Loading…
Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology
Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a solvent-free system. Response Surface Methodology (R...
Saved in:
Published in: | PloS one 2015-12, Vol.10 (12), p.e0144664-e0144664 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433 |
---|---|
cites | cdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433 |
container_end_page | e0144664 |
container_issue | 12 |
container_start_page | e0144664 |
container_title | PloS one |
container_volume | 10 |
creator | Jumbri, Khairulazhar Al-Haniff Rozy, Mohd Fahruddin Ashari, Siti Efliza Mohamad, Rosfarizan Basri, Mahiran Fard Masoumi, Hamid Reza |
description | Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a solvent-free system. Response Surface Methodology (RSM) based on central composite rotatable design (CCRD) was used to optimise the main important reaction variables, such as enzyme amount, reaction temperature, substrate molar ratio, and reaction time along with immobilised lipase from Candida Antarctica (Novozym 435) as a biocatalyst. The RSM data indicated that the reaction temperature was less significant in comparison to other factors for the production of a KMO ester. By using this statistical analysis, a quadratic model was developed in order to correlate the preparation variable to the response (reaction yield). The optimum conditions for the enzymatic synthesis of KMO were as follows: an enzyme amount of 2.0 wt%, reaction temperature of 83.69°C, substrate molar ratio of 1:2.37 (mmole kojic acid:oleic acid) and a reaction time of 300.0 min. Under these conditions, the actual yield percentage obtained was 42.09%, which is comparably well with the maximum predicted value of 44.46%. Under the optimal conditions, Novozym 435 could be reused for 5 cycles for KMO production percentage yield of at least 40%. The results demonstrated that statistical analysis using RSM can be used efficiently to optimise the production of a KMO ester. Moreover, the optimum conditions obtained can be applied to scale-up the process and minimise the cost. |
doi_str_mv | 10.1371/journal.pone.0144664 |
format | article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1748873449</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A437466043</galeid><doaj_id>oai_doaj_org_article_1e5f4fc9560b4ad8b67993c0b33083ad</doaj_id><sourcerecordid>A437466043</sourcerecordid><originalsourceid>FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433</originalsourceid><addsrcrecordid>eNqNk1Fv0zAQxyMEYmPwDRBEQkLw0GLHjpO8IE3VBhWbJm3Aq3Vxzq0rNy62M9HvwQfGXbupRXtAeXB097u_7b_vsuw1JWPKKvpp4Qbfgx2vXI9jQjkXgj_JjmnDipEoCHu693-UvQhhQUjJaiGeZ0eFEGVFGDnO_lytolmaANG4Poe-yydz8KAi-vug0_mFWUHA0QQi2HXALr9Z93GOwYRNFvJvbmFUful65yxCxPwsJIHcJMX8xtlb7OPo3COmupRY5u06v8aQTh5SaPAaFOaXGOeuc9bN1i-zZxpswFe79ST7cX72ffJ1dHH1ZTo5vRgp0RRxJAQtFBSUtSW0KFRb1DV0SnRNVdWoOaCuBTTIK6gVCK1rrbqiQWBVAYIzdpK93equrAtyZ2iQtOJ1XTHOm0RMt0TnYCFX3izBr6UDI-8Czs8k-GiURUmx1FyrphSk5dDVraiahinSMkZqBl3S-rzbbWiX2Klkigd7IHqY6c1cztyt5KKmJaNJ4MNOwLtfA4Yo08MptBZ6dMPm3CUhhJa0Sui7f9DHb7ejZpAuYHrt0r5qIypPOatSR5E7l8aPUOnrcGlU6j5tUvyg4ONBQWIi_o4zGEKQ05vr_2evfh6y7_fYOYKN8-DssOnScAjyLai8C8GjfjCZErkZnns35GZ45G54Utmb_Qd6KLqfFvYXCl8XOQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1748873449</pqid></control><display><type>article</type><title>Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology</title><source>Access via ProQuest (Open Access)</source><source>PubMed Central</source><creator>Jumbri, Khairulazhar ; Al-Haniff Rozy, Mohd Fahruddin ; Ashari, Siti Efliza ; Mohamad, Rosfarizan ; Basri, Mahiran ; Fard Masoumi, Hamid Reza</creator><contributor>van Berkel, Willem J.H.</contributor><creatorcontrib>Jumbri, Khairulazhar ; Al-Haniff Rozy, Mohd Fahruddin ; Ashari, Siti Efliza ; Mohamad, Rosfarizan ; Basri, Mahiran ; Fard Masoumi, Hamid Reza ; van Berkel, Willem J.H.</creatorcontrib><description>Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a solvent-free system. Response Surface Methodology (RSM) based on central composite rotatable design (CCRD) was used to optimise the main important reaction variables, such as enzyme amount, reaction temperature, substrate molar ratio, and reaction time along with immobilised lipase from Candida Antarctica (Novozym 435) as a biocatalyst. The RSM data indicated that the reaction temperature was less significant in comparison to other factors for the production of a KMO ester. By using this statistical analysis, a quadratic model was developed in order to correlate the preparation variable to the response (reaction yield). The optimum conditions for the enzymatic synthesis of KMO were as follows: an enzyme amount of 2.0 wt%, reaction temperature of 83.69°C, substrate molar ratio of 1:2.37 (mmole kojic acid:oleic acid) and a reaction time of 300.0 min. Under these conditions, the actual yield percentage obtained was 42.09%, which is comparably well with the maximum predicted value of 44.46%. Under the optimal conditions, Novozym 435 could be reused for 5 cycles for KMO production percentage yield of at least 40%. The results demonstrated that statistical analysis using RSM can be used efficiently to optimise the production of a KMO ester. Moreover, the optimum conditions obtained can be applied to scale-up the process and minimise the cost.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0144664</identifier><identifier>PMID: 26657030</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Browning ; Catalysis ; Chemical properties ; Chemical synthesis ; Design optimization ; Enzymatic synthesis ; Enzymes ; Esterification ; Esters ; Esters - chemical synthesis ; Fatty acids ; Food industry ; Kojic acid ; Lipase ; Lipase - chemistry ; Mathematical models ; Methods ; Oleic acid ; Oleic Acid - chemistry ; Production processes ; Pyrones - chemistry ; Reaction time ; Response surface methodology ; Response surfaces ; Science ; Skin care products ; Solvents ; Statistical analysis ; Substrates ; Temperature ; Temperature effects ; Tyrosinase ; Yield</subject><ispartof>PloS one, 2015-12, Vol.10 (12), p.e0144664-e0144664</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Jumbri et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Jumbri et al 2015 Jumbri et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433</citedby><cites>FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1748873449/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1748873449?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26657030$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>van Berkel, Willem J.H.</contributor><creatorcontrib>Jumbri, Khairulazhar</creatorcontrib><creatorcontrib>Al-Haniff Rozy, Mohd Fahruddin</creatorcontrib><creatorcontrib>Ashari, Siti Efliza</creatorcontrib><creatorcontrib>Mohamad, Rosfarizan</creatorcontrib><creatorcontrib>Basri, Mahiran</creatorcontrib><creatorcontrib>Fard Masoumi, Hamid Reza</creatorcontrib><title>Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a solvent-free system. Response Surface Methodology (RSM) based on central composite rotatable design (CCRD) was used to optimise the main important reaction variables, such as enzyme amount, reaction temperature, substrate molar ratio, and reaction time along with immobilised lipase from Candida Antarctica (Novozym 435) as a biocatalyst. The RSM data indicated that the reaction temperature was less significant in comparison to other factors for the production of a KMO ester. By using this statistical analysis, a quadratic model was developed in order to correlate the preparation variable to the response (reaction yield). The optimum conditions for the enzymatic synthesis of KMO were as follows: an enzyme amount of 2.0 wt%, reaction temperature of 83.69°C, substrate molar ratio of 1:2.37 (mmole kojic acid:oleic acid) and a reaction time of 300.0 min. Under these conditions, the actual yield percentage obtained was 42.09%, which is comparably well with the maximum predicted value of 44.46%. Under the optimal conditions, Novozym 435 could be reused for 5 cycles for KMO production percentage yield of at least 40%. The results demonstrated that statistical analysis using RSM can be used efficiently to optimise the production of a KMO ester. Moreover, the optimum conditions obtained can be applied to scale-up the process and minimise the cost.</description><subject>Acids</subject><subject>Browning</subject><subject>Catalysis</subject><subject>Chemical properties</subject><subject>Chemical synthesis</subject><subject>Design optimization</subject><subject>Enzymatic synthesis</subject><subject>Enzymes</subject><subject>Esterification</subject><subject>Esters</subject><subject>Esters - chemical synthesis</subject><subject>Fatty acids</subject><subject>Food industry</subject><subject>Kojic acid</subject><subject>Lipase</subject><subject>Lipase - chemistry</subject><subject>Mathematical models</subject><subject>Methods</subject><subject>Oleic acid</subject><subject>Oleic Acid - chemistry</subject><subject>Production processes</subject><subject>Pyrones - chemistry</subject><subject>Reaction time</subject><subject>Response surface methodology</subject><subject>Response surfaces</subject><subject>Science</subject><subject>Skin care products</subject><subject>Solvents</subject><subject>Statistical analysis</subject><subject>Substrates</subject><subject>Temperature</subject><subject>Temperature effects</subject><subject>Tyrosinase</subject><subject>Yield</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk1Fv0zAQxyMEYmPwDRBEQkLw0GLHjpO8IE3VBhWbJm3Aq3Vxzq0rNy62M9HvwQfGXbupRXtAeXB097u_7b_vsuw1JWPKKvpp4Qbfgx2vXI9jQjkXgj_JjmnDipEoCHu693-UvQhhQUjJaiGeZ0eFEGVFGDnO_lytolmaANG4Poe-yydz8KAi-vug0_mFWUHA0QQi2HXALr9Z93GOwYRNFvJvbmFUful65yxCxPwsJIHcJMX8xtlb7OPo3COmupRY5u06v8aQTh5SaPAaFOaXGOeuc9bN1i-zZxpswFe79ST7cX72ffJ1dHH1ZTo5vRgp0RRxJAQtFBSUtSW0KFRb1DV0SnRNVdWoOaCuBTTIK6gVCK1rrbqiQWBVAYIzdpK93equrAtyZ2iQtOJ1XTHOm0RMt0TnYCFX3izBr6UDI-8Czs8k-GiURUmx1FyrphSk5dDVraiahinSMkZqBl3S-rzbbWiX2Klkigd7IHqY6c1cztyt5KKmJaNJ4MNOwLtfA4Yo08MptBZ6dMPm3CUhhJa0Sui7f9DHb7ejZpAuYHrt0r5qIypPOatSR5E7l8aPUOnrcGlU6j5tUvyg4ONBQWIi_o4zGEKQ05vr_2evfh6y7_fYOYKN8-DssOnScAjyLai8C8GjfjCZErkZnns35GZ45G54Utmb_Qd6KLqfFvYXCl8XOQ</recordid><startdate>20151214</startdate><enddate>20151214</enddate><creator>Jumbri, Khairulazhar</creator><creator>Al-Haniff Rozy, Mohd Fahruddin</creator><creator>Ashari, Siti Efliza</creator><creator>Mohamad, Rosfarizan</creator><creator>Basri, Mahiran</creator><creator>Fard Masoumi, Hamid Reza</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151214</creationdate><title>Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology</title><author>Jumbri, Khairulazhar ; Al-Haniff Rozy, Mohd Fahruddin ; Ashari, Siti Efliza ; Mohamad, Rosfarizan ; Basri, Mahiran ; Fard Masoumi, Hamid Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acids</topic><topic>Browning</topic><topic>Catalysis</topic><topic>Chemical properties</topic><topic>Chemical synthesis</topic><topic>Design optimization</topic><topic>Enzymatic synthesis</topic><topic>Enzymes</topic><topic>Esterification</topic><topic>Esters</topic><topic>Esters - chemical synthesis</topic><topic>Fatty acids</topic><topic>Food industry</topic><topic>Kojic acid</topic><topic>Lipase</topic><topic>Lipase - chemistry</topic><topic>Mathematical models</topic><topic>Methods</topic><topic>Oleic acid</topic><topic>Oleic Acid - chemistry</topic><topic>Production processes</topic><topic>Pyrones - chemistry</topic><topic>Reaction time</topic><topic>Response surface methodology</topic><topic>Response surfaces</topic><topic>Science</topic><topic>Skin care products</topic><topic>Solvents</topic><topic>Statistical analysis</topic><topic>Substrates</topic><topic>Temperature</topic><topic>Temperature effects</topic><topic>Tyrosinase</topic><topic>Yield</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jumbri, Khairulazhar</creatorcontrib><creatorcontrib>Al-Haniff Rozy, Mohd Fahruddin</creatorcontrib><creatorcontrib>Ashari, Siti Efliza</creatorcontrib><creatorcontrib>Mohamad, Rosfarizan</creatorcontrib><creatorcontrib>Basri, Mahiran</creatorcontrib><creatorcontrib>Fard Masoumi, Hamid Reza</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale_Opposing Viewpoints In Context</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jumbri, Khairulazhar</au><au>Al-Haniff Rozy, Mohd Fahruddin</au><au>Ashari, Siti Efliza</au><au>Mohamad, Rosfarizan</au><au>Basri, Mahiran</au><au>Fard Masoumi, Hamid Reza</au><au>van Berkel, Willem J.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-12-14</date><risdate>2015</risdate><volume>10</volume><issue>12</issue><spage>e0144664</spage><epage>e0144664</epage><pages>e0144664-e0144664</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a solvent-free system. Response Surface Methodology (RSM) based on central composite rotatable design (CCRD) was used to optimise the main important reaction variables, such as enzyme amount, reaction temperature, substrate molar ratio, and reaction time along with immobilised lipase from Candida Antarctica (Novozym 435) as a biocatalyst. The RSM data indicated that the reaction temperature was less significant in comparison to other factors for the production of a KMO ester. By using this statistical analysis, a quadratic model was developed in order to correlate the preparation variable to the response (reaction yield). The optimum conditions for the enzymatic synthesis of KMO were as follows: an enzyme amount of 2.0 wt%, reaction temperature of 83.69°C, substrate molar ratio of 1:2.37 (mmole kojic acid:oleic acid) and a reaction time of 300.0 min. Under these conditions, the actual yield percentage obtained was 42.09%, which is comparably well with the maximum predicted value of 44.46%. Under the optimal conditions, Novozym 435 could be reused for 5 cycles for KMO production percentage yield of at least 40%. The results demonstrated that statistical analysis using RSM can be used efficiently to optimise the production of a KMO ester. Moreover, the optimum conditions obtained can be applied to scale-up the process and minimise the cost.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26657030</pmid><doi>10.1371/journal.pone.0144664</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2015-12, Vol.10 (12), p.e0144664-e0144664 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1748873449 |
source | Access via ProQuest (Open Access); PubMed Central |
subjects | Acids Browning Catalysis Chemical properties Chemical synthesis Design optimization Enzymatic synthesis Enzymes Esterification Esters Esters - chemical synthesis Fatty acids Food industry Kojic acid Lipase Lipase - chemistry Mathematical models Methods Oleic acid Oleic Acid - chemistry Production processes Pyrones - chemistry Reaction time Response surface methodology Response surfaces Science Skin care products Solvents Statistical analysis Substrates Temperature Temperature effects Tyrosinase Yield |
title | Optimisation and Characterisation of Lipase-Catalysed Synthesis of a Kojic Monooleate Ester in a Solvent-Free System by Response Surface Methodology |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T12%3A25%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Optimisation%20and%20Characterisation%20of%20Lipase-Catalysed%20Synthesis%20of%20a%20Kojic%20Monooleate%20Ester%20in%20a%20Solvent-Free%20System%20by%20Response%20Surface%20Methodology&rft.jtitle=PloS%20one&rft.au=Jumbri,%20Khairulazhar&rft.date=2015-12-14&rft.volume=10&rft.issue=12&rft.spage=e0144664&rft.epage=e0144664&rft.pages=e0144664-e0144664&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0144664&rft_dat=%3Cgale_plos_%3EA437466043%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1748873449&rft_id=info:pmid/26657030&rft_galeid=A437466043&rfr_iscdi=true |