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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...

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Published in:PloS one 2015-12, Vol.10 (12), p.e0144664-e0144664
Main Authors: Jumbri, Khairulazhar, Al-Haniff Rozy, Mohd Fahruddin, Ashari, Siti Efliza, Mohamad, Rosfarizan, Basri, Mahiran, Fard Masoumi, Hamid Reza
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cited_by cdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433
cites cdi_FETCH-LOGICAL-c692t-6612ca213b5abe6cb288adc6d9778ef4aef86a9e47a8ca6ff8fcd29ea372a6433
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creator Jumbri, Khairulazhar
Al-Haniff Rozy, Mohd Fahruddin
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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
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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>
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1932-6203
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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
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