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Structure and Function of Lipids

Author: Sophia

what's covered
In this lesson, you will learn about lipids, or fats. Specifically, this lesson will cover:

Table of Contents

1. The Function of Lipids

Lipids (or fats) include a diverse group of compounds that are largely nonpolar in nature. The reason lipids are nonpolar is that they are hydrocarbons that include mostly nonpolar carbon–carbon or carbon–hydrogen bonds. Nonpolar molecules are hydrophobic (“water fearing”), or insoluble in water.

key concept
Lipids perform many different functions in our bodies and in our cells. Cells store long-term energy in the form of fats. Lipids also provide insulation from the environment for plants and animals (Figure 1). Lipids are also the building blocks of many hormones and include fats, oils, waxes, phospholipids, and steroids.

Diagram that shows different types of lipids. Triglycerides are on the left, phospholipids are in the center, steroids and waxes are on the right. Triglycerides include fats and oils. There is an image of the chemical structure of fatty acid chains. Structural fatty acid includes cheese. Double bonds include nuts. In the phospholipids section, it shows hydrophilic head water leaving and the hydrophobic tails water heating. Beneath that shows the phosphate group, hydrophilic water leaving, and hydrophobic water heating. Under the steroids section, it shows the 4 carbs based rings. Those transform into cholesterol, testosterone, estrogen, vitamin D, and cortisone. In the waxes section it shows long carbon chains, solid at room temperature, repel water, plants, ears, and bee cones.
Figure 1

term to know
Lipids
Fats that include a diverse group of compounds that are largely nonpolar in nature.


2. The Major Types of Lipids

A fat molecule consists of two main components—glycerol and fatty acids. Glycerol is an organic compound (alcohol) with three carbons, five hydrogens, and three hydroxyl (OH) groups. Fatty acids contain a long chain of hydrocarbons with a carboxyl group attached, hence the name “fatty acid.” The number of carbons in the fatty acid may range from 4 to 36; most common are those containing 12–18 carbons. In a fat molecule, the fatty acids are attached to each of the three carbons of the glycerol molecule with an ester bond through an oxygen atom (Figure 2).

Chemical structures of glycerol, fatty acid, and triacylglycerol.
Figure 2. Triacylglycerol is formed by the joining of three fatty acids to a glycerol backbone in a dehydration reaction. Three molecules of water are released in the process.

IN CONTEXT

During this ester bond formation, three water molecules are released. The three fatty acids in the triacylglycerol may be similar or dissimilar. Fats are also called triacylglycerols or triglycerides because of their chemical structure. Some fatty acids have common names that specify their origin.

EXAMPLE

Palmitic acid, a saturated fatty acid, is derived from the palm tree. Arachidic acid is derived from Arachis hypogea, the scientific name for groundnuts or peanuts.

Fatty acids may be saturated or unsaturated. In a fatty acid chain, if there are only single bonds between neighboring carbons in the hydrocarbon chain, the fatty acid is said to be saturated. Saturated fatty acids are saturated with hydrogen; in other words, the number of hydrogen atoms attached to the carbon skeleton is maximized. Stearic acid is an example of a saturated fatty acid (Figure 3).

Chemical structure of stearic acid.
Figure 3. Stearic acid is a common saturated fatty acid.

When the hydrocarbon chain contains a double bond, the fatty acid is said to be unsaturated. Oleic acid is an example of an unsaturated fatty acid (Figure 4).

Chemical structure of hydrocarbon chain with a double bond.
Figure 4. Oleic acid is a common unsaturated fatty acid.

term to know
Glycerol
An organic compound (alcohol) with three carbons, five hydrogens, and three hydroxyl (OH) groups.

2a. Unsaturated Fats

Most unsaturated fats are liquid at room temperature and are called oils. If there is one double bond in the molecule, then it is known as a monounsaturated fat (e.g., olive oil), and if there is more than one double bond, then it is known as a polyunsaturated fat (e.g., canola oil).

When a fatty acid has no double bonds, it is known as a saturated fatty acid because no more hydrogen may be added to the carbon atoms of the chain. A fat may contain similar or different fatty acids attached to glycerol. Long straight fatty acids with single bonds tend to get packed tightly and are solid at room temperature. Animal fats with stearic acid and palmitic acid (common in meat) and the fat with butyric acid (common in butter) are examples of saturated fats.

IN CONTEXT

Mammals store fats in specialized cells called adipocytes, where globules of fat occupy most of the cell’s volume. In plants, fat or oil is stored in many seeds and is used as a source of energy during seedling development. Unsaturated fats or oils are usually of plant origin and contain cis unsaturated fatty acids. Cis and trans indicate the configuration of the molecule around the double bond. If hydrogens are present in the same plane, it is referred to as a cis fat; if the hydrogen atoms are on two different planes, it is referred to as a trans fat. The cis double bond causes a bend or a “kink” that prevents the fatty acids from packing tightly, keeping them liquid at room temperature (Figure 5). Olive oil, corn oil, canola oil, and cod liver oil are examples of unsaturated fats. Unsaturated fats help to lower blood cholesterol levels, whereas saturated fats contribute to plaque formation in the arteries.

Chemical structure of saturated fatty acid. Beneath that is the chemical structure of Unsaturated fatty acids. Beneath that image is the chemical structure of trans oleic acid.
Figure 5. Saturated fatty acids have hydrocarbon chains connected by single bonds only.

Unsaturated fatty acids have one or more double bonds. Each double bond may be in a cis or trans configuration. In the cis configuration, both hydrogens are on the same side of the hydrocarbon chain. In the trans configuration, the hydrogens are on opposite sides. A cis double bond causes a kink in the chain.

terms to know
Monounsaturated Fat
When there is one double bond in the molecule. An example of this is olive oil.
Polyunsaturated Fat
When there is more than one double bond in the molecule. An example of this is canola oil.

2b. Trans Fats

In the food industry, oils are artificially hydrogenated to make them semi-solid and of a consistency desirable for many processed food products. Simply speaking, hydrogen gas is bubbled through oils to solidify them. During this hydrogenation process, double bonds of the cis–conformation in the hydrocarbon chain may be converted to double bonds in the trans–conformation.

Margarine, some types of peanut butter, and shortening are examples of artificially hydrogenated trans fats. Recent studies have shown that an increase in trans fats in the human diet may lead to an increase in levels of low-density lipoproteins (LDL), or “bad” cholesterol, which in turn may lead to plaque deposition in the arteries, resulting in heart disease. Many fast food restaurants have recently banned the use of trans fats, and food labels are required to display the trans fat content.

2c. Omega Fatty Acids

Alpha-linolenic acid (Figure 6) is an example of an omega-3 fatty acid. It has three cis double bonds and, as a result, a curved shape. For clarity, the carbons are not shown. Each singly bonded carbon has two hydrogens associated with it, also not shown.

Chemical structure of omega-3 fatty acid.
Figure 6

Essential fatty acids are fatty acids that are required but not synthesized by the human body. Consequently, they have to be supplemented through ingestion via the diet. Omega-3 fatty acids (like that shown in Figure 6) fall into this category and are one of only two known for humans (the other being omega-6 fatty acids). These are polyunsaturated fatty acids and are called omega-3 because the third carbon from the end of the hydrocarbon chain is connected to its neighboring carbon by a double bond.

The farthest carbon away from the carboxyl group is numbered as the omega (ω) carbon, and if the double bond is between the third and fourth carbon from that end, it is known as an omega-3 fatty acid. Omega-3 fatty acids—which are nutritionally important since the body does not make them—include alpha-linoleic acid (ALA), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA), all of which are polyunsaturated.

hint
Salmon, trout, and tuna are good sources of omega-3 fatty acids. Research indicates that omega-3 fatty acids reduce the risk of sudden death from heart attacks, reduce triglycerides in the blood, lower blood pressure, and prevent thrombosis by inhibiting blood clotting. They also reduce inflammation and may help reduce the risk of certain cancers in animals.

Like carbohydrates, fats have received a lot of bad publicity. It is true that eating an excess of fried foods and other “fatty” foods leads to weight gain. However, fats do have important functions. Many vitamins are fat soluble, and fats serve as a long-term storage form of fatty acids: a source of energy. They also provide insulation for the body. Therefore, “healthy” fats in moderate amounts should be consumed on a regular basis.

term to know
Essential Fatty Acids
Fatty acids that are required but not synthesized by the human body.

2d. Waxes

Wax covers the feathers of some aquatic birds and the leaf surfaces of some plants. Because of the hydrophobic nature of waxes, they prevent water from sticking on the surface (Figure 7). Waxes are made up of long fatty acid chains esterified to long-chain alcohols.

Figure 7. Waxy coverings on some leaves are made of lipids. (credit: Roger Griffith)

2e. Phospholipids

Phospholipids are major constituents of the plasma membrane, the outermost layer of animal cells. Like fats, they are composed of fatty acid chains attached to a glycerol or sphingosine backbone. Instead of three fatty acids attached as in triglycerides, however, there are two fatty acids forming diacylglycerol, and the third carbon of the glycerol backbone is occupied by a modified phosphate group (Figure 8).

Figure 8. A phospholipid is a molecule with two fatty acids and a modified phosphate group attached to a glycerol backbone. The phosphate may be modified by the addition of charged or polar chemical groups. Two chemical groups that may modify the phosphate—choline and serine—are shown here. Both choline and serine attach to the phosphate group at the position labeled R.

key concept
A phosphate group alone attached to a diacylglycerol does not qualify as a phospholipid; it is phosphatidate (diacylglycerol 3-phosphate), the precursor of phospholipids. The phosphate group is modified by alcohol. Phosphatidylcholine and phosphatidylserine are two important phospholipids that are found in plasma membranes. A phospholipid is an amphipathic molecule, meaning it has a hydrophobic and a hydrophilic part. The fatty acid chains are hydrophobic and cannot interact with water, whereas the phosphate-containing group is hydrophilic and interacts with water (Figure 9).

Figure 9. The phospholipid bilayer is the major component of all cellular membranes. The hydrophilic head groups of the phospholipids face the aqueous solution. The hydrophobic tails are sequestered in the middle of the bilayer.

The head is the hydrophilic part, and the tail contains the hydrophobic fatty acids. In a membrane, a bilayer of phospholipids forms the matrix of the structure, the fatty acid tails of phospholipids face inside, away from water, whereas the phosphate group faces the outside, aqueous side (Figure 9).

Phospholipids are responsible for the dynamic nature of the plasma membrane. If a drop of phospholipids is placed in water, it spontaneously forms a structure known as a micelle, where the hydrophilic phosphate heads face the outside and the fatty acids face the interior of this structure.

term to know
Phospholipids
Major constituents of the plasma membrane, the outermost layer of animal cells.

2f. Steroids

Unlike the phospholipids and fats discussed earlier, steroids have a fused ring structure. Although they do not resemble the other lipids, they are grouped with them because they are also hydrophobic and insoluble in water. All steroids have four linked carbon rings, and several of them, like cholesterol, have a short tail (Figure 10). Many steroids also have the –OH functional group, which puts them in the alcohol classification (sterols).

The image of the chemical structure of cholesterol. Next to it is the chemical structure of cortisol.
Figure 10. Steroids such as cholesterol and cortisol are composed of four fused hydrocarbon rings.

2g. Cholesterol

Cholesterol is the most common steroid. Cholesterol is mainly synthesized in the liver and is the precursor to many steroid hormones such as testosterone and estradiol, which are secreted by the gonads and endocrine glands. It is also the precursor to Vitamin D. Cholesterol is also the precursor of bile salts, which help in the emulsification of fats and their subsequent absorption by cells. Although commonly viewed negatively, cholesterol is necessary for the proper functioning of the body. It is a component of the plasma membrane of animal cells and is found within the phospholipid bilayer. Being the outermost structure in animal cells, the plasma membrane is responsible for the transport of materials and cellular recognition, and it is involved in cell-to-cell communication.

summary
In this lesson, you learned about the structure and function of lipids. Lipids are a class of macromolecules that are nonpolar and hydrophobic in nature. The major types of lipids include fats and oils, waxes, phospholipids, and steroids. Fats are a stored form of energy and are also known as triacylglycerols or triglycerides. Fats are made up of fatty acids and either glycerol or sphingosine. Fatty acids may be unsaturated or saturated, depending on the presence or absence of double bonds in the hydrocarbon chain. If only single bonds are present, they are known as saturated fatty acids. Unsaturated fatty acids may have one or more double bonds in the hydrocarbon chain. Trans fats are used in the food industry. These are made when oils are artificially hydrogenated to make them semi-solid and of a consistency desirable for many processed food products. Phospholipids make up the matrix of membranes. They have a glycerol or sphingosine backbone to which two fatty acid chains and a phosphate-containing group are attached. Waxes cover the feathers of some aquatic birds and the leaf surfaces of some plants. Steroids are another class of lipids. Their basic structure has four fused carbon rings. Cholesterol is a type of steroid and is an important constituent of the plasma membrane, where it helps to maintain the fluid nature of the membrane. It is also the precursor of steroid hormones such as testosterone.

Source: THIS TUTORIAL HAS BEEN ADAPTED FROM LUMEN LEARNING’S “NUTRITION FLEXBOOK”. ACCESS FOR FREE AT https://courses.lumenlearning.com/suny-nutrition/. LICENSE: creative commons attribution 4.0 international.

Terms to Know
Essential Fatty Acids

Fatty acids that are required but not synthesized by the human body.

Glycerol

An organic compound (alcohol) with three carbons, five hydrogens, and three hydroxyl (OH) groups.

Lipids

Fats that include a diverse group of compounds that are largely nonpolar in nature.

Monounsaturated Fat

When there is one double bond in the molecule. An example of this is olive oil.

Phospholipids

Major constituents of the plasma membrane, the outermost layer of animal cells.

Polyunsaturated Fat

When there is more than one double bond in the molecule. An example of this is canola oil.