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Hydrolases-mediated transformation of oleuropein into demethyloleuropein
[Display omitted] •Demethyloleuropein was synthesized from oleuropein via the screening of a panel of hydrolases (EC 3).•α-chymotrypsin was the best biocatalyst, thus revealing a classical example of enzyme promiscuity.•The enzymatic reaction proceeded with complete chemoselectivity at pH 7 and 4 °C...
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Published in: | Bioorganic chemistry 2019-03, Vol.84, p.384-388 |
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container_title | Bioorganic chemistry |
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creator | Cariati, Luca Oliverio, Manuela Mutti, Francesco G. Bonacci, Sonia Knaus, Tanja Costanzo, Paola Procopio, Antonio |
description | [Display omitted]
•Demethyloleuropein was synthesized from oleuropein via the screening of a panel of hydrolases (EC 3).•α-chymotrypsin was the best biocatalyst, thus revealing a classical example of enzyme promiscuity.•The enzymatic reaction proceeded with complete chemoselectivity at pH 7 and 4 °C.
Phenolic compounds present in extra virgin olive oil have recently attracted considerable attention due to their pharmacological activities. Among them oleacein (3,4-DHPEA-EDA), structurally related to oleochantal (4-HPEA-EDA), is one of the most studied. 3,4-DHPEA-EDA has been synthesized through decarboxylation of demethyloleuropein catalyzed by Er(OTf)3. Demethyloleuropein is extracted from black olives drupes in very limited amounts and only in particular periods of the year. The availability of demethyloleuropein could be increased by a selective hydrolysis of the methyl ester moiety of oleuropein, a secoiridoid present in large amount in olive leaves. In this work we describe a new enzymatic method for carrying out a selective hydrolysis of oleuropein via the screening of a panel of hydrolases (lipases, esterases and proteases). Among all the enzymes tested the best results was obtained using α-chymotrypsyn from bovine pancreas as biocatalyst, thus revealing a classic example of catalytic enzyme promiscuity. |
doi_str_mv | 10.1016/j.bioorg.2018.12.005 |
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•Demethyloleuropein was synthesized from oleuropein via the screening of a panel of hydrolases (EC 3).•α-chymotrypsin was the best biocatalyst, thus revealing a classical example of enzyme promiscuity.•The enzymatic reaction proceeded with complete chemoselectivity at pH 7 and 4 °C.
Phenolic compounds present in extra virgin olive oil have recently attracted considerable attention due to their pharmacological activities. Among them oleacein (3,4-DHPEA-EDA), structurally related to oleochantal (4-HPEA-EDA), is one of the most studied. 3,4-DHPEA-EDA has been synthesized through decarboxylation of demethyloleuropein catalyzed by Er(OTf)3. Demethyloleuropein is extracted from black olives drupes in very limited amounts and only in particular periods of the year. The availability of demethyloleuropein could be increased by a selective hydrolysis of the methyl ester moiety of oleuropein, a secoiridoid present in large amount in olive leaves. In this work we describe a new enzymatic method for carrying out a selective hydrolysis of oleuropein via the screening of a panel of hydrolases (lipases, esterases and proteases). Among all the enzymes tested the best results was obtained using α-chymotrypsyn from bovine pancreas as biocatalyst, thus revealing a classic example of catalytic enzyme promiscuity.</description><identifier>ISSN: 0045-2068</identifier><identifier>EISSN: 1090-2120</identifier><identifier>DOI: 10.1016/j.bioorg.2018.12.005</identifier><identifier>PMID: 30543985</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Biocatalysis ; Cattle ; Chymotrypsin - metabolism ; Demethyloleuropein ; Enzyme promiscuity ; Hydrolases ; Hydrolases - metabolism ; Hydrolysis ; Iridoid Glucosides - chemistry ; Iridoid Glucosides - metabolism ; Iridoids - chemistry ; Iridoids - metabolism ; Olea - chemistry ; Olea - metabolism ; Oleuropein ; Pancreas - enzymology</subject><ispartof>Bioorganic chemistry, 2019-03, Vol.84, p.384-388</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-e021d10ef199c9725bb7a986d7b6668826213499e3f67691a343b238e33195d33</citedby><cites>FETCH-LOGICAL-c408t-e021d10ef199c9725bb7a986d7b6668826213499e3f67691a343b238e33195d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30543985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cariati, Luca</creatorcontrib><creatorcontrib>Oliverio, Manuela</creatorcontrib><creatorcontrib>Mutti, Francesco G.</creatorcontrib><creatorcontrib>Bonacci, Sonia</creatorcontrib><creatorcontrib>Knaus, Tanja</creatorcontrib><creatorcontrib>Costanzo, Paola</creatorcontrib><creatorcontrib>Procopio, Antonio</creatorcontrib><title>Hydrolases-mediated transformation of oleuropein into demethyloleuropein</title><title>Bioorganic chemistry</title><addtitle>Bioorg Chem</addtitle><description>[Display omitted]
•Demethyloleuropein was synthesized from oleuropein via the screening of a panel of hydrolases (EC 3).•α-chymotrypsin was the best biocatalyst, thus revealing a classical example of enzyme promiscuity.•The enzymatic reaction proceeded with complete chemoselectivity at pH 7 and 4 °C.
Phenolic compounds present in extra virgin olive oil have recently attracted considerable attention due to their pharmacological activities. Among them oleacein (3,4-DHPEA-EDA), structurally related to oleochantal (4-HPEA-EDA), is one of the most studied. 3,4-DHPEA-EDA has been synthesized through decarboxylation of demethyloleuropein catalyzed by Er(OTf)3. Demethyloleuropein is extracted from black olives drupes in very limited amounts and only in particular periods of the year. The availability of demethyloleuropein could be increased by a selective hydrolysis of the methyl ester moiety of oleuropein, a secoiridoid present in large amount in olive leaves. In this work we describe a new enzymatic method for carrying out a selective hydrolysis of oleuropein via the screening of a panel of hydrolases (lipases, esterases and proteases). Among all the enzymes tested the best results was obtained using α-chymotrypsyn from bovine pancreas as biocatalyst, thus revealing a classic example of catalytic enzyme promiscuity.</description><subject>Animals</subject><subject>Biocatalysis</subject><subject>Cattle</subject><subject>Chymotrypsin - metabolism</subject><subject>Demethyloleuropein</subject><subject>Enzyme promiscuity</subject><subject>Hydrolases</subject><subject>Hydrolases - metabolism</subject><subject>Hydrolysis</subject><subject>Iridoid Glucosides - chemistry</subject><subject>Iridoid Glucosides - metabolism</subject><subject>Iridoids - chemistry</subject><subject>Iridoids - metabolism</subject><subject>Olea - chemistry</subject><subject>Olea - metabolism</subject><subject>Oleuropein</subject><subject>Pancreas - enzymology</subject><issn>0045-2068</issn><issn>1090-2120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMo7vrxD0R69NI6k7RpchFE1BUEL3oOaTvVLG2zJl1h_71ddtWbp4HheedlHsYuEDIElNfLrHLeh_eMA6oMeQZQHLA5goaUI4dDNgfIi5SDVDN2EuMSADEv5TGbCShyoVUxZ4vFpgm-s5Fi2lPj7EhNMgY7xNaH3o7OD4lvE9_ROvgVuSFxw-iThnoaPzbd3_6MHbW2i3S-n6fs7eH-9W6RPr88Pt3dPqd1DmpMCTg2CNSi1rUueVFVpdVKNmUlpVSKS44i15pEK0up0YpcVFwoEgJ10Qhxyq52d1fBf64pjqZ3saauswP5dTQci1LmCngxofkOrYOPMVBrVsH1NmwMgtk6NEuzc2i2Dg1yMzmcYpf7hnU1KfkN_UibgJsdQNOfX46CibWjoZ70BapH03j3f8M3A_uETw</recordid><startdate>201903</startdate><enddate>201903</enddate><creator>Cariati, Luca</creator><creator>Oliverio, Manuela</creator><creator>Mutti, Francesco G.</creator><creator>Bonacci, Sonia</creator><creator>Knaus, Tanja</creator><creator>Costanzo, Paola</creator><creator>Procopio, Antonio</creator><general>Elsevier Inc</general><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>201903</creationdate><title>Hydrolases-mediated transformation of oleuropein into demethyloleuropein</title><author>Cariati, Luca ; Oliverio, Manuela ; Mutti, Francesco G. ; Bonacci, Sonia ; Knaus, Tanja ; Costanzo, Paola ; Procopio, Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-e021d10ef199c9725bb7a986d7b6668826213499e3f67691a343b238e33195d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Biocatalysis</topic><topic>Cattle</topic><topic>Chymotrypsin - metabolism</topic><topic>Demethyloleuropein</topic><topic>Enzyme promiscuity</topic><topic>Hydrolases</topic><topic>Hydrolases - metabolism</topic><topic>Hydrolysis</topic><topic>Iridoid Glucosides - chemistry</topic><topic>Iridoid Glucosides - metabolism</topic><topic>Iridoids - chemistry</topic><topic>Iridoids - metabolism</topic><topic>Olea - chemistry</topic><topic>Olea - metabolism</topic><topic>Oleuropein</topic><topic>Pancreas - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cariati, Luca</creatorcontrib><creatorcontrib>Oliverio, Manuela</creatorcontrib><creatorcontrib>Mutti, Francesco G.</creatorcontrib><creatorcontrib>Bonacci, Sonia</creatorcontrib><creatorcontrib>Knaus, Tanja</creatorcontrib><creatorcontrib>Costanzo, Paola</creatorcontrib><creatorcontrib>Procopio, Antonio</creatorcontrib><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>Bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cariati, Luca</au><au>Oliverio, Manuela</au><au>Mutti, Francesco G.</au><au>Bonacci, Sonia</au><au>Knaus, Tanja</au><au>Costanzo, Paola</au><au>Procopio, Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrolases-mediated transformation of oleuropein into demethyloleuropein</atitle><jtitle>Bioorganic chemistry</jtitle><addtitle>Bioorg Chem</addtitle><date>2019-03</date><risdate>2019</risdate><volume>84</volume><spage>384</spage><epage>388</epage><pages>384-388</pages><issn>0045-2068</issn><eissn>1090-2120</eissn><abstract>[Display omitted]
•Demethyloleuropein was synthesized from oleuropein via the screening of a panel of hydrolases (EC 3).•α-chymotrypsin was the best biocatalyst, thus revealing a classical example of enzyme promiscuity.•The enzymatic reaction proceeded with complete chemoselectivity at pH 7 and 4 °C.
Phenolic compounds present in extra virgin olive oil have recently attracted considerable attention due to their pharmacological activities. Among them oleacein (3,4-DHPEA-EDA), structurally related to oleochantal (4-HPEA-EDA), is one of the most studied. 3,4-DHPEA-EDA has been synthesized through decarboxylation of demethyloleuropein catalyzed by Er(OTf)3. Demethyloleuropein is extracted from black olives drupes in very limited amounts and only in particular periods of the year. The availability of demethyloleuropein could be increased by a selective hydrolysis of the methyl ester moiety of oleuropein, a secoiridoid present in large amount in olive leaves. In this work we describe a new enzymatic method for carrying out a selective hydrolysis of oleuropein via the screening of a panel of hydrolases (lipases, esterases and proteases). Among all the enzymes tested the best results was obtained using α-chymotrypsyn from bovine pancreas as biocatalyst, thus revealing a classic example of catalytic enzyme promiscuity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30543985</pmid><doi>10.1016/j.bioorg.2018.12.005</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biocatalysis Cattle Chymotrypsin - metabolism Demethyloleuropein Enzyme promiscuity Hydrolases Hydrolases - metabolism Hydrolysis Iridoid Glucosides - chemistry Iridoid Glucosides - metabolism Iridoids - chemistry Iridoids - metabolism Olea - chemistry Olea - metabolism Oleuropein Pancreas - enzymology |
title | Hydrolases-mediated transformation of oleuropein into demethyloleuropein |
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