Fermented Milk Lactose Reduction via pH-Stable Lactase

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Solution Overview

Problem

Current methods for producing fermented milk products fail to effectively reduce lactose content while maintaining sweetness and texture, and often result in post-acidification issues, which are problematic for lactose-intolerant consumers.

Innovation Solution

A process involving a starter culture with lactose-deficient lactic acid bacteria and a low pH stable lactase, where the lactase is added during or after fermentation to convert lactose into glucose and galactose, reducing lactose content and post-acidification, and enhancing sweetness and texture.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If conventional lactase is used to reduce lactose content, then lactose content is reduced, but the lactase loses activity at low pH during fermentation

Engineering Contradiction:
Improvelactose contentVSAvoidlactase activity stability
Core Design Contradiction:
Quantity of substanceVSReliability

Solution Approach 1:

The patent applies parameter changes by selecting a lactase enzyme with optimized pH stability characteristics. The low pH stable lactase maintains catalytic activity across a broader pH range (pH 3-6), allowing it to function effectively during the acidic fermentation process while converting lactose to glucose and galactose. This parameter optimization resolves the contradiction between lactose reduction and enzyme stability.

Inventive Principle:
Principle #35Parameter changes

2Stability of the object's composition

If lactose-deficient lactic acid bacteria are used, then post-acidification is reduced, but lactose content is not effectively reduced

Engineering Contradiction:
Improvepost-acidification levelVSAvoidlactose content
Core Design Contradiction:
Stability of the object's compositionVSQuantity of substance

Solution Approach 1:

The patent merges two functional components: lactose-deficient lactic acid bacteria (which control post-acidification by metabolizing non-lactose carbohydrates) and low pH stable lactase (which converts lactose to glucose and galactose). This combination allows simultaneous achievement of reduced post-acidification and effective lactose reduction, as each component performs its specialized function without interfering with the other.

Inventive Principle:
Principle #5Merging (Combining)

3Quantity of substance

If fermentation is extended to reduce lactose, then lactose content is reduced, but sweetness is lost due to lactose depletion

Engineering Contradiction:
Improvelactose contentVSAvoidproduct sweetness
Core Design Contradiction:
Quantity of substanceVSEase of manufacture

Solution Approach 1:

The patent replaces the mechanical/biological process of extended fermentation (which depletes all carbohydrates including sweet ones) with an enzymatic system. The low pH stable lactase specifically targets and converts lactose to glucose and galactose, which are sweeter than lactose. This substitution allows lactose reduction while simultaneously enhancing sweetness, as the enzymatic conversion produces sweeter monosaccharides rather than depleting all carbohydrates.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

4Duration of action of stationary object

If non-lactose carbohydrate is added to support lactose-deficient bacteria, then bacterial growth is maintained, but post-acidification increases

Engineering Contradiction:
Improvebacterial growth periodVSAvoidpost-acidification
Core Design Contradiction:
Duration of action of stationary objectVSObject-generated harmful factors

Solution Approach 1:

The patent extracts the lactose metabolism function from the lactic acid bacteria by using lactose-deficient strains that cannot metabolize lactose. Instead, these bacteria metabolize added non-lactose carbohydrates (like glucose or sucrose), while the low pH stable lactase separately handles lactose conversion. This separation allows controlled use of non-lactose carbohydrates for bacterial growth without the bacteria converting them to excessive acid during post-fermentation storage, as the lactase continues to convert remaining lactose independently.

Inventive Principle:
Principle #2Taking out (Extraction)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The process results in fermented milk products with reduced lactose content, increased sweetness, and improved texture, catering to lactose-intolerant consumers while maintaining product quality.

Implementation Method 1

a low pH stable lactase added to the process either at the start, during or at the end of the fermentation step, wherein the low pH stable lactase retains its activity at a pH of 5.0 and a temperature of 37 °C

Methodology Applied
Scientific EffectHydrolysis: Hydrolysis

Implementation Method 2

the starter culture comprises at least one lactose-deficient strain, which is capable of metabolizing a non-lactose carbohydrate

Methodology Applied
Scientific EffectFermentation: Fermentation

Data Source

PatentEP3821712B1Fermented milk product obtained by an improved process
Publication Date: 2022.11.09 KERRY GRP SERVICES INT LTD
  • EP3821712B1 patent drawing
  • EP3821712B1 patent drawing

AI summary

A fermented milk product comprising the starter culture of step 3) and the low pH stable lactase added in step 4) produced by the process comprising the steps of: 1) adding a starter culture comprising at least one lactic acid bacteria strain to a milk base, 2) fermenting the milk for a period of time until a target pH is reached, 3) wherein the starter culture comprises at least one lactose-deficient strain, which is capable of metabolizing a non-lactose carbohydrate, and 4) adding a low pH stable lactase to the process either at the start, during or at the end of the fermentation step, wherein the low pH stable lactase retains its activity at a pH of 5.0 and a temperature of 37°C at a level of at least 5% as compared to its activity at the optimum pH of the lactase.