ABSTRACT
Metabólitos do fungo entomopatogênico Nomuraea rileyi produzidos em culturas submersas em caldo Sabouraud sacarose extrato de levedura foram extraídos com diclorometano. O extrato bruto foi fracionado por cromatografia em coluna e em camada espessa de fluxo contínuo utilizando benzeno-clorofórmio-acetato de etila 18:1:1 (v:v:v) como eluentes. Amostras de Saccharomyces cerevisiae e de bactérias (18 cepas hospitalares e 5 estirpes fitopatogênicas) foram testadas frente ao metabólito empregando-se o método de difusäo em ágar pelo sistema de discos (Kirby-Bauer). Aproximadamente (40 por cento) (9/23) das amostras bacterianas ensaiadas tiveram seu crescimento inibido na presença do metabólito produzido pelo fungo Nomuraea rileyi, sugerindo uma possível atividade antibacteriana deste metabólito
Subject(s)
Antifungal Agents/metabolism , Gram-Negative Bacteria/growth & development , Gram-Positive Bacteria/growth & development , Mitosporic Fungi/isolation & purification , MycotoxinsABSTRACT
It has been found that the pigment-I from Chromobacterium violaceum, 3 [1,2 dihydro 5 (5 hydroxy 1H indol 3 yl) 2 oxo 3H pyrrol-3 ylidiene] 1,3 dihydro 2H indol 2 one, has trypanocide activity. The formylated derivatives, pigment-III, immobilized 100% of the Trypanosoma cruzi at a level of 46 micronM after 48h of interaction with a total growth inhibition in the same period. Pigment I exhibited low toxicity and a DNA synthesis inhibition similar to that of Nifurtimox, a known trypanocide compound
Subject(s)
Amino Acid Sequence , Protease Inhibitors/analysis , Trypsin Inhibitor, Bowman-Birk Soybean/analysis , Trypsin InhibitorsABSTRACT
Chromobacterium violaceum, Brazilian or Chilean strain, produces a pigment 3 [1,2-dihydro-5 (5-hydroxy-JH-indo) 2-oxo-3H-pyrrol-3-ylidene] 1,3-dihydro-2H-indol-2-one (Violacein). Violacein was isolated from acetone extract in both cases and identified by ultraviolet-visible., infrared, nuclear magnetic rosonance spectroscopy and by mass spectrometry. A derivative of violacein, the tetracetyl-violacein was synthetized in order to confirm the violacein structure. The biosynthesis of C=violacein is also reported