We specialize in bespoke D-tagatose production, leveraging cutting-edge biotechnology and proprietary enzyme engineering to deliver high-purity, cost-effective D-tagatose tailored to your specific industrial or research needs.
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DTEase, a member of the ketose 3-epimerase family, serves as a critical Glycosyl Functional Enzyme in the stereospecific interconversion of rare sugars. This Epimerase exhibits broad substrate specificity, catalyzing the reversible epimerization of ketoses at the C-3 position through a deprotonation-reprotonation mechanism mediated by a conserved histidine residue. Specifically, DTEase enables the efficient interconversion between D-tagatose and D-sorbose, as well as between D-fructose and D-allulose.
Fig.1 Various physiological functions of D-tagatose in the human body.1
Are you currently facing low conversion rates, thermal instability of enzymes, or cost-intensive purification cycles in your rare sugar manufacturing? Our custom DTEase production service helps you obtain high-activity, thermotolerant enzymes and achieve up to 85% conversion rates through our AI-augmented rational design and certified Bacillus subtilis expression platforms. We streamline your path from molecular design to industrial-scale D-allulose and D-tagatose production.
Discover How We Support High-Impact Discoveries
We leverage advanced AI-guided design methods to precisely identify structural "hotspots" in the DTE scaffold. These hotspots are targeted to significantly boost the enzyme's thermotolerance, allowing it to function effectively at higher temperatures, and enhance its substrate affinity for improved binding and conversion efficiency. This focused approach ensures superior enzyme performance for industrial use.
The optimized gene sequence, crafted through extensive genetic engineering and modeling, is synthesized with precision and integrated into high-secretion vectors. These vectors are designed to facilitate efficient extracellular secretion of the enzyme, simplifying downstream processing by reducing the need for complex purification and enhancing overall yield and quality.
Through controlled fed-batch fermentation experiments, we explore the impact of metal ion concentrations and pH buffers on enzymatic activity. By systematically varying these conditions and analyzing the data, we determine the optimal combination that maximizes enzyme activity, ensuring consistent and high-quality production.
To ensure long-term durability and reusability, the DTE enzyme is immobilized on advanced resin supports with high surface area and chemical stability. Rigorous stability testing evaluates the enzyme's half-life and recycling stability over multiple 24-hour cycles, verifying its ability to maintain activity and structural integrity under repeated use for reliable and cost-effective industrial applications.
A 10-liter scale run validates the enzyme's performance in a realistic industrial setting, bridging the gap between lab research and full-scale production. We aim for a conversion rate exceeding 85%, demonstrating high efficiency, and closely monitor product purity to meet stringent quality standards. Successful validation confirms the enzyme's reliability, paving the way for final delivery and commercialization.
Fig.2 DTEase production procedure.
Collaborating to Amplify Your Scientific Impact!
Efficiently converting bulk fructose into D-allulose, providing a 70% sweetness profile with nearly zero calories.
Synthesizing rare sugar backbones used in the development of antiviral agents and specific glycoproteins.
Producing D-tagatose for use in low-glycemic index (GI) products and prebiotic formulations.
Enabling the cost-effective synthesis of rare hexoses that exhibit unique anti-inflammatory or antioxidant properties.
Serving as a primary catalytic component in engineered microbial consortia for complex carbon source utilization.
DTE Facilitation
"Using the custom DTE production service in our research has significantly facilitated our high-density substrate trials. The enzyme's stability at 70°C allowed us to run continuous batches without the usual loss of activity seen with wild-type strains."- 2 weeks ago, Dr. Al*rt M.
Low Endotoxin
"The transition to the certified expression host improved our downstream processing speed by 40%. The lack of endotoxins made our D-tagatose application much safer for food-grade testing."- 6 weeks ago, Prof. Sa*ah L.
A: Off-the-shelf enzymes often lack the thermal stability needed for industrial runs. Our custom service uses AI to "harden" the enzyme for your specific reactor conditions, ensuring longer half-lives and higher cumulative yields.
A: Absolutely. We offer several immobilization options (adsorption, covalent bonding, etc.) to ensure the enzyme can be reused across multiple batches, significantly lowering your COGS.
A: Our engineered DTE variants are designed for high specificity. We provide HPLC data with every batch to verify that side-product formation (like D-glucose or D-fructose residues) is within your required tolerances.
A: Our rational design process includes "pH-shifting" engineering. Please contact our team so we can discuss the specific mutations required to maintain activity at your desired pH range.
We specialize in bespoke D-tagatose production, leveraging cutting-edge biotechnology and proprietary enzyme engineering to deliver high-purity, cost-effective D-tagatose tailored to your specific industrial or research needs.
Our comprehensive glycan and glycoprotein structure and profiling services employ state-of-the-art analytical techniques to provide in-depth insights into the complex carbohydrate structures and their functional roles.
Creative Biolabs provides an end-to-end custom DTEase production service that combines cutting-edge AI protein design with robust industrial fermentation. From increasing conversion rates to 85% to ensuring GRAS-certified safety, we empower your R&D to lead the rare sugar market. For detailed project discussions, technical consultations, or to receive a formal quotation, please reach out to our specialist team.
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