Egg Yolk Phosvitin Separation Using Selective HDL Hydrolysis

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Solution Overview

Problem

Current methods for extracting phosvitin from egg yolks are costly, inefficient, and often denature the protein, making it unsuitable for commercial use due to the need for solvents and high amounts of water, which also affect the functional properties of the protein.

Innovation Solution

A method involving controlled enzymatic hydrolysis of high-density lipoprotein (HDL) using proteolytic enzymes like pepsin and acid-stable protease to break the bond with phosvitin, followed by centrifugation and ultrafiltration to isolate phosvitin without solvents or high heat, resulting in a concentrated, salt-free solution.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If salt and heat are used to disrupt phosphocalcic bridges between HDL and phosvitin, then phosvitin is freed from HDL, but the protein structure is denatured and functional properties are lost

Engineering Contradiction:
Improvephosvitin functional propertiesVSAvoidprotein denaturation
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent uses proteolytic enzymes (pepsin and acid-stable protease) as intermediary substances to selectively hydrolyze HDL proteins and disrupt phosphocalcic bridges, replacing direct harsh treatment with a mediated biochemical process that preserves phosvitin structure

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the chemical parameters by controlling pH levels (using acid-stable protease at low pH) and enzyme concentration to selectively target HDL protein hydrolysis while preserving phosvitin integrity, achieving selective disruption without denaturation

Inventive Principle:
Principle #35Parameter changes

2Quantity of substance

If solvents are used to remove lipids from granules, then lipid removal is achieved, but solvent residues make the product unsuitable for food applications

Engineering Contradiction:
Improvelipid removal efficiencyVSAvoidsolvent residue contamination
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The patent extracts and removes lipids from egg yolk granules through differential centrifugation and density gradient centrifugation before protein hydrolysis, physically separating lipid phases without introducing chemical solvents, thus achieving lipid removal while maintaining food safety

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent replaces chemical solvent-based lipid removal with a physical/mechanical separation system using centrifugation and density gradients, achieving the same lipid removal effect through mechanical forces rather than chemical extraction

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

3Manufacturing precision

If large amounts of water are used to dilute and remove salt, then salt is removed from solution, but the process becomes costly and inefficient

Engineering Contradiction:
Improvesalt removal efficiencyVSAvoidextraction efficiency
Core Design Contradiction:
Manufacturing precisionVSProductivity

Solution Approach 1:

The patent extracts and removes salt from the phosvitin solution through ultrafiltration using semi-permeable membranes that selectively allow salt ions to pass through while retaining phosvitin, achieving efficient salt removal without requiring large volumes of water for dilution

Inventive Principle:
Principle #2Taking out (Extraction)

4Reliability

If proteolytic enzymes are used to hydrolyze HDL proteins, then HDL-phosvitin bond is broken, but enzyme cost increases production expense

Engineering Contradiction:
ImproveHDL-phosvitin bond disruptionVSAvoidproduction cost
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent segments the protein hydrolysis process into two stages: first using pepsin to initiate HDL protein hydrolysis and bond disruption, then using acid-stable protease to complete the hydrolysis, allowing optimized enzyme selection and potential process simplification

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent changes operational parameters such as pH, temperature, and enzyme incubation time to optimize enzyme activity and reduce required enzyme quantities, minimizing production costs while achieving complete HDL-phosvitin bond disruption

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

This method allows for the cost-effective production of high-quality phosvitin and HDL-derived products with improved bioavailability and functional properties, reducing mineral depletion risks and enhancing their value as nutritional supplements.

Implementation Method 1

introducing a hydrolysing agent into the egg yolk granules to preferentially partially hydrolyse the HDL protein bound to the phosvitin molecule

Methodology Applied
Scientific EffectHydrolysis: Hydrolysis

Implementation Method 2

centrifuging to separate the precipitate from the supernatant, the supernatant comprising unbound phosvitin, LDL, and peptides

Methodology Applied
Scientific EffectCentrifugal separation: Centrifugal Separation

Implementation Method 3

The supernatant is then subjected to ultrafiltration to separate phosvitin from the solution to produce a concentrated phosvitin product

Methodology Applied
Scientific EffectUltrafiltration: Semipermeable Membrane

Data Source

PatentUS12351608B2Methods of separating phosvitin and HDL from an egg yolk product and resulting compositions
Publication Date: 2025.07.08 ECOVATEC SOLUTIONS INC
  • US12351608B2 patent drawing
  • US12351608B2 patent drawing
  • US12351608B2 patent drawing

AI summary

There is a method of separating phosvitin and HDL proteins from an egg yolk composition. The egg yolk composition includes HDL proteins bound to phosvitin. At least a portion of the HDL proteins are hydrolysed to cause the HDL proteins and phosvitin to become unbound and forming a hydrolysed solution comprising hydrolysed HDL, phosvitin and peptides. The hydrolysed HDL is separated from the phosvitin and peptides to form a separated hydrolysed HDL composition and a separated phosvitin and peptide solution. One resulting product is an egg yolk composition formed having at least 20% solids by mass of phosvitin phosphopeptides unbound from HDL. Another resulting product is an egg yolk composition having at least 80% hydrolysed HDL-derived lipopeptide solids by mass.