Minimized Byproduct Formation
Knockouts ensure high selectivity for SA production, leading to a much higher yield and purity.
Succinic Acid (SA) is a crucial platform chemical used in the synthesis of polymers, resins, biodegradable plastics, and pharmaceutical intermediates. Traditional production via petrochemical synthesis requires high energy consumption and relies on non-renewable feedstocks. While microbial fermentation offers a sustainable alternative, it is often plagued by many by-products (such as acetic acid, lactic acid, and ethanol), which reduce the yield and increase the cost of purification.
CD Biosynsis offers a synthetic biology service focused on enhancing the microbial production of SA. Our core strategy involves modification of the metabolic pathway of Actinobacillus succinogenes , a high-potential native SA producer, to eliminate competing pathways and maximize carbon flux towards SA. This is combined with the optimization of anaerobic fermentation conditions (e.g., pH control, CO2 concentration, and nutrient feeding) to ensure the engineered strain performs robustly and achieves high titer and yield. This integrated approach aims to deliver a high-purity, sustainable, and cost-effective bioproduction route for this vital chemical.
Get a QuoteAchieving cost-competitive and high-yield Succinic Acid production through fermentation faces these major hurdles:
A cost-effective solution must eliminate by-product formation and maximize the specific production rate.
CD Biosynsis utilizes advanced metabolic engineering to optimize Succinic Acid production in A. succinogenes :
Modification of Metabolic Pathway of Actinobacillus succinogenes
We employ genome editing to knock out competing pathways (e.g., genes for lactate, acetate, and ethanol production) to dedicate carbon flux exclusively to SA synthesis.
Optimization of Anaerobic Fermentation Conditions
We tailor the fermentation parameters, including pH and CO2 sparging rates , to maintain optimal SA production while mitigating cell stress and ensuring high CO2 fixation.
Enhancement of CO2 Fixation and NAD(H) Balance
We engineer the strain to overexpress key CO2 fixing enzymes (PEP carboxykinase) and ensure a balanced NADH supply required for the final SA reduction steps.
Tolerance and Excretion Improvement
We explore engineering the cell membrane or overexpressing membrane transporters to improve the cell's tolerance to SA and facilitate product excretion.
This systematic approach is focused on overcoming internal metabolic flux diversion and ensuring robust performance under high-titer conditions.
Our Succinic Acid engineering service is dedicated to pursuing the following production goals:
Minimized Byproduct Formation
Knockouts ensure high selectivity for SA production, leading to a much higher yield and purity.
High Carbon Efficiency and CO2 Utilization
Optimized pathways ensure efficient use of feedstock and consume CO2 as a reactant , contributing to environmental sustainability.
Reduced Purification Costs
High purity crude broth resulting from byproduct elimination simplifies downstream processing and lowers costs significantly. [Image of Cost Reduction Icon]
Renewable Feedstock Use
Fermentation utilizes low-cost sugars (glucose, xylose) as feedstock, decoupling production from fossil fuel prices .
Robust Anaerobic Performance
The engineered A. succinogenes is designed to maintain high viability and productivity under industrial anaerobic conditions.
We provide an integrated platform aimed at maximizing the quality and cost-effectiveness of sustainable Succinic Acid production.
Our Succinic Acid strain engineering service follows a standardized, iterative research workflow:
Technical communication is maintained throughout the process, focusing on timely feedback regarding purity and yield.
Explore the potential for a high-purity, sustainable Succinic Acid supply. CD Biosynsis provides customized strain engineering solutions:
Why is Succinic Acid considered a platform chemical?
It is classified as one of the top 12 building block chemicals by the DOE because it can be readily converted into a wide variety of valuable downstream products , including 1,4-butanediol, THF, and biodegradable polymers.
How does byproduct formation increase purification costs?
Removing chemically similar byproducts like acetic acid and lactic acid from the SA solution requires complex and energy-intensive separation steps (e.g., fractional crystallization, solvent extraction, chromatography), which greatly increases the overall manufacturing cost.
Why is Actinobacillus succinogenes a preferred host?
A. succinogenes is a highly robust, native SA producer known for its ability to utilize a wide range of carbon sources and achieve high SA titers and yields under anaerobic conditions, making it an excellent industrial starting point.
What is the role of CO2 fixation in SA production?
SA synthesis requires the carboxylation of PEP (Phosphoenolpyruvate) using CO2 as a reactant. This step not only increases the final carbon yield but also helps balance the cell's NADH}/\text{NAD ratio, which is essential for anaerobic growth.
What is the estimated project timeline?
A project involving dedicated metabolic pathway engineering (multiple gene modifications) and fermentation optimization typically requires 22-26 weeks for final strain delivery and comprehensive performance validation.
CRISPR-Cas9 technology represents a transformative advancement in gene editing techniques. The main function of the system is to precisely cut DNA sequences by combining guide RNA (gRNA) with the Cas9 protein. This technology became a mainstream genome editing tool quickly after its 2012 introduction because of its efficient, simple and low-cost nature.
The CRISPR gene editing system with its Cas9 version stands as a vital instrument for current biological research. CRISPR technology enables gene knockout (KO) through permanent gene expression blockage achieved by sequence disruption. Various scientific domains including disease modeling and drug screening employ this technology to study gene functions. CRISPR KO technology demonstrates high efficiency and precision but requires confirmation and verification post-implementation because unsatisfactory editing may produce off-target effects or incomplete gene knockouts which impact experimental result reliability. For precise and efficient Gene Editing Services - CD Biosynsis, Biosynsis offers comprehensive solutions tailored to your research needs.
The CRISPR-Cas9 knockout cell line was developed using CRISPR/Cas9 gene editing to allow scientists to remove genes accurately for research on gene function and disease models and pharmaceutical discovery. Genetic research considers this technology essential due to its high efficiency together with simple operation and broad usability.
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CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.