Allergen-Free and Vegan Source Icon
Using fungal fermentation eliminates allergy concerns related to shellfish and expands market viability.
Chitin and its derivative, Chitosan, are biocompatible polysaccharides used widely in Medical Textiles/Fibers, water treatment, and drug delivery due to their unique properties. The traditional source faces major drawbacks: Traditional source shellfish is allergenic, non-vegan, and requires harsh chemical deacetylation. This severely limits its purity, sustainability, and applicability in medical fields.
CD Biosynsis offers a revolutionary, non-animal-based biomanufacturing route: Metabolic Engineering: Ferment Aspergillus or Rhizopus fungi that naturally produce chitin in their cell walls. This provides a reliable, non-allergenic, and vegan-friendly source of Chitin. For the conversion step, we employ Enzymatic Deacetylation: Utilize specific microbial Chitin Deacetylase in a mild enzymatic process to produce high-purity Chitosan. This enzymatic process replaces harsh chemical treatment, yielding a consistent, high-purity Chitosan with a precisely controlled degree of deacetylation.
Get a QuoteThe traditional production of Chitosan and Chitin faces these key challenges:
A sustainable solution must transition to a non-animal source and a green, precise conversion method.
CD Biosynsis utilizes fermentation and enzyme technology to achieve superior Chitosan production:
Fungal Chitin Bioproduction
We implement controlled fermentation of specific fungi e.g. Aspergillus or Rhizopus, which naturally produce Chitin in their cell walls, providing an allergen-free and vegan-friendly source.
Precision Enzymatic Deacetylation
We use specific Chitin Deacetylase CDA enzymes produced by engineered microbes e.g. Bacillus subtilis to catalyze Chitin to Chitosan conversion under mild conditions.
Precise DDA Control
By controlling the concentration and reaction time of the Chitin Deacetylase enzyme, we achieve unprecedented, uniform control over the Degree of Deacetylation DDA of the final Chitosan.
Optimized Fungal Harvest
We develop optimized cell lysis and separation protocols e.g. mild acid treatment to efficiently harvest high-purity Chitin from the fungal biomass.
This biological route ensures a safe, high-quality, and highly consistent supply of Chitosan.
Our Chitosan Chitin engineering service is dedicated to pursuing the following production goals:
Allergen-Free and Vegan Source Icon
Using fungal fermentation eliminates allergy concerns related to shellfish and expands market viability.
Green, Enzymatic Conversion Icon
The CDA-based process replaces the need for harsh, corrosive alkali treatment, reducing environmental impact.
Precise DDA Control Icon
Enzymatic deacetylation allows for the precise tuning of the Degree of Deacetylation DDA, ensuring tailored functionality.
High Polymer Purity Icon
The fermentation route yields a cleaner starting material with fewer impurities than shellfish waste.
Consistent Batch Quality Icon
Controlled fungal fermentation provides a consistent feedstock for enzymatic conversion.
We deliver a truly modern, high-quality Chitosan solution for biomedical and high-value applications.
Our Chitosan Chitin 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 high-purity, non-animal-based Chitosan supply. CD Biosynsis provides customized strain and process engineering solutions:
Why is enzymatic deacetylation superior to chemical deacetylation?
Chemical deacetylation uses hot, concentrated sodium hydroxide NaOH, which is corrosive and non-specific, leading to polymer degradation lowering molecular weight and a broad DDA range. Enzymatic deacetylation uses Chitin Deacetylase CDA, which operates under mild conditions e.g. near neutral pH and ambient temperature, preserving the molecular weight and allowing for precise control over the final DDA.
How does the Degree of Deacetylation DDA affect Chitosan functionality?
The DDA is the percentage of amine groups NH}_2$ that are unsubstituted deacetylated on the polymer backbone. This value is critical because it determines the solubility, charge density, and biocompatibility of the Chitosan. For example, high DDA is often required for medical applications like wound dressings due to improved antimicrobial activity.
Why use fungi Aspergillus or Rhizopus as the Chitin source?
These fungi naturally produce Chitin as a structural component of their cell walls, providing a renewable, microbial source. Unlike shellfish, the fungal biomass is non-allergenic, vegan, and can be produced year-round in a controlled fermentation setting, ensuring supply stability and purity.
How is Chitin separated from the fungal biomass?
Chitin is part of the fungal cell wall, along with other polysaccharides and proteins. We use a mild pretreatment protocol involving dilute acid and alkali or enzymatic lysis to selectively remove the other cell wall components, leaving behind a high-purity Chitin fiber for the deacetylation step.
What is the estimated project timeline?
A comprehensive project involving fungal strain optimization, CDA enzyme production, and enzymatic conversion optimization typically requires 30-40 weeks for final Chitosan product delivery and validated protocol.
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.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
|
There is no product in your cart. |
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.