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Production of Structured Phosphatidylcholine with High Content of Myristic Acid by Lipase-Catalyzed Acidolysis and Interesterification

التفاصيل البيبلوغرافية
العنوان: Production of Structured Phosphatidylcholine with High Content of Myristic Acid by Lipase-Catalyzed Acidolysis and Interesterification
المؤلفون: Anna Chojnacka, Witold Gładkowski
المصدر: Catalysts, Vol 8, Iss 7, p 281 (2018)
بيانات النشر: MDPI AG, 2018.
سنة النشر: 2018
المجموعة: LCC:Chemical technology
LCC:Chemistry
مصطلحات موضوعية: immobilized lipases, structured phosphatidylcholine, myristic acid, trimyristin, acidolysis, interesterification, egg-yolk phosphatidylcholine, Chemical technology, TP1-1185, Chemistry, QD1-999
الوصف: Synthesis of structured phosphatidylcholine (PC) enriched with myristic acid (MA) was conducted by acidolysis and interesterification reactions using immobilized lipases as catalysts and two acyl donors: trimyristin (TMA) isolated from ground nutmeg, and myristic acid obtained by saponification of TMA. Screening experiments indicated that the most effective biocatalyst for interesterification was Rhizomucor miehei lipase (RML), whereas for acidolysis, the most active were Thermomyces lanuginosus lipase (TLL) and RML. The effect of the molar ratio of substrates (egg-yolk PC/acyl donor), enzyme loading, and different solvent on the incorporation of MA into PC and on PC recovery was studied. The maximal incorporation of MA (44 wt%) was achieved after 48 h of RML-catalyzed interesterification in hexane using substrates molar ratio (PC/trimyristin) 1/5 and 30% enzyme load. Comparable results were obtained in toluene with 1/3 substrates molar ratio. Interesterification of PC with trimyristin resulted in significantly higher MA incorporation than acidolysis with myristic acid, particularly in the reactions catalyzed by RML.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2073-4344
Relation: http://www.mdpi.com/2073-4344/8/7/281; https://doaj.org/toc/2073-4344
DOI: 10.3390/catal8070281
URL الوصول: https://doaj.org/article/05b74414d3d04777a0e63e203641880f
رقم الأكسشن: edsdoj.05b74414d3d04777a0e63e203641880f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20734344
DOI:10.3390/catal8070281