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Polysaccharide

Polysaccharide is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Polysaccharide rather than just read about it. In short: Polysaccharides (; from Ancient Greek πολύς (polús) 'many, much' and σάκχαρ (sákkhar) 'sugar') are "compounds consisting of a large number of monosaccharides linked glycosidically". They are the most abundant carbohydrates in food.

Polysaccharide — main illustration
Polysaccharide — illustration

Key takeaways

  • Polysaccharide belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Polysaccharide to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Polysaccharide from memory before moving on to harder problems.

Reference excerpt

Polysaccharides (; from Ancient Greek πολύς (polús) 'many, much' and σάκχαρ (sákkhar) 'sugar') are "compounds consisting of a large number of monosaccharides linked glycosidically". They are the most abundant carbohydrates in food. Their structures range from linear to highly branched polymers. Examples include storage polysaccharides such as starch, glycogen, and galactogen and structural polysaccharides such as hemicellulose and chitin. The term "glycan" is synonymous with polysaccharide, but often glycans are discussed in the context of glycoconjugates, i.e. hybrids of polysaccharides and proteins or lipids. Polysaccharides are often heterogeneous, containing slight modifications of the repeating unit. They may be amorphous (e.g. starch) or insoluble in water (e.g. cellulose). Saccharides are generally composed of simple carbohydrates called monosaccharides with the general formula (CH2O)n where n is three or more. Examples of monosaccharides are glucose, fructose, and glyceraldehyde. Polysaccharides, meanwhile, have a general formula of Cx(H2O)y where x and y are usually large numbers between 200 and 2500. When the repeating units in the polymer backbone are six-carbon monosaccharides, as is often the case, the general formula simplifies to (C6H10O5)n, where typically 40 ≤ n ≤ 3000. Polysaccharides are highly branched. In fact, starch holds I2iodine molecules in the helical portion. The starch-I2 is dark blue in colour. Cellulose does not contain complex helices and hence cannot hold I2; as a result, a colour change is not observed when placed in an I2-dye. This colour-changing property is a unique character test for polysaccharides

As a rule of thumb, polysaccharides contain more than ten monosaccharide units, whereas oligosaccharides contain three to ten monosaccharide units, but the precise cutoff varies according to the convention. Polysaccharides are an important class of biological polymers. Their function in living organisms is usually either structure- or storage-related. Starch (a polymer of glucose) is used as a storage polysaccharide in plants, being found in the form of both amylose and the branched amylopectin. In animals, the structurally similar glucose polymer is the more densely branched glycogen, sometimes called "animal starch". Glycogen's properties allow it to be metabolized more quickly, which suits the active lives of moving animals. In bacteria, they play an important role in bacterial multicellularity. Cellulose and chitin are examples of structural polysaccharides. Cellulose is used in the cell walls of plants and other organisms and is said to be the most abundant organic molecule on Earth. It has many uses such as a significant role in the paper and textile industries and is used as a feedstock for the production of rayon (via the viscose process), cellulose acetate, celluloid, and nitrocellulose. Chitin has a similar structure but has nitrogen-containing side branches, increasing its strength. It is found in arthropod exoskeletons and in the cell walls of some fungi. It also has multiple uses, including surgical threads. Polysaccharides also include callose or laminarin, chrysolaminarin, xylan, arabinoxylan, mannan, fucoidan, and galactomannan.

Cellulose and dietary fiber

Structure Nutritional polysaccharides are common sources of energy. Many organisms can easily break down starches into glucose. By contrast, few organisms can metabolize cellulose. Some bacteria and protists can metabolize these carbohydrate types. Ruminants and termites, for example, use microorganisms to process cellulose. Some polysaccharides are not very digestible, but in the form of dietary fiber, they enhance digestion. Soluble fiber binds to bile acids in the small intestine, making them less likely to enter the body; this, in turn, lowers cholesterol levels in the blood. Soluble fiber also attenuates the absorption of sugar, reduces sugar response after eating, normalizes blood lipid levels and, once fermented in the colon, produces short-chain fatty acids as byproducts with wide-ranging physiological activities (discussion below). Although insoluble fiber is associated with reduced diabetes risk, the mechanism by which this occurs is unknown. Dietary fiber is nevertheless regarded as important for the diet, with regulatory authorities in many developed countries recommending increases in fiber intake.

Storage polysaccharides

Starch

Starch is a glucose polymer in which glucopyranose units are bonded by alpha-linkages. It is made up of a mixture of amylose (15–20%) and amylopectin (80–85%). Amylose consists of a linear chain of several hundred glucose molecules, and amylopectin is branched made of several thousand glucose units (every chain of 24–30 glucose units is one unit of Amylopectin). Starches are insoluble in water. They can be digested by breaking the alpha-linkages (glycosidic bonds). Humans and other animals have amylases so that they can digest starches. Potato, rice, wheat, and maize are major sources of starch in the human diet. The formations of starches are the ways that plants store glucose.

Glycogen

… excerpt ends here. Continue reading the full article.

Illustrations

Polysaccharide: 3D structure of cellulose, a beta-glucan polysaccharide
3D structure of cellulose, a beta-glucan polysaccharide
Polysaccharide: Amylose is a linear polymer of glucose mainly linked with α(1→4) bonds. It can be made of several thousands of glucose units. It is one of the two components of starch, the other being amylopectin.
Amylose is a linear polymer of glucose mainly linked with α(1→4) bonds. It can be made of several thousands of glucose units. It is one of the two components of starch, the other being amylopectin.
Polysaccharide illustration
Polysaccharide illustration
Polysaccharide: Some important natural structural polysaccharides
Some important natural structural polysaccharides

Worked examples

Example 1 — a first encounter with Polysaccharide

Start with the simplest possible case. Write down what Polysaccharide claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Polysaccharide before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Polysaccharide ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Polysaccharide

In research
Polysaccharide appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Polysaccharide in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Polysaccharide is common in secondary-school and first-year university syllabi. It links to neighbouring topics Carbohydrate chemistry, Polysaccharides, so understanding it makes those chapters shorter.
In everyday life
Look for Polysaccharide outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.

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How to study Polysaccharide in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Polysaccharide means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Polysaccharide out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Polysaccharide in simple terms?

Polysaccharides (; from Ancient Greek πολύς (polús) 'many, much' and σάκχαρ (sákkhar) 'sugar') are "compounds consisting of a large number of monosaccharides linked glycosidically". They are the most abundant carbohydrates in food.

Why does Polysaccharide matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Polysaccharide?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Polysaccharide.

Tags

  • Carbohydrate chemistry
  • Polysaccharides

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