Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Recombinant histolytic clostridium type II collagenase, preparation method and application thereof

A technology of Clostridium histolyticum and collagenase, which is applied in the field of bioengineering, can solve the problems of complex refolding process, high technical difficulty, and high production cost, and achieve the effects of purification, soluble expression, and increased yield

Pending Publication Date: 2021-06-11
重庆科润生物医药研发有限公司
View PDF11 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The renaturation process of inclusion bodies is complex, technically difficult, low in yield, and high in production cost, so it cannot be applied to industrial production at present

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Recombinant histolytic clostridium type II collagenase, preparation method and application thereof
  • Recombinant histolytic clostridium type II collagenase, preparation method and application thereof
  • Recombinant histolytic clostridium type II collagenase, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Example 1 Construction of Recombinant Clostridium histolytica Type II Collagenase Fusion Protein Engineering Bacteria

[0046] 1. Construction of pET30-a(+)-ColH / BL21(DE3) engineering bacteria

[0047] The mature protein of Clostridium histolyticum type II collagenase contains 991 amino acids, and the sequence of the Clostridium histolyticum type II collagenase gene is shown in SEQ ID NO.1.

[0048] The tag protein is selected from Fasciola hepatica calcium-binding protein Fh8 (GenBank accession number: AAF31420.1); the amino acid sequence of the tag protein protein is shown in SEQ ID NO.2, and its nucleotide sequence is shown in SEQ ID NO. 3.

[0049] The linker sequence was designed as SEQ ID NO: 7-GSGSGHMHHHHHHSSGPDLDDDDK-, and the C-terminus of the above-mentioned Fh8 tagged protein was connected to the N-terminus of the mature protein sequence of Clostridium histolyticum type II collagenase through the linker. The amino acid sequence of the obtained fusion protein...

Embodiment 2

[0055] Example 2 Fermentation of Recombinant Clostridium histolyticum Type II Collagenase Engineering Bacteria

[0056] Seed liquid activation: transfer 60ul of pET30-a(+)-ColH / BL21(DE3) glycerol tube strain into 100ml 2xYT medium, kan+100ug / ml; culture temperature 33℃, 220r / min, culture for about 12h (OD value 4.5-5.5).

[0057] Fermentation process: use 5L Baoxing fermenter for fermentation, set the temperature at 37°C, ventilate at 3vvm, insert 4ml of trace elements, kan+0.06g sterile filter, then insert into the fermenter pH7.0; take LB culture medium stored at 4°C The prepared seeds are inoculated into 2L of fermentation medium (M9 improved medium) according to the proportion of 5% (100ml); the initial speed is 300rpm, start the speed dissolved oxygen linkage, the dissolved oxygen value is set to 30%, and the speed is increased to 600r / min, the dissolved oxygen value is set to 15%, and the speed is increased to 800r / min. At this time, the ventilation volume is adjusted ...

Embodiment 3

[0058] Example 3 Separation and Purification of Recombinant Clostridium Histolyticum Type II Collagenase

[0059] 1. Bacterial crushing and clarification

[0060] The bacteria were collected by high-speed freezing and centrifugation, and the bacteria were suspended according to the ratio of 1:10 (1g:10ml buffer: 20mM Tris-HClpH7.6). Break the bacteria 3 times, then refrigerate and centrifuge at high speed, collect the supernatant, and discard the precipitate; use a 0.65 μm hollow fiber column to clarify the bacteriostasis solution by ultrafiltration.

[0061] 2. Ni 2+ Chelation chromatography

[0062] Use equilibration buffer 25mM Tris-HCl pH8.0, equilibrate the chromatography column, load the bacteriostasis solution, then use elution buffer 25mM Tris-HCl pH8.0 10mM imidazole to elute impurity protein; use elution buffer 25mM Tris-HCl pH8 .0 50mM imidazole to elute the fusion protein of interest.

[0063] 3. Enterokinase enzymolysis

[0064] In the above fusion protein so...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
purityaaaaaaaaaa
Login to View More

Abstract

The invention discloses and provides a recombinant histolytic clostridium type II collagenase. The recombinant histolytic clostridium type II collagenase comprises a histolytic clostridium type II collagenase and a tag protein connected to an N end of the histolytic clostridium type II collagenase, the tag protein comprises fasciola hepatica calcium binding protein (Fh8); preferably, the amino acid sequence of the fasciola hepatica calcium binding protein is SEQ ID NO: 2. The invention also provides an expression vector and recombinant engineering bacteria for expressing the recombinant clostridium histolyticum type II collagenase, and also provides a preparation method of the clostridium histolyticum type II collagenase. The recombinant clostridium histolyticum type II collagenase can be efficiently expressed, does not form inclusion bodies, is easy to separate and purify, and is beneficial to industrial production of the clostridium histolyticum type II collagenase.

Description

technical field [0001] The invention relates to the field of bioengineering, in particular to a high-purity recombinant Clostridium histolyticum type II collagenase and its preparation method and application. Background technique [0002] Collagenase Clostridium Histolyticum (Collagenase Clostridium Histolyticum) is a drug originally developed by BioSpecifics Technologies Group, which was approved by the US Food and Drug Administration (FDA) on February 2, 2010, and obtained by the European Medicines Agency on February 28, 2011 (EMA) approval, and on July 3, 2015, it was approved for marketing by the Japanese Medicines and Medical Devices Agency (PMDA). product name The products of Auxilium Pharmaceuticals (now Endo Pharmaceuticals, Endo International) are sold in the US market, and by Asahi Kasei (Aasahi Kasei) in the Japanese market. product name The products are sold in the European market by Swedish Orphan Biovitrum (SOBI). In addition, the trade name and produ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12N9/52C07K19/00C12N15/62C12N15/70C12N1/21A61K38/48A61P19/04A61P21/00A61P17/00A61P15/00C12R1/19
CPCC12N9/52C07K14/43559C12N15/70C12Y304/24003A61P19/04A61P21/00A61P17/00A61P15/00C07K2319/00A61K38/00Y02A50/30
Inventor 李树刚张伟龚会英但国平邓永康刘涛程丹凝辛渝杨丹丹于廷和
Owner 重庆科润生物医药研发有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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