Relevant bibliographies by topics / Lipase catalyzed esterification

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Lipase catalyzed esterification'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Lipase catalyzed esterification"

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Rajendran, Aravindan, Anbumathi Palanisamy, and Viruthagiri Thangavelu. "Lipase catalyzed ester synthesis for food processing industries." Brazilian Archives of Biology and Technology 52, no. 1 (2009): 207–19. http://dx.doi.org/10.1590/s1516-89132009000100026.

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Lipases are one of the most important industrial biocatalyst which catalyzes the hydrolysis of lipids. It can also reverse the reaction at minimum water activity. Because of this pliable nature, it is widely exploited to catalyze the diverse bioconversion reactions, such as hydrolysis, esterification, interesterification, alcoholysis, acidolysis and aminolysis. The property to synthesize the esters from the fatty acids and glycerol promotes its use in various ester synthesis. The esters synthesized by lipase finds applications in numerous fields such as biodiesel production, resolution of the
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GANDHI, NEENA N., NITIN S. PATIL, SUDHIRPRAKASH B. SAWANT, JYESHTHARAJ B. JOSHI, PRAMOD P. WANGIKAR, and D. MUKESH. "Lipase-Catalyzed Esterification." Catalysis Reviews 42, no. 4 (2000): 439–80. http://dx.doi.org/10.1081/cr-100101953.

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Zhang, Yuyang, Yan Yan, Zhiyuan Lin, et al. "Advancements in the Esterification of Phytosterols Catalyzed by Immobilized Lipase." Catalysts 15, no. 3 (2025): 225. https://doi.org/10.3390/catal15030225.

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Phytosterol exhibits cholesterol-lowering, cardiovascular-protecting, anti-inflammatory, and anticancer efficacies but has low bioavailability due to its high melting point and poor solubility. Esterification with fatty acids enhances liposolubility, improving absorption and utilization fivefold. Industrial production of phytosterol esters mainly relies on chemical synthesis, which faces challenges in separation, purification, and quality assurance due to side reactions. Enzymatic synthesis, featuring mild conditions, environmental friendliness, and high selectivity, has gained attention from
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Pang, Na, Fang Qin Wang, Hong Sheng Cui, et al. "Lipase-Catalyzed Synthesis of Caffeic Acid Propyl Ester in Ionic Liquid." Advanced Materials Research 634-638 (January 2013): 555–58. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.555.

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Lipase-catalyzed esterification of caffeic acid with 1-propanol, to form caffeic acid propyl ester (CAPE), was investigated in ionic liquid using immobilized lipase. Ten ILs were used as the reaction medium; three types of lipases were selected as biocatalysts, and the lipase-catalyzed synthesis properties of CAPE were measured systematically in order to enhance the yield of CAPE. The results indicated that when [Bmim][Tf2N] was selected as reaction media, Novozym 435 was used as catalyst, the molar ratio of 1-propanol to CA was 10:1, the reaction temperature was 80 °C, and the mass ratio of c
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Ponnarasy, G., Md Maksudur Rahman Khan, Md Abul Kalam, and Mohd Sabri Mahmud. "Light Induced Esterification of Oleic Acid Catalyzed by Pseudomonas Cepacia Lipase." International Journal of Environmental Science and Development 5, no. 4 (2014): 344–46. http://dx.doi.org/10.7763/ijesd.2014.v5.506.

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Hari Krishna, S., and N. G. Karanth. "LIPASES AND LIPASE-CATALYZED ESTERIFICATION REACTIONS IN NONAQUEOUS MEDIA." Catalysis Reviews 44, no. 4 (2002): 499–591. http://dx.doi.org/10.1081/cr-120015481.

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Zhong, Hui, Zheng Fang, Bao Hua Zou, Xin Li, and Kai Guo. "Studies on the Esterification Synthesis of Alkyl Oleates in Solvent-Free System by Candida Sp. Lipase." Advanced Materials Research 634-638 (January 2013): 599–603. http://dx.doi.org/10.4028/www.scientific.net/amr.634-638.599.

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The alkyl oleates were prepared by esterification of oleic acid with alkyl alcohols catalyzed by the lipase from Candida sp. 99-125 in solvent-free system. The influence of several factors, including enzyme concentration, temperature, molar ratio between oleic acid and alkyl alcohols and the structures of alcohols, was also investigated. The results indicated that the reactions catalyzed by lipase at 20 oC, in the presence of 5% (w/w) lipase, on the molar ratio of 1:1 between oleic acid and alcohols, afforded products in high yield and showed high selectivity to the alcohols with less hindranc
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Zhong, Hui, Zheng Fang, Bao Hua Zou, Xin Li, and Kai Guo. "Studies on the Immobilized-Lipase-Catalyzed Esterification of Alkyl Oleates in Solvent-Free Systems." Advanced Materials Research 645 (January 2013): 19–23. http://dx.doi.org/10.4028/www.scientific.net/amr.645.19.

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The esterification of oleic acid with alkyl alcohols in solv ent-free systems was catalyzed by an immobilized lipase from Candida sp . 99-125. The influence of several factors, including enzyme concentration, temperature, molar ratio between oleic acid and alkyl alcohols, and structure of alcohol was also investigated. The results indicated that the reactions catalyzed by lipase at 20 o C, in the presence of 3% (w/w) lipase, on the molar ratio of 1:1 between oleic acid and alcohols, afforded products in high yield. It showed high selectivity to primary and low selectivity to secondary alcohols
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Zhou, Juntong, Qingqing Tian, Yuezhu Ma, Yue Wang, and Qing Huo. "Lipase-catalyzed selective esterification of catechin." Materials Express 11, no. 6 (2021): 995–1000. http://dx.doi.org/10.1166/mex.2021.1971.

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Catechins show strong antioxidant, antitumoral, antiviral, and anti-inflammatory activities. The uses of catechins in food, cosmetic, and pharmaceutical formulations seem very attractive. Unfortunately, solubility and stability of catechins are poor in apolar media, which limits their efficient uses. In order to improve the solubility of catechins in the oil phase and maintain their oxidation resistance, a regioselective enzymatic acylation was investigated. The effects of reaction medium, water content, carbon chain length of acyl donor and other factors on the acylation reaction were studied
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DUCRET, A., P. PEPIN, M. TRANI, and R. LORTIE. "Lipase-catalyzed Selective Esterification of Ibuprofen." Annals of the New York Academy of Sciences 799, no. 1 Enzyme Engine (1996): 747–51. http://dx.doi.org/10.1111/j.1749-6632.1996.tb33285.x.

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Dissertations / Theses on the topic "Lipase catalyzed esterification"

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Tarantino, Riccardo. "Lipase-catalyzed synthesis of esters and amides for cosmetic uses." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2022.

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This work focuses on the Lipase-catalyzed synthesis of esters and amides of great interest for the cosmetic sector, by employing enzymes Lipozyme® 435 and Novozym® 435, respectively. The esterification reactions yielded very high conversion of substrates in solvent-free systems within a short time interval. Regarding the synthesis of amides, Lauric and Oleic acid monoethanolamine (LMEA and OMEA) were successfully synthetized both with and without the use of organic solvents. The most promising results were obtained through the transacylation reactions in tert-butanol between the ethyl esters o
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Nguyen, Ba-Vu. "Chiral building blocks for synthesis of pine sawfly sex pheromones Enantioselective Lipase Catalysed Acylations and Esterifications of Primary Alcohols and Acids and Synthesis of the Sex Pheromone of the Pine Sawfly Microdiprion pallipes." Doctoral thesis, KTH, Chemistry, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3024.

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<p>This thesis describes the development of new methods for thepreparation of enantiomerically pure methyl branched alkylcompounds and their use as building blocks in the synthesis ofstereoisomerically pure pheromones of pine sawflies.</p><p>The high regioselectivity, enantioselectivity and activityof lipases in organic solvent in conjunction withenvironmentally compatible reaction conditions have madelipase-catalysed synthesis an attractive alternative toconventional synthetic methods in organic chemistry. The lipasefrom<i>Pseudomonas cepacia</i>(PCL) was used in kineticresolutions of primary
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Leszczak, Jean-Pierre. "Synthèse d'esters de l'acide benzoïque par catalyse enzymatique en milieu hétérogène microaqueux." Grenoble INPG, 1998. https://theses.hal.science/tel-00841819.

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La synthèse d'esters de l'acide benzoïque par voie enzymatique en milieu hétérogène microaqueux est envisagée. Cette estérification est possible et est catalysée par la lipase de Candida rugosa en suspension dans un mélange hexane/toluène. Le toluène permet la solubilisation de l'acide benzoique. De nombreux paramètres influencent la synthèse des benzoates de méthyle et de butyle. La teneur en eau initiale agit uniquement sur la cinétique de réaction sans modifier de manière notable la position de l'équilibre de réaction. Il est préférable, dans la mesure du possible, de travailler à une activ
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Yang, Yung-Ching, and 楊永慶. "Synthesis of Monostearin via Lipase-catalyzed Esterification." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/47186518242228902478.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>90<br>Monoglyceride (MG) is one type of derivative of acylglycerol, in which one of the hydroxyl group of glycerol is esterified with fatty acid. MGs are most widely used as additives and emulsifiers in the food, cosmetic and pharmaceutical products. The conventional chemical methods to produce MG in industry are usually carried out at higher temperatures (220-250℃) under nitrogen atmosphere by employing inorganic alkaline catalysts. The major disadvantages of these processes are: it needs high energy, it produces several undesirable by products and also the quality
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Kaur, Jasmedh. "Studies on Lipase catalyzed esterification reactions in microaqueous environment." Thesis, 1996. http://localhost:8080/xmlui/handle/12345678/2725.

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Yang, Cheng Kang, and 楊正剛. "Optimal Lipase-Catalyzed Esterification of Hexyl Laurate by Continuous Packed Bed Reactor." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/56711506854591237736.

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碩士<br>大葉大學<br>生物產業科技學系<br>94<br>Hexyl esters, a medium-chain ester, with a fruity flavor are primarily used in personal care formulations as an important emollient for cosmetic applications. Packed bed reactors, are the most frequently used reactors for immobilized lipases. They are best used continuously on a commercial scale so as to minimize labor and overhead costs. Enzymatic synthesis with a continuous packed bed reactor can either satisfy consumers’ need for “natural quality” or lower production cost on industrial applications. The ability of lipase from Rhizomucor miehei (Lipase IM77) t
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HUONG, DINH THI MY, and 林美香. "Liquid Lipase Catalyzed Esterification for Biodiesel Production in The Presence of Superabsorbent Polymer." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/u7a9u3.

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碩士<br>明志科技大學<br>化學工程系生化工程碩士班<br>107<br>Biodiesel, a renewable and environmental friendly energy has replaced for diesel in the engine vehicles. Mostly biodiesel on the world is produced by alkaline catalyzed transesterification of edible oils, which causes the high price of biodiesel and the competition in the food supplement. None-edible oils and waste cooking oils are the potential feedstocks because of their cheap price. The esterification of fatty acids with methanol seems to be a suitable process for biodiesel production from these feedstocks. In this study, the esterification of Oleic ac
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Cheng, Yu-Chi, and 鄭育奇. "Acyl transfer catalyzed by lipases in organic solvents; I. Theoretical study of side-reaction effects on lipase-catalyzed transesterification, II. Esterification resolution of (R, S)- phenoxypropionic acid by Carica papaya lipase." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/55801606957079300809.

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博士<br>國立成功大學<br>化學工程學系碩博士班<br>93<br>(I) An analytical solution for the dynamic kinetic resolution of enzyme-catalyzed irreversible acyl transfer was employed to study the side-reaction effects on the yield and optical purity of the desired enantiomeric product. A lipase-catalyzed enantioselective thiotransesterification between (R, S)-naproxen 2,2,2-trifluoroethyl thioester and 4-morpholine ethanol with in situ racemization of (R)-thioester using trioctylamine as the racemization catalyst in isooctane was designed as a model system to compare the theoretical predictions. Under an initial water
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Hsu, Chin-Shuo, and 徐景碩. "Lipase-catalyzed enantioselective esterification of (S)-hydroxyalkyl ester of non-steroidal drugs in organic media." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/95944807831705817669.

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碩士<br>南台科技大學<br>化學工程系<br>91<br>A lipase-catalyzed enantioselective esterification process in organic solvents was developed for the synthesis of (S)-naproxen hydroxyalkyl ester and (S)-ketoprofen hydroxyalkyl ester. With the selection of lipase (Candida rugosa lipase and Lipase MY) and reaction medium (isooctane and cyclohexane), a high enantiomeric ratio of >100 for the enzyme were obtained for the synthesis of (S)-Naproxen hydroxyalkyl ester. 1,4-Butanediol was the best acyl acceptor. The carbon chain length of the alcohol had a major effect on the enzyme activity and enantioselectivity of
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Hwang, Jenq Woei, and 黃政偉. "Enrichment of Gamma-linolenic acid from borage oil and evening primrose oil via lipase-catalyzed hydrolysis and esterification." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/45737289923350162550.

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碩士<br>國立臺灣科技大學<br>化學工程研究所<br>84<br>Lipase(triacylglycerol ester hydrolase, E.C.3.1.1.3) from Candida rugosa was immobilized on hydrophobic microporous polypropylene supports by physical adsorption. The immobilized enzyme catalysts were employed for the selective hydrolysis and esterification of borage oil and evening primrose oil to contrate their GLA contents in glycerides. The Michaelis constant Km and the maximum rate constant Vm for the lipolysis of borage oil by Candida rugosa are 0.10
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Book chapters on the topic "Lipase catalyzed esterification"

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Baldessari, Alicia, and Guadalupe García Liñares. "Lipase-Catalyzed Acetylation and Esterification of Bile Acids." In Lipases and Phospholipases. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8672-9_18.

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Hollenbach, Rebecca, Katrin Ochsenreither, and Christoph Syldatk. "Parameters Influencing Lipase-Catalyzed Glycolipid Synthesis by (Trans-)Esterification Reaction." In Advances in Biochemical Engineering/Biotechnology. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/10_2021_173.

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Stamatis, H., A. Xenakis, H. Sztajer, U. Menge, and F. N. Kolisis. "Studies on the Specificity of Penicillium Simplicissimum Lipase Catalyzed Esterification Reactions in Microemulsions." In Progress in Biotechnology. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-444-89046-7.50105-3.

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Robles Medina, A., L. Esteban Cerdán, A. Giménez Giménez, B. Camacho Páez, M. J. Ibáñez González, and E. Molina Grima. "Lipase-catalyzed esterification of glycerol and polyunsaturated fatty acids from fish and microalgae oils." In Progress in Industrial Microbiology. Elsevier, 1999. http://dx.doi.org/10.1016/s0079-6352(99)80131-3.

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Procter, Garry. "Hydrolysis and esterification." In Asymmetric Synthesis. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198557265.003.0009.

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Abstract There are two general approaches to the use of hydrolysis and esterification in asymmetric synthesis, and usually both involve the use of enzymes as asymmetric catalysts. In one case the asymmetric catalyst is used in a kinetic resolution process in which one enantiomer of a racemic mixture reacts more rapidly than its antipode. In the example shown (Fig. 9.1) the lipase-catalysed hydrolysis of the (1R,2R)-enantiomer of 9.1 is rapid. In effect, the (1S,.2S) enantiomer is not a substrate for the enzyme, and essentially all of the fastreacting antipode is hydrolysed to the alcohol. As i
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Knez, Ž., and M. Habulin. "Lipase Catalysed Esterification in Supercritical Carbon Dioxide." In Progress in Biotechnology. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-444-89046-7.50061-8.

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Taber, Douglass F. "Carbon–Carbon Bond Formation: The Petrov Synthesis of Combretastatin A-4." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0025.

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Janine Cossy of ESPCI Paris (Org. Lett. 2011, 13, 4084) and Yasushi Obora of Kansai University (Chem. Lett. 2011, 40, 1055) independently developed conditions for the “borrowed hydrogen” condensation of acetonitrile with an alcohol 1 to give the nitrile 2. Akio Baba of Osaka University showed (Angew. Chem. Int. Ed. 2011, 50, 8623) that a ketene silyl acetal 4 could be condensed with a carboxylic acid 3 to give the β-keto ester 5. Timothy W. Funk of Gettysburg College found (Tetrahedron Lett. 2010, 51, 6726) that the cyclopropanol 6, readily prepared by Kulinkovich condensation of an alkene wit
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Valivety, Rao H., Peter J. Halling, and Alasdair R. Macrae. "Effect of Water Activity on Rate of Lipase Catalysed Esterification." In Progress in Biotechnology. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-444-89046-7.50080-1.

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Sarazin, C., C. Roblot, B. Decagny, F. Ergan, J. N. Barbotin, and J. P. Séguin. "NMR study of hydration of liquid phase during lipase catalysed esterification in non aqueuous media." In Progress in Biotechnology. Elsevier, 1998. http://dx.doi.org/10.1016/s0921-0423(98)80107-x.

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Conference papers on the topic "Lipase catalyzed esterification"

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Kim, In-Hwan, Dongchan Oh, and Suhyeon Choi. "Production of value-added oleochemicals via Eversa immobilized lipase-catalyzed esterification." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/lqbh2911.

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Eversa lipase (from Themomyces lanuginosus) as a liquid type was developed to produce biodiesel. In our previous study, diisononyl adipate was effectively synthesized with an immobilized lipase prepared from Eversa lipase using Lewatit VP OC 1600 as a carrier. In this study, two oleochemicals, palmitoleic acid rich triacylglycerol (TAG) and 2-ethylhexyl palmitate, were successfully synthesized by Eversa immobilized lipase-catalyzed esterification. The palmitoleic acid rich TAG was synthesized from macadamia nut oil via two-step enzymatic reactions, which are C. rugosa lipase-catalyzed hydrolys
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Kim, In-Hwan, and Suhyeon Choi. "Efficient Synthesis of 2-ethylhexyl Palmitate via an Immobilized Lipase-catalyzed Esterification." In Virtual 2021 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2021. http://dx.doi.org/10.21748/am21.162.

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Kang, Jeanne, and In-Hwan Kim. "Concentration of eicosapentaenoic acid via Candida rugosa lipase-catalyzed esterification with phytosterol and fatty acid from anchovy oil." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/wyzv8794.

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Eicosapentaenoic acid (EPA, 20:5n3), which is one of the well-known polyunsaturated fatty acids (PUFAs), is contained abundantly in anchovy oil among marine oils. EPA, along with docosapentaenoic acid (DPA, 22:5n3) and docosahexaenoic acid (DHA, 22:6n3), provide several health benefits such as reducing the risk of cardiovascular disease, cancer, and stroke, protecting vision, and increasing immunity. In the present study, EPA was concentrated efficiently in the unesterified fatty acid when Candida rugosa lipase-catalyzed esterification with phytosterol and fatty acid from anchovy oil was carri
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Lee, Yu Jin, Changhwan Ju, and In-Hwan Kim. "Novel Strategy for Synthesis of Stearidonic Acid Enriched Triacylglycerol from Ahiflower Seed Oil via a Two-step Enzyme Reaction." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/uhjd7801.

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Stearidonic acid (SDA) is a plant-based n-3 polyunsaturated fatty acids (PUFAs) with several positive therapeutic effects on human health such as reducing risks of cardiovascular diseases, obesity, inflammation, and cancer. Moreover, the conversion efficiency of SDA to EPA is significantly higher than α-linolenic acid to EPA, in the human body. Plant oils with SDA, such as ahiflower seed oil and echium seed oil, exhibit substantially higher oxidative stability than fish oil with EPA and DHA, the most popular n-3 PUFA. The present study has successfully carried out the enrichment of SDA and the
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Yoon, Hui su, та In-Hwan Kim. "Lipozyme TL IM-catalyzed synthesis of γ-linolenic acid rich triacylglycerol from borage oil as a novel strategy". У 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/sgec7971.

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Lipozyme TL IM from Thermomyces lanuginosus is widely employed for various enzymatic reactions such as esterification, hydrolysis, and alcoholysis. However, none of the publications is using Lipozyme TL IM as a biocatalyst to synthesize triacylglycerol (TAG) with fatty acid and glycerol because the silica gel carrier in Lipozyme TL IM aggregates with glycerol. Thus, most studies regarding the synthesis of TAG via lipase-catalyzed esterification have employed Novozym 435, one of the most expensive enzymes. In present study, we attempted to synthesize TAG using Lipozyme TL IM with glyceride, ins
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John, George, Jose James, Malick Samateh, Siddharth Marwaha, and Vikas Nanda. "Sucralose Hydrogels: Peering into the Reactivity of Sucralose versus Sucrose Using Lipase Catalyzed Trans-Esterification." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/xkza4963.

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Sucralose differs from sucrose only by virtue of having three Cl groups instead of OH groups. Its intriguing features include being noncaloric, noncariogenic, 600 times sweeter than sucrose, stable at high temperatures/acidic pH's, and void of disagreeable aftertastes. These properties are attractive as food additive, one of which is as hydrogel obtainable via the technique of molecular gelation using a sucralose-derived low-molecular weight gelator (LMWG). The process of molecular gelation entails using specially designed lipid-like amphiphilic molecules capable of self-assembling in a liquid
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Park, Mi Soon, Yu Jin Lee, and In-Hwan Kim. "Synthesis of Pinolenic Acid Enriched Triacylglycerol from Pine Nut Oil via a Two-step Consecutive Enzyme Reaction." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/jlcw3538.

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Pinolenic acid (PLA), Δ‐5,9,12‐octadecatrienoic acid-C18:3, is a plant origin polyunsaturated fatty acid and is contained abundantly in pine nut oil. PLA has several health benefits, such as the reduction of atherosclerosis, inflammation, and blood pressure. In addition, PLA may work as an appetite suppressant by increasing the effect of satiety hormones, such as cholecystokinin and glucagon-like peptide-1. The aim of this study was to synthesize PLA-enriched TAG from pine nut oil via a two-step lipase-catalyzed reaction, which is ethanolysis and esterification. In the first step, PLA was enri
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Zapata-Romero, Gilberto A., Markus Doerr, and Martha C. Daza. "Enantioselective lipase-catalyzed O-acylation of (RS)-propranolol: analysis of the hydrogen bonds essential for catalysis." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020131.

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We investigated the effect of the acyl group size in the enantioselectivity of the acylation of propranolol, an amino alcohol used as β-adrenergic blocking agent. We applied a methodology frequently used to model enantioselectivity that is based on the hydrogen bonds present in the tetrahedral intermediate, which occurs in lipase-catalyzed reactions. We sampled the conformations of the tetrahedral intermediate corresponding to the esterification of both enantiomers of propranolol with ethanoyl and butanoyl, employing molecular dynamics simulation together with a quantum mechanics/molecular mec
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Bassi, Jaquelinne de Jorge, Larissa Midiane Todero, Flávia Arantes Pires Lage, Maria Carolina Cucatti Corradini, DANIELA B. HIRATA, and Adriano Aguiar Mendes. "ENZYMATIC SYNTHESIS OF BANANA FLAVOR (ISOAMYL BUTYRATE) BY ESTERIFICATION REACTION CATALYZED BY IMMOBILIZED LIPASE ON POLY-METHACRYLATE PARTICLES." In Simpósio Nacional de Bioprocessos e Simpósio de Hidrólise Enzimática de Biomassa. Galoá, 2015. http://dx.doi.org/10.17648/sinaferm-2015-33466.

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Bhushan, Indu. "Efficient media for high production of microbial lipase from Bacillus subtilis (BSK-L) using response surface methodology for enantiopure synthesis of drug molecules." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.044.

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Lipases are a multipurpose enzyme that holds a significant position in industrial applications due to its ability to catalyse a large number of reactions such as hydrolysis, esterification, interesterification, transesterification which makes it a potential candidate. It is also used for the separation of chiral drugs from the racemic mixture and this property of lipase is considered very important in pharmaceutical industries for the synthesis of enantiopure bioactive molecules. Assuming the tremendous importance of lipases, as stereoselective biocatalysts, in pharmaceuticals and various othe
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