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What are examples of disaccharides?

3 min read

Disaccharides, also known as 'double sugars,' are carbohydrates formed when two monosaccharides, or simple sugars, join together through a condensation reaction. For instance, the common disaccharides sucrose, lactose, and maltose are responsible for the sweetness found in table sugar, milk, and malted grains, respectively.

Quick Summary

Disaccharides are carbohydrates composed of two monosaccharide units connected by a glycosidic bond. Common examples include sucrose (glucose + fructose), lactose (glucose + galactose), and maltose (glucose + glucose). These molecules serve as energy sources and are broken down by enzymes during digestion.

Key Points

  • Sucrose: A disaccharide made of glucose and fructose, commonly known as table sugar.

  • Lactose: Composed of glucose and galactose, lactose is the primary sugar found in milk.

  • Maltose: A reducing sugar formed from two glucose units, found in malted grains and produced from starch breakdown.

  • Cellobiose: Consists of two glucose units with a $\beta$-linkage, similar to the structure of cellulose, and is indigestible by humans.

  • Trehalose: A non-reducing disaccharide of two glucose units, acting as an energy source in many fungi and insects.

  • Glycosidic Bond: The covalent bond linking the two monosaccharides in a disaccharide, formed during dehydration synthesis.

In This Article

Common Examples of Disaccharides

Disaccharides are a fundamental part of a balanced diet and are present in a wide range of natural and processed foods. While the three most common examples are sucrose, lactose, and maltose, there are other, less familiar disaccharides that play important roles in biology and industry.

Sucrose: The Table Sugar Disaccharide

Sucrose is a non-reducing disaccharide composed of one molecule of glucose and one molecule of fructose. This versatile sugar is found naturally in many fruits, vegetables, and grains, but it is most famously extracted and refined from sugarcane and sugar beets to produce common table sugar. Due to its non-reducing nature, the glycosidic bond links the reactive anomeric carbons of both sugar units, preventing the molecule from easily undergoing oxidation.

Sources of sucrose:

  • Fruits like mangoes and watermelons
  • Vegetables such as sweet potatoes and carrots
  • Refined products like candy, ice cream, and sweetened beverages

Lactose: The Milk Sugar Disaccharide

Lactose is the disaccharide found primarily in the milk of mammals, including humans and cows. It is formed by a $\beta$(1→4) glycosidic bond linking one molecule of galactose and one molecule of glucose. Lactose is a reducing sugar because it retains a free hemiacetal unit on its glucose component. For the body to absorb lactose, it must be broken down by the enzyme lactase in the small intestine. Individuals with lactose intolerance lack sufficient amounts of this enzyme, leading to digestive issues.

Sources of lactose:

  • Milk and milk products like yogurt and cheese
  • Some baked goods, cereals, and processed foods

Maltose: The Malt Sugar Disaccharide

Maltose, or malt sugar, is a reducing disaccharide consisting of two glucose units joined by an $\alpha$(1→4) glycosidic bond. It is not very abundant in nature but is produced during the partial hydrolysis of starch, a process facilitated by the enzyme amylase. This is why crackers and other starchy foods can taste sweet after being chewed for a while. Maltose plays a crucial role in brewing beer and is also used as a sweetener in some foods.

Sources of maltose:

  • Germinating grains like barley
  • Hydrolyzed starch products, such as corn syrup
  • Malted beverages and certain candies

Other Notable Disaccharides

Beyond the most common examples, other disaccharides exist that have unique properties and applications:

  • Cellobiose: Formed from two glucose units linked by a $\beta$(1→4) glycosidic bond, identical to the bonds in cellulose. Unlike maltose, humans cannot digest cellobiose, but it is produced during the breakdown of cellulose.
  • Trehalose: Composed of two glucose units connected by an $\alpha$(1→1)α glycosidic bond. It is a non-reducing sugar found in fungi, insects, and yeast, where it serves as a source of energy.
  • Lactulose: A synthetic, non-natural disaccharide made from galactose and fructose. The human body cannot break it down, and it is used medicinally to treat constipation.

Comparison of Common Disaccharides

Feature Sucrose Lactose Maltose
Component Monosaccharides Glucose + Fructose Galactose + Glucose Glucose + Glucose
Glycosidic Bond Type $\alpha$(1→2)β $\beta$(1→4) $\alpha$(1→4)
Reducing Sugar? No (non-reducing) Yes (reducing) Yes (reducing)
Primary Sources Table sugar, fruits, sugar cane Milk and dairy products Germinating grains, starch hydrolysis
Sweetness Very Sweet Mildly Sweet Less Sweet than sucrose

Conclusion

Understanding what are examples of disaccharides and their composition provides a clearer picture of the different kinds of sugars we consume. From the ubiquitous sweetness of sucrose to the milk sugar lactose and the malt sugar maltose, these double sugars are crucial as energy sources in our diet. Their distinct properties, determined by their monosaccharide building blocks and glycosidic linkages, dictate not only their taste and texture but also how our bodies digest and utilize them. This knowledge helps us appreciate the intricate biochemistry behind our food and metabolism.

For more detailed information on the chemical properties and classification of disaccharides, consult authoritative resources such as the entry on carbohydrates from Chemistry LibreTexts.

Frequently Asked Questions

A disaccharide is a type of carbohydrate formed when two monosaccharides, or simple sugars, are joined together by a glycosidic bond, with the loss of a water molecule.

The three most common disaccharides are sucrose (table sugar), lactose (milk sugar), and maltose (malt sugar).

Lactose is composed of one molecule of glucose and one molecule of galactose.

Sucrose is a non-reducing sugar because the glycosidic bond links the anomeric carbons of both the glucose and fructose units, meaning neither has a free aldehyde or ketone group available to act as a reducing agent.

Maltose is found in foods like germinating grains, corn syrup, certain cereals, and is a key ingredient in brewing beer.

No, humans cannot digest cellobiose because they lack the specific enzymes required to break the beta-glycosidic bond linking its two glucose units.

Both maltose and cellobiose are made of two glucose units. The key difference is their glycosidic linkage: maltose has an $\alpha$(1→4) bond, while cellobiose has a $\beta$(1→4) bond.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.