Sustainability Focus
The bio-based route significantly reduces the dependence on fossil fuels and the associated high emissions of petrochemical synthesis.
Acrylic Acid (AA) is a high-volume industrial chemical crucial for producing superabsorbent polymers, coatings, and adhesives. The market is overwhelmingly dominated by petrochemical synthesis, which results in high emissions and significant environmental impact . Furthermore, current bio-based efforts are hampered by incomplete biosynthesis pathways and the toxicity of the product to microbial hosts, leading to low titers.
CD Biosynsis offers a targeted metabolic engineering service to establish a more sustainable production route for acrylic acid. Our approach centers on the reconstruction of a functional metabolic pathway in Pseudomonas putida , leveraging its robustness and ability to utilize diverse feedstocks. This is coupled with the directed evolution of the 3-hydroxypropionate dehydratase (3-HPDH) enzyme , a critical bottleneck, to enhance its activity and stability. We aim to establish a platform that explores high-flux biosynthesis of acrylic acid, offering a sustainable alternative to traditional methods.
Get a QuoteTransitioning acrylic acid production to a biological platform faces several critical technical obstacles:
Addressing these challenges requires a robust host and targeted pathway and enzyme optimization efforts.
CD Biosynsis provides a systematic metabolic engineering approach focused on feasibility and efficiency:
Reconstruction of the Metabolic Pathway in Pseudomonas putida
We establish a complete, high-flux pathway from central metabolism to 3-HP in the robust host P. putida, a microorganism known for its solvent tolerance and high growth rate.
Directed Evolution of 3-Hydroxypropionate Dehydratase
We employ directed evolution and saturation mutagenesis to screen for 3-HPDH variants with enhanced catalytic turnover and improved thermal resilience , aiming to relieve the pathway bottleneck.
Host Tolerance Engineering
We explore techniques to modify the host cell envelope and efflux pumps, aiming to increase the host's tolerance to the inherently toxic acrylic acid product.
Dynamic Pathway Control
We implement dynamic gene expression systems (e.g., biosensors) that aim to balance cell growth and production phase , potentially mitigating the toxicity effects during accumulation.
Our systematic approach explores the potential for more efficient and sustainable acrylic acid bioproduction.
Our acrylic acid engineering service is committed to achieving the following value proposition:
Sustainability Focus
The bio-based route significantly reduces the dependence on fossil fuels and the associated high emissions of petrochemical synthesis.
Enhanced Pathway Efficiency
Directed evolution aims to reduce the 3-HPDH bottleneck, potentially leading to a more rapid conversion of the precursor ( 3-HP ).
Robust Host Performance
P. putida is a naturally resilient host, offering potential advantages in tolerance and industrial scale-up compared to standard hosts like E. coli.
Customized Strain Design
All pathway and enzyme modifications are tailored, representing a focused attempt to address specific efficiency bottlenecks for clients.
Process Optimization Potential
The engineered system offers a potential platform for advanced fermentation strategies to maximize final productivity under toxic conditions.
We provide a biosynthetic platform aimed at transitioning toward sustainable acrylic acid production.
Our Acrylic Acid strain engineering service follows a standardized, investigative research workflow:
Technical communication is maintained throughout the process, focusing on timely feedback regarding efficiency and feasibility milestones.
Explore the potential for sustainable acrylic acid production. CD Biosynsis provides customized strain engineering solutions:
Why is acrylic acid production generally considered challenging?
Acrylic acid is highly reactive and chemically toxic to most microbial cells. This toxicity severely limits the maximum concentration (titer) that can be achieved in a fermentation batch, making it difficult to achieve industrial yields comparable to petrochemical processes.
What is the role of 3-hydroxypropionate dehydratase (3-HPDH)?
3-HPDH catalyzes the crucial final step: the dehydration of the precursor 3-HP to acrylic acid. It is frequently the rate-limiting enzyme in the pathway, meaning its activity and stability largely determine the overall pathway flux.
Why choose Pseudomonas putida for this challenging synthesis?
P. putida is naturally tolerant to solvents and various inhibitory compounds , making it a more resilient host for the production of toxic chemicals like acrylic acid, compared to sensitive organisms like E. coli or yeast.
How do you address the instability of 3-HPDH?
We use directed evolution , which is a powerful screening methodology. By introducing controlled mutations and selecting the best variants, we aim to discover enzyme structures that exhibit higher intrinsic stability and catalytic rate under industrial conditions.
What is the expected project timeline?
A project involving pathway construction, complex directed evolution of a rate-limiting enzyme, and toxicity engineering typically requires 22-26 weeks for final strain delivery and initial performance assessment.
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.