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 |
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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. 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><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf102871g</identifier><identifier>PMID: 20886886</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>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</subject><ispartof>Journal of agricultural and food chemistry, 2010-10, Vol.58 (20), p.10886-10892</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a411t-eb3f5dac96f2169a30c8439801aa0a359a2c04527a098ff78090624eb0d98f9c3</citedby><cites>FETCH-LOGICAL-a411t-eb3f5dac96f2169a30c8439801aa0a359a2c04527a098ff78090624eb0d98f9c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf102871g$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf102871g$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23352611$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20886886$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, Hyun Ju</creatorcontrib><creatorcontrib>Ahn, Hyung Jin</creatorcontrib><creatorcontrib>Ji, Geun Eog</creatorcontrib><title>Transformation of Rutin to Antiproliferative Quercetin-3-glucoside by Aspergillus niger</title><title>Journal of agricultural and food chemistry</title><addtitle>J. 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. Technologies</subject><subject>Quercetin - analogs & derivatives</subject><subject>Quercetin - metabolism</subject><subject>Quercetin - pharmacology</subject><subject>Rutin - metabolism</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1LAzEQhoMotlYP_gHZi6CH1Zlkd5scS_ELCqJUPC7ZbFJStpua7Ar990Za24swMAzvw8zwEHKJcIdA8X5pYuNjXByRIeYU0hyRH5MhxDDleYEDchbCEgB4PoZTMqDAeRFrSD7nXrbBOL-SnXVt4kzy3ne2TTqXTNrOrr1rrNE-pt86eeu1VzrGKUsXTa9csLVOqk0yCWvtF7Zp-pC0dqH9OTkxsgn6YtdH5OPxYT59TmevTy_TySyVGWKX6oqZvJZKFIZiISQDxTMmOKCUIFkuJFWQ5XQsQXBjxhwEFDTTFdRxFoqNyM12b3z0q9ehK1c2KN00stWuDyVmQiDNOLKI3m5R5V0IXpty7e1K-k2JUP56LPceI3u1W9tXK13vyT9xEbjeATIo2ZhoUdlw4BjLaYF44KQK5dL1vo02_jn4AzJPhlM</recordid><startdate>20101027</startdate><enddate>20101027</enddate><creator>You, Hyun Ju</creator><creator>Ahn, Hyung Jin</creator><creator>Ji, Geun Eog</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20101027</creationdate><title>Transformation of Rutin to Antiproliferative Quercetin-3-glucoside by Aspergillus niger</title><author>You, Hyun Ju ; Ahn, Hyung Jin ; Ji, Geun Eog</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a411t-eb3f5dac96f2169a30c8439801aa0a359a2c04527a098ff78090624eb0d98f9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aspergillus niger - enzymology</topic><topic>Aspergillus niger - metabolism</topic><topic>Bioactive Constituents</topic><topic>Bioconversions. 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 & 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. 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.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>20886886</pmid><doi>10.1021/jf102871g</doi><tpages>7</tpages></addata></record> |
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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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