Literature DB >> 20886886

Transformation of rutin to antiproliferative quercetin-3-glucoside by Aspergillus niger.

Hyun Ju You1, Hyung Jin Ahn, Geun Eog Ji.   

Abstract

The flavonol quercetin in plants and foods occurs predominantly in the form of glycoside whose sugar moiety affects the bioavailability and the mechanism of its biological activities. The antiproliferative activities of quercetin derivatives such as quercetin aglycone, quercetin-3-β-D-glucoside (Q3G), and rutin were compared using six different cancer cell lines including colon, breast, hepatocellular, and lung cancer. The IC50 value of Q3G ranged between 15 and 25 μM in HT-29, HCT 116, MCF-7, HepG2, and A549 cells. In these five cell lines, Q3G showed the most potent growth inhibition, whereas rutin showed the least potency. Transformation of rutin to Q3G was conducted by controlling α-L-rhamnosidase and β-D-glucosidase activities from crude enzyme extract of Aspergillus niger. Carbon sources during culture and transformation conditions such as pH, temperature, and heat-stability were optimized. After 4 h biotransformation, 99% of rutin was transformed to Q3G and no quercetin was detected. This study presented an efficient biotransformation for the conversion of rutin to Q3G which was newly shown to have more potent antiproliferative effect than quercetin and rutin.

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Year:  2010        PMID: 20886886     DOI: 10.1021/jf102871g

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  19 in total

1.  A spectrophotometric method for high-throughput screening of α-l-rhamnosidase activity on rutin coupled with a β-d-glucosidase assay.

Authors:  Bin-Chun Li; Bo Peng; Tian Zhang; Yan-Qin Li; Guo-Bin Ding
Journal:  3 Biotech       Date:  2019-05-21       Impact factor: 2.406

2.  Biotransformation of Rutin Using Crude Enzyme from Rhodopseudomonas palustris.

Authors:  Chun-Jie Guan; Yu-Jia Ji; Jia-Lin Hu; Chao-Nan Hu; Fei Yang; Guan-E Yang
Journal:  Curr Microbiol       Date:  2017-02-17       Impact factor: 2.188

3.  Characterization of a glycoside hydrolase family 78 α-l-rhamnosidase from Bacteroides thetaiotaomicron VPI-5482 and identification of functional residues.

Authors:  Binchun Li; Yaru Ji; Yanqin Li; Guobin Ding
Journal:  3 Biotech       Date:  2018-02-08       Impact factor: 2.406

Review 4.  Review of anticancer mechanisms of isoquercitin.

Authors:  Guilherme di Camillo Orfali; Ana Carolina Duarte; Vivien Bonadio; Natalia Peres Martinez; Maria Elisa Melo Branco de Araújo; Fernanda Bruschi Marinho Priviero; Patricia Oliveira Carvalho; Denise Gonçalves Priolli
Journal:  World J Clin Oncol       Date:  2016-04-10

5.  Hydrolyzed Flavonoids from Cyrtosperma johnstonii with Superior Antioxidant, Antiproliferative, and Anti-Inflammatory Potential for Cancer Prevention.

Authors:  Ornchuma Naksuriya; Krai Daowtak; Singkome Tima; Siriporn Okonogi; Monika Mueller; Stefan Toegel; Ruttiros Khonkarn
Journal:  Molecules       Date:  2022-05-18       Impact factor: 4.927

6.  Flavonol Glycosides from Euphorbia microsciadia Bioss. with their Immunomodulatory Activities.

Authors:  Syed Mustafa Ghanadian; Abdul Majid Ayatollahi; Suleiman Afsharypour; Sumaira Hareem; Omer Mohamed Abdalla; Jean Jules Kezetas Bankeu
Journal:  Iran J Pharm Res       Date:  2012       Impact factor: 1.696

Review 7.  Improved release and metabolism of flavonoids by steered fermentation processes: a review.

Authors:  Nguyen Thai Huynh; John Van Camp; Guy Smagghe; Katleen Raes
Journal:  Int J Mol Sci       Date:  2014-10-24       Impact factor: 5.923

8.  An effective biphase system accelerates hesperidinase-catalyzed conversion of rutin to isoquercitrin.

Authors:  Jun Wang; An Gong; Cai-Feng Yang; Qi Bao; Xin-Yi Shi; Bei-Bei Han; Xiang-Yang Wu; Fu-An Wu
Journal:  Sci Rep       Date:  2015-03-03       Impact factor: 4.379

Review 9.  Cytotoxicity of dietary flavonoids on different human cancer types.

Authors:  Katrin Sak
Journal:  Pharmacogn Rev       Date:  2014-07

Review 10.  Flavonoids from the Genus Euphorbia: Isolation, Structure, Pharmacological Activities and Structure-Activity Relationships.

Authors:  Douglas Kemboi Magozwi; Mmabatho Dinala; Nthabiseng Mokwana; Xavier Siwe-Noundou; Rui W M Krause; Molahlehi Sonopo; Lyndy J McGaw; Wilma A Augustyn; Vuyelwa Jacqueline Tembu
Journal:  Pharmaceuticals (Basel)       Date:  2021-05-02
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