Abstract

The cytotoxicity of extracts from Alternaria alternata against tobacco Bright Yellow-2 (BY-2) cells was investigated by a simultaneous double-staining procedureusing fluorescein diacetate and propidium iodide. The active fraction from a 10-day-old culture filtrate of the fungus was purified by ammonium sulfate precipitation, ultrafiltration, gel filtration on Sephadex G-10, and reversed-phase HPLC, in sequence. The partially purified principle appears to be heat- and acid-stable, as neither incubation at 100°C for 30 min nor overnight treatment at pH2 altered the cytotoxicity. The cytotoxicity of the principle was abolished after treatment with proteinase K or trypsin, while the dithiothreitol treatment showed reduced cytotoxicity.

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