Sustainable Feedstock Utilization Icon
Utilization of crude glycerol and sugar-derived intermediates replaces fossil fuel dependence.
Epoxy Resin Precursors are foundational chemical building blocks for high-performance Coatings/Composites e.g. aerospace materials, protective paints, wind turbine blades. Production challenges stem from the traditional route: they are Traditionally petrochemical-derived Bisphenol A/Epichlorohydrin and the starting materials and products often carry high toxicity and environmental risk. This drives the need for sustainable, bio-based alternatives.
CD Biosynsis offers a two-pronged metabolic engineering strategy to produce bio-based resin precursors: Metabolic Engineering: Biosynthesis of Epichlorohydrin from Glycerol a biodiesel by-product using engineered microbes. Glycerol is a cheap, abundant feedstock. We also focus on developing sustainable Bisphenol A substitutes via Develop bio-based Bisphenol alternatives e.g., from Tyrosine via Phenylpropanoid pathway engineering . This strategy replaces the two primary petrochemical components with non-toxic, bio-based alternatives, significantly reducing environmental and health hazards.
Get a QuoteThe transition to sustainable epoxy resin precursors faces these key hurdles:
A successful solution requires replacing both petrochemical precursors with high-purity, bio-derived alternatives.
CD Biosynsis utilizes comprehensive metabolic engineering to produce bio-based epoxy precursors:
Biosynthesis of Epichlorohydrin
We engineer microbes to efficiently convert crude glycerol through intermediates like 3-chloropropanediol into the Epichlorohydrin ECH precursor in a sustainable process.
Bio-Bisphenol Alternatives
We use phenylpropanoid pathway engineering to synthesize Bisphenol alternatives e.g. Tyrosinol-based compounds from cheap carbon sources or Tyrosine, eliminating the need for toxic BPA.
Multi-Enzyme Cascade Optimization
The biosynthesis of these precursors involves multi-step enzyme cascades . We optimize enzyme expression and balance the flux to ensure high yield and minimal byproduct formation for polymer-grade purity.
Halogenation Pathway Control
For ECH production, we manage the in-vivo halogenation reaction to control product toxicity and maximize the efficiency of the final cyclization to Epichlorohydrin.
This systematic approach replaces the toxic petrochemical value chain with a safe, sustainable bioproduction platform.
Our Epoxy Resin Precursor engineering service is dedicated to pursuing the following production goals:
Sustainable Feedstock Utilization Icon
Utilization of crude glycerol and sugar-derived intermediates replaces fossil fuel dependence.
Eliminate High Toxicity Precursors Icon
Replacement of BPA and petrochemical ECH removes major health and environmental hazards.
High Polymer-Grade Purity Icon
Precision metabolic engineering ensures the final bio-monomer meets the strict purity requirements for polymerization.
Improved Pathway Efficiency Icon
Enzyme and flux optimization leads to high conversion yields of feedstock to bio-precursor product.
Safer Bioprocess Icon
Microbial production operates under mild conditions, reducing the risk associated with hazardous chemical synthesis.
We deliver an innovative and safe platform for next-generation bio-based epoxy resins.
Our Epoxy Resin Precursor engineering service follows a rigorous, multi-stage research workflow:
Technical communication is maintained throughout the process, focusing on timely feedback regarding yield and product quality attributes.
Explore the potential for a sustainable, low-toxicity epoxy resin value chain. CD Biosynsis provides customized strain and process engineering solutions:
Why is Epichlorohydrin ECH biosynthesis important?
Epichlorohydrin is a key monomer for virtually all epoxy resins. Traditional production uses hazardous petrochemicals. Biologically producing ECH from glycerol a readily available biodiesel byproduct offers a route that is both sustainable and safer , avoiding the harsh chemical intermediates and conditions of the traditional process.
How are Bisphenol A BPA alternatives developed?
We use Metabolic Engineering to introduce or enhance pathways e.g. the Phenylpropanoid pathway in microbes to synthesize aromatic compounds structurally similar to BPA but without its toxic endocrine disrupting properties . These compounds, often derived from amino acids like Tyrosine, maintain the necessary reactive sites for polymerization while being bio-based and safer.
How is the multi-step pathway complexity addressed?
We use advanced synthetic biology tools to coordinate the expression of all necessary enzymes. This involves optimizing gene promoters and ribosome binding sites to ensure that the flux through the cascade is balanced , preventing the accumulation of toxic intermediates and ensuring the highest possible yield of the final precursor product.
What is the main challenge in using crude glycerol feedstock?
Crude glycerol is cheap but contains various impurities e.g. methanol, salts, which can inhibit microbial growth and product formation . Our engineering focuses on developing robust strains that can tolerate these impurities and possess highly efficient glycerol uptake and conversion pathways, ensuring the economic benefits of the low-cost feedstock are realized.
What is the estimated project timeline?
A comprehensive project involving two independent pathway engineering efforts ECH and aromatic precursor and fermentation optimization typically requires 30-40 weeks for final strain delivery and validated high-titer bioprocess protocols.
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.