Transformation of Rutin to Antiproliferative Quercetin-3-glucoside by Aspergillus niger

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...

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Veröffentlicht in:Journal of agricultural and food chemistry 2010-10, Vol.58 (20), p.10886-10892
Hauptverfasser: You, Hyun Ju, Ahn, Hyung Jin, Ji, Geun Eog
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container_title Journal of agricultural and food chemistry
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creator You, Hyun Ju
Ahn, Hyung Jin
Ji, Geun Eog
description 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.
doi_str_mv 10.1021/jf102871g
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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. 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Agric. Food Chem</addtitle><description>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.</description><subject>Aspergillus niger - enzymology</subject><subject>Aspergillus niger - metabolism</subject><subject>Bioactive Constituents</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Biotransformation</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal Proteins - metabolism</subject><subject>Growth Inhibitors - metabolism</subject><subject>Growth Inhibitors - pharmacology</subject><subject>Humans</subject><subject>Methods. Procedures. 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Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Biotransformation</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal Proteins - metabolism</topic><topic>Growth Inhibitors - metabolism</topic><topic>Growth Inhibitors - pharmacology</topic><topic>Humans</topic><topic>Methods. Procedures. Technologies</topic><topic>Quercetin - analogs &amp; derivatives</topic><topic>Quercetin - metabolism</topic><topic>Quercetin - pharmacology</topic><topic>Rutin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>You, Hyun Ju</creatorcontrib><creatorcontrib>Ahn, Hyung Jin</creatorcontrib><creatorcontrib>Ji, Geun Eog</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, Hyun Ju</au><au>Ahn, Hyung Jin</au><au>Ji, Geun Eog</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transformation of Rutin to Antiproliferative Quercetin-3-glucoside by Aspergillus niger</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2010-10-27</date><risdate>2010</risdate><volume>58</volume><issue>20</issue><spage>10886</spage><epage>10892</epage><pages>10886-10892</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><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. 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subjects Aspergillus niger - enzymology
Aspergillus niger - metabolism
Bioactive Constituents
Bioconversions. Hemisynthesis
Biological and medical sciences
Biotechnology
Biotransformation
Cell Line, Tumor
Cell Proliferation - drug effects
Food industries
Fundamental and applied biological sciences. Psychology
Fungal Proteins - metabolism
Growth Inhibitors - metabolism
Growth Inhibitors - pharmacology
Humans
Methods. Procedures. Technologies
Quercetin - analogs & derivatives
Quercetin - metabolism
Quercetin - pharmacology
Rutin - metabolism
title Transformation of Rutin to Antiproliferative Quercetin-3-glucoside by Aspergillus niger
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