Enzyme Engineering and Optimization Services

CD Biosynsis provides integrated Enzyme Engineering and Optimization services, leveraging the convergence of rational design, de novo protein design, and directed evolution to create novel or hyper-functional biocatalysts. Our platform is designed to address the fundamental challenges faced by native enzymes, enabling their transformation into robust, highly selective, and efficient tools suitable for demanding industrial and therapeutic applications. We offer comprehensive solutions that range from generating high-diversity mutant libraries to performing structure-guided amino acid substitutions, ensuring that every project is tackled with the most suitable and cutting-edge methodology for achieving maximized enzyme activity, thermal stability, and substrate specificity.

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Bridging Rational Design and Directed Evolution

Enzyme engineering is a multidisciplinary field focused on improving or altering the functions of natural enzymes for practical utility. Our platform offers a balanced approach, employing Rational Design when structural information is available to precisely guide mutations, and utilizing Directed Evolution when structural guidance is limited, relying on high-throughput screening of massive genetic diversity. For entirely new functions, our De Novo Design capabilities allow us to construct functional proteins from scratch. This integrated strategy ensures that whether you need to subtly adjust stability, drastically alter substrate specificity, or invent a new catalytic capability, we possess the tools and expertise to deliver customized, optimized enzymes for your specific biomanufacturing or therapeutic application.

Integrated Enzyme Engineering Approaches

Rational Design and De Novo Synthesis Directed Evolution and Library Construction Specific Functional Optimization

Structure-Guided Modification and Creation

Rational and De Novo Design

Utilizes computational tools and structural biology data (e.g., crystallography, cryo-EM) to predict and test specific mutations for targeted improvements in function.

In Silico Modeling

Molecular dynamics simulations and docking studies to model enzyme-substrate interactions and identify key residues for mutagenesis, minimizing experimental workload.

De Novo Enzyme Design

Designing enzymes from fundamental principles to catalyze reactions not found in nature, opening new avenues for synthetic chemistry.

Creating and Screening Genetic Diversity

Directed Evolution

Full-cycle evolution from high-diversity library construction (DNA Shuffling, Saturation Mutagenesis) to ultra-high-throughput screening (Phage, Yeast, mRNA Display).

High-Diversity Library Generation

Ensuring maximum coverage of the sequence space using advanced mutagenesis techniques like NNS/NNK codon randomization and gene recombination.

Ultra-High-Throughput Screening

Leveraging automated robotics and display technologies for rapid identification of rare, improved variants from populations up to 10^13.

Targeted Performance Enhancement

Optimization Services

Targeted engineering to improve specific traits, including thermal and solvent stability, pH tolerance, substrate specificity, and enantioselectivity (chiral purity).

Enzyme Cascade Design

Optimization and integration of multi-enzyme systems, addressing cofactor regeneration and intermediate channeling for efficient one-pot synthesis.

Immobilization Engineering

Modifying enzyme surfaces for enhanced linkage to solid supports, improving operational stability and reusability for industrial bioreactors.

The Integrated Enzyme Engineering Process

A multi-strategy approach for high-impact enzyme solutions.

Project Definition and Structural Analysis

Strategy Selection (Rational vs. Directed)

Engineering Execution and Screening

Validation, Delivery, and Iteration

Target Identification: Define the native enzyme's limitations and desired performance goals (e.g., 10X activity increase, 99 percent ee).

Structural & Sequence Analysis: Gather relevant structural data, homology models, and sequence conservation information.

Strategy Selection: Decide on the optimal path: Rational Design (precise, structure-based) or Directed Evolution (blind search, high diversity).

Design/Library Build: Perform CADD modeling for rational variants or generate high-diversity libraries via mutagenesis/shuffling.

Assay Development: Customize HTS assays (e.g., colorimetric, fluorescent, FACS) to precisely measure the desired performance trait.

Screening: Execute HTS or display technology screening on the generated variants to identify top-performing 'hits'.

  • Characterization: Validate selected variants for kinetics, stability, and specificity under industrial conditions.
  • Delivery: Provide final optimized gene sequence, expression vector, and a comprehensive data report.
  • Iteration: Integrate the best mutations into the next engineering round to achieve further gains.

Why Choose Our Enzyme Engineering Platform

Integrated Expertise

           

Seamless combination of computational modeling and ultra-high-throughput experimental screening.

Highest Diversity

           

Access to 10^13 library variants via mRNA Display, ensuring no superior variant is missed.

Custom Screening Assays

           

Ability to develop specialized HTS and FACS assays for complex traits like chemoselectivity or non-natural substrates.

Industrial Ready

           

Enzymes are optimized against real-world industrial parameters, ensuring robustness and scalability.

Client Testimonials on Enzyme Engineering Services

"The combination of rational design and directed evolution yielded a 25-fold increase in our target enzyme's turnover rate, which was critical for process economics."

Dr. Alan Cooper, Biocatalysis Lead

"We struggled to find a lipase with sufficient solvent tolerance. Their comprehensive optimization service delivered a variant stable in 40 percent organic solvent, a game-changer for our synthesis."

Ms. Sofia Perez, Senior Process Chemist

"The De Novo Design service successfully engineered an initial scaffold for a completely novel C-H activation reaction, an area previously considered impossible for biocatalysis."

Prof. Dr. Kenji Tanaka, Principal Investigator

FAQs about Enzyme Engineering and Optimization

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What is the difference between Rational Design and Directed Evolution?

Rational Design is knowledge-driven, relying on structural and biochemical data to predict specific beneficial mutations. Directed Evolution is blind, mimicking natural selection by screening vast numbers of randomly generated mutants to find the best performers.

Which approach is better for optimizing enzyme stability?

Often, a combination is best. Rational design can introduce known stabilizing elements (like disulfide bonds or optimized salt bridges), while directed evolution can find subtle, synergistic mutations that significantly enhance stability.

What is De Novo Enzyme Design used for?

De Novo Design is used to create enzymes from scratch to catalyze non-natural reactions or to serve as highly robust, minimal scaffolds for future engineering, especially when no suitable native enzyme exists.

How do you handle the problem of cofactor dependence in multi-enzyme cascades?

We integrate a dedicated, efficient cofactor regeneration system (e.g., using formate dehydrogenase for NAD(P)H) into the cascade, ensuring the required cofactor is continuously recycled, minimizing input costs.

How much does Metabolic Engineering services cost?

The cost of Metabolic Engineering services depends on the project scope, complexity of the target compound, the host organism chosen, and the required yield optimization. We provide customized quotes after a detailed discussion of your specific research objectives.

Do your engineered strains meet regulatory standards?

We adhere to high quality control standards in all strain construction and optimization processes. While we do not handle final regulatory approval, our detailed documentation and compliance with best laboratory practices ensure your engineered strains are prepared for necessary regulatory filings (e.g., GRAS, FDA).

What to look for when selecting the best gene editing service?

We provide various gene editing services such as CRISPR-sgRNA library generation, stable transformation cell line generation, gene knockout cell line generation, and gene point mutation cell line generation. Users are free to select the type of service that suits their research.

Does gene editing allow customisability?

Yes, we offer very customised gene editing solutions such as AAV vector capsid directed evolution, mRNA vector gene delivery, library creation, promoter evolution and screening, etc.

What is the process for keeping data private and confidential?

We adhere to the data privacy policy completely, and all customer data and experimental data are kept confidential.