Back to Search
Start Over
Regio-specific biotransformation of alizarin to alizarin methoxide with enhanced cytotoxicity against proliferative cells
- Source :
- Journal of industrial microbiologybiotechnology. 47(6-7)
- Publication Year :
- 2019
-
Abstract
- Alizarin has been reported to have an antigenotoxic activity along with an inhibitory effect on the tumor cell growth of human colon carcinoma cells. Alizarin was biotransformed into an O-methoxide derivative using O-methyltransferase from Streptomyces avermitilis MA4680 (SaOMT2) to enhance its bioefficacy. The biotransformed product was extracted, purified, and characterized using various chromatographic and spectroscopic analyses, and confirmed to be an alizarin 2-O-methoxide. The antiproliferative activity of the compound against gastric cancer cells (AGS), uterine cervical cancer (Hela), liver cancer (HepG2), and normal cell lines was investigated. Alizarin 2-O-methoxide showed an inhibitory effect on all three cancer-cell lines at very low concentrations, from 0.078 µM, with no cytotoxicity against 267B1 (human prostate epithelial) and MRC-5 (normal human fetal lung fibroblast).
- Subjects :
- Magnetic Resonance Spectroscopy
Bioengineering
Anthraquinones
Antineoplastic Agents
02 engineering and technology
Alizarin
01 natural sciences
Applied Microbiology and Biotechnology
HeLa
chemistry.chemical_compound
Industrial Microbiology
Inhibitory Concentration 50
Biotransformation
Cell Line, Tumor
Neoplasms
medicine
Escherichia coli
Humans
Cytotoxicity
Fibroblast
Cell Proliferation
biology
010405 organic chemistry
Chemistry
Hep G2 Cells
021001 nanoscience & nanotechnology
biology.organism_classification
medicine.disease
Molecular biology
Streptomyces
0104 chemical sciences
medicine.anatomical_structure
Cancer cell
sense organs
0210 nano-technology
Liver cancer
Streptomyces avermitilis
Biotechnology
HeLa Cells
Subjects
Details
- ISSN :
- 14765535
- Volume :
- 47
- Issue :
- 6-7
- Database :
- OpenAIRE
- Journal :
- Journal of industrial microbiologybiotechnology
- Accession number :
- edsair.doi.dedup.....6dd048cd6c20e43e8b3c164766e43144