Antiproliferative polyketides from fungus Xylaria cf. Longipes SWUF08-81 in different culture media.
Kittiwan SresuksaiSasiphimol SawadsitangPhongphan JantaharnPakin NoppawanAudomsak ChuratNuttika SuwannasaiWiyada MongkolthanarukThanaset SenawongSarawut TontaphaPairot MoontragoonVittaya AmornkitbamrungSirirath McCloskeyPublished in: Natural products and bioprospecting (2024)
Bioactive compounds from the wood-decay fungus Xylaria cf. longipes SWUF08-81, cultivated in three different culture media (GM, YM and PDB), were isolated. Their structures and stereochemistry were deduced from spectroscopic and MS data analysis, together with quantum chemical calculations of 13 C NMR chemical shifts and electronic circular dichroism (ECD) spectra. Five undescribed polyketides including dibenzofuran (1), mellein (2), dihydroisocoumarin (15), and two pyrans (16, 17), together with twenty-three compounds were determined. Compounds 18 and 20 were significantly toxic against cancer cell lines (HCT116, HT29, MCF-7 and HeLa) based on the MTT assay. Quantification by HPLC showed that 18 was produced three-fold higher in the broth of PDB than YM. These studies showed that the production of different compounds were primarily dependent on nutrition sources and it has given a starting point for the growth optimization conditions for the scaling up of bioactive compounds production.
Keyphrases
- data analysis
- cystic fibrosis
- ms ms
- molecular dynamics
- density functional theory
- high resolution
- mass spectrometry
- multiple sclerosis
- magnetic resonance
- papillary thyroid
- physical activity
- simultaneous determination
- high throughput
- cell cycle arrest
- drinking water
- molecular dynamics simulations
- high performance liquid chromatography
- breast cancer cells
- monte carlo
- cell death
- squamous cell carcinoma
- tandem mass spectrometry