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Antimicrobial butyrolactone I derivatives from the Ecuadorian soil fungus Aspergillus terreus Thorn. var terreus

Abstract:

The fungus Aspergillus terreus Thorn var. terreus isolated from an Ecuador soil sample was cultured in liquid and solid media and yielded three main metabolites identified as terreic acid (1), butyrolactone I (2) and lovastatin (3). The natural products as well as three synthetic butyrolactone I derivatives were assessed for antimicrobial activity against Gram-positive and Gram-negative bacteria and fungi as well as for seed germination and seedling growth. Furthermore, the compounds were assessed as inhibitors towards the enzymes acetylcholinesterase, β-glucosidase, and β-glucuronidase. Terreic acid, butyrolactone I, butyrolactone 4′,4″-diacetate (2.1), and 3′-(3-methylbutyl)-butyrolactone II (2.2) were active towards the phytopathogenic bacteria Erwinia carotovora with IC<inf>50</inf> of 5 and 4-18 μg/ml, respectively. Under the same experimental conditions, the IC <inf>50</inf> of streptomycin was 1.9 μg/ml. 3′-(3-Methylbutyl)- butyrolactone II was moderately active against Pseudomonas syringae and Botrytis cinerea with IC<inf>50</inf> of 21μg/ml and MIC of 15.6 μg/ml, respectively. Butyrolactone I also inhibited germination of the dicot Lactuca sativa with an IC<inf>50</inf> of 5 × 10<sup>-5</sup> M. The IC <inf>50</inf> of reference herbicide acetochlor was 1 × 10<sup>-5</sup> M. The effect of 2.2 and 2.3, known as butyrolactone III on Panicum millaceum germination and growth was stronger than that of 2 and 2.1. Reduction of the double bond in the isoprenyl side chain of butyrolactone I increased the antibacterial effect against E. carotovora as well as acetylation. To our best knowledge, this is the first report on the antibacterial effect of butyrolactone derivatives towards Erwinia carotovora and the phytopathogenic fungus Botrytis cinerea. The butyrolactone I derivative 2.2 presented a moderate inhibitory effect against the enzyme acetylcholinesterase with an IC<inf>50</inf> of 47 μg/ml. Under the same experimental conditions, the reference inhibitor galanthamine had an IC<inf>50</inf> of 3 μg/ml. © Springer 2005.