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1.
Braz. j. microbiol ; 46(3): 937-941, July-Sept. 2015. ilus
Article in English | LILACS | ID: lil-755825

ABSTRACT

In this study, we evaluated the effect of low and high molecular weight polycyclic aromatic hydrocarbons (PAHs), i.e., Phenanthrene, Pyrene and Benzo[a]pyrene, on the radial growth and morphology of the PAH-degrading fungal strains Aspergillus nomius H7 and Trichoderma asperellum H15. The presence of PAHs in solid medium produced significant detrimental effects on the radial growth of A. nomius H7 at 4,000 and 6,000 mg L−1 and changes in mycelium pigmentation, abundance and sporulation ability at 1,000–6,000 mg L−1. In contrast, the radial growth of T. asperellum H15 was not affected at any of the doses tested, although sporulation was observed only up to 4,000 mg L−1 and as with the H7 strain, some visible changes in sporulation patterns and mycelium pigmentation were observed. Our results suggest that fungal strains exposed to high doses of PAHs significantly vary in their growth rates and sporulation characteristics in response to the physiological and defense mechanisms that affect both pigment production and conidiation processes. This finding is relevant for obtaining a better understanding of fungal adaptation in PAH-polluted environments and for developing and implementing adequate strategies for the remediation of contaminated soils.

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Subject(s)
Aspergillus/growth & development , Benzo(a)pyrene/pharmacology , Mycelium/drug effects , Phenanthrenes/pharmacology , Polycyclic Aromatic Hydrocarbons/pharmacology , Pyrenes/pharmacology , Spores, Fungal/drug effects , Trichoderma/growth & development , Aspergillus/drug effects , Aspergillus/metabolism , Biodegradation, Environmental , Polycyclic Aromatic Hydrocarbons/metabolism , Soil Microbiology , Soil Pollutants , Trichoderma/drug effects , Trichoderma/metabolism
2.
Mem. Inst. Oswaldo Cruz ; 104(7): 980-985, Nov. 2009. ilus, tab
Article in English | LILACS | ID: lil-534162

ABSTRACT

The in vitro activity of four 2-nitropropene derivatives, 1-(3-benzothienyl)-2-nitropropene (N1), 1-(3-thienyl)-2-nitropropene (N2), 1-(5-bromo-2-thienyl)-2-nitropropene (N3) and 1-(4-bromo-2-thienyl)-2-nitropropene (N4), were tested against cultures of the parasite Trypanosoma cruzi. Cytotoxicity studies were performed using Vero cells. The blood trypomastigotes, amastigotes and epimastigotes showed differential degrees of sensitivity towards the four tested compounds; the highest activity against the epimastigotes and blood tripomastigotes was exhibited by N1, followed by N3, N4 and finally N2. In contrast, whereas the compounds N1, N3 and N4 exerted similar magnitudes of activity against amastigotes, N2 was found to be a much less potent compound. According to our results, the compound N1 had the highest level of activity (IC50: 0.6 ìM) against epimastigotes.


Subject(s)
Animals , Antiprotozoal Agents/pharmacology , Nitro Compounds/pharmacology , Trypanosoma cruzi/drug effects , Analysis of Variance , Chlorocebus aethiops , Pyrenes/pharmacology , Trypanosoma cruzi/growth & development , Vero Cells
3.
Indian J Biochem Biophys ; 1990 Dec; 27(6): 359-62
Article in English | IMSEAR | ID: sea-28852

ABSTRACT

Administration of pyrene-linked fatty acids and lipids to cultured cells or an enveloped (vesicular stomatitis) virus induced photosensitization which, following irradiation with a long ultra-violet light (LUV), resulted in killing of the cells and loss of the infectivity of the virus with the following specific effects. (i) LUV illumination of the pyrene-sphingomyelin administered cultured skin fibroblasts derived from normal individuals and patients with Niemann-Pick disease permitted selective killing of the latter. (ii) Similarly LUV illumination of pyrenedodecanoic acid (P12) incubates of leukemic cell lines mixed with human bone marrow cells permitted selective killing of the former. (iii) LUV illumination of P12 incubates of vesicular stomatitis virus decreased the infectivity of the virus by up to 12 logs.


Subject(s)
Cell Survival/drug effects , Cells, Cultured , Fibroblasts , Lauric Acids/pharmacology , Leukemia, Myeloid/pathology , Niemann-Pick Diseases/pathology , Pyrenes/pharmacology , Sphingomyelins/pharmacology , Tumor Cells, Cultured , Ultraviolet Rays , Vesicular stomatitis Indiana virus/growth & development
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