Lipids

Question 1

Fill in the blank.

The four main classes of biological macromolecules are proteins, carbohydrates, nucleic acids, and ____________.

Answer 1

lipids

These are a class of water-insoluble organic molecules that includes triglycerides, cholesterol, waxes, and more.

Question 2

Name three roles that lipids play in the human body.

Answer 2

1. maintaining cell structure (via lipid-based membranes)
2. participating in biological signaling
3. serving as energy storage molecules

Question 3

Fill in the blank.

Most fat stored in the human body, as well as the majority of dietary fat, exists in the form of _____________.

Answer 3

triglycerides

Triglycerides, or triacylglycerols, are molecules consisting of a glycerol backbone and three fatty acids.

Question 4

In a triglyceride, each fatty acid is attached to the glycerol backbone via which functional group?

Answer 4

ester

As such, triglycerides contain three ester linkages: one for each fatty acid chain on the molecule.

Question 5

Fill in the blank.

The hydrolysis of a triglyceride using a strong base (such as NaOH) is termed _____________.

Answer 5

saponification

Saponification gets its name from “soap-making,” due to the soaplike nature of the products. (In fact, the process is sometimes actually used to make soap.)

Question 6

Name the products of a complete saponification reaction in which NaOH was used.

Answer 6

• glycerol
• three fatty acid salts

These are “salts” (here, deprotonated fatty acids associated with sodium atoms) rather than actual fatty acids because saponification utilizes a strong base (here, NaOH), which causes the products to be deprotonated. However, if acid is added in a later step, these salts will be protonated to form fatty acids.

Question 7

How many molecules of NaOH are required to completely saponify an unsaturated triglyceride?

Answer 7

three

Since all triglycerides contain three fatty acid tails, complete saponification always requires three units of NaOH: one for each tail. (The fact that this triglyceride is unsaturated is actually irrelevant to the correct answer.)

Question 8

True or false.

Saponification involves the breakage of ester linkages.

Answer 8

True

In a triglyceride, the three fatty acid tails are attached to the glycerol backbone via ester linkages. These bonds are broken during saponification.

Question 9

Fill in the blank.

________ fatty acids are those that contain no carbon-carbon double bonds in their fatty acid chains. In these fatty acids, all carbons except the carbonyl carbon are bound to ________ other atoms.

Answer 9

Saturated, four

Question 10

Fill in the blank.

________ fatty acids are those that contain at least one carbon-carbon double bond in their fatty acid chains. In these fatty acids, at least one carbon in the chain is bound to only ________ other atoms.

Answer 10

Unsaturated, three

Since carbon is saturated when it is attached to four other atoms (via single bonds), it is considered unsaturated when attached to fewer than four atoms.

Question 11

Which has a higher melting point: a typical saturated fat or a typical unsaturated fat?

Answer 11

typical saturated fat

Saturated fats (composed of saturated fatty acids) can stack well due to their lack of “kinks” caused by double bonds. In contrast, unsaturated fats have double-bond kinks, weakening their stacking. As such, saturated fats are more difficult to melt (meaning that they have higher melting points) than unsaturated fats.

Question 12

A free fatty acid at physiological pH would be most likely to carry what charge (if any)?

Answer 12

negative charge

Free fatty acids are composed of a nonpolar hydrocarbon tail (uncharged) and a carboxylic acid group. At physiological pH, carboxylic acid groups tend to be negatively-charged (COO⁻).

Question 13

Glycerol, which forms the backbone of a triglyceride, is a molecule that contains three -OH groups. What name is given to such molecules?

Answer 13

triols

Triols are molecules that contain three hydroxyl (-OH) groups. (In contrast, diols are molecules that contain two -OH groups.)

Question 14

Define:

amphipathic

Answer 14

They are molecules that possess both polar and nonpolar properties.

Fatty acids, which contain a polar (hydrophilic) head and a nonpolar (hydrophobic) tail, exemplify amphipathic compounds.

Question 15

Fill in the blank.

Fatty acids are often named using “lipid numbers,” where they are designated in the form of C:D.

In this system, C represents the number of ________, and D represents the number of ________.

Answer 15

carbons, double bonds

For instance, oleic acid contains 18 carbons and 1 double bond, so its lipid-number nomenclature is 18:1.

Question 16

When described in lipid-number format, all saturated fatty acids have what number after the colon?

Answer 16

0

In lipid-number format, the number before the colon refers to the number of carbons (which varies), while the number after the colon denotes the number of double bonds in the chain (which is 0 for all saturated fatty acids).

Question 17

Fill int he blank.

Fatty acids that contain fewer than six carbon atoms are termed ________-______ _______ _______.

Answer 17

short-chain fatty acids

These are the shortest (smallest) fatty acid molecules.

Question 18

Fill in the blank.

Medium-chain fatty acids are those that contain between ________ and ________ carbon atoms.

Answer 18

six, twelve

Medium-chain FAs are longer than short-chain FAs (<6 carbons) but shorter than long-chain FAs (13-21 carbons).

Question 19

Stearic acid, a saturated fatty acid, has a chemical formula of C₁₈H₃₆O₂. With regard to chain length, how is stearic acid classified?

Answer 19

long-chain fatty acid

Long-chain fatty acids are those that contain between 13 and 21 carbon atoms.

Question 20

Melissic acid, a saturated fatty acid, has a chemical formula of C₃₀H₆₀O₂. With regard to chain length, how is melissic acid classified?

Answer 20

very long-chain fatty acid

Very long-chain fatty acids are those that contain more than 21 carbon atoms.

Question 21

In a fatty acid chain, a certain carbon atom is bound to three hydrogen atoms. This carbon atom is denoted with which Greek letter?

Answer 21

omega

(ω)

The only carbon atom in a fatty acid chain that is attached to three hydrogen atoms is the terminal (end) carbon. This carbon is designated as the omega (ω) carbon, since omega is the last letter in the Greek alphabet.

Question 22

In a form of fatty acid notation termed delta-x notation, linoleic acid is described as cis-Δ9, cis-Δ12 octadecadienoic acid. What do the delta (Δ) symbols represent in this notation?

Answer 22

Double bonds

This should be answerable even if you aren’t familiar with delta notation, as the delta symbols are preceded by “cis,” which in this context is used to designate double bonds in which the carbon substituents fall on the same side of the double bond.

Question 23

Name the structure shown below.

Answer 23

cholesterol

It is a lipid and the precursor to steroid hormones, is recognizable from its structure containing four fused rings.

Question 24

Cholesterol is found in the cell membranes of which of the following?

Choose from eukaryotic cells, prokaryotic cells, or viruses.

Answer 24

eukaryotic cells

Make sure you understand that the membranes of prokaryotic cells (bacteria) do not contain cholesterol! The AAMC has been known to ask questions about this in their practice materials.

Viruses do not have cell membranes at all, so that option can be easily eliminated.

Question 25

Name the class of lipid molecules that serves as the **primary lipid** component of cell membranes.

Answer 25

phospholipids ## Footnote This is a lipid molecule that contains a phosphate group. Phospholipids are the main component of cell membranes, which exist as lipid bilayers with the polar phospholipid heads pointing outward and the nonpolar tails facing inward.

Question 26

Describe the structure of a **phospholipid**.

Answer 26

They contain a **phosphate group** attached to at least one (usually two) fatty acid tails via a **backbone**. ## Footnote Most commonly, that backbone is **glycerol**, a three-carbon alcohol. Additionally, phospholipids may be modified via the addition of various molecules to the phosphate head group.

Question 27

# Fill in the blank. Esters consisting of both long-chain alcohols and long-chain fatty acids are lipids termed \_\_\_\_\_\_\_\_\_\_.

Answer 27

waxes ## Footnote These are very large molecules (the alcohol chains alone are typically between 12 and 32 carbon atoms long). Plants and animals (such as honeybees) secrete waxes for various reasons, usually related to their hydrophobic nature.

Question 28

What is the name of the molecule shown below?

Answer 28

isoprene ## Footnote It is a hydrocarbon compound with the chemical formula C₅H₈. Terpenes, which are highly biologically important lipids, have structures that consist of repeating isoprene units.

Question 29

# Define: terpenes

Answer 29

They are strong-smelling **hydrocarbon** lipids that are composed of repeating units of isoprene. ## Footnote While terpenes serve a variety of functions in plants as well as animals, for the MCAT, it is most important that you be able to recognize their isoprene-based structure.

Question 30

The smallest and simplest terpenes are termed **monoterpenes**. How many **isoprene units** comprise a monoterpene?

Answer 30

two ## Footnote This can be remembered because *one* isoprene unit wouldn't be a terpene at all; it would just be isoprene. Since isoprene has a chemical formula of C₅H₈, monoterpenes have chemical formulae of C₁₀H₁₆.

Question 31

A **diterpene** would be expected to contain how many carbon atoms?

Answer 31

20 ## Footnote As its name indicates, a diterpene is essentially twice the size (and formula) of a monoterpene. Monoterpenes have 10 carbon atoms, so diterpenes would be expected to have 20.

Question 32

Name the **triterpene** that serves as a precursor to all steroid hormones (as well as to cholesterol itself).

Answer 32

squalene ## Footnote We often remember that cholesterol is the precursor to steroid hormones, but we may not realize that cholesterol itself has a precursor! That precursor is squalene, a triterpene. Like all terpenes, squalene has abundant double bonds, which allow it to easily act as a reactant in various reactions.

Question 33

Which of the following hormones is derived from squalene? * oxytocin * estrogen * antidiuretic hormone

Answer 33

estrogen ## Footnote All steroid hormones are derived from squalene (more specifically, they are derived from cholesterol, which is derived from squalene). Estrogen is the only steroid hormone listed.

Question 34

Which of the following hormones is **not** derived from squalene? * cortisol * aldosterone * melatonin

Answer 34

melatonin ## Footnote This question is essentially asking "which of the following is not a steroid hormone?" Melatonin is an amino acid-derived hormone, not a steroid. Even if you didn't know that (although you should!), you can recall that all MCAT-relevant steroid hormones end in "-ol," "-one," or "-en." Melatonin ends in "-in," so it can't be a steroid.

Question 35

# Fill in the blank. **Terpenes** that have been chemically modified, often in a way that makes them oxygen-containing, can be termed \_\_\_\_\_\_\_\_\_\_\_.

Answer 35

terpenoids ## Footnote While the terms "terpene" and "terpenoid" have been increasingly used interchangeably in scientific and informal literature, you should understand the distinction on the front of this card for the MCAT.

Question 36

Name the **class of lipids** in which the molecule below is categorized.

Answer 36

prostaglandin ## Footnote Prostaglandins are lipids that contain exactly 20 carbon atoms. Their structures always include a five-membered ring. Although that alone is enough to answer this question, note that they also are carboxylic acids and always contain carbon-carbon double bonds.

Question 37

**Prostaglandins** are derived from which fatty acid?

Answer 37

arachidonic acid ## Footnote While you don't need to be familiar with the structure of this unsaturated fatty acid for the MCAT, you should understand its relationship to prostaglandins, and you may see it referenced in a passage.

Question 38

Name the **fat-soluble** vitamins.

Answer 38

1. vitamin A 2. vitamin D 3. vitamin E 4. vitamin K ## Footnote All other vitamins are water-soluble.

Question 39

Name the process that facilitates **lipid digestion** in the small intestine. ## Footnote Hint: This process is assisted by the presence of bile, the amphipathic nature of which allows fatty acids to be mixed with water and spread apart.

Answer 39

emulsification ## Footnote While emulsification is not digestion per se, it facilitates digestion by spreading apart larger clumps of dietary fat. This is accomplished by bile, a substance produced in the liver and stored in the gall bladder.

Question 40

Name the main **enzyme** that catalyzes the digestion of fats in the small intestine.

Answer 40

pancreatic lipase ## Footnote As its name implies, lipase catalyzes the breakdown of lipids (fats). If you chose bile instead, note that bile is not an enzyme! Bile simply emulsifies (spreads out) fats to allow the water-soluble pancreatic lipase to access them.

Question 41

What **spherical/cluster-like structures** form in the lumen of the **small intestine** and carry lipids to brush border cells for absorption?

Answer 41

micelles ## Footnote Micelles are spherical, amphipathic structures in which fats are carried from the interior (lumen) of the small intestine to the brush borders of small intestinal cells.

Question 42

Is the interior of a micelle **hydrophobic** or **hydrophilic**?

Answer 42

hydrophobic ## Footnote As we've seen with globular proteins, micelles form based on hydrophobic effects. This means that hydrophobic (nonpolar) portions cluster in the structure's interior, while hydrophilic (polar) portions face the aqueous environment.

Question 43

A **micelle** reaches the brush border, is broken down into its component lipids, and is absorbed into the mucosa. What happens next?

Answer 43

The components are **re-esterified**. ## Footnote In other words, the lipids (which had previously been broken down into fundamental components such as fatty acids) are reacted to re-form triglycerides and cholesteryl esters.

Question 44

Re-esterified lipid components in the intestinal mucosa are then packaged into what **structures**?

Answer 44

chylomicrons ## Footnote These are lipoprotein particles that transport lipids from the intestines to other areas throughout the body.

Question 45

Name **four** types of molecules that are found in **chylomicrons**.

Answer 45

1. Triglycerides 2. Phospholipids 3. Cholesterol 4. Proteins ## Footnote The first three of these molecules are dietary lipids (with triglycerides comprising the bulk of dietary lipids), so it should be logical that they would be found in chylomicrons. Chylomicrons are lipo*proteins*, so proteins should also make sense on this list.

Question 46

# Fill in the blank. Lymphatic vessels found within intestinal villi are called \_\_\_\_\_\_\_\_\_\_\_.

Answer 46

lacteals ## Footnote These are the small lymphatic vessels that chylomicrons travel through to move away from the intestine and toward the thoracic duct.

Question 47

# Fill in the blank. Chylomicrons exit the lymphatic system via the thoracic duct, which is a lymphatic vessel that empties into the \_\_\_\_\_\_\_\_ system.

Answer 47

circulatory ## Footnote Specifically, the thoracic duct drains into the left subclavian vein, but as the MCAT isn't an anatomy exam, you're unlikely to be asked for that detail in particular.

Question 48

# Fill in the blank. Beta-oxidation is the process of \_\_\_\_\_\_\_\_, or breakdown, of fatty acids. ## Footnote Choose from either "catabolism" or "anabolism."

Answer 48

catabolism ## Footnote An easy way to remember that catabolism refers to breakdown is to note the similarity of its opposite, anabolism, to "anabolic steroids." Anabolic steroids are meant to build up mass, so anabolism must refer to the buildup of larger macromolecules, while catabolism refers to their breakdown.

Question 49

In **eukaryotes**, most beta-oxidation occurs in which organelle?

Answer 49

mitochondria ## Footnote Note that in addition to mitochondrial beta-oxidation, a small amount of beta-oxidation (mainly of very long-chain fatty acids) does occur in peroxisomes.

Question 50

In **prokaryotes**, where does beta-oxidation occur?

Answer 50

cytosol ## Footnote Prokaryotes lack membrane-bound organelles, so they have neither mitochondria nor peroxisomes (the two organelles in which beta-oxidation occurs in eukyarotes). Instead, beta-oxidation happens in the cytosol.

Question 51

Name the **three** main products of **beta-oxidation**.

Answer 51

1. Acetyl-CoA 2. NADH 3. FADH₂

Question 52

# Fill in the blank. Beta-oxidation gets it name from the carbon on a fatty acid molecule that is positioned \_\_\_\_\_\_\_\_ carbon(s) away from the carbonyl carbon.

Answer 52

two ## Footnote The beta carbon is adjacent to the alpha carbon, which is adjacent to the carbonyl carbon.

Question 53

# True or false. Free fatty acids in the cell cytosol can diffuse into the mitochondria, where they later undergo beta-oxidation.

Answer 53

False ## Footnote A free fatty acid is negatively-charged due to the presence of a carboxylate group. Such charged (and therefore highly polar) molecules cannot diffuse directly across the mitochondrial membrane(s).

Question 54

Free fatty acids in the **cytosol** must undergo what **process** before they can be transported into the **mitochondria**?

Answer 54

activation ## Footnote This process renders the fatty acid uncharged, after which short-chain activated FAs can simply diffuse into the mitochondria, while larger activated FAs are brought in via a specialized shuttle system.

Question 55

In fatty acid activation, a free fatty acid is transformed into a molecule called a fatty **acyl-CoA**. Predictably, this is simply the fatty acid attached to coenzyme A (CoA). Which **enzyme** catalyzes this reaction?

Answer 55

long-chain fatty acyl-CoA synthetase ## Footnote This enzyme is alternatively termed long-chain fatty acyl-CoA ligase. This is in keeping with the definition of a ligase, which is an enzyme that catalyzes the attachment of two molecules into a single, larger molecule.

Question 56

# True or false. Fatty acid activation requires ATP.

Answer 56

True ## Footnote Fatty acid activation, or the transformation of a free fatty acid into a fatty acyl-CoA, does require energy input in the form of ATP hydrolysis. In fact, ATP is a reactant of this process, and AMP is a product.

Question 57

# Fill in the blank. Unlike small- to medium-chain fatty acids, small- to medium-chain fatty acyl-CoA molecules can diffuse directly into the mitochondria because they are less \_\_\_\_\_\_\_\_\_\_.

Answer 57

polar ## Footnote Polarity is the most important determinant of whether a substance can diffuse across a biological membrane. The less polar the molecule, the more easily it can diffuse.

Question 58

What is the purpose of the **carnitine shuttle**?

Answer 58

It functions to **transport long-chain** and very long-chain fatty acids (FAs) across the **inner mitochondrial membrane**. ## Footnote Short- and medium-chain FAs, once activated, can simply diffuse into the inner compartment of the mitochondria, but longer FAs are too large and must be specifically transported.

Question 59

Once a fatty acid is activated and transported into the mitochondria, **beta-oxidation** takes place as a repeated series of how many steps?

Answer 59

four ## Footnote Put simply, beta-oxidation is essentially a series of four steps repeated over and over. Each four-step cycle releases one acetyl-CoA, one NADH, and one FADH₂ molecule.

Question 60

The first of the four key steps of beta-oxidation involves the formation of a *trans* double bond between the second and third carbons and the associated reduction of FAD to FADH₂. A member of which class of **enzyme** catalyzes this reaction?

Answer 60

oxidoreductase | (dehydrogenase) ## Footnote The full name of the enzyme that catalyzes this step is fatty acyl-CoA dehydrogenase. However, you are much more likely to be asked to realize that the reduction of FAD must be performed by an oxidoreductase than to be asked the specific identity of this enzyme.

Question 61

The second of the four key steps of beta-oxidation involves the addition of -OH to one side of the double bond between carbons 2 and 3, rendering it a single bond. What **molecule** is also involved in this reaction?

Answer 61

water | (H₂O) ## Footnote The enzyme that catalyzes this step is enoyl-CoA hydratase, the name of which may help answer this question. However, even without this information, we know that an -OH was added to one side of the bond. To render it a single bond, an -H must have been added to the other side, indicating that H₂O was involved.

Question 62

The third main step of beta-oxidation, catalyzed by β-hydroxyacyl-CoA dehydrogenase, produces which **high-value molecule**?

Answer 62

NADH ## Footnote The enzyme name here tells us that this reaction is a redox reaction. Overall, each round of beta-oxidation produces one molecule each of FADH₂, NADH, and acetyl-CoA. FADH₂ was produced in step 1, and acetyl-CoA is produced in step 4, leaving NADH to be produced here, in step 3.

Question 63

# Fill in the blank. The final step of beta-oxidation involves breakage of the molecule into a shorter acyl-CoA and \_\_\_\_\_\_\_-\_\_\_.

Answer 63

acetyl-CoA ## Footnote Acetyl-CoA, a biologically important molecule, is the main product of beta-oxidation. This molecule can then be used in other metabolic processes, such as the Krebs cycle.