Pectinase Enzyme Selective Conversion of Ginsenoside Rb1 to Rd

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Solution Overview

Problem

Conventional methods for producing specific ginseng saponins, such as ginsenoside Rd, result in low yields due to non-specific enzyme activity, requiring large enzyme amounts and additional purification steps, increasing costs and limiting large-scale application.

Innovation Solution

A method using pectinase isolated from Trichoderma reesei to selectively convert ginsenoside Rb1 into ginsenoside Rd, optimizing enzyme specificity and reaction conditions for high-yield production.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional enzymes are used for converting ginsenoside Rb1, then the conversion reaction occurs, but the enzyme shows non-specific activity causing low yield of desired ginsenoside Rd

Engineering Contradiction:
Improveyield of ginsenoside RdVSAvoidspecificity of enzyme conversion
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The patent changes the key parameter of enzyme type from conventional cellulases to pectinase, which has different substrate specificity. This parameter change enables selective conversion of ginsenoside Rb1 to Rd while minimizing non-specific reactions, thereby simultaneously improving both productivity (yield) and manufacturing precision (specificity)

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces a specific enzyme (pectinase) as an intermediary catalyst that mediates the conversion reaction. This intermediary enables selective transformation of ginsenoside Rb1 to Rd through its specific catalytic activity, avoiding the non-specific activity problems of conventional enzymes

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If large amount of enzyme is used to compensate for non-specific activity, then the conversion reaction proceeds, but the cost increases significantly

Engineering Contradiction:
Improveconversion efficiencyVSAvoidamount of enzyme required
Core Design Contradiction:
ProductivityVSQuantity of substance

Solution Approach 1:

The patent changes the enzyme type parameter to pectinase, which has inherent high specificity for the substrate. This eliminates the need to use large amounts of enzyme to compensate for non-specific activity, thereby reducing both the quantity of enzyme required and the associated costs while maintaining high conversion efficiency

Inventive Principle:
Principle #35Parameter changes

3Manufacturing precision

If additional purification steps are performed to isolate desired ginsenoside, then pure product is obtained, but the process complexity and cost increase

Engineering Contradiction:
Improvepurity of ginsenoside RdVSAvoidpurification process complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The patent performs preliminary action by selecting an enzyme with high substrate specificity before the conversion reaction. This preliminary selection of pectinase ensures that the conversion reaction itself produces high purity product with minimal byproducts, thereby eliminating the need for complex additional purification steps and reducing process complexity

Inventive Principle:
Principle #10Preliminary action

4Adaptability or versatility

If non-specific enzyme reaction occurs, then various ginseng saponins are produced, but the desired ginsenoside Rd cannot be obtained in high yield

Engineering Contradiction:
Improverange of ginseng saponins producedVSAvoidyield of specific ginsenoside Rd
Core Design Contradiction:
Adaptability or versatilityVSProductivity

Solution Approach 1:

The patent changes the enzyme specificity parameter by selecting pectinase instead of conventional cellulases. This parameter change restricts the reaction to produce primarily the desired ginsenoside Rd with minimal other saponins, thereby improving the yield of specific ginsenoside Rd while maintaining controlled versatility

Inventive Principle:
Principle #35Parameter changes

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 method achieves high-yield production of ginsenoside Rd with high specificity, reducing costs and simplifying the purification process, enabling larger quantities of desired saponins to be obtained efficiently.

Implementation Method 1

the enzymatic hydrolysis of aqueous mixtures comprising homogenized ginseng roots containing mixtures of saponins with an enzyme composition comprising cellulase from Trichoderma reesei

Methodology Applied
Scientific EffectEnzymatic hydrolysis: Hydrolysis

Implementation Method 2

treating ginsenoside Rb1, obtained from ginseng, with particular enzymes to structurally convert the saponin

Methodology Applied
Scientific EffectEnzyme catalysis: Enzyme

Data Source

PatentEP3351639B1Method for selectively producing ginsenoside rd from saponins of ginseng through enzymatic method
Publication Date: 2020.05.27 AMOREPACIFIC CORP
  • EP3351639B1 patent drawingFigure 1
  • EP3351639B1 patent drawing
  • EP3351639B1 patent drawing

AI summary

The present invention relates to a method for selectively producing ginsenoside Rd, which is originally present in ginseng in a trace amount, from panaxadiol-type saponins of ginseng, and more specifically to a method capable of obtaining a desired target compound, that is, ginsenoside Rd, in high yields, by treating a panaxadiol-type saponin obtained from ginseng, with particular enzymes to structurally convert the saponins.