Food Additives E Codes

Food Additive E1105 Lysozyme

A scientific review of E1105 lysozyme, covering egg-white enzyme identity, peptidoglycan hydrolysis, cheese and wine use, Gram-positive control, dose, residual allergen risk and labelling.

Food Additive E1105 Lysozyme
Technical review by FSTDESKLast reviewed: May 14, 2026. Rewritten as a specific technical review using the sources listed below.

Additive E1105 Lysozyme technical scope

E1105 lysozyme is a protein enzyme, most commonly obtained from hen egg white, that hydrolyses beta-1,4 glycosidic bonds in bacterial peptidoglycan. This weakens the cell wall and can lyse susceptible bacteria. The mechanism explains both the value and the limitation of the additive. Lysozyme is most effective against many Gram-positive organisms, while the outer membrane of Gram-negative bacteria often protects them unless other hurdles or treatments increase access. A food manufacturer should therefore not describe lysozyme as a broad universal preservative. It is a targeted antimicrobial enzyme.

The food-additive file must identify source, activity, carrier, allergen origin and intended use. EFSA opinions on hen-egg lysozyme treat it as a food enzyme and emphasize intended processes such as cheese, brewing, wine and vinegar production. The source is central because egg lysozyme is a known allergen. Safety for the general population does not remove the need to protect egg-allergic consumers through correct labelling and residual-risk evaluation.

Additive E1105 Lysozyme mechanism and product variables

In cheese, lysozyme is used mainly to inhibit unwanted Gram-positive bacteria such as Clostridium tyrobutyricum, which can contribute to late blowing and gas defects in hard and semi-hard cheeses. It can reduce spoilage risk without replacing milk quality, hygiene, starter control and ripening management. Dose should be validated in the cheese type because pH, salt, moisture, fat, ripening time and microbial ecology change enzyme performance.

In wine, lysozyme can control lactic acid bacteria and help manage malolactic fermentation or spoilage. EFSA's wine opinion is important because residual lysozyme was detected in treated wines and could trigger allergic reactions in susceptible individuals. A winery using lysozyme should therefore document dose, addition point, clarification, residual presence where relevant and allergen label decision. The same concept applies to beer, vinegar or other fermented products: antimicrobial purpose and allergen communication must be aligned.

Additive E1105 Lysozyme measurement evidence

Lysozyme activity is affected by pH, ionic strength, temperature, substrate organism and matrix binding. Heat can reduce enzyme activity; proteins, polyphenols or particles can bind or remove active enzyme; salt and pH can alter antimicrobial performance. If lysozyme is added before severe heat treatment, it may lose function. If it is added into a matrix with high phenolic content, it may interact differently than in a simple aqueous system. The plant trial should measure the target microbiological outcome, not only assume activity from the supplier certificate.

Effective use is hurdle-based. Lysozyme may be combined with pH, salt, starter culture, temperature control, packaging, nisin or other antimicrobial strategies depending on the product. The combination must be validated because some hurdles complement lysozyme while others reduce activity. For example, a low pH may support microbial control but can also change protein stability. A cheese or wine trial should include retain samples and microbiological testing through the relevant shelf-life or ripening period.

Additive E1105 Lysozyme failure interpretation

Quality control should include enzyme activity units, source declaration, microbiological quality, storage condition, lot traceability, dose calculation and addition record. Finished-product release should include the target microbiological evidence and allergen labelling review. If an allergen claim or exemption is considered, it should be supported by the applicable regulation and analytical or process evidence. A generic "natural preservative" statement is not enough.

Typical failures include late gas defect despite treatment, over-reliance on lysozyme while hygiene is poor, inactivation during processing, wrong microbial target and missing egg-allergen communication. The corrective action depends on the failure: verify activity, check dose and addition point, identify organisms, review pH and salt, and confirm label compliance. E1105 is a valuable enzyme when the target organism and allergen responsibility are both clearly managed.

Additive E1105 Lysozyme release and change-control limits

Minimum effective use is important because lysozyme is both active and allergenic. Adding more enzyme than needed may not improve safety if the limiting organism is resistant, but it can increase residual allergen exposure. The validation should therefore identify the target organism, the expected reduction or inhibition, and the dose that achieves it under the real pH, salt, temperature and storage conditions. If the target is late blowing in cheese, measure ripening outcome. If the target is lactic acid bacteria in wine, measure residual microbial risk and residual enzyme concern.

Additive E1105 Lysozyme practical production review

Analytical follow-up depends on the product. In cheese, the decisive evidence is microbiological and defect-related: gas formation, spoilage organisms, texture, flavour and ripening condition. In wine, the file may also need residual protein or allergen-related information because consumers drink the product directly. In enzyme-treated products where lysozyme is expected to remain active or residual, the company should not assume that clarification, filtration or aging removes the allergen. The risk assessment should be product-specific.

Lysozyme also needs change control. A switch in supplier, enzyme activity, egg source, carrier, pasteurization step, starter culture, salt level or ripening temperature can change performance. If the product historically relies on E1105 to control a defect, any of these changes should trigger a small verification trial. This prevents the additive from becoming an unexamined inherited ingredient.

Additive E1105 Lysozyme review detail

Operators should know that lysozyme is not a flavour, colour or inactive processing aid in the ordinary sense. It is an active enzyme and an egg-derived material. Wrong storage, wrong addition temperature or wrong batch identification can change both function and allergen control.

Additive E1105 Lysozyme review detail

Food Additive E1105 Lysozyme needs a narrower technical lens in Food Additives E Codes: ingredient identity, process history, analytical method, storage condition and release decision. This is where the article moves from naming the subject to explaining which variable should be controlled, why that variable moves and what would make the evidence unreliable.

This Food Additive E1105 Lysozyme page should help the reader decide what to do next. If unexplained variation, weak release logic, complaint recurrence or poor transfer from trial to production is observed, the strongest response is to confirm the mechanism, protect the lot from premature release and adjust only the variable supported by the evidence.

Additive E1105 Lysozyme: additive-function specification

Food Additive E1105 Lysozyme should be handled through additive identity, purity, legal food category, maximum permitted level, carry-over, matrix compatibility, declaration and technological function. Those words are not filler; they define the evidence that proves whether the product, lot or process is still inside its intended control boundary.

For Food Additive E1105 Lysozyme, the decision boundary is dose approval, label check, market restriction, substitute selection or supplier requalification. The reviewer should trace that boundary to assay, purity statement, formulation dose calculation, finished-product check, label review and matrix performance test, then record why those data are sufficient for this exact product and title.

In Food Additive E1105 Lysozyme, the failure statement should name wrong additive class, excessive dose, weak function, regulatory mismatch, undeclared carry-over or poor compatibility with pH and heat history. The follow-up record should preserve sample point, method condition, lot identity, storage age and corrective action so another reviewer can repeat the conclusion.

FAQ

What does E1105 lysozyme do?

It hydrolyses peptidoglycan in susceptible bacterial cell walls, especially many Gram-positive organisms.

Why is lysozyme an allergen concern?

Commercial food lysozyme is often derived from hen egg white, so residual enzyme may affect egg-allergic consumers.

Sources