作者: Tanja Schirmeister , Christine Beemelmanns , Thorsten Heinzel , Michael Poulsen , Soohyun Um
DOI: 10.1039/D1RA00997D
关键词:
摘要: Targeted HRMS2-GNPS-based metabolomic analysis of Pseudoxylaria sp. X187, a fungal antagonist the fungus-growing termite symbiosis, resulted in identification two lipopeptidic congeners xylacremolides, named xylacremolide C and D, which are built from d-phenylalanine, l-proline an acetyl-CoA starter unit elongated by four malonyl-CoA derived ketide units. The putative xya gene cluster was identified draft genome generated Illumina PacBio sequencing RNAseq studies. Biological activities A B were evaluated revealed weak histone deacetylase inhibitory (HDACi) antifungal activities, as well moderate protease inhibition activity across panel nine human, viral bacterial proteases.