How are Mono and Diglycerides metabolized without the Free Fatty Acids of Triglycerides?

How are Mono and Diglycerides metabolized without the Free Fatty Acids of Triglycerides?

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Having difficulty figuring out what the body does with ingested mono and diglycerides if the usual process of TAG metabolism includes the FFA released from the TAG returning to the MAG to recreate a TAG in the enterocyte, whereas with MAG and DAG consumption, those FFA don't exist. There are many studies (Nagao, 2000, Takatoshi, 2002 and others) confirming that DAG oil consumption leads to weight loss, which is seemingly obvious as the fat cannot be stored without the FFA getting repackaged into TAGs for storage in the adipose tissue. I have not found any studies on what actually happens to the MAGs in lieu of its normal course. I would much appreciate if someone could direct me to literature discussing this process or help me better understand it. Many thanks! Anyone?

Inside the intestinal lumen, di- and triacylglycerol are hydrolysed to free fatty acid and monoglyceride by lipase.

These diffuse through the plasma membrane of enterocyte where they will used to resynthetize triacylglycerol, and ultimately the lipoprotein chylomicron for transport into the general circulation.

Contrary to what your question seems to imply, the glycerol to which the free fatty acid are affixed is not necessarily coming from the food: glycerol is routinely produced by glycolysis. (This notably also happens in the adypocytes). There is no requirement that food contain a ratio three fatty acid to one glycerol to be fully absorbed - if the weight loss property of DAG are true, it may be through a different mechanism.

Fats and Fatty Acids

Most of us are bombarded with information about fats (much of it conflicting or confusing) and the healthiest way to eat. The terms “saturated fats,” “omega-3 fats,” and “trans fats” are familiar parts of our collective vocabularies. But, what do these terms really mean and how are they significant in terms of eating healthy and in a Paleo-appropriate way? If you take a little time to read this primer on fats and fatty acids, you will soon become familiar with these essential nutrients, their nomenclature and how they affect your health and well-being.

Going to the Bloodstream

As stomach contents enter the small intestine, the digestive system sets out to manage a small hurdle, namely, to combine the separated fats with its own watery fluids. The solution to this hurdle is bile. Bile contains bile salts, lecithin, and substances derived from cholesterol so it acts as an emulsifier. It attracts and holds onto fat while it is simultaneously attracted to and held on to by water. Emulsification increases the surface area of lipids over a thousand-fold, making them more accessible to the digestive enzymes.

Once the stomach contents have been emulsified, fat-breaking enzymes work on the triglycerides and diglycerides to sever fatty acids from their glycerol foundations. As pancreatic lipase enters the small intestine, it breaks down the fats into free fatty acids and monoglycerides. Yet again, another hurdle presents itself. How will the fats pass through the watery layer of mucus that coats the absorptive lining of the digestive tract? As before, the answer is bile. Bile salts envelop the fatty acids and monoglycerides to form micelles. Micelles have a fatty acid core with a water-soluble exterior. This allows efficient transportation to the intestinal microvillus. Here, the fat components are released and disseminated into the cells of the digestive tract lining.

Figure 5.11 Micelle Formation

Scheme of a micelle formed by phospholipids in an aqueous solution by Emmanuel Boutet / CC BY-SA 3.0

Figure 5.12 Schematic Diagram Of A Chylomicron

Chylomicrons Contain Triglycerides Cholesterol Molecules and other Lipids by OpenStax College / CC BY 3.0

Just as lipids require special handling in the digestive tract to move within a water-based environment, they require similar handling to travel in the bloodstream. Inside the intestinal cells, the monoglycerides and fatty acids reassemble themselves into triglycerides. Triglycerides, cholesterol, and phospholipids form lipoproteins when joined with a protein carrier. Lipoproteins have an inner core that is primarily made up of triglycerides and cholesterol esters (a cholesterol ester is a cholesterol linked to a fatty acid). The outer envelope is made of phospholipids interspersed with proteins and cholesterol. Together they form a chylomicron, which is a large lipoprotein that now enters the lymphatic system and will soon be released into the bloodstream via the jugular vein in the neck. Chylomicrons transport food fats perfectly through the body’s water-based environment to specific destinations such as the liver and other body tissues.

Cholesterols are poorly absorbed when compared to phospholipids and triglycerides. Cholesterol absorption is aided by an increase in dietary fat components and is hindered by high fiber content. This is the reason that a high intake of fiber is recommended to decrease blood cholesterol. Foods high in fiber such as fresh fruits, vegetables, and oats can bind bile salts and cholesterol, preventing their absorption and carrying them out of the colon.

If fats are not absorbed properly as is seen in some medical conditions, a person’s stool will contain high amounts of fat. If fat malabsorption persists the condition is known as steatorrhea. Steatorrhea can result from diseases that affect absorption, such as Crohn’s disease and cystic fibrosis.

Figure 5.13 Cholesterol and Soluble Fiber

Image by Allison Calabrese / CC BY 4.0

How are Mono and Diglycerides metabolized without the Free Fatty Acids of Triglycerides? - Biology

Department of Chemistry, Faculty of Science and Engineering, Nusa Cendana University

Department of Pharmacy, Health Polytechnic of Kupang

Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada

Department of Chemistry, Faculty of Science and Engineering, Nusa Cendana University

2020 Volume 69 Issue 4 Pages 277-295

  • Published: 2020 Received: June 21, 2019 Released on J-STAGE: April 03, 2020 Accepted: January 21, 2020 Advance online publication: - Revised: -

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Fatty acid and monoglyceride are examples of lipid compounds that can be founded in vegetable oils. The fatty acid has an important role in the human diet, lubricants, detergents, cosmetics, plastics, coatings, and resin. Monoglyceride has a wide function in the food industry in particular as natural emulsifier, pharmaceuticals, cosmetics, antioxidant, and antibacterial. Therefore, isolation and preparation of fatty acid and monoglyceride are the crucial step. This article focuses on providing the chemical reaction paths of isolation fatty acid and synthesis of monoglyceride from vegetable oils. Fatty acids could be isolated by Colgate-Emery steam hydrolysis, hydrolysis of vegetable oils using inorganic base catalyst or lipase, and base-catalyzed hydrolysis of pure fatty acid methyl ester. There are three steps in the synthesis of pure fatty acid methyl ester which are neutralization, transesterification, and fractional distillation. There are four reactions paths in preparing monoglyceride from vegetable oils. They are glycerolysis, ethanolysis using lipase enzyme (sn-1,3), esterification of fatty acid with glycerol in the presence of inorganic acid catalyst or lipase, transesterification of fatty acid methyl ester with glycerol, transesterification of fatty acid methyl ester with protected glycerol (1,2-O-isopropylidene glycerol), and deprotection using an acid resin (Amberlyst-15).

Fatty acids and monoglycerides are two groups of lipid compounds that can be produced from vegetable oils or animal fats. Vegetable oil is a triglyceride compound, also known as triacylglycerol or glycerol triester, with the acyl group that comes from a fatty acid. The type of vegetable oil is determined by the kind of fatty acid that is bound to triglycerides. Triglycerides of vegetable oils comprises of certain major fatty acids with some other minor fatty acids. For example, the coconut oil (Cocos nucifera L.), the castor oil (Ricinus communis L.), the olive oil, the sunflower oil, the palm oil contains 54% lauric acid 1) , 93% ricinoleic acid 2) , oleic acids 3) , oleic and linoleic acid 4) and palmitic acid 5) , respectively.

Some types of fatty acids such as EPA and DHA have essential functions in health such as reducing coronary heart disease risk factors, preventing certain cancers and improving the functioning of the body’s immune system 6) . There is also another type of fatty acid known as Linoleic acid (C18: 2, ῲ6) that is essential for human health 7) . Medium chain fatty acids, especially lauric acid, has been reported to have antibacterial activity 8) . Hydroxy fatty acids ricinoleic acid is known as a multifunctional compound in the industry for producing soap, adhesive, surfactants, cosmetics, other personal care products, wax, ink, perfume, plastic materials, paints, coatings, lubricants, food ingredients, fine chemicals and pharmaceuticals 9) .

Several methods that generally used to produce fatty acids from vegetable oils are hydrolysis at high temperatures and pressures (Colgate-Emery Process) and hydrolysis reactions using either alkaline or lipase as catalysts 10) . The fatty acid plays an important role in human life and hence the availability of fatty acids needs to be prioritized to ensure sustainability production in industries. Therefore, isolation or manufacture of fatty acids from vegetable oils, as one of the sources of fatty acid, needs to be considered and studied.

Monoglyceride is an important lipid compound from vegetable oil. Based on the position of the ester linkage that covalently bonded to glycerol, monoglycerides can be divided into two categories, 1-monoglyceride (α-monoglyceride) and 2-monoglyceride (β-monoglyceride) as shown in Fig. 1. Structure of 1-monoglyceride or α-monoglycerides is determined by the positions of carboxylate anion on C1 or C3 atoms of the glycerol molecule. Otherwise, it will produce 2-monoglyceride or β-monoglyceride if the acyl group attached to the C2 atom.

Structure of 1-monoglyceride and 2-monoglyceride.

The structure of monoglycerides consist of a head that is hydrophilic and tail that is hydrophobic or lipophilic. Due to these particular properties, monoglycerides can be categorized as a surfactant, and it is included as non-ionic surfactants. As a non-ionic surfactant, monoglycerides display excellent emulsifying properties, especially for combining oil and water. Thus, monoglyceride compounds have a wide application in human life.

Monoglyceride compounds have important applications as emulsifiers in the food, cosmetics, pharmaceuticals, detergents and petroleum industries 11) , 12) , 13) , 14) , 15) . Monoglycerides are safe and non-toxic emulsifiers because they are produced from vegetable oils. Around 75% of the total emulsifiers in the food industry worldwide come from monoglyceride compounds 4) . It is estimate that the annual monoglycerides consumptions in the United States was 85,000,000 Kg 16) . Moreover, the global emulsifier market offered natural emulsifier ingredients is up to 2.6 million tons in 2017 and it is expected to grow annually. There are also biological activities in monoglycerides. It has been reported that monoglycerides including monolaurin, monomyristin, monocaprin, monoolein, and monolinolein shown antimicrobial activities 1) , 17) , 18) , 19) . Monomiristin and monopalmitin showed promising bioactivity against E. coli O157: H7 at a concentration of 20 ppm (60-80%) and monolaurin could inhibit the growth of Yersinia enterocolitica and E. coli O157: H7 at 50 ppm (>90%) 20) . Monocaprin and monolaurin exhibited strong activity to Helicobacter pylori 21) . Hydrolyzed virgin coconut oil that contains both lauric acid and monolaurin have been reported to actively inhibit Salmonella typhimurium 22) . Monocaprin also has been revealed to have microbicidal activities to the Food-Borne bacteria i.e. Campylobacter jejuni, Salmonella spp., as well as Escherichia coli and showed the best activity toward C. jejuni. Some monoglyceride from the root extract of Ibervillea Sonorae Greene (in DCM) also displayed hypoglycemic activity 23) . The antibacterial activity of monoglyceride compounds is determined by the chemical structure and hydrophilic and lipophilic properties that are expected to interact with cell walls of both Gram-positive and Gram-negative bacteria.

Some novel utility of monoglyceride, palm fatty acid distillate (PFAD) with minor amounts of glycerides, can be used as a sustainable feedstock to produce an eco-friendly alkyl resin 24) . Monoglyceride function as an intermediate compound in the synthesis of a novel Gemini surfactant for the Enhanced Oil Recovery process 25) . Monoglycerides from omega-3 polyunsaturated fatty acid (PUFA) were also beneficial effects to some human disorder condition such as cancer and inflammation disease 26) . Monoglycerides from EPA and DHA are likewise very useful for human health base on their nutritive value 6) , role in there regulation of inflammation, cholesterol metabolism, and brain functions 27) , their influence to erythrocyte fatty acid profiles and the expression levels of inflammatory circulating mediators 28) . Long Chain Poly Unsaturated Fatty Acid (LC-PUFA) monoglycerides oil also increased LC-PUFA levels in erythrocytes, plasma, and chylomicrons 29) .

Monoolein also has shown antioxidant activity and anti-atherosclerosis 30) . In the pharmaceutical industry, besides being used as an antibacterial ingredient, monoglyceride also used as a binder in drug tablets, skin moisturizing agents, and slow drug release in the body. In the food industry, monoglyceride is an excellent emulsifier for cake, bread, and margarine products. In addition, monoglycerides have lubricating and plastic properties which are widely applied in the textile and plastic industries. In the cosmetics industry, monoglycerides have consistency used to improve the quality of creams and lotions 4) .

A variety of application of monoglycerides has led to an increasing demand for monoglyceride. As a result, it affects the availability of monoglyceride. Monoglycerides are conventionally made by chemical glycerolysis reactions of vegetable oils at high temperatures using inorganic alkaline catalysts. This process produces monoglyceride in a low yield and characterized to have a darker color and charred smell. This process requires high energy consumption and is not suitable for the manufacture of heat-sensitive monoglycerides such as monoglycerides from EPA and DHA. Therefore, production of monoglycerides from vegetable oils is an alternative approach to meet the demand. Both researcher and industry players can employ alternative rational chemical reaction approach.

Although world vegetable oil production increased to 184×106 tons in 2016-2020 30) , it does not guarantee the availability of natural fatty acids and emulsifiers such as monoglycerides. This problem is caused by various drawbacks in the process of isolation and synthesis of fatty acids and monoglycerides in vegetable oils. Thus, the topic of discussion in this article will focus on presenting various approaches and chemical reactions to isolate and synthesize both fatty acids and monoglycerides from vegetable oils.

Vegetable oil is rich in fatty acids that bound to triglycerides or present as free fatty acids (FFA). The amount of free fatty acids in vegetable oil is expressed in acid value. The acid value represents the content of free fatty acids. Since the fatty acid plays an important role in human life, the isolation or production of fatty acids from vegetable oil is an important aspect to be considered. In this section, we will discuss in detail several approaches to isolate or synthesis of fatty acids from vegetable oils.

Fatty acids can be produced from the hydrolysis of triglycerides with subcritical water or supercritical CO2 30) . This process involves some steps which are the breaking down of triglycerides to diglycerides and FFA, then breaking off diglycerides to monoglycerides and FFA, and finally the breaking down of monoglycerides to glycerol and FFA. The conventional method in producing fatty acids from vegetable oils is steam fat-splitting at high temperatures and pressures that are known as Colgate-Emery Steam Hydrolysis 31) and Foster-Wheeler process 30) . This hydrolysis reaction requires operating temperature at 250°C and pressure at 50 atm. The advantage of these two hydrolysis processes is that the process can take place without catalyst, produces a high-quality FFA, in term of its high yield and purity, and also minimum waste.

Despite some advantages of the Colgate-Emery method, this process has major drawbacks here it needs extreme and intensive reaction conditions, is costly because it requires a specific breaking column that must be resistant to high temperatures and pressures, as well as corrosive to the produced fatty acids. This method is also not suitable for the production of heat-sensitive fatty acids, or fatty acids bearing hydroxyl groups such as ricinoleic acid. At an extreme reaction condition, ricinoleic acid can be dehydrated or might undergo undesired thermal decomposition. The Colgate-Emery method is also limited to be applied to vegetable oil containing unsaturated fatty acids (PUFA) with high iodine numbers due to polymerization 10) .

Fatty acids can also be obtained through base-catalyzed hydrolysis reactions of a vegetable oil sample by using a strong base catalyst such as KOH and NaOH. This method is too costly and needs acidification step to the soap formed so that free fatty acids can be afforded 10) . Recent research regarding the isolation of fatty acids from a vegetable oil sample has also been successfully published by Jumina et al 32) . In this research, corn oil as a source of linoleic acid and oil as a source of oleic acid are used as raw materials in the process of isolating fatty acids. Corn oil and coconut oil are each heated with KOH 11% (b/v) in ethanol solvent. The reaction takes place at room temperature for 90 minutes. Product of hydrolyzed reaction that is catalyzed by base toward corn oil and palm oil was isolated in n-hexane solvent. Acidified product in n-hexane is carried out in sulfuric acid until the pH of the aqueous phase reaches pH=1. The fatty acid product that was isolated was in the n-hexane phase. Based on chromatography analysis, it shows oil corn containing linoleic acid (57.74%), and palmitate acid (19.88%) that is measured as ethyl linoleic and ethyl palmitate, respectively.

The enzymatic hydrolysis by employing lipase enzyme has been developed to overcome the weaknesses of the production of fatty acids from vegetable oils through Colgate-Emery and alkaline catalyzed hydrolysis. In this reaction process, the hydrolysis reaction of vegetable oil will take place at lower temperatures and atmospheric pressure, thus can minimize the energy consumption, and it follows the green chemical reaction. Lipase enzymes are also more effective at catalyzing reactions in a water solution, are reusable and produce a high-quality free fatty acid. The effective lipase enzyme used for the hydrolysis of triglycerides to produce free fatty acids is sn-1,3-selective lipases 33) , such as porcine pancreas lipase (PPL), Rhizopus arrhizus, and Rhizomucor miehei. This enzyme is also effective in the production of heat-sensitive fatty acids such as erucic acid.

Products from the hydrolysis of triglycerides from vegetable oils using lipase enzyme catalysts are fatty acids and glycerol. Lipase enzymes can be separated easily through the decantation process and it can be reused. The separating process of fatty acids can be done by extracting the products of hydrolysis with a non-polar organic solvent and washed it with water. Free fatty acids are easily dissolved in the organic phase and can be separated by solvent evaporation. Glycerol as a by-product will dissolve in the water phase with other impurities.

Vegetable oil can be a source of fatty acid methyl esters (FAME), an ester form of fatty acid. A fatty acid ester can be obtained by alkaline catalyst transesterification reactions from triglycerides of vegetable oil. The presence of free fatty acids in vegetable oil can interfere with the transesterification reaction to produce (FAME). For this reason, neutralizing vegetable oils with a weak base solution aid in eliminating the free fatty acids 8) . Based on this fact, vegetable oil with an acid number less than one (<1) is qualified as a raw material for transesterification reactions.

Alkaline-catalyzed transesterification reactions from vegetable oils using methanol will produce FAME and glycerol. The reaction mixture of FAME can be easily separated through the extraction process using a non-polar solvent. Each fatty acid methyl ester can be easily separated by fractional distillation based on their different boiling point properties. After the separation of fatty acid methyl ester, then a base-catalyzed hydrolysis process is carried out to produce free fatty acids. The chemical reactions scheme of the synthesis of fatty acid from vegetable oil through the formation of FAME is presented in Fig. 2.

Reaction scheme of synthesis of fatty acid from FAME.

Vegetable oil can be one of the sources for producing monoglycerides cause it is rich in fatty acids. Fatty acids are present as esters in the glycerol framework and it is known as triglycerides or glycerol triesters. In general, the chemical structure of triglycerides from vegetable oils is shown in Fig. 3. Almost all of the fatty acids (RCO-) in vegetable oils have an even number of carbon atoms. Hydrocarbon chains (-R) of fatty acids can be present in saturated (no double bonds), and unsaturated (with double bonds) and their types (-R) can be the same or differ in triglyceride molecules.

Structure of triglyceride from vegetable oil.

From its chemical structure, triglycerides from vegetable oils appear as ester compounds (RCOOR). As a derivative of carboxylic acid, the ester compound has a carbonyl (C=O) functional group which stands as the center of the chemical reactivity. It means that a chemical reaction can occur in the carbonyl group with the presence of specific reagents such as nucleophile (Nu − ) or electrophile (E + ) and therefore the ester compound can be converted into another compound according to the type of reaction. Triglycerides as triester compounds can also react with an electrophile and nucleophile to produce another compound with broader applications.

Common reactions of triglycerides in vegetable oil are hydrolysis and transesterification reactions. These reactions require water and alcohol as reagents and are catalyzed by a base (homogeneous and heterogeneous) catalyst or lipase enzyme catalyst. If triglycerides are hydrolyzed with water, it will produce fatty acids and glycerol. However, if triglycerides undergo a transesterification reaction with an alcohol, new esters will be obtained, such as monoglycerides, diglycerides, fatty acid methyl esters (FAME) and glycerol.

Several chemical reactions approaches in the synthesis of monoglycerides from vegetable oils are discussed in the following section. Chemical reactions involved for obtaining monoglycerides from vegetable oils are glycerolysis, ethanolysis, esterification of free fatty acids and glycerol, transesterification of glycerol with fatty acid methyl esters, and transesterification of fatty acid methyl esters with protected glycerol 1,2-acetonide glycerol followed by deprotection reactions using an acid resin.

Glycerolysis reaction involves he breaking down of triglycerides from oil using glycerol, polyalcohol (1,2,3-propanetriol) molecules. Glycerol has three hydroxyl groups (-OH), which are the sources of nucleophiles (Fig. 4). Glycerol is a polar compound, with nontoxic property, and mainly a by-product of biodiesel production 34) . Utilizing glycerol as a raw material in monoglyceride synthesis is an effort to increase the sale value of glycerol and the efficiency of the biodiesel industry. Glycerol as a biodiesel byproduct finally does not accumulate as waste which pollutes the environment, but it can be developed into a valuable product.

Synthesis of monoglycerides from vegetable oils through glycerolysis reactions with glycerol as a nucleophile (electron donor) is also known as transesterification. This transesterification reaction between triglycerides and glycerol is performed in the presence of a base catalyst or lipase enzyme catalyst to produce new ester compounds, monoglycerides and diglycerides. The reaction scheme of the glycerolysis of vegetable oil is shown in Fig. 5.

Base-catalyzed glycerolysis of vegetable oil.

The transesterification reaction of vegetable oil via glycerolysis with glycerol is accelerated by using strong base catalyst. This reaction can be considered as an irreversible reaction when the use of excess glycerol allows the formation of more monoglycerides. This reaction must take place at a high temperature (200-260°C) because both glycerol and triglycerides physicochemical properties have very high boiling points and by the end of the reaction, the product must be neutralized. It is considered that this process has high energy consumption, produce poor quality and a low yield product. The reaction product is a mixture of monoglycerides, diglycerides, triglycerides, free fatty acid (FFA), and also their alkali metal salt. The purification is usually needed to afford a high purity of monoglycerides.

Some homogeneous inorganic base catalysts that are commonly used in glycerolysis of vegetable oils are NaOH, KOH, and Ca(OH)2. Galucio et al. reported that the synthesis of monoacylglycerol from sunflower was carried out using Ca(OH)2 as a catalyst 7) . Monoolein and monolinolein obtained were characterized by HPLC and yields about 48.3%. While the heterogeneous base catalysts are Cs-MCM-41, Cs-Sepiolite, MgO, and calcined hydrotalcite 35) . Corma et al. have successfully synthesized of monoacylglycerol using MgO as a catalyst and this reaction gives 65% 35) . The utilization of the alkyl guanidine compound as a catalyst for synthesizing of monoacylglycerol has been carried out by Aguiar et al 36) . Monostearin that is product reaction gives a low yield of about 10%. Monoglycerides from Neem seed oil can be prepared via reaction of the refined neem oil and glycerol (ratio 1:2) at 220°C using 0.05% CaO in an inert atmospheric N2 condition. Monoglyceride obtained was soluble in methanol after cooled to 80°C 37) .

There are disadvantages of using homogeneous inorganic base catalysts and high temperatures reaction where it produces dark monoglyceride with charred odors, requires high capital investments, the catalysts are non-reusable, and are not suitable for the production of heat-sensitive monoglycerides (EPA and DHA). The advantage of using heterogeneous base catalysts is high conversion rates and the catalyst can be reused.

The use of lipase enzyme catalyst (EC, an sn-1,3 selective lipase, is the best alternative for overcoming various weaknesses of glycerolysis of vegetable oils using alkaline catalysts. By utilizing enzymatic catalyst, glycerolysis reaction can take place well at temperatures under 80°C, and it can improve the quality and purity of monoglyceride products, and suitable for the manufacture of heat-sensitive monoglycerides 6) . Lipase enzymes also show good activity and stability in hydrophobic solvents for the synthesis of monoglycerides through glycerolysis 38) .

At present, the potential and abundant specific lipase enzyme (sn-1.3) for glycerolysis reaction of vegetable oil are Lipozyme TL IM 39) , 40) . Some of the other lipase enzymes used are Novozym 435 and Fermase CALB 10000 4) Pseudomonas sp. (lipase PS), Pseudomonas fluorescens (lipase AK), Candida rugosa (AY lipase), Rhizopus delemar (lipase D), Mucor javanicus (lipase M), Rhizopus oryzae (lipase F), C. rugosa (lipase OF) Alcaligenes sp. (PL lipase) and Chromobacterium viscosum (lipase LP) 41) . Some of these enzymes are immobilized on supporting materials such as Celite, silica gel, CaCO3, Accurel EP100, and activated charcoal. Lipase PS enzyme is the best enzyme for producing monoglycerides from palm oil through glycerolysis reactions, while Accurel EP100 is the best as supporting material 42) . McNeill et al. was performed glycerolysis reaction of vegetable oil using lipase to give the mixed product such as monoacylglycerol, diacylglycerol, and triacylglycerol 43) . This reaction yields 90% monoacylglycerol. On another reaction, Rosu et al. modify lipase by immobilized with CaCO3 as material support to generate monoacylglycerol for 96% purity 44) .

Some monoglycerides from vegetable oil samples and heat-sensitive monoglycerides (containing PUFA) have been successfully synthesized through the glycerolysis reaction using lipases. Anchovy oil and Tuna oil are two oil samples that can produce monoglycerides that are rich in PUFA such as EPA and DHA. Under various reaction conditions, several types of lipase enzymes such as Lipozyme TL IM 45) and Novozym 435 46) have advantages in converting vegetable oils to monoglycerides (Table 1). Of these, the Lipozym TL IM enzyme produced by Novozym Inc. is a relatively cheap and has potential and extensive applications in lipid modification included in catalysis glycerolysis reaction of vegetable oils 40) . Lipozym TL IM enzyme is Thermomyces lanuginosus (TLL) which is embedded to silica through an ionic adsorption process. Lipozyme TL IM as an sn-1,3-selective lipases enzyme is not suitable when the reaction temperature above 60°C 39) . On the other hand, Novozym 435 as a type of lipase produced by Novozym can show its superiority as a catalyst in the conversion of tuna oil to monoglyceride which is rich in EPA and DHA 47) . The success of various types of lipase as a catalyst in the conversion of vegetable oils and animal fats into monoglycerides through the glycerolysis reaction can be seen in Table 1.

There are several drawbacks of glycerolysis reactions using lipase enzyme catalysts that are taking long reaction times, costly (an expensive enzyme), and low mixing rates of glycerol and triglyceride reactants. A suitable solvent will improve the reaction system to be more homogeneous to increase the substrate conversion rate, reaction rate, and formation of monoglyceride products. Some suitable solvents for enzymatic catalyst glycerolysis reactions are n-hexane, n-heptane, dioxane, acetonitrile, acetone, isooctane, tert-butanol, and tert-pentanol. These weaknesses are also being considered in their application in the manufacturing industry of monoglyceride, foremost because of its high cost and the enzyme reusability aspect. The reaction scheme of glycerolysis reaction using a specific lipase enzyme catalyst is presented in Fig. 6. A by-product (diglycerides) is also formed from the glycerolysis reaction, so a purification process is needed to separate monoglycerides from diglycerides.

Glycerolysis reaction of vegetable oil using lipase enzyme as a catalyst.

Ethanolysis reaction of vegetable oil, also known as transesterification, is breaking down the reaction of triglyceride using ethanol. Transesterification is the reaction of an ester with excess alcohol involving lipase as a catalyst to produce monoglyceride, a new ester derivative. This reaction is quite beneficial because it is irreversible (one way) reaction so we can afford monoglyceride abundantly. By using excess alcohol, it can increase the yield of the product. The by-product of the ethanolysis reaction pathway of a vegetable oil sample using lipase as a catalyst is ethyl ester of fatty acids. This is because the acyl group released from triglycerides can react with ethanol to form esters from fatty acids.

The ethanolysis reaction of vegetable oil using a lipase enzyme is a specific reaction to produce a regioisomer 2-monoglyceride or β-monoglyceride (see Fig. 1). The lipase enzyme catalyst suitable for the use in the ethanolysis reaction is sn-1,3-regiospecific lipase 8) , 48) , 49) . The sn-1,3-regiospecific lipase is only initiated lysis reaction of the acyl group in position 1 and 3 of the glycerol backbone. The acyl group in position 2 of the glycerol backbone will be maintained so the reaction will produce 2-monoglyceride. For this explanation, Munio et al. reported that the synthesis of 2-monoacylglycerol is reacted excess 96% ethanol with cod liver oil using Lipase D (from Rhizopus oryzae) and Lipase Rd (from Rhizopus delemar) that supported at MP-1000 to give a good yield of 2-MAG (72,1 and 70%) 50) . This result was achieved in experimental conditions as follows 500 mg Cold Liver Oil, 500 mg dry absolute ethanol (22 ethanol/oil molar ratio), 60 mg lipase and 3 mL acetone (6 mL / g oil) at 37 8C, 200 rpm and 24 h. Purification of 2-MAG compounds rich in PUFA was carried out with silica gel chromatography to produce 2-MAG with 85% yield and 96% purity. Purification with solvent extraction (hydroethanolic phase, Ethanol: H2O 90:10) produced 2-MAG with 89% purity and 77% yield. The solvent extraction technique is more beneficial because it uses a small amount of solvent.

Some types of alcohol using the synthesis of 2-monoacylglycerol was performed by Lee et al. 51) . This reaction catalyzed Lipase that is obtained from Pseudomonas fluorescence. The results of this reaction indicate that the type of alcohol can provide results with various compositions that are 85% monoacetin, 96% monobutyrin, 50% monocaprylin, 48% monolaurin, and 45% monopalmitin. Monoglyceride can also be afforded through selective ethanolysis of sunflower oil with Lipozyme RM IM (a Rhizomucor miehei lipase immobilized on macroporous anion exchange resins). Ethanolysis of sunflower takes place in condition: volume ratio of sunflower oil to ethanol 12 : 3.5 mL, 50 mL of aqueous solution of 10 N NaOH, temperature 40°C and 40 mg of Lipozyme RM IM. High conversion of triglyceride to a fatty acid ethyl ester and monoglyceride can be obtained under the mild condition in the mixture of 2 mole fatty acid ethyl ester and 1 mol monoglycerides 52) . Immobilized lipase from Mucor miehei has been worked to catalyze 2-MAG synthesis reaction from Canarium oil. This reaction consists of a mixture of 750 mg of canarium oil and 3 g of dry ethanol (1: 4 w/w) to act as a substrate of 375 mg lipase enzyme (10% of the total substrate) 53) . The reaction took place in the orbital water bath shaker at a temperature of 35°C for 6 hours with a speed of 248 rpm for 6 hours. The 2-MAG produced from Canarium oil is 74% yield which is rich in oleic acid and linoleic acid.

The selective preparation of 2-monolaurin with a yield of 30.1% and purity of 100% was successfully carried out from the ethanolysis reaction of coconut oil using lipozyme TL IM, an sn-1.3 regioselective lipase enzyme 8) . A total of 750 mg of coconut oil was reacted with 3 g of dry ethanol and catalyzed by 375 mg of the TL IM Lipozyme enzyme (10% (w/w) of total reactants). The reaction was carried out at 55°C for 6 hours. The crude 2-monolaurin compound is separated by extraction using a hydroalcoholic solution (Ethanol: water 80:20) and the by-products are washed with n-hexane. Purification of the 2-monolaurin product was carried out by TLC using a mixture of chloroform: acetone: methanol (9.5: 0.45: 0.05) as a mobile phase and silica plate as a stationary phase.

The Pacific oyster (Crassostrea Gigas) oil which is rich in ω-3 PUFAs has been successfully extracted using supercritical carbon dioxide (SC-CO2) techniques. The optimum of temperature and pressure for SC-CO2 extractions of oyster oil was 50°C and 30 Mpa. Oil extracted has been used in the ethanolysis reaction catalyzed by Novozymes-435, Lipozyme TL IM, and Lipozyme RM IM to produce 2-MAG rich with 3-3 PUFAs 54) . Reaction was mixtured by 1.50 grams of oyster oil, 6 grams of ethanol (94%), and 0.75 grams of enzyme. The mixture was placed it in a shaking incubator and maintained at 250 rpm and 37°C for 3 h. The ω-3 PUFAs content significantly increased in 2-MAG obtained from Novozymes 435, Lipozyme TL IM, and Lipozyme RM IM to 43.03%, 45.95%, and 40.50%.

The ethanolysis reaction of trimyristin using lipozyme TL IM also could selectively produce 2-monomyristin as a yellowish liquid with a yield of 18%. Trimyristin was prepared from the esterification reaction of myristic acid and glycerol in the presence of H2SO4 as a catalyst 19) . Trimyristin (1 mmol) was reacted with dry ethanol (3 mL) at 308 K for 24 h using catalyst from TL IM (0.38 g). After the filtration process to separate the enzyme, the 2-monomiristin compound was isolated in an 80% ethanol solution and the by-products were washed using n-hexane. The 2-monomiristin compound was purified with PTLC using chloroform : acetone : methanol=9.5:0.45:0.05 as the mobile phase. Jumina et al. 19) have also synthesized 2-monopalmitin from tripalmitin using TL IM as a catalyst via the same procedure and reaction conditions as in the synthesis of 2-monomiristin from trimiristin. The 2-monopalmitin product after purification is in the form of yellow solids and has a yield of 8%.

The schematic reaction of an ethanolysis of vegetable oil is presented in Fig. 7. Selective preparation of 2-monoglyceride can be performed trough alcoholysis of triglyceride from an oil or pure triglyceride using an sn-1.3 regioselective lipase enzyme, lipozyme TL IM and lipozyme RM IM. The reported studies revealed the success of the synthesis of 2-monoglyceride using sn-1.3 regioselective lipase enzyme and showed that this enzyme is selectively breaking down the acyl groups from a triglyceride only in positions 1 and 3. Thus, sn-1.3 regioselective lipase enzyme was recommended in the synthesis of 2-monoglyceride via ethanolysis of triglycerides. Avoiding the use of methanol was suggested to produce a non-toxic 2-monoglycerides. The lipase enzymes that commonly used in the production of 2-monoglycerides are Rhizopus arrhizus lipase immobilized on celite 55) , Rhizomucor miehei, Rhizopus delamar, Rhizopus javanicus 56) , Pseudomonas fluorescence 51) , Novozym 435 12) , 57) , Lipase DF from Rhizopus oryzae 48) . Initially, the lipase enzyme will cause a deacylation reaction of triglycerides to form an acyl-enzyme complex. The presence of ethanol will further deacylated the acyl-enzyme complex to form fatty acid ethyl esters. The diglyceride product, produced further, will also form an acyl-enzyme complex and the second deacylation of the acyl-enzyme complex is happen so the final product formed is 2-monoglyceride.

Ethanolysis reaction of vegetable oil using lipase enzyme catalyst.

The advantage of the ethanolysis reaction of vegetable oils using specific lipase enzymes is that it is capable of producing monoglycerides with certain regioisomers. This reaction pathway is essential to produce a monoglyceride that is heat sensitive but has great benefits for human health such as 2-arachidonoylglycerol 49) , 2-monoglycerides from EPA and DHA 48) , 2-monolaurin 8) , 2-monomiristin 19) . The ethanolysis reaction is also important in preparing a structured triacylglycerol for nutritional functions. In this case, the ethanolysis reaction provides a synthesis technique of 2-monoglyceride compounds from polyunsaturated fatty acid (PUFA). Furthermore, 2-monoglycerides of PUFA are esterified with a medium chain fatty acid (lauric acid, capric acid, and myristic acid) to produce a structured triacylglycerol.

The esterification reaction of a free fatty acid with glycerol using an acid catalyst or lipase enzyme catalyst can also produce monoglyceride compounds. The approach of this reaction is the fatty acids from a vegetable oil must be isolated before reacting with glycerol. The use of glycerol as raw materials is remarkable because it utilizes the byproducts of the biodiesel industry 34) .

The esterification reaction of glycerol and free fatty acids takes place at a temperature of 100-120°C and make it more efficient than glycerolysis reactions. However, the acid-catalyzed esterification is a reversible reaction in which the formed ester can be hydrolyzed again into a reactant, so it only produces a low yield product. One effort to increase the yield of ester products is to distillate the water as a side product during the reaction using Dean-Stark Water Collector. Schematic of the esterification of free fatty acids and glycerol in the presence of an acid catalyst is shown in Fig. 8.

Esterification reaction of free fatty acid and glycerol using an acid catalyst.

The homogeneous acid catalyst used can be derived from H2SO4 and pTSA 18) , 34) . The weakness of using this catalyst is its non-reusable aspect and it becomes a waste in the environment. The use of strong acid catalysts tends to regenerate triglycerides such as trimyristin 19) if the mole ratio of the reactants, temperature, and reaction time are not optimized. Triglycerides are formed because all the -OH groups in glycerol are stabilized by the presence of acyl groups from free fatty acids. Limiting the amount of free fatty acids is probably one solution to increase the formation of monoglycerides.

To improve the quality and amount of monoglycerides formed through the esterification of FFA, the catalyst is replaced by a heterogeneous acid catalyst. The advantage of this catalyst is that it can be reused. Bossaert et al. have successfully synthesized of monoacylglycerol to yield 53% using MCM-41-SO3H 58) . The innovation by supporting material to MCM-41 was performed by D’iaz et al 59) , 60) . The product of this reaction is monolaurin (63%) and monoolein compound (45%). The other substance for supporting material to create a new catalyst that is MMS-H mesoporous is aluminum and zirconium 60) . Monolaurin and dilaurin can be produced of this reaction with a yield of 93%. Nakamura et al. have also used a heterogeneous catalyst that is ZrOCl2·8H2O and AlCl3·6H2O to generate monolaurin with good yield 61) . Hoo and Abdulah have used other catalyst that is mesoporous 12-tungstophosphoric acid SBA-15 to synthesized monolaurin to give 50% 62) . Synthesis of monolaurin and dilaurin has also conducted by using Mg-Al-CO3 layered double hydroxide 63) . The good yield has obtained from this reaction of about 99%. The previous effort to generate monoacylglycerol with good yield has also worked by Kotwal et al 64) . This reaction used solid Fe-Zn double metal cyanide (DMC) as a catalyst. The product of this reaction is monolaurin (66%), monomiristin (75.9%), monostearin (62.2%), and monoolein (63.4%). Zeolite Imidazolate Framework-8 (ZIF-8) has been applied as a heterogeneous catalyst in the esterification reaction oleic acid and glycerol to produce monoolein. The esterification reaction was carried out for 22 hours in t-butanol as the solvent at 423 K with 1.8 g of oleic acid, 6 g of glycerol, 85 g of t-butanol, and 3 g of ZIF, resulted in the conversion rate of 60% and catalyst recovery 97 wt% 65) . The rp-SBA-15-Pr-SO3H catalyst exhibited the highest catalytic activity for the esterification of oleic acid with glycerol to produce monoolein 66) . The high yield obtained by Pr-SO3H-functionalized rope-shaped SBA-15 silica was proposed by a large specific surface area, high acid amount, and suitable pore size of the catalyst. -SO3H functionalized carbon catalysts were successfully used as a heterogeneous catalyst in esterification reaction between glycerol with lauric acid and oleic acid to produce monolaurin and monoolein respectively. The reaction lasted for 7-24 hours at 100-125°C, with a ratio of glycerol and free fatty acid was 1:1, and at the end of the reaction, the catalyst was reusable 67) .

All heterogeneous acid catalysts have Brønsted acid sites which serve to catalyze the esterification reaction of free fatty acid. In the first step, Brønsted acid sites in the heterogeneous catalyst will protonate oxygen atoms from carbonyl groups in free fatty acids. This protonation step makes the carbonyl group is more easily attacked by nucleophiles in the form of alcohol from glycerol. The -OH group which is bound to C1 and C3 atoms of glycerol has more potential to attack carbonyl groups than those that bound to C2. The -OH group on C2 atoms is more sterically hindered when it attacks the carbonyl group. Therefore, the possibility of forming a 1-monoglyceride product is greater than 2-monoglyceride. If the reaction time is not well controlled, it is also possible to form diglyceride molecules due to the lack of strerical barriers for the -OH group in C1 and C3 from glycerol.

An attempt to reduce the energy consumption level in the esterification reaction of free fatty acids and glycerol is to replace the acid catalyst with the lipase enzyme catalyst. Replacement of the catalysts into lipase enzymes provides several advantages such as producing monoglyceride with a high yield, good quality, and the reaction take place in mild conditions 68) . In the esterification reaction, water molecules are produced as a by-product. To shift the equilibrium to the formation of monoglyceride molecules compared to the hydrolysis reaction, the esterification reaction should be carried out in a non-water solvent or microaqueous solvent. The esterification reaction scheme of glycerol and free fatty acids with lipase enzyme catalyst is shown in Fig. 9.

Esterification reaction of fatty acid with glycerol using lipase enzyme.

Lipase enzymes has much application because it can interact with various substrates. This interaction was obtained from binding the active site of amino acid to the ester substrate so that it provides catalysis of transesterification and esterification reaction.

Some advantages of using lipase enzymes in the esterification reaction of fatty acid to produce monoglycerides:

1. are selective (to the certain substrate)

2. have catalytic activity under moderate reaction conditions such as low pressure and temperature, also takes place in water media

3. are easily separated from the product

4. do not produce side products that are harmful to the environment (green chemistry)

6. decompose in the environment

Lipase enzymes included in sn-1,3-selective lipases can be used in esterification reactions of fatty acids and glycerol to produce monoglycerides. These enzymes are like Novozyme 435, Candida antarctica lipase B, Lipozym RM IM, Lipase L9 (Penicillium camembertii lipase), Lipase GH1 (cloned from Penicillium cyclopium and expressed in Pichiapastoris strain GS115), Candida sp.99-125 lipase and Lipozyme IM-20. Each type of lipase displays the ability to catalyze the reaction of making monoglycerides from various types of fatty acids and glycerol under various reaction conditions. Informations related to the esterification reaction between various types of fatty acids and glycerol, the type of lipase catalyst, reaction conditions, yield and selectivity of the monoglyceride produced, are described in full in Table 2. Novozym 435 as a biocatalyst, can catalyze the reaction of capric acid and capric acid esterification each with glycerol to produce monoglycerides with a product yield reaching 92 wt% 30) . Lipase G also has an advantage as a catalyst in the esterification reaction of some fatty acids with glycerol to produce monoglycerides with a selectivity level>60% 16) . Lipozyme RM IM has also succeeded in converting the reaction of lauric acid and glycerol into monoglycerides in the form of monolaurin with conversion rates reaching 93.23% and monoglyceride yield 53.67% 69) . Monoolein as an unsaturated monoglyceride with a yield of 84 wt% has been successfully carried out through the reaction of oleic acid and glycerol catalyzed by Lipase GH1 70) . Yadav et al. 71) have also succeeded in making glyceryl monoundecylenate with a yield of 92% through the reaction of undecylenic acid with glycerol using Immobilized Candida antarctica lipase B (PyCal). Also, the using of Candida sp. 99-125 enzyme for synthesizing monoacylglycerol has conducted by Zhao et al 72) .

Transesterification reactions are very simple reactions in producing a monoglyceride from vegetable oil. In this synthetic route, monoglycerides are afforded from transesterification of fatty acid ethyl esters with glycerol. This reaction is quite effective because both of the fatty acid ethyl esters and glycerol can be obtained through base-catalyzed transesterification reactions of vegetable oil with ethanol. Ethanol is particularly preferred than methanol because it can produce non-toxic or food grade monoglycerides. Purification of fatty acids ethyl ester from the glycerol as a by-product can be performed by fractional distillation technique. The reaction scheme for the formation of fatty acid ethyl esters from vegetable oils is presented in Fig. 10.

Base-catalyzed transesterification reaction of vegetable oil.

Pure fatty acid ethyl ester such as ethyl laurate can be reacted with glycerol using alkaline catalyst or lipase enzyme catalyst to produce monoglyceride. Some of the catalysts that can be used in this reaction are NaOH, KOH, Na etoxide, MgO 73) , 74) , 75) and also an sn-1,3-selective lipase catalyst that specifically for transesterification reactions such as Lipozym TL IM. Some monoglyceride can be synthesized from the reaction of glycerol and fatty methyl ester at low temperature catalyzed by supported guanidine catalyst, where the catalyst was reusable without altering its reactivity 76) . Reaction scheme of transesterification of fatty acid ethyl ester and glycerol is displayed in Fig. 11.

Transesterification reaction scheme of fatty acid ethyl ester with glycerol.

The transesterification reaction is quite beneficial because it is an irreversible reaction so that monoglyceride can be produced at a higher yield. The formation of monoglyceride via transesterification of purified fatty acid ethyl ester with glycerol is considered to be more efficient than glycerolysis of vegetable oil because the fatty acid ethyl ester itself is obtained from the conversion of vegetable oil. This weakness of this reaction is that has huge potential for the formation of diglyceride molecules. The reason is that there are 3-OH groups in glycerol which have the potential to undergo a transesterification reaction, especially the -OH group bound to C1 and C3. To improve the yield of monoglyceride produced, it is necessary to optimize the transesterification reaction of fatty acid ethyl esters with glycerol in the reactant mole ratio, catalyst amount, temperature and reaction time so it will minimize the diglyceride products formed. Another strategy for increasing monoglyceride compared with the diglycerides is by employing a protective group of alcohol such as acetal group.

Using a protective group in the synthesize reaction of a particular material is one of the efforts to increase the amount of the desired products. In connection with the synthesis of monoglycerides, glycerol as raw material should be protected first to increase the yield of the product. Protection of glycerol as a polyalcohol compound by converting it into an acetal compound is considered as a notable approach. The acetal group is quite stable in alkaline conditions. By assuming that the -OH group in C1 from glycerol can act as a nucleophile, it can attack the ketone compounds (dimethyl ketone or acetone) which have been protonated first by a proton ion of an acid catalyst. In the first stage, a hemiacetal compound will be formed. Furthermore, the -OH group in C2 can react with the intermediate hemiacetal to form an acetal product of glycerol that is known as 1,2-acetonide glycerol or 1,2-O-isopropylidene glycerol. The protection reaction of glycerol to 1,2-acetonide glycerol is shown in Fig. 12. Protected glycerol or 1,2-acetonide glycerol or 1,2-O-Isopropylidene glycerol can be made easily from the reaction of glycerol and acetone using a p-TSA catalyst. On a large scale, the glycerol protection reaction to 1,2-O-Isopropylidene glycerol can work well in a chloroform solvent. The reaction taking place at a temperature of 120°C for 6.5 hours and the compound 1,2-O-Isopropylidene glycerol is a clear liquid (colorless liquid) produced with a yield of 94% by Yu et al. 77) 33.71% yield and 100% purity by Jumina et al. 19) and 66.7% yield and 99.07% purity by Nitbani et al 8) .

The protection reaction of glycerol to 1,2-acetonide glycerol.

In the synthesis of monoglycerides, the 1,2-acetonide glycerol compound will be reacted with a fatty acid ethyl ester using a weak base catalyst such as Na2CO3 8) , 19) , 77) and K2CO3 19) . In this transesterification reaction, alcohol is derived from 1,2-acetonide glycerol. For example, the reaction of fatty acids ethyl ester from ethyl capric with 1,2-acetonide glycerol using Na2CO3 as a catalyst will produce 1,2-acetonide-3-capryl glycerol compound 78) . Usually, the transesterification of fatty acids ethyl ester (ethyl capric 18) , ethyl myristic 19) ) with 1,2-acetonide glycerol took place at 110°C for approximately 24 hours. The 1,2-acetonide-3-alkyl glycerol product will be formed with high yield when the 1,2-acetonide glycerol compound is made excess with the mole ratio of fatty acid ethyl ester to 1,2-acetonide glycerol is 1:8 and 1:4. Alcohol as a by-product of this reaction can be easily separated by washing with water, as well as the remaining base catalyst. Base catalysts can be replaced with lipase enzyme catalysts, which specific catalyzed the transesterification reactions. Lipozyme TL IM enzyme is considered as one of the affordable lipase enzymes with high catalytic activity in transesterification reactions 40) .

The monoglyceride product in the form of 1-monocaprin or 1-monomyristin will be obtained after deprotection reaction of 1,2-acetonide-3-capryl glycerol or 1,2-acetonide-3-myristyl glycerol using Amberlyst-15 in ethanol as a solvent. Especially for 1-monocaprin, this reaction gives rendement 78.34% and purity 100% after purification of crude monocaprin using Preparatif Thin Layer Chromatography. The mixture of n-hexane and ethyl acetate (7:3) was used as an eluen for purification. The reaction scheme is shown in Fig. 13. In the synthesis of 1-monomiristin19, it does not involve purification steps with Preparative Thin Layer Chromatography. 1-monomiristin compound with 100% purity is only produced from filtration and evaporation of the product of the 1,2-acetonide-3-myristyl glycerol deprotection reaction using Amberlyst-15. Synthesis of 1-monolinolein as an unsaturated monoglyceride was also successfully carried out by Jumina et al. 32) using protected glycerol (1,2-O-isopropylidene glycerol) via an intermediate isopropylidene glycerol linoleate. Isolation of 1-monolinolein product is only carried out through the extraction process of isopropylidene glycerol linoleate deprotection reaction using a dichloromethane solvent. The results of the analysis with Gas Chromatography showed that the 1-monolinolein product produced was cis-monolinolein (41.3% purity) and trans-monolinolein (41.93% purity) 32) .

Reaction scheme of the synthesis of monocaprin using 1,2-acetonide glycerol.

Deprotection reactions of 1,2-acetonide-3-alkyl glycerol can take place at room temperature for 24 hours using Amberlyst-15 in methanol 12) and ethanol 78) . The deprotection reaction in ethanol solvents is more advantageous because it can avoid the toxicity of the monoglyceride compounds produced. This consideration is important because monoglyceride compounds have wide applications that come into direct contact with humans, such as food and medicine ingredients. Isolation of the final product 1-monoglyceride can be carried out by column chromatography 12) . Other purification method is extraction in a hydroalcoholic solution (water-ethanol solution mixture 80:20) 34) and washed with n-hexane to separate the by-products which are usually fatty acids or fatty acids ethyl ester 79) . The isolation technique by liquid-liquid extraction is more advantageous because it uses safe solvents simple equipment, and is easy to do. In summary, the reaction conditions related to the synthesis of monoglycerides using protected glycerol which includes types of esters of fatty acids, types of catalysts, reaction temperatures, solvents, and purification techniques can be seen in Table 3.

The synthesis of monoglycerides through reaction approach using protected glycerol is very effective and beneficial. However, this achievment only would be regarded as the organic synthesis in academic laboratory scale research. There are no references that indicate about the practical engineering processes in preparing monoglycerides using protected glycerol. Various reaction conditions related to the use of protected glycerol in monoglyceride synthesis (Table 3) illustrate that this synthesis pathway might be easily applied on an industrial scale. The process of isolating monoglyceride final products which are quite simple both by filtration and liquid-liquid extraction (using dichloromethane solvents or hydroalcoholic solutions) is a promising consideration in the design for scale-up in the Industry.

Vegetable oil is a natural ingredient that is rich in saturated and unsaturated fatty acids which are present as triglycerides as well as free fatty acids. The major fatty acids type contain in the vegetable oil and it determines whether they are edible or non-edible oil. Fatty acids with their wide range application in human life can be isolated from vegetable oils. The Colgate-Emery steam hydrolysis can produce high-quality fatty acids, but it takes place under extreme conditions (high temperature and pressure) and is also not suitable for heat-sensitive fatty acids. Another alternative process that is quite precise is the hydrolysis of vegetable oils via enzymatic catalysis using the sn-1,3-specific lipase enzyme. The other alternative is through alkaline hydrolysis of a fatty acid methyl ester that has been isolated first from vegetable oil.

The synthesis of monoglyceride from vegetable oils can also be carried out through various chemical reaction approaches such as glycerolysis, ethanolysis using sn-1,3 lipase enzyme, esterification of fatty acids with glycerol using inorganic acid or lipase enzyme as a catalyst, transesterification of fatty acids methyl ester with glycerol and transesterification of fatty acids methyl esters with protected glycerol compound (1,2-O-isopropylidene glycerol) followed by deprotection using an acid resin (Amberlyst-15). To date, employing the protected glycerol (1,2-acetonide glycerol) followed by deprotection reactions using Amberlyst-15 is the most effective route for obtaining 1-monoglyceride but only in academic laboratory scale research. Purification of monoglycerides with hydroalcoholic solutions is found to be the most effective and easiest method. Meanwhile, 2-monoglyceride compounds are recommended to be synthesized through the ethanolysis reaction of vegetable oils using sn-1,3-selective lipases enzyme.

Palmitate and oleate modify membrane fluidity and kinase activities of INS-1E β-cells alongside altered metabolism-secretion coupling

Chronic exposure to elevated levels of glucose and free fatty acids impairs beta-cell function, leading to insulin secretion defects and eventually beta-cell failure. Using a semi-high throughput approach applied to INS-1E beta-cells, we tested multiple conditions of chronic exposure to basal, intermediate and high glucose, combined with saturated versus mono- and polyunsaturated fatty acids in order to assess cell integrity, lipid metabolism, mitochondrial function, glucose-stimulated calcium rise and secretory kinetics. INS-1E beta-cells were cultured for 3 days at different glucose concentrations (5.5, 11.1, 25 mM) without or with BSA-complexed 0.4 mM saturated (C16:0 palmitate), monounsaturated (C18:1 oleate) or polyunsaturated (C18:2 linoleate, C18:3 linolenate) fatty acids, resulting in 0.1-0.5 μM unbound fatty acids. Accumulation of triglycerides in cells exposed to fatty acids was glucose-dependent, oleate inducing the strongest lipid storage and protecting against glucose-induced cytotoxicity. The combined chronic exposure to both high glucose and either palmitate or oleate altered mitochondrial function as well as glucose-induced calcium rise. This pattern did not directly translate at the secretory level since palmitate and oleate exhibited distinct effects on the first and the second phases of glucose-stimulated exocytosis. Both fatty acids changed the activity of kinases, such as the MODY-associated BLK. Additionally, chronic exposure to fatty acids modified membrane physicochemical properties by increasing membrane fluidity, oleate exhibiting larger effects compared to palmitate. Chronic fatty acids differentially and specifically exacerbated some of the glucotoxic effects, without promoting cytotoxicity on their own. Each of the tested fatty acids functionally modified INS-1E beta-cell, oleate inducing the strongest effects.

Keywords: Fatty acids Glucose Insulin Lipotoxicity Membrane/fluidity Pancreas.


Like triglycerides, phospholipids have a glycerol backbone. But unlike triglycerides, phospholipids are diglycerides (two fatty-acid molecules attached to the glycerol backbone) while their third fatty-acid chain has a phosphate group coupled with a nitrogen-containing group. This unique structure makes phospholipids water soluble. Phospholipids are what we call amphiphilic&mdashthe fatty-acid sides are hydrophobic (dislike water) and the phosphate group is hydrophilic (likes water).

In the body phospholipids bind together to form cell membranes. The amphiphilic nature of phospholipids governs their function as components of cell membranes. The phospholipids form a double layer in cell membranes, thus effectively protecting the inside of the cell from the outside environment while at the same time allowing for transport of fat and water through the membrane.

Figure 5.7 The Structure of a Phospholipid

Image by Allison Calabrese / CC BY 4.0

Phospholipids are ideal emulsifiers that can keep oil and water mixed. Emulsions are mixtures of two liquids that do not mix. Without emulsifiers, the fat and water content would be somewhat separate within food. Lecithin (phosphatidylcholine), found in egg yolk, honey, and mustard, is a popular food emulsifier. Mayonnaise demonstrates lecithin&rsquos ability to blend vinegar and oil to create the stable, spreadable condiment that so many enjoy. Food emulsifiers play an important role in making the appearance of food appetizing. Adding emulsifiers to sauces and creams not only enhances their appearance but also increases their freshness.

Lecithin&rsquos crucial role within the body is clear, because it is present in every cell throughout the body 28 percent of brain matter is composed of lecithin and 66 percent of the fat in the liver is lecithin. Many people attribute health-promoting properties to lecithin, such as its ability to lower blood cholesterol and aid with weight loss. There are several lecithin supplements on the market broadcasting these claims. However, as the body can make most phospholipids, it is not necessary to consume them in a pill. The body makes all of the lecithin that it needs.

Figure 5.8 The Difference Between Triglycerides and Phospholipids

Image by Allison Calabrese / CC BY 4.0

Results and discussion

The intervention resulted in a −9.5±0.6% weight loss (101.8±5.8 vs 92.0±4.9 kg before and after weight loss, respectively, P<0.05) and had a duration range from 17 to 32 weeks. A significant improvement in glucose control indices was observed after weight loss, accompanied by a non-statistically significant, but noteworthy reduction in HOMA-IR (P=0.08) (Table 1). The intervention had a small positive impact in blood lipid profile, except a significant decrease in high-density lipoprotein. Figure 1 presents intramyocellular lipids and their fatty acid residues before and after weight loss. A remarkable decrease by 77.7±13.1% in intramyocellular triglyceride content was observed (P<0.05). Similar decreases were observed in all triglyceride fatty acid residues (that is, saturated, mono-unsaturated and poly-unsaturated fatty acids). Changes in intramyocellular diglycerides before and after weight loss did not show a uniform pattern with three negative and two positive ranks. Mean values before and after weight loss were 8.25±1.71 vs 5.91±0.76 nmol/mg dry tissue (change in range, −6.24 to 2.41) and changes were not significantly different (P=0.686).

Intramyocellular triglycerides and diglycerides before and after weight loss. Values are means±s.e. * Indicates statistically significant difference compared with values before weight loss.

Our results reveal that moderate weight loss depletes intramyocellular lipid storage, without significantly affecting diglyceride levels in diabetes mellitus. The marked decrease in intramyocellular triglycerides may be attributed to the fact that subjects at the end of the protocol were still on a hypocaloric diet. To this perspective, it is not clear whether the observed reduction may be attributed to the weight loss per se or it was the effect of negative energy balance. However, even under these conditions, no such clear effect was observed for intramyocellular diglycerides. A reduction of the overall flux to lipid uptake and esterification at fasting that has been observed after weight loss (Kelley et al., 1999), along with a modest reduction in the availability of substrates from the systemic circulation, may explain at least in part the depletion of intramyocellular lipid storage, without affecting intermediate molecules of lipid metabolism, such as diglycerides. In this perspective, the well-known effects of weight loss on insulin sensitivity and glucose homeostasis may not be mediated by changes in these intermediate molecules.

Oxidation of fatty acids

The process of beta-oxidation occurs in mitochondria to break down fatty acids into 2-carbon acetyl-CoA molecules which can then enter the citric acid cycle. Each cleavage, which takes place at the second (beta) carbon from the end of the hydrocarbon chain, produces 1 FADH2 and 1 NADH to go on to the electron transport chain. Finally, the 3-carbon glycerol backbone is converted to a glycolysis intermediate or used for gluconeogenesis. The liver can also convert acetyl-CoA to water-soluble ketone bodies that can travel through the blood to be converted back to acetyl-CoA for the citric acid cycle in other cells.

Saturated fats

Saturated fats are characterized as being fully reduced with the maximum number of bonds to hydrogen and single C—C bonds along its fatty acid tail. These molecules have greater reducing potential than unsaturated fats, providing greater energy storage.

Unsaturated fats

Unsaturated fats contain one or more double C=C bonds in their fatty acid tails, a less than fully reduced (partially oxidized) form compared to saturated fats. Most of the double bonds are found in the Z/cis conformation.

[edit] Metabolism

Triglycerides, as major components of very low density lipoprotein (VLDL) and chylomicrons, play an important role in metabolism as energy sources and transporters of dietary fat. They contain more than twice as much energy (9 kcal/g) as carbohydrates and proteins. In the intestine, triglycerides are split into monoacylglycerol and free fatty acids (this process is called lipolysis) (with the help of lipases and bile secretions), which are then moved into the cells lining the intestines (absorptive enterocytes). The triglycerides are rebuilt in the enterocytes from their fragments and packaged together with cholesterol and proteins to form chylomicrons. These are excreted from the cells and collected by the lymph system and transported to the large vessels near the heart before being mixed into the blood. Various tissues can capture the chylomicrons, releasing the triglycerides to be used as a source of energy. Fat and liver cells can synthesize and store triglycerides. When the body requires fatty acids as an energy source, the hormone glucagon signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids. As the brain cannot utilize fatty acids as an energy source (unless converted to a ketone), the glycerol component of triglycerides can be converted into glucose, via gluconeogenesis, for brain fuel when it is broken down. Fat cells may also be broken down for that reason, if the brain's needs ever outweigh the body's.

Triglycerides cannot pass through cell membranes freely. Special enzymes on the walls of blood vessels called lipoprotein lipases must break down triglycerides into free fatty acids and glycerol. Fatty acids can then be taken up by cells via the fatty acid transporter (FAT).

How are Mono and Diglycerides metabolized without the Free Fatty Acids of Triglycerides? - Biology

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