Regio-specific biotransformation of alizarin to alizarin methoxide with enhanced cytotoxicity against proliferative cells

Author:

Nguyen Trang Thi Huyen1,Han Jang Mi1,Jung Hye Jin12,Pandey Ramesh Prasad12,Park Yong Il3,Sohng Jae Kyung12

Affiliation:

1. grid.412859.3 0000 0004 0533 4202 Department of Life Science and Biochemical Engineering Sun Moon University 70 Sunmoon-ro 221, Tangjeong-myeon 31460 Asan-si Chungnam Republic of Korea

2. grid.412859.3 0000 0004 0533 4202 Department of Pharmaceutical Engineering and Biotechnology Sun Moon University 70 Sunmoon-ro 221, Tangjeong-myeon 31460 Asan-si Chungnam Republic of Korea

3. grid.411947.e 0000 0004 0470 4224 Department of Biotechnology The Catholic University of Korea 14662 Bucheon Gyeonggi-do Republic of Korea

Abstract

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).

Funder

National research foundation of korea

Next-Generation BioGreen 21 Program

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,Biotechnology,Bioengineering

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