Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate

Kojic acid (5-hydroxy-2-hydroxymethyl-4-pyrone) is an organic acid produced from various carbon sources in an aerobic fermentation by many species of Aspergillus, Penicillium and Acetobacter. The importance of kojic acid (KA) is recently focused on its role as whitening agent in cosmetic formu...

Full description

Saved in:
Bibliographic Details
Main Author: Ishak, Nurazwa
Format: Thesis
Language:English
Published: 2015
Subjects:
Online Access:http://psasir.upm.edu.my/id/eprint/71060/1/FBSB%202015%20175%20-%20IR.pdf
http://psasir.upm.edu.my/id/eprint/71060/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.upm.eprints.71060
record_format eprints
spelling my.upm.eprints.710602019-11-12T08:11:56Z http://psasir.upm.edu.my/id/eprint/71060/ Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate Ishak, Nurazwa Kojic acid (5-hydroxy-2-hydroxymethyl-4-pyrone) is an organic acid produced from various carbon sources in an aerobic fermentation by many species of Aspergillus, Penicillium and Acetobacter. The importance of kojic acid (KA) is recently focused on its role as whitening agent in cosmetic formulation. Kojic acid is water soluble and has low stability towards light exposure. KA has also been criticized for weak depigmenting effect and unstable for long storage. The hydrophilic property of KA has restricted its application in cosmetic, oily food and pharmaceutical products. In order to improve the chemical and biological activities of KA, its derivatives with new and improved chemical properties and biological activities needs to be developed. Various KA derivatives such as KA esters have been synthesized at industrial scale. KA esters are normally produced via chemical process where strong acid or alkali is used. This chemical process is not environmentally friendly and also produces complex mixtures that make the product purification difficult and high cost. The possibility of using lipase, lipozyme RMIM, in the esterification of KA with palmitic acid (PA) in acetone to synthesize KA palmitate (KAP) was investigated in this study. Preliminary, the effects of organic solvent, substrate ratio, enzyme loading, temperature and reaction time on the yield of KAP were evaluated. The appropriate ranges for each variable were subsequently used for optimization using response surface methodology (RSM). The optimal reaction condition for ester production was then applied in 500 mL stirred tank reactor (STR) using two types of impeller [Rushton turbine (RT) and Pitch blade disc turbine (PBDT)] to investigate the effect of agitation speed on the esterification performance. Among the organic solvent tested for esterification to synthesize KAP, acetone was the preferred solvent. Optimal conditions for esterification as suggested by RSM were as follows: PA to KA ratio, 6.74; enzyme loading, 0.59 g; reaction temperature, 45.9°C and reaction time, 20 h, which gave the percentage of esterification of 64.47%. For the esterification in STR, the percentage yield of KAP was significantly higher for RT than PBDT at all agitation speeds tested (150 to 450 rpm). The highest yield of KAP (82.14%) was obtained in STR with RT agitated at 250 rpm. Results from this study have demonstrated that substantially high yield of KA esters could be produced by enzymatic esterification using lipase. This alternative method has potential to be used industrially. Since the use of hazardous chemical can be minimized, enzymatic synthesis of KA esters is more natural and appears to be more appealing to the customers than the chemical process. 2015-04 Thesis NonPeerReviewed text en http://psasir.upm.edu.my/id/eprint/71060/1/FBSB%202015%20175%20-%20IR.pdf Ishak, Nurazwa (2015) Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate. Masters thesis, Universiti Putra Malaysia. Lipase Enzymes Esters
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
topic Lipase
Enzymes
Esters
spellingShingle Lipase
Enzymes
Esters
Ishak, Nurazwa
Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
description Kojic acid (5-hydroxy-2-hydroxymethyl-4-pyrone) is an organic acid produced from various carbon sources in an aerobic fermentation by many species of Aspergillus, Penicillium and Acetobacter. The importance of kojic acid (KA) is recently focused on its role as whitening agent in cosmetic formulation. Kojic acid is water soluble and has low stability towards light exposure. KA has also been criticized for weak depigmenting effect and unstable for long storage. The hydrophilic property of KA has restricted its application in cosmetic, oily food and pharmaceutical products. In order to improve the chemical and biological activities of KA, its derivatives with new and improved chemical properties and biological activities needs to be developed. Various KA derivatives such as KA esters have been synthesized at industrial scale. KA esters are normally produced via chemical process where strong acid or alkali is used. This chemical process is not environmentally friendly and also produces complex mixtures that make the product purification difficult and high cost. The possibility of using lipase, lipozyme RMIM, in the esterification of KA with palmitic acid (PA) in acetone to synthesize KA palmitate (KAP) was investigated in this study. Preliminary, the effects of organic solvent, substrate ratio, enzyme loading, temperature and reaction time on the yield of KAP were evaluated. The appropriate ranges for each variable were subsequently used for optimization using response surface methodology (RSM). The optimal reaction condition for ester production was then applied in 500 mL stirred tank reactor (STR) using two types of impeller [Rushton turbine (RT) and Pitch blade disc turbine (PBDT)] to investigate the effect of agitation speed on the esterification performance. Among the organic solvent tested for esterification to synthesize KAP, acetone was the preferred solvent. Optimal conditions for esterification as suggested by RSM were as follows: PA to KA ratio, 6.74; enzyme loading, 0.59 g; reaction temperature, 45.9°C and reaction time, 20 h, which gave the percentage of esterification of 64.47%. For the esterification in STR, the percentage yield of KAP was significantly higher for RT than PBDT at all agitation speeds tested (150 to 450 rpm). The highest yield of KAP (82.14%) was obtained in STR with RT agitated at 250 rpm. Results from this study have demonstrated that substantially high yield of KA esters could be produced by enzymatic esterification using lipase. This alternative method has potential to be used industrially. Since the use of hazardous chemical can be minimized, enzymatic synthesis of KA esters is more natural and appears to be more appealing to the customers than the chemical process.
format Thesis
author Ishak, Nurazwa
author_facet Ishak, Nurazwa
author_sort Ishak, Nurazwa
title Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
title_short Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
title_full Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
title_fullStr Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
title_full_unstemmed Enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
title_sort enzymatic esterification of kojic acid and palmitic acid by immobilized lipase for synthesis of kojic acid palmitate
publishDate 2015
url http://psasir.upm.edu.my/id/eprint/71060/1/FBSB%202015%20175%20-%20IR.pdf
http://psasir.upm.edu.my/id/eprint/71060/
_version_ 1651869148394815488
score 13.211869