Ruminant Enzyme Product Without Amylase for Forage Digestion

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Solution Overview

Problem

Current ruminant enzyme products are inadequate as they often contain amylase, which can lead to glucose deficiency and acidosis in ruminants, and lack a complete enzyme profile including beta-glucanase, pectinase, mannanase, and alpha-galactosidase, limiting the digestibility of forage cell walls and overall energy release.

Innovation Solution

A unique enzyme product combining cellulase, xylanase, beta-glucanase, pectinase, mannanase, and alpha-galactosidase, excluding amylase to enhance fiber digestibility in ruminant diets, with specific activity ranges per gram to optimize energy release and prevent glucose deficiencies.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If amylase is included in ruminant enzyme products, then starch degradation is enhanced, but glucose deficiency and acidosis occur in ruminants

Engineering Contradiction:
Improvestarch degradation efficiencyVSAvoidglucose deficiency and acidosis
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

The patent removes amylase from the enzyme product formulation entirely, extracting the harmful element that causes glucose deficiency and acidosis while retaining beneficial fibrolytic enzymes for fiber digestion enhancement

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent changes the enzyme composition parameters by specifying exact activity ranges for six fibrolytic enzymes (cellulase: 200-800 U/g, xylanase: 750-3000 U/g, beta-glucanase: 225-890 U/g, pectinase: 1-100 U/g, mannanase: 50-800 U/g, alpha-galactosidase: 1-100 U/g) while maintaining zero amylase activity

Inventive Principle:
Principle #35Parameter changes

2Productivity

If a complete enzyme profile including beta-glucanase, pectinase, mannanase, and alpha-galactosidase is provided, then forage cell wall digestibility is improved, but enzyme product complexity increases

Engineering Contradiction:
Improveforage cell wall digestibilityVSAvoidenzyme product composition
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent combines six different fibrolytic enzymes into a single integrated enzyme product formulation, merging multiple functions (cellulose, hemicellulose, pectin, mannan, and galactan degradation) into one comprehensive solution for complete cell wall digestion

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent creates a composite enzyme product containing multiple enzyme types with specific activity ratios, forming a composite catalytic system that addresses all major cell wall components simultaneously through coordinated enzymatic actions

Inventive Principle:
Principle #40Composite materials

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

Significantly improves the digestibility of forage diets, increasing organic matter digestibility and gas production, thereby enhancing animal productivity and health by ensuring adequate energy availability without risking acidosis.

Implementation Method 1

The enzyme product represents a unique combination of several cellulolytic and hemicellulolytic enzymes... cellulase, xylanase, pectinase, beta-glucanase, mannanase and alpha-galactosidase

Methodology Applied
Scientific EffectHydrolysis: Hydrolysis

Data Source

PatentUS8815316B2Enzyme product for ruminants
Publication Date: 2014.08.26 KEMIN IND ZHUHAI
  • US8815316B2 patent drawing
  • US8815316B2 patent drawing
  • US8815316B2 patent drawing

AI summary

A method is described for improving the digestibility of a forage diet for ruminant animals. A forage, including alfalfa, Chinese wildrye, corn silage, straw silage, corn stover, ryegrass or TMR, is treated with an enzyme product having cellulase, xylanase, beta-glucanase, pectinase, mannanase and alpha-galactosidase activities.