene, hyphae of F. solani contained numerous lipid vesicles which could be stained by the lipid-specific dyes: Sudan III and Rhodamine B. The fluorescence produced by Rhodamine B and PAH benzo[a]pyrene were at the same locations in the fungal hyphae, indicating that F. solani stored PAH in pre-existing lipid vesicles. A passive temperature-independent process is involved in the benzo[a]pyrene uptake and storage. Sodium azide, a cytochrome c oxidation inhibitor, and the two cytoskeleton inhibitors colchicine and cytochalasin did not prevent the transport and accumulation of PAH in lipid vesicles of F. solani hyphae. F. solani degraded a large range of PAHs at different rates. PAH intracellular storage in lipid vesicles was not necessarily accompanied by degradation and was common to numerous other fungi.
Insights
The fungus Fusarium solani stores polycyclic aromatic hydrocarbons (PAHs) in lipid vesicles via a passive process. This storage mechanism is common in fungi and not always linked to PAH degradation.
Area of Science:
- Environmental microbiology
- Bioremediation
- Fungal metabolism
Background:
- Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants.
- Fungal species are increasingly recognized for their potential in bioremediation.
- Understanding PAH accumulation mechanisms in fungi is crucial for developing effective remediation strategies.
Purpose of the Study:
- To investigate the accumulation and elimination of PAHs in the fungus Fusarium solani.
- To elucidate the cellular mechanisms underlying PAH storage in fungal hyphae.
- To determine the relationship between PAH storage and degradation in F. solani.
Main Methods:
- Culturing Fusarium solani on a synthetic medium supplemented with benzo[a]pyrene.
- Utilizing lipid-specific dyes (Sudan III, Rhodamine B) to identify storage sites.
- Microscopic analysis to observe fluorescence localization of Rhodamine B and benzo[a]pyrene.
- Testing the effect of metabolic inhibitors (sodium azide, colchicine, cytochalasin) on PAH transport.
Main Results:
- Fusarium solani hyphae contain numerous lipid vesicles that accumulate benzo[a]pyrene.
- PAH accumulation occurs via a passive, temperature-independent process.
- Inhibitors of cellular respiration and cytoskeleton did not impede PAH transport and storage.
- F. solani demonstrated degradation of various PAHs at different rates.
- Intracellular PAH storage was observed in numerous other fungal species.
Conclusions:
- Fusarium solani stores polycyclic aromatic hydrocarbons (PAHs) within pre-existing lipid vesicles.
- PAH uptake and storage by F. solani is a passive process independent of cellular metabolism.
- Lipid vesicle storage of PAHs is a widespread phenomenon in fungi, not always coupled with degradation.
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