Genetically Modified Candida for Hydroxy Fatty Acid Production

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for producing α,ω-hydroxyacids and diacids are limited by harsh chemical reagents, lack of selectivity, and inefficiencies in ricinoleic acid production, which also pose safety concerns due to allergenic compounds and toxic byproducts, while there is a need for a broader range of agro-based hydroxyl fatty acids for various industrial applications.

Innovation Solution

Genetically modified strains of the yeast Candida are used to biocatalytically convert fatty acids into ω-hydroxy fatty acids and α,ω-dicarboxylic acids with additional functional groups, allowing for the production of ricinoleic acid analogs that can be used as monomers for polymer synthesis, offering higher reactivity and broader applicability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If castor oil is used as the primary source of ricinoleic acid, then hydroxyl functional groups are provided for chemical derivatization, but allergenic compounds and toxic byproducts harm workers and create safety concerns

Engineering Contradiction:
Improveavailability of hydroxyl functional groupsVSAvoidallergenic compounds and toxic byproducts
Core Design Contradiction:
Ease of manufactureVSObject-affected harmful factors

Solution Approach 1:

The patent extracts and eliminates the harmful components (allergenic compounds and toxic byproducts) from the castor oil production system by using genetically modified Candida strains that selectively produce hydroxyl functional groups without the associated harmful substances, thereby separating the useful function from the harmful effects

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent introduces genetically modified Candida yeast strains as intermediary biocatalysts that mediate the conversion of fatty acids to hydroxyl functional groups, replacing the direct chemical processing of castor oil and thereby eliminating exposure to harmful compounds while maintaining the desired chemical functionality

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If chemical routes are used to produce ricinoleic acid analogs, then production capacity is achieved, but multiple steps and harsh chemical reagents are required with poor selectivity

Engineering Contradiction:
Improveproduction capacityVSAvoidmultiple process steps and harsh reagents
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent replaces complex chemical synthesis systems with a biological system (genetically modified Candida strains) that performs the same function through enzymatic catalysis, eliminating the need for multiple chemical steps and harsh reagents while maintaining production capacity

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

Solution Approach 2:

The patent changes the fundamental parameters of the production system from chemical to biological, using living cells with engineered metabolic pathways to perform the synthesis, thereby achieving high selectivity and simplified process conditions while maintaining productivity

Inventive Principle:
Principle #35Parameter changes

3Quantity of substance

If ricinoleic acid is produced from castor oil, then high-volume products are obtained, but the spectrum of agro-based hydroxyl fatty acids is limited

Engineering Contradiction:
Improvehigh-volume productionVSAvoidspectrum of hydroxyl fatty acids
Core Design Contradiction:
Quantity of substanceVSAdaptability or versatility

Solution Approach 1:

The patent creates a universal biocatalytic platform using genetically modified Candida strains that can process various fatty acid substrates to produce different hydroxyl fatty acid products, thereby achieving both high-volume production and broad product spectrum from a single system

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The patent introduces dynamic flexibility to the production system by enabling the same biological platform to be adjusted and reconfigured to produce different hydroxyl fatty acid analogs based on the substrate fed to the cells, allowing adaptation to various product requirements while maintaining high-volume production capability

Inventive Principle:
Principle #15Dynamics

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 approach enables the production of ricinoleic acid analogs with high yield and selectivity, suitable for a wide range of industrial applications, including biodegradable polymers and medical materials, under mild reaction conditions without the need for harsh chemicals.

Implementation Method 1

Genetically modified strains of the yeast Candida are used to biocatalytically convert fatty acids into ω-hydroxy fatty acids and α,ω-dicarboxylic acids

Methodology Applied
Scientific EffectBiocatalysis: Enzyme

Implementation Method 2

producing an α-carboxyl-ω-hydroxy fatty acid by fermenting the genetically modified Candida host cell

Methodology Applied
Scientific EffectFermentation: Fermentation

Data Source

PatentUS8158391B2Production of an α-carboxyl-ω-hydroxy fatty acid using a genetically modified Candida strain
Publication Date: 2012.04.17 DNA TWOPOINTO INC
  • US8158391B2 patent drawing
  • US8158391B2 patent drawing
  • US8158391B2 patent drawing

AI summary

A substantially pure Candida host cell for the production of a α-carboxyl-ω-hydroxy fatty acid having a carbon chain length in the range from C6 to C22, a α,ω-dicarboxylic fatty acid having a carbon chain length in the range from C6 to C22, or mixtures thereof, is provided. The Candida host cell is characterized by a first genetic modification class and a second genetic modification class. The first genetic modification class comprises one or more genetic modifications that disrupt the peroxisomal β-oxidation pathway. The second genetic modification class comprises one or more genetic modifications that collectively or individually disrupt at least one gene selected from the group consisting of a CYP52A type cytochrome P450, a fatty alcohol oxidase, and an alcohol dehydrogenase.