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Digestive enzymes

Enzymes are globular proteins that control biological reactions. Digestive enzymes speed up the breakdown (hydrolysis) of food molecules into their ‘building block’ components. These reactions occur outside of the cells lining the gut.

Diagram of stages in action of sucrase on sucrose.

Action of sucrase on sucrose

Sucrose binds to the active site on sucrase, and this puts stress on the bond between the 2 sugars that make up sucrose. The bond breaks, releasing glucose and fructose.

Rights: University of Waikato. All rights reserved.

Naming and classification of enzymes

There are 2 systems used for naming enzymes:

  • The suffix ‘-ase’ is used with the root name of the substance being acted upon, for example, when sucrose (sugar) is digested, it is acted upon by an enzyme called sucrase.

  • The type of chemical reaction involved as the enzyme functions, for example, when sucrase acts on sucrose, it breaks it into a molecule of glucose and a molecule of fructose. This reaction involves adding a water molecule to break a chemical bond and so the enzyme is a hydrolase. All digestive enzymes belong to this hydrolase class.

Enzymes are classified according to the type of chemical reaction catalysed. All digestive enzymes are hydrolases, whereas most of the enzymes involved in energy release for muscular contraction are oxidation-reduction enzymes such as oxidases, hydrogenases and dehydrogenases.

Chemical structure of enzymes

Enzymes are large protein molecules, all of which have their own specific 3D shape. Embedded within the shape is a region known as the ‘active site’, which can attract other suitably shaped molecules to bind to the site. The analogy that is often used to describe this mechanism is that of a key fitting into a lock. The enzyme serves as the lock and the attracted molecule (called the substrate) is the key.

Once the chemical reaction within this lock and key arrangement has been completed, the products are released and the enzyme is free to attract another substrate molecule.

The rate of reaction for such a process is thousands of substrate molecules per minute. If a solution of sugar is left in a sealed container, it breaks down into glucose and fructose extremely slowly. In the presence of a small amount of the enzyme sucrase, the rate of breakdown is millions of times faster.

Sometimes, chemical substances other than substrates can bind with the active sites of enzymes, blocking their normal function. For example, water-soluble compounds of arsenic and mercury are extremely poisonous because they can permanently bind to some enzyme systems, markedly reducing their efficiency. Depending on the dose, the end result could be death.

Digestive enzymes

Digestive enzymes all belong to the hydrolase class, and their action is one of splitting up large food molecules into their ‘building block’ components. Another unique property is that they are extracellular enzymes that mix with food as it passes through the gut. The majority of other enzymes function within the cytoplasm of the cell.

The chemical digestion of food is dependent on a whole range of hydrolase enzymes produced by the cells lining the gut as well as associated organs such as the pancreas. The end goal is to break large food molecules into very much smaller ‘building block’ units. These can then be readily and rapidly absorbed through the gut wall and into the bloodstream for transport to the liver and from there to other parts of the body.

The main enzyme-producing structures of the human digestive system are the salivary glands, stomach, pancreas, liver and small intestine.

Digestive juices and enzymes

Substance digested

Product formed

Saliva Amylase

Starch

Maltose

Gastric juice Protease (pepsin) and hydrochloric acid

Proteins

Partly digested proteins

Pancreatic juice Proteases (trypsin) Lipases Amylase

Proteins Fats emulsified by bile Starch

Peptides and amino acids Fatty acids and glycerol Maltose

Intestinal enzymes Peptidases Sucrase Lactase Maltase

Peptides Sucrose (sugar) Lactose (milk sugar) Maltose

Amino acids Glucose and fructose Glucose and galactose Glucose

Bile from the liver Bile salts

Fats globules

Fat droplets

The following pathway summarises how starch present in a food like bread is broken down chemically into glucose, which can then be absorbed through the intestinal wall and into the bloodstream for transport to the liver and from there to other parts of the body.

Mouth and duodenum

Starch hydrolysed into maltose through the action of the enzyme amylase.

Diagram of how starch is broken down chemically into glucose

Starch to glucose pathway

The following pathway summarises how starch present in a food like bread is broken down chemically into glucose, which can then be absorbed through the intestinal wall and into the bloodstream for transport to the liver and from there to other parts of the body.

Rights: University of Waikato. All Rights Reserved.

Jejunum

Maltose hydrolysed into glucose through the action of the enzyme maltase.

Related content

Use these articles below to explore some of the science ideas and concepts fundemental to the understanding of digestion chemisty.

The article Catalysing chemical reactions with enzymes includes an animated video outlining in detail how enzymes work.

Activity ideas

Try one of more of these activities with your students.

  • Enzyme action – investigate the effect that fruit purees (pineapple, kiwifruit, peach) have on the setting of party jellies.

  • Salivary amylase and starch – explore the action of salivary amylase on starch present in cooked rice with simple tests for starch and its digestion product, maltose, are applied.

  • Lactose intolerance – investigate the effect of the digestive enzyme lactase on a sugar found in milk called lactose. The digestive system condition known as lactose intolerance will also be looked at.

See our Enzymes Pinterest board for more resource ideas.

Useful link

Read Digestive Enzymes on Biology Online for more information about the various digestive enzymes and the digestion process.

Published: 13 July 2011