Surface-Displayed Enzyme Yeast for Lignocellulosic Ethanol Production

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Solution Overview

Problem

Current methods for producing ethanol from lignocellulosic biomass face challenges in achieving high yields with low initial cell concentrations and reduced enzyme usage, often requiring high cell concentrations and large amounts of enzymes, which increase costs and complicate enzyme recovery.

Innovation Solution

A method involving yeast transformed to display enzymes such as endoglucanase, cellobiohydrolase, and β-glucosidase on its surface for hydrolyzing lignocellulosic biomass, combined with finely pulverizing and hydrothermal treatments of biomass, to enhance saccharification efficiency and ethanol production.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Loss of substance

If a small amount of enzyme is used for saccharification, then production cost is reduced, but saccharification efficiency and fermentation yield become significantly poor

Engineering Contradiction:
Improveenzyme usage amountVSAvoidsaccharification efficiency
Core Design Contradiction:
Loss of substanceVSProductivity

Solution Approach 1:

The yeast cell surface itself serves as the enzyme carrier, with cellulase and other hydrolytic enzymes directly anchored on the cell surface. This eliminates the need for separate enzyme addition, as the yeast cells perform saccharification autonomously during fermentation, converting cellulose to glucose and then to ethanol in a self-sufficient manner

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent combines the saccharification function and fermentation function into a single yeast cell system. The yeast cells simultaneously perform cellulose hydrolysis (via surface-anchored enzymes) and ethanol fermentation, merging two previously separate processes into one integrated system that improves efficiency while reducing enzyme requirements

Inventive Principle:
Principle #5Merging (Combining)

2Productivity

If many types of enzymes are expressed at high level on cell surface, then ethanol yield increases, but production cost increases

Engineering Contradiction:
Improveethanol yieldVSAvoidproduction cost
Core Design Contradiction:
ProductivityVSLoss of substance

Solution Approach 1:

The yeast cell surface is engineered to display multiple types of hydrolytic enzymes (cellulase, hemicellulase, pectinase, lignin peroxidase) that can degrade various components of lignocellulosic biomass. This multi-functional enzyme system allows a single yeast strain to process complex biomass substrates efficiently, achieving high ethanol yield from diverse feedstocks without requiring separate enzyme treatments for each component

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

Solution Approach 2:

The patent optimizes enzyme expression levels and cell concentration parameters to achieve cost-effective ethanol production. By controlling the expression level of surface-anchored enzymes and maintaining appropriate cell concentrations, the system achieves high saccharification efficiency and ethanol yield while avoiding the need for excessive enzyme addition or very high cell concentrations that would increase costs

Inventive Principle:
Principle #35Parameter changes

3Quantity of substance

If very high initial cell concentration is used, then cellulase activity on cell surface increases, but ethanol production cost increases

Engineering Contradiction:
Improvecellulase activity on cell surfaceVSAvoidethanol production cost
Core Design Contradiction:
Quantity of substanceVSLoss of substance

Solution Approach 1:

The yeast cells are pre-engineered to have cellulase and other hydrolytic enzymes anchored on their cell surfaces before fermentation begins. This preliminary preparation ensures that when the yeast cells are added to the fermentation system, they immediately possess the necessary enzymatic activity to degrade cellulose, eliminating the need to use very high cell concentrations to achieve sufficient surface cellulase activity

Inventive Principle:
Principle #10Preliminary action

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 allows for efficient ethanol production from lignocellulosic biomass at lower yeast concentrations and reduced enzyme amounts, improving yield and reducing production costs while simplifying enzyme recovery processes.

Implementation Method 1

yeast transformed so as to display an enzyme on the cell surface... the enzyme is an enzyme involved in hydrolysis of the lignocellulosic biomass

Methodology Applied
Scientific EffectEnzyme hydrolysis: Enzyme

Implementation Method 2

endoglucanase, cellobiohydrolase, and β-glucosidase on its surface for hydrolyzing lignocellulosic biomass

Methodology Applied
Scientific EffectCellulose hydrolysis: Hydrolysis

Implementation Method 3

culturing yeast transformed so as to display an enzyme on the cell surface in a medium containing particles of lignocellulosic biomass, thereby producing ethanol

Methodology Applied
Scientific EffectFermentation: Fermentation

Implementation Method 4

combined with finely pulverizing and hydrothermal treatments of biomass

Methodology Applied
Scientific EffectHydrothermal treatment: Heat Treatment

Data Source

PatentUS9816113B2Method for producing ethanol
Publication Date: 2017.11.14 KANSAI CHEM ENG CO LTD
  • US9816113B2 patent drawing
  • US9816113B2 patent drawing
  • US9816113B2 patent drawing

AI summary

Disclosed is a method for producing ethanol, including: culturing yeast transformed so as to display an enzyme on the cell surface in a medium containing particles of lignocellulosic biomass, thereby producing ethanol, wherein the enzyme is an enzyme involved in hydrolysis of the lignocellulosic biomass. The present invention makes it possible to provide a method for producing ethanol by which a high ethanol yield can be achieved from lignocellulosic biomass with lower initial cell concentration and added enzyme amount.