A Novel Hyaluronic Acid Fusion Enzyme Anti-feedback Inhibition and Its Preparation Method and Enzyme Cutting Process
A hyaluronic acid, feedback inhibition technology, applied in biochemical equipment and methods, enzymes, introduction of foreign genetic material using vectors, etc., can solve the limitation of hyaluronic acid thorough enzyme digestion preparation and production, animal immune source infection, substrate Low affinity and other problems, to achieve the effect of solving the inhibition of enzyme cleavage substrate, improving the efficiency of enzyme cleavage and high expression efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] This embodiment is a preparation method of a novel hyaluronic acid fusion enzyme resistant to feedback inhibition. The novel hyaluronic acid fusion enzyme is obtained by recombining the gene encoding hyaluronan-binding protein and the gene encoding hyaluronan hydrolase into yeast for fusion expression, and the hyaluronic acid-binding protein part can be combined with the substrate hyaluronic acid The specific binding is beneficial to the function of the hyaluronan hydrolase part, solves the problem of the inhibition of the enzyme cleavage substrate existing in the hyaluronidase catalyzed reaction, and significantly improves the enzyme cleavage efficiency.
[0043] In this example, Saccharomyces cerevisiae is used as the host, and the genes of hyaluronan-binding protein and leech hyalurolase are introduced into the host through genetic engineering technology, and the repeated amino acid sequences of 9 glycines and serines (9 GS sequences) are used as Linker Linking bindi...
Embodiment 2
[0055] This example is to investigate the effect of the addition amount of the inducer galactose on the induced expression of the novel hyaluronic acid fusion enzyme. The fusion enzyme gene sequence construction and plasmid recombination were carried out according to the preparation method in Example 1, and the obtained recombinant plasmid was introduced into Saccharomyces cerevisiae, and then inoculated into a 500 mL conical flask containing 50 mL of YPD medium. The speed of the shaker was 200 r / min, and the culture was carried out for 24 hours to obtain the seed solution of the expression bacteria; then the seed solution of the expression bacteria was transferred to a 10L shake flask containing 3L YPD medium according to the volume concentration of 10%, and continued at 32 °C, 200 r / Fermentation was carried out for about 10 hours under the condition of 7 When cells / ml, different concentrations of galactose were added overnight at 30°C to induce the expression of the novel ...
Embodiment 3
[0060] In this example, the enzymatic activity of the novel hyaluronic acid fusion enzyme prepared in Example 1 was detected by the plate diffusion method. The principle of plate diffusion detection of enzyme activity is: using the permeability of agarose plate, the permeated enzyme solution undergoes enzymatic hydrolysis reaction with macromolecular hyaluronic acid in the plate, and using cetylpyridine chloride and macromolecular hyaluronic acid. The non-colored part (hydrolyzed transparent circle) can be visually seen in the color development, so as to judge the enzymatic activity of hyaluronic acid.
[0061] In this example, the novel hyaluronic acid fusion enzyme was introduced into Saccharomyces cerevisiae after the recombinant plasmid constructed by linking the hyaluronic acid-binding protein and the leech hyaluronic acid hydrolase gene according to the preparation method in Example 1, containing 50 mL of YPD In a 500 mL Erlenmeyer flask of culture medium, at a temperatu...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com