Accelerated Dechlorination Rate
Enhanced RDase activity significantly speeds up the conversion of TCE and the toxic intermediates (DCE, VC) to ethene.
Trichloroethylene (TCE) is a widespread and hazardous groundwater contaminant, often resisting conventional treatment. Bioremediation, specifically reductive dechlorination by specialized anaerobic bacteria (like Dehalococcoides), offers a powerful solution to convert TCE into harmless ethene. However, this process is often slow and relies heavily on expensive, manually injected co-substrates (electron donors).
We provide specialized Genetic and Metabolic Engineering services to optimize TCE degradation. Our core strategy involves enhancing the expression and activity of critical Reductive Dehalogenases (RDases) in robust strains (e.g., Dehalococcoides) to accelerate the complete dechlorination of TCE to ethene. Furthermore, we engineer strains to synthesize their own necessary electron donors (like Lactate) from cheap, simple sugars, significantly reducing the cost and complexity of field application for effective groundwater remediation.
Get a QuoteThe biological remediation of TCE in groundwater faces critical technical and economic barriers:
A successful solution must improve the speed and completeness of the reaction while ensuring a stable, cost-effective supply of electron donors.
We apply advanced Genetic and Metabolic Engineering to create highly effective TCE remediation platforms:
Enhanced RDase Expression and Activity
Engineer strains to highly express and improve the catalytic activity of key Reductive Dehalogenases (RDases) responsible for the complete conversion of TCE to ethene.
In Situ Electron Donor Production
Engineer the TCE degrader or a co-culture helper strain to metabolize cheap, simple sugars and internally produce the necessary electron donors (e.g., Lactate), eliminating external feeding.
Intermediate Toxicity Tolerance
Enhance the strain's tolerance to the toxic intermediates (e.g., Vinyl Chloride, VC) and accelerate the expression of the RDases responsible for their rapid final breakdown.
Genetic Stability and Viability Enhancement
Optimize the strain's core metabolism for robust growth and long-term genetic stability in the nutrient-poor, subsurface environment.
Our systematic strategy ensures complete and rapid TCE degradation with a reduced long-term operational cost.
Our TCE Degraders Engineering service offers the following key benefits for groundwater remediation:
Accelerated Dechlorination Rate
Enhanced RDase activity significantly speeds up the conversion of TCE and the toxic intermediates (DCE, VC) to ethene.
Complete Conversion to Ethene
Engineered strains eliminate the risk of stalling at toxic intermediates (VC), ensuring full, safe remediation.
Reduced Operational Cost
Internal production of electron donors from cheap sugars drastically reduces the long-term cost of co-substrate injection.
Robust Field Performance
Optimized metabolism ensures the viability and colonization ability of the specialized strains in the subsurface environment.
Sustainable Solution
Offers a green, in situ method that permanently detoxifies the groundwater, avoiding mass excavation or pump-and-treat methods.
We provide a specialized platform for robust, highly efficient biological remediation of Trichloroethylene and other chlorinated solvents in groundwater.
Our TCE Degraders Engineering service follows a rigorous, multi-stage research workflow:
Technical communication is maintained throughout the process, focusing on timely feedback regarding dechlorination kinetics and donor utilization efficiency.
Explore the potential for a fast, cost-effective in situ TCE remediation. We provide customized microbial solutions:
What is Reductive Dechlorination?
Reductive dechlorination is an anaerobic process where the microbe uses chlorinated solvents (like TCE) as terminal electron acceptors, replacing chlorine atoms with hydrogen atoms until a harmless product (ethene) is formed.
Why are electron donors necessary?
Electron donors (like Lactate or H2) provide the energy and reducing power that the microbe needs to drive the dechlorination reaction and maintain its own cellular functions under anaerobic conditions.
Why is Vinyl Chloride (VC) stalling dangerous?
VC is highly carcinogenic and significantly more toxic than TCE itself. If the remediation stalls at VC, the treatment is incomplete and creates a greater health hazard, making the final conversion to ethene essential.
How do you engineer a strain to produce its own electron donors?
We introduce or enhance fermentative pathways (e.g., Lactic Acid fermentation) that allow the strain to break down simple sugars (which are cheap to inject) into the necessary electron donors (like Lactate) for internal use or secretion.
What is the estimated project timeline?
A project focusing on enzyme and metabolic pathway engineering typically requires 28-34 weeks for final engineered strain delivery and validated remediation 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.