Clostridium autoethanogenum Bacteria for Ethanol Fermentation

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Solution Overview

Problem

Current microbial fermentation processes for ethanol production from carbon monoxide (CO) gases suffer from inefficiencies, including co-production of acetate, which can lead to greenhouse gas emissions and reduced ethanol yield, especially when CO-containing gases have high CO and low H2 concentrations.

Innovation Solution

A novel biologically pure isolate of bacteria, such as Clostridium autoethanogenum strain LBS1560, capable of anaerobic fermentation of substrates with greater than 65% CO and less than 20% H2 by volume, achieving an ethanol to acetate ratio of at least 1.0 and producing ethanol concentrations up to 3.4 g/L, with enhanced productivity and reduced acetate production.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional yeast-based fermentation processes are used to produce ethanol from carbohydrate feed stocks, then ethanol production is achieved, but the cost is influenced by the value of feed stocks as human food or animal feed and cultivation is not economically sustainable in all geographies

Engineering Contradiction:
Improveethanol production efficiencyVSAvoidcost of carbohydrate feed stocks
Core Design Contradiction:
ProductivityVSQuantity of substance

Solution Approach 1:

The patent changes the carbon source parameter from carbohydrate feed stocks to CO-containing gases, fundamentally altering the substrate type. This allows utilization of industrial waste gases (steel industry, coal gasification, biomass gasification) that are abundant and low-cost, eliminating the economic constraints of traditional crop-based fermentation

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses bacterial fermentation pathways (acetyl-CoA pathway) that replicate the ethanol production capability traditionally associated with yeast, but applies it to a different substrate (CO gases instead of carbohydrates). This copying of the fermentation function on an alternative substrate enables sustainable ethanol production from non-food resources

Inventive Principle:
Principle #26Copying

2Productivity

If micro-organisms are used to convert CO gases into ethanol, then ethanol production from abundant carbon resources is achieved, but acetate is co-produced which reduces ethanol yield and can lead to greenhouse gas emissions

Engineering Contradiction:
Improveethanol production from COVSAvoidacetate co-production and greenhouse gas emissions
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The patent optimizes the gas composition parameters (high CO concentration >65%, low H2 concentration <20%) to favor ethanol production pathways over acetate production. This parameter optimization shifts the metabolic balance toward ethanol, achieving ethanol to acetate ratios of at least 1.0:1, thereby reducing harmful emissions while maintaining productivity

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent converts the previously harmful acetate by-product into a manageable component by optimizing conditions to minimize its formation. The acetate that is produced can be further utilized or disposed of, but the primary strategy is to convert the harmful emission problem into a controlled fermentation outcome with minimal acetate formation through precise gas composition control

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

3Adaptability or versatility

If conventional fermentation processes are used with high CO and low H2 concentrations, then substrate utilization is improved, but ethanol production efficiency decreases due to co-production of acetate

Engineering Contradiction:
Improveability to utilize high CO low H2 substratesVSAvoidethanol production efficiency
Core Design Contradiction:
Adaptability or versatilityVSProductivity

Solution Approach 1:

The patent identifies and optimizes specific parameter ranges for gas composition (CO >65%, H2 <20%) that simultaneously enable both substrate utilization and high ethanol productivity. This parameter optimization resolves the contradiction by finding the sweet spot where high CO tolerance does not compromise ethanol yield

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs dynamic control of fermentation conditions, including pH control (maintaining pH 5.0-6.5), temperature control (30-40°C), and gas flow rate optimization, to adapt the fermentation process to the specific substrate composition. This dynamic adjustment ensures high ethanol production efficiency even when utilizing substrates with varying CO and H2 concentrations

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

The bacteria efficiently convert CO-rich substrates into ethanol with improved ethanol to acetate ratios and productivity, reducing waste and greenhouse gas emissions, and can operate in the absence of H2, making the process more sustainable and economically viable.

Implementation Method 1

A novel biologically pure isolate of bacteria, such as Clostridium autoethanogenum strain LBS1560, capable of anaerobic fermentation of substrates with greater than 65% CO and less than 20% H2 by volume

Methodology Applied
Scientific EffectAnaerobic fermentation: Fermentation

Data Source

PatentUS8852918B2Bacteria and methods of use thereof
Publication Date: 2014.10.07 LANZATECH NZ INC
  • US8852918B2 patent drawing
  • US8852918B2 patent drawing

AI summary

A biologically pure isolate of a selected bacterium derived from Clostridium autoethanogenum is described which has improved efficiency in the production of ethanol by anaerobic fermentation of substrates comprising carbon monoxide. The bacterium can produce ethanol and acetate at an ethanol to acetate ratio of at least 1.0 and has a productivity of at least 1.2 g of ethanol/l of fermentation broth per day. The bacterium is also characterized in that it has substantially no ability to sporulate.