Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate

학위논문 (석사)-- 서울대학교 대학원 : 농생명공학부, 2012. 2. 장판식. Erythorbic acid, a stereoisomer of L-ascorbic acid, has been extensively been used as an antioxidant, but cannot be applied to lipid-base foods due to poor lipophilicity. For this reason, synthesis of erythorbyl laurate (6-O-lauroyl-erythorbate) was perf...

Full description

Bibliographic Details
Main Author: 이다은
Other Authors: 장판식, Lee, Da Eun, 농생명공학부
Format: Doctoral or Postdoctoral Thesis
Language:English
Published: 서울대학교 대학원 2012
Subjects:
630
Online Access:http://hdl.handle.net/10371/154796
http://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000001493
id ftseoulnuniv:oai:s-space.snu.ac.kr:10371/154796
record_format openpolar
spelling ftseoulnuniv:oai:s-space.snu.ac.kr:10371/154796 2023-05-15T13:39:24+02:00 Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate 이다은 장판식 Lee, Da Eun 농생명공학부 2012 62 http://hdl.handle.net/10371/154796 http://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000001493 eng eng 서울대학교 대학원 000000001493 http://hdl.handle.net/10371/154796 http://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000001493 000000000006▲000000000011▲000000001493▲ 630 Thesis Dissertation 2012 ftseoulnuniv 2019-06-28T00:20:26Z 학위논문 (석사)-- 서울대학교 대학원 : 농생명공학부, 2012. 2. 장판식. Erythorbic acid, a stereoisomer of L-ascorbic acid, has been extensively been used as an antioxidant, but cannot be applied to lipid-base foods due to poor lipophilicity. For this reason, synthesis of erythorbyl laurate (6-O-lauroyl-erythorbate) was performed in acetonitrile using an immobilized lipase from Candidia antartica as a biocatalyst to increase its lipophilicity. Response surface methodology was used to optimize the erythorbyl laurate synthesis conditions in terms of enzyme content (1,000-5,000 propyl laurate unit, PLU), molar ratio of laurate to erythorbate (5-25), and reaction temperature (25-65°C). The central composite experimental results showed the conditions for maximum molar conversion yield were as follows: enzyme content, 2,994 PLU; 24.33 laurate to erythorbate molar ratio, and reaction temperature, 53.03°C. The maximum molar conversion yield reached 77.81%, which was in agreement with the predicted value (76.92%). The erythorbyl laurate was purified and identified by MALDI-TOF and FT-IR. Erythorbyl laurate was continuously synthesized by esterification in a pack-bed enzyme reactor with immobilized-lipase from Candida antarctica. Response surface methodology (RSM) based on 5-level 3-factor central composite design was adopted to optimize conditions for the enzymatic esterification. The reaction variables, such as reaction temperature (10-70oC), substrate molar ratio ([lauric acid]/[erythorbic acid], 5-15), and residence time (8-40 min) were evaluated and optimum conditions were found to be 56.2oC, 14.3, and 24.2 min, respectively. Under the optimum conditions, the degree of esterification was predicted as the value of 86.3%. In addition, removal of water by adsorption on ion exchange resins in potassium form has been used to improve esterification, and erythorbyl laurate typed powder was stable at a temperature not exceeding 50 oC for 30 days. This research could help to develop an economical method for production of erythorbyl laurate for use as a novel food-grade emulsifier with antioxidant activity. Master Doctoral or Postdoctoral Thesis Antarc* Antarctica antartic* Seoul National University: S-Space
institution Open Polar
collection Seoul National University: S-Space
op_collection_id ftseoulnuniv
language English
topic 630
spellingShingle 630
이다은
Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
topic_facet 630
description 학위논문 (석사)-- 서울대학교 대학원 : 농생명공학부, 2012. 2. 장판식. Erythorbic acid, a stereoisomer of L-ascorbic acid, has been extensively been used as an antioxidant, but cannot be applied to lipid-base foods due to poor lipophilicity. For this reason, synthesis of erythorbyl laurate (6-O-lauroyl-erythorbate) was performed in acetonitrile using an immobilized lipase from Candidia antartica as a biocatalyst to increase its lipophilicity. Response surface methodology was used to optimize the erythorbyl laurate synthesis conditions in terms of enzyme content (1,000-5,000 propyl laurate unit, PLU), molar ratio of laurate to erythorbate (5-25), and reaction temperature (25-65°C). The central composite experimental results showed the conditions for maximum molar conversion yield were as follows: enzyme content, 2,994 PLU; 24.33 laurate to erythorbate molar ratio, and reaction temperature, 53.03°C. The maximum molar conversion yield reached 77.81%, which was in agreement with the predicted value (76.92%). The erythorbyl laurate was purified and identified by MALDI-TOF and FT-IR. Erythorbyl laurate was continuously synthesized by esterification in a pack-bed enzyme reactor with immobilized-lipase from Candida antarctica. Response surface methodology (RSM) based on 5-level 3-factor central composite design was adopted to optimize conditions for the enzymatic esterification. The reaction variables, such as reaction temperature (10-70oC), substrate molar ratio ([lauric acid]/[erythorbic acid], 5-15), and residence time (8-40 min) were evaluated and optimum conditions were found to be 56.2oC, 14.3, and 24.2 min, respectively. Under the optimum conditions, the degree of esterification was predicted as the value of 86.3%. In addition, removal of water by adsorption on ion exchange resins in potassium form has been used to improve esterification, and erythorbyl laurate typed powder was stable at a temperature not exceeding 50 oC for 30 days. This research could help to develop an economical method for production of erythorbyl laurate for use as a novel food-grade emulsifier with antioxidant activity. Master
author2 장판식
Lee, Da Eun
농생명공학부
format Doctoral or Postdoctoral Thesis
author 이다은
author_facet 이다은
author_sort 이다은
title Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
title_short Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
title_full Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
title_fullStr Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
title_full_unstemmed Lipase-catalyzed Esterification between Erythorbic Acid and Lauric Acid for the Production of Erythorbyl Laurate
title_sort lipase-catalyzed esterification between erythorbic acid and lauric acid for the production of erythorbyl laurate
publisher 서울대학교 대학원
publishDate 2012
url http://hdl.handle.net/10371/154796
http://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000001493
genre Antarc*
Antarctica
antartic*
genre_facet Antarc*
Antarctica
antartic*
op_relation 000000001493
http://hdl.handle.net/10371/154796
http://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000001493
000000000006▲000000000011▲000000001493▲
_version_ 1766118005287157760