Wanrudee Hiranrat, Asadhawut Hiranrat, P. Supaphon
{"title":"Antimicrobial Activity of Secondary Metabolites from Endophytic Fungus Fusarium sp. Isolated from Eichhornia crassipes Linn.","authors":"Wanrudee Hiranrat, Asadhawut Hiranrat, P. Supaphon","doi":"10.55164/ajstr.v24i3.244115","DOIUrl":null,"url":null,"abstract":"The active metabolites producing endophytic fungus, Fusarium sp., was isolated from Eichhornia crassipes Linn. yielded four compounds: “altersolanol (1)”, “4-hydroxydihydronorjavanicin (2)”, “5-hydroxy-7-methoxy-2-isopropylchromone (3)” and “fusaraichromenone (4)”. Structures of 1-4 were elucidated by analysis of their spectroscopic data. The antimicrobial activity was tested by using four bacteria; methicillin-resistant Staphylococcus aureus (MRSA SK1), Staphylococcus aureus (SA), Escherichia coli (EC) and Pseudomonas aeruginosa ATCC27853 (PA)and two yeast; Cryptococcus neoformans ATCC90112 flucytosine – resistant (CN90112) and Candida albicans ATCC 90028 (CA90028) to adverse effect showed that compound 1 and 3 had moderate antibacterial activity against MRSA, SA, PA and SK1 with same MIC value 16 μg/mL. However, all pure compounds showed relatively low activities to inhibit the growth of CA90028 and CN91112 yeast.","PeriodicalId":426475,"journal":{"name":"ASEAN Journal of Scientific and Technological Reports","volume":"20 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ASEAN Journal of Scientific and Technological Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55164/ajstr.v24i3.244115","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
The active metabolites producing endophytic fungus, Fusarium sp., was isolated from Eichhornia crassipes Linn. yielded four compounds: “altersolanol (1)”, “4-hydroxydihydronorjavanicin (2)”, “5-hydroxy-7-methoxy-2-isopropylchromone (3)” and “fusaraichromenone (4)”. Structures of 1-4 were elucidated by analysis of their spectroscopic data. The antimicrobial activity was tested by using four bacteria; methicillin-resistant Staphylococcus aureus (MRSA SK1), Staphylococcus aureus (SA), Escherichia coli (EC) and Pseudomonas aeruginosa ATCC27853 (PA)and two yeast; Cryptococcus neoformans ATCC90112 flucytosine – resistant (CN90112) and Candida albicans ATCC 90028 (CA90028) to adverse effect showed that compound 1 and 3 had moderate antibacterial activity against MRSA, SA, PA and SK1 with same MIC value 16 μg/mL. However, all pure compounds showed relatively low activities to inhibit the growth of CA90028 and CN91112 yeast.