There are three expression hosts of Escherichia coli, yeast, and Streptomyces. The following is the development process of expressing proteins in Escherichia coli.
1.Select promoters, tags and vectors (promoters, tags, vectors)
The core R&D personnel have many years of experience in biocatalysis, structural biology and directed evolution, and have published papers in well-known journals such as PNAS, PLoS Pathogens, FEBS J, JMB, JAFC, Biotechnology for Biofuels, etc. We have integrated (semi-) rational design, directed evolution, multi-enzyme fusion and other enzyme engineering methods to change the expression level, thermal stability, substrate specificity and catalytic efficiency of enzymes. At present, it has been applied in many projects for subtances such as coenzyme factor, steviol glycoside RD and psicose.
For in vitro enzyme catalysis, we have independently developed a variety of purification resins and immobilized resins suitable for mass production. Common groups include NTA, IDA, epoxy, amino and composite groups. Different resin substrates can also be screened according to protein properties and reaction conditions.
If substrates and products can enter and exit cells freely and are not easily degraded by hybrid enzymes, whole-cell catalysis is often the better choice.
Based on mature experience, the optimization process of reaction conditions including reaction pH, reaction temperature, metal ions, substrate concentration, enzyme amount, reaction time, whole-cell/enzyme preservation and application can be completed in about 1-3 months.
For in vitro enzyme catalysis, we have independently developed a variety of purification resins and immobilized resins suitable for mass production. Common groups include NTA, IDA, epoxy, amino and composite groups. Different resin substrates can also be screened according to protein properties and reaction conditions.
If substrates and products can enter and exit cells freely and are not easily degraded by hybrid enzymes, whole-cell catalysis is often the better choice.