Partially Hydrolyzed Guar Gum With Low Viscosity and Prebiotic Activity

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Solution Overview

Problem

Existing guar gum products face limitations due to high viscosity and the inability to balance viscosity with bioregulatory activity, making them unsuitable for use in large quantities in food products.

Innovation Solution

A method involving enzymatic hydrolysis of guar gum using β-mannanase, specifically glycosyl hydrolase 5 family enzymes, to produce a partially hydrolyzed guar gum (PHGG) with controlled molecular weights and reduced oligosaccharide content, achieving a balance between viscosity and bioactivity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If guar gum is used as a water-soluble dietary fiber, then prebiotic physiological functions are achieved, but high viscosity limits its use in food products

Engineering Contradiction:
Improveprebiotic physiological functionVSAvoidviscosity
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The guar gum polysaccharide chains are segmented through partial hydrolysis using beta-mannanase, breaking long chains into shorter segments. This reduces molecular weight and viscosity while preserving the prebiotic functional properties of the polysaccharide structure.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The molecular weight parameter of guar gum is changed through controlled enzymatic hydrolysis. By adjusting hydrolysis time, temperature, and enzyme concentration, the viscosity is reduced to an acceptable range while maintaining the prebiotic functionality requiring certain polysaccharide integrity.

Inventive Principle:
Principle #35Parameter changes

2Ease of operation

If guar gum is hydrolyzed to reduce viscosity, then solubility improves, but bioregulatory activity is lost

Engineering Contradiction:
ImprovesolubilityVSAvoidbioregulatory activity
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

Partial hydrolysis is performed rather than complete hydrolysis. The hydrolysis is controlled to achieve only the necessary degree of chain shortening for improved solubility, stopping before the point where bioregulatory activity is compromised. This partial action maintains the balance between solubility and functionality.

Inventive Principle:
Principle #16Partial or excessive action

Solution Approach 2:

The hydrolysis process uses feedback control by monitoring molecular weight reduction and stopping the reaction when optimal solubility is achieved while preserving bioregulatory activity. The process parameters are adjusted based on real-time assessment of polysaccharide chain integrity.

Inventive Principle:
Principle #23Feedback

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 PHGG product maintains low viscosity and high solubility while retaining biological regulatory activities, allowing its use in larger amounts without palatability issues, suitable for various food products and dietary supplements.

Implementation Method 1

performing enzymatic hydrolysis on a guar gum sample using a β-mannanase

Methodology Applied
Scientific EffectEnzymatic hydrolysis: Hydrolysis

Implementation Method 2

β-mannanase may include a glycosyl hydrolase 5 family β-mannanase

Methodology Applied
Scientific EffectEnzyme catalysis: Enzyme

Data Source

PatentUS20260078204A1Composition containing partially hydrolyzed guar gum and method for preparing the same
Publication Date: 2026.03.19 ZYMEBASE INC
  • US20260078204A1 patent drawing
  • US20260078204A1 patent drawing
  • US20260078204A1 patent drawing

AI summary

The present disclosure disclosed a method for preparing a PHGG sample and a composition containing the PHGG sample. The method may include performing enzymatic hydrolysis on a guar gum sample using a β-mannanase to obtain a reaction mixture. The method may also include processing the reaction mixture to obtain the PHGG sample. The PHGG sample may include a plurality of polysaccharides, and more than 70% by weight of the plurality of polysaccharides may have molecular weights higher than 5,000 Daltons. The PHGG sample includes one or more oligosaccharides that have degrees of polymerization (DP) less than or equal to 10, and in the PHGG sample, a mass concentration of the one or more oligosaccharides having DP less than or equal to 10 is less than 3%.