Skip to main content
Food Science Daily

Food science glossary

25 terms

Amylopectin

Food Chemistry

The highly branched fraction of starch, with α-1,4 chains joined by α-1,6 branch points roughly every 20–25 units.

Real-life application

The branched starch that makes rice sticky and gives bread its soft crumb; waxy rice varieties are almost pure amylopectin.

See also: Amylose, Starch gelatinisation

Amylose

Food Chemistry

The essentially linear fraction of starch, made of α-1,4-linked glucose units. Typically 20–30% of common starches.

Real-life application

The straight-chain starch behind the firm, separate grains in basmati rice and the hard set of cooled boiled potatoes.

See also: Amylopectin, Retrogradation

Antioxidant

Food Chemistry

A substance that delays oxidative rancidity. Primary antioxidants (BHA, BHT, TBHQ, tocopherols) donate hydrogen to break the radical chain; secondary antioxidants (citric acid, EDTA) chelate pro-oxidant metals.

Real-life application

Added to potato chips, cooking oils and butter — as BHA, BHT or vitamin E — to stop them turning rancid on the shelf.

See also: Rancidity, Peroxide value

Caramelisation

Food Chemistry

Thermal degradation of sugars in the absence of amino groups, producing colour and flavour compounds. It requires much higher temperatures than the Maillard reaction.

Real-life application

What gives roasted onions, seared steak crust and toffee their brown colour and flavour — distinct from the browning caused by a Maillard reaction.

See also: Maillard reaction

Casein

Food Chemistry

The main phosphoprotein of milk, about 80% of milk protein, existing as micelles stabilised by κ-casein. Precipitates at pH 4.6 or on rennet action.

Real-life application

The protein that curdles when lemon juice is added to hot milk to make paneer or cheese; also why milk clots when it reaches an acidic stomach.

See also: Isoelectric point, Whey protein

Degree of esterification DE

Food Chemistry

The percentage of galacturonic acid carboxyl groups in pectin that are methyl-esterified.

Real-life application

Determines whether a fruit jam needs added sugar and acid to set (high-ester pectin) or can be made as a low-sugar spread (low-ester pectin).

See also: Pectin

Denaturation

Food Chemistry

Loss of a protein's secondary, tertiary and quaternary structure without breaking peptide bonds, caused by heat, pH change, salts, solvents or shear.

Real-life application

Why an egg turns solid when fried or boiled, and why milk proteins clump together if boiled with lemon juice.

See also: Isoelectric point, Protein coagulation

Emulsifier

Food Chemistry

A surface-active molecule with hydrophilic and lipophilic regions that lowers interfacial tension and stabilises an emulsion.

Real-life application

What keeps mayonnaise, ice cream and chocolate from separating into oil and water layers while sitting on a shelf.

See also: Emulsion, HLB

Emulsion

Food Chemistry

A dispersion of one immiscible liquid in another, stabilised by an emulsifier. Oil-in-water as in milk and mayonnaise, or water-in-oil as in butter and margarine.

Real-life application

Milk, mayonnaise, butter and salad dressings are everyday examples — mixtures of oil and water that would otherwise separate.

See also: Emulsifier, HLB, Homogenisation

Enzymatic browning

Food Chemistry

Browning catalysed by polyphenol oxidase, which oxidises phenolic compounds to quinones that polymerise into brown melanins. It requires oxygen, the enzyme, and a phenolic substrate.

Real-life application

Why a cut apple or potato turns brown within minutes, and why a squeeze of lemon juice slows it down.

See also: Polyphenol oxidase, Blanching, Maillard reaction

HLB Hydrophilic-Lipophilic Balance

Food Chemistry

A number from 0 to 20 describing an emulsifier's relative affinity for water and oil.

Real-life application

Used by food formulators to pick the right emulsifier for a product — a low-HLB emulsifier suits butter-type spreads, a high-HLB one suits salad dressings.

See also: Emulsifier, Emulsion

Hydrogenation

Food Chemistry

Addition of hydrogen across double bonds of unsaturated fatty acids using a nickel catalyst, raising melting point and oxidative stability.

Real-life application

What turns liquid vegetable oil into solid vanaspati or margarine — and why health advisories now warn about the trans fat it can create.

See also: Trans fat, Iodine value

Invert sugar

Food Chemistry

The equimolar mixture of glucose and fructose produced by hydrolysing sucrose, so called because the optical rotation inverts from positive to negative.

Real-life application

Used in commercial baking and sweet-making, including Indian mithai syrups, to stop sugar crystals forming and keep the product moist.

See also: Reducing sugar

Isoelectric point pI

Food Chemistry

The pH at which a protein carries no net electrical charge, so electrostatic repulsion between molecules is minimal.

Real-life application

Why paneer and cheese are made by adjusting milk's acidity — the proteins clump together and separate from the whey at this exact pH.

See also: Denaturation, Casein

Maillard reaction

Food Chemistry

A non-enzymatic browning reaction between a reducing sugar's carbonyl group and a free amino group of an amino acid or protein, producing melanoidin pigments and a wide range of flavour compounds.

Real-life application

What gives bread crust, roasted coffee, fried onions and a seared tandoori chicken their brown colour and flavour — distinct from sugar caramelising on its own.

See also: Caramelisation, Enzymatic browning, Reducing sugar, Acrylamide

Moisture content

Food Chemistry

The total amount of water in a food, expressed on a wet basis (mass of water per mass of wet sample) or dry basis (mass of water per mass of dry solids).

Real-life application

What determines whether a bag of wheat, rice or spice powder is safe to store long-term or will spoil and grow mould.

See also: Water activity

Pectin

Food Chemistry

A structural polysaccharide of plant cell walls based on galacturonic acid. High-methoxyl pectin (DE > 50%) gels with sugar and acid; low-methoxyl pectin gels with calcium.

Real-life application

The setting agent in homemade jam — naturally present in fruits like apple and citrus peel, or added as a powder when a fruit's own pectin is too low.

See also: Degree of esterification, Syneresis

Polyphenol oxidase PPO

Food Chemistry

A copper-containing enzyme responsible for enzymatic browning in cut fruit and vegetables. Optimum pH is around 6–7 and it is largely inactivated above about 80 °C.

Real-life application

The enzyme responsible for cut apples, bananas and potatoes turning brown — the same reaction as enzymatic browning, named for the enzyme that drives it.

See also: Enzymatic browning, Blanching

Protein coagulation

Food Chemistry

The aggregation of denatured protein molecules into an insoluble network, following denaturation and driven by newly exposed hydrophobic groups.

Real-life application

Why beating and heating egg whites turns a runny liquid into a firm meringue or omelette.

See also: Denaturation, Isoelectric point, Casein

Rancidity

Food Chemistry

Deterioration of fats producing off-flavours. Hydrolytic rancidity releases free fatty acids by lipase or water; oxidative rancidity is a free-radical chain reaction with oxygen at unsaturated bonds.

Real-life application

The “off” smell and taste in old cooking oil, stale namkeen or biscuits made with old ghee — caused by fat breaking down over time.

See also: Peroxide value, Antioxidant, Free fatty acid

Reducing sugar

Food Chemistry

A sugar with a free aldehyde or ketone group that can act as a reducing agent — glucose, fructose, lactose and maltose are reducing sugars. Sucrose is not, because both anomeric carbons are involved in the glycosidic bond.

Real-life application

Involved in the Maillard browning of bread crust and biscuits, and the basis of the test strips used to check sugar levels in some quality labs.

See also: Maillard reaction, Invert sugar

Retrogradation

Food Chemistry

The re-association of gelatinised starch chains, mainly amylose, into an ordered crystalline structure during cooling and storage, expelling water (syneresis).

Real-life application

Why rice and bread go hard and stale in the fridge faster than at room temperature — the starch re-crystallises as it cools.

See also: Starch gelatinisation, Syneresis, Amylose

Starch gelatinisation

Food Chemistry

The irreversible swelling of starch granules when heated in water above a characteristic temperature, in which the crystalline structure is lost, amylose leaches out and viscosity rises sharply.

Real-life application

Why raw rice and raw atta dough have to be cooked with water and heat before becoming soft rice or roti — the starch granules swell and burst.

See also: Retrogradation, Amylose, Amylopectin

Water activity aw

Food Chemistry

The ratio of the vapour pressure of water in a food to the vapour pressure of pure water at the same temperature. It measures how much water is available for microbial growth and chemical reactions — not how much water is present.

Real-life application

Why honey and jam don't need refrigeration despite containing a lot of water, while fresh bread does — bacteria and mould need “available” water, not just any water.

See also: Moisture content, Hurdle technology, Water sorption isotherm

Whey protein

Food Chemistry

The soluble milk proteins remaining after casein removal — chiefly β-lactoglobulin and α-lactalbumin. Heat-labile but acid-stable.

Real-life application

The liquid left over from making paneer or cheese, now sold separately as a popular protein supplement powder in gyms and nutrition stores.

See also: Casein, Denaturation

Know the terms? Put them to the test.

Definitions only get you so far. The free General Aptitude test shows you how you handle the real thing under a clock.

Start the free test