Broad-Spectrum Degradation
Directed evolution yields Azoreductases capable of cleaving diverse Azo dye structures, offering a universal solution for complex effluent.
Azo dyes constitute the largest and most complex class of synthetic colorants used in the textile industry. Their discharge into wastewater poses a significant environmental threat due to their toxicity, color, and resistance to conventional treatment. Biological treatment using Azo Dye-degrading Enzymes, specifically Laccases and Azoreductases, offers a highly selective and environmentally friendly alternative to chemical processes.
We specialize in advanced Enzyme Engineering and Biocatalyst Immobilization to overcome the current limitations. Our core strategy involves directed evolution of Azoreductases to broaden their substrate spectrum and enhance stability in harsh, high-salt wastewater environments. Furthermore, we develop co-immobilization systems that integrate both Laccase (for aromatic ring cleavage) and Azoreductase (for Azo bond cleavage), ensuring efficient, sequential degradation of complex dyes, leading to complete decolorization and detoxification of textile effluent.
Get a QuoteThe enzymatic treatment of textile wastewater faces several key technical and economic constraints:
Commercial success requires robust, low-cost enzymes capable of treating diverse, complex dye compositions under harsh conditions.
We apply advanced Enzyme Engineering and Biocatalyst Development for robust Azo dye degradation:
Directed Evolution of Azoreductases
Engineer Azoreductases using directed evolution to significantly broaden the range of Azo bonds they can cleave and enhance stability in high-salt wastewater.
Sequential Co-Immobilization
Co-immobilize Laccase (for aromatic cleavage) and Azoreductase onto a single support matrix to enable a stable, reusable, and sequential detoxification process.
Enhanced Enzyme Production
Optimize gene expression and host strains (e.g., Pichia, E. coli) for high-yield, low-cost production of the engineered recombinant Laccase and Azoreductase enzymes.
Process Robustness Engineering
Introduce thermostability and pH-stability mutations to ensure the enzymes retain high activity throughout the entire wastewater treatment process.
Our integrated enzyme approach achieves complete decolorization and detoxification simultaneously.
Our Azo Dye-degrading Enzymes Engineering service offers the following key benefits:
Broad-Spectrum Degradation
Directed evolution yields Azoreductases capable of cleaving diverse Azo dye structures, offering a universal solution for complex effluent.
Complete Decolorization and Detoxification
The Laccase/Azoreductase system ensures both the removal of color and the breakdown of toxic aromatic amine byproducts.
Reusable Biocatalyst
Co-immobilized enzymes can be easily recovered and reused over multiple cycles, significantly reducing reagent costs.
High Tolerance to Harsh Conditions
Engineered enzymes retain activity and stability in high-salt and high-temperature industrial wastewater, ensuring reliability.
Green Chemistry Solution
Replaces polluting chemical treatments (e.g., coagulation, oxidation) with a non-toxic, highly specific biological process.
We provide a specialized platform for developing robust, cost-effective enzymatic solutions for textile wastewater treatment.
Our Azo Dye-degrading Enzyme Engineering service follows a rigorous, multi-stage research workflow:
Technical communication is maintained throughout the process, focusing on timely feedback regarding activity and stability.
Explore the potential for a green, effective textile wastewater treatment solution. We provide customized biocatalytic solutions:
What is the difference between Azoreductase and Laccase functions?
Azoreductase cleaves the Azo bond (-N=N-), leading to decolorization and the formation of colorless aromatic amines. Laccase is an oxidase that further breaks down these toxic aromatic amines into non-toxic compounds.
Why is high salinity a problem for enzymes?
High salt concentrations (ionic strength) can disrupt the hydrophobic and electrostatic interactions that maintain the enzyme's complex 3D structure (tertiary structure), leading to denaturation and loss of activity.
How does co-immobilization reduce treatment cost?
Immobilization fixes the enzymes to a solid support, allowing them to be retained within the reactor and reused many times, dramatically reducing the expense of enzyme addition.
What is directed evolution?
Directed evolution is a protein engineering technique that mimics natural selection in a laboratory setting to create mutant enzymes with desired traits (e.g., higher activity or stability) through iterative rounds of mutation, expression, and screening.
What is the estimated project timeline?
A project involving enzyme engineering, directed evolution, and biocatalyst immobilization typically requires 28-36 weeks for final engineered enzyme and validated reactor 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.