Enzymatic preparation of food-grade l-alpha-glycerylphosphorylcholine from soy phosphatidylcholine or fractionated soy lecithinopen access
- Authors
- Kim, Jeongeun; Song, Yejin; Lee, Soo Jeong; Lee, Jung Eun; Chung, Min-Yu; Kim, In-Hwan; Kim, Byung Hee
- Issue Date
- Jan-2020
- Publisher
- WILEY
- Keywords
- food-grade cognitive enhancer; lecithin; l-alpha-glycerylphosphorylcholine; Novozym 435; phosphatidylcholine
- Citation
- BIOTECHNOLOGY PROGRESS, v.36, no.1, pp 1 - 9
- Pages
- 9
- Journal Title
- BIOTECHNOLOGY PROGRESS
- Volume
- 36
- Number
- 1
- Start Page
- 1
- End Page
- 9
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/1693
- DOI
- 10.1002/btpr.2910
- ISSN
- 8756-7938
1520-6033
- Abstract
- l-alpha-Glycerylphosphorylcholine (l-alpha-GPC) is a biosynthetic precursor for the neurotransmitter acetylcholine in humans, making it a useful as a cognitive enhancer for treating patients with stroke and dementia, including Alzheimer's disease. The aim of this study was to prepare l-alpha-GPC via Novozym 435 (an immobilized Candida antarctica lipase B)-catalyzed hydrolysis of soy phosphatidylcholine or a fractionated soy lecithin, from which triacylglycerols were completely removed, followed by food-grade solvent extraction of l-alpha-GPC from the reaction products. The reaction was performed in n-hexane-water biphasic media in a stirred-batch reactor. Phosphatidylcholine was completely hydrolyzed to l-alpha-GPC under optimal conditions: temperature, 55 degrees C; water content, 100 wt% of the substrate weight; enzyme loading, 10 wt% of the substrate weight; and reaction time of 6 hr (for soy phosphatidylcholine) or 8 hr (for fractionated soy lecithin). Water-soluble fractions of the reaction products containing 98.6 area% l-alpha-GPC (from soy phosphatidylcholine) or 52.4 area% glycerophosphodiesters, including l-alpha-GPC (from fractionated soy lecithin), were obtained after phase separation of the media. The resulting products would be suitable for use as food-grade cognitive enhancers because of the use of enzymatic reaction and food-grade solvent extraction.
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