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

Disulfide bond reinforced folding based lipase mutant with high heat stability and construction method thereof

A construction method and lipase technology, applied in the field of enzyme engineering, can solve the problem of low thermal stability

Active Publication Date: 2013-10-16
宁夏夏盛实业集团有限公司
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the lipase produced by the above-mentioned strains has the problem of low thermal stability.

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
  • Disulfide bond reinforced folding based lipase mutant with high heat stability and construction method thereof
  • Disulfide bond reinforced folding based lipase mutant with high heat stability and construction method thereof
  • Disulfide bond reinforced folding based lipase mutant with high heat stability and construction method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] First, through the software SWISS-MODEL ( http: / / swissmodel.expasy.org / ) to establish the structure model of Rhizopus sinensis lipase, and use the software disulfide by design to predict the disulfide bonds that may be generated in the lipase structure. The prediction results indicated that two pairs of disulfide bonds may be formed in the lid hinge region of lipase, which are Phe95Cys / Phe214Cys and Asn84Cys / Gly266Cys respectively. NOTE: The lid of Rhizopus sinensis lipase and its hinge region are 82 GTNS FRSAIT DMVFT 96 , the lid region consists of 6 amino acids, underlined. Combined with the analysis of the structural model of the lipase, it was found that Asn84Cys / Gly266Cys is too close to the lid region, and the analysis may affect the opening of the lid, thereby causing a huge impact on the lipase activity. Therefore, a pair of disulfide bonds Phe95Cys / Phe214Cys, which is also located in the hinge region of the lid, but relatively far away, was selected for ...

Embodiment 2

[0020] The plasmid template pPIC9K-proRCL used in the present invention was constructed for previous studies [Wang Lele, Yu Xiaowei, Xu Yan, Cloning of Rhizopus chinensis leader peptide lipase gene and its expression in Pichia pastoris, High Technology Communications, ( 2009), 19(10):105], containing the lipase gene (proRCL) of Rhizopus chinensis CCTCC M201021. Two cysteine ​​mutations Phe95Cys and Phe214Cys were introduced by overlap extension PCR, and the primers used were as follows:

[0021]

[0022]

[0023] PCR amplification conditions: 94°C for 3min; 94°C for 1min, 55°C for 1min, 72°C for 2min, 30 cycles; 72°C for 10min.

[0024] The amplified sequence was connected with pMD19-T simple, and the competent cells of large intestine were transformed by heat shock method. The positive strains were amplified and cultured, and the E. coli strains containing the plasmid pPIC9K were expanded at the same time. The plasmids were extracted from the two, digested with AvrⅡ a...

Embodiment 3

[0026] After the positive strains were expanded and cultivated, the plasmids were extracted and digested with Sal Ⅰ to make them linear. The total amount was 5-10 μg for electroporation of Pichia pastoris competent. The electrorotator was set to a voltage of 1500V, a capacitance of 25μF, and a resistance of 200Ω. After electroporation, add 1 mL of sorbitol solution, revive at 30°C for 1 h, and spread a YPD plate with a G418 concentration of 0.25 mg / mL. The grown single colony is inoculated with YPD liquid medium and expanded to extract the genome. The genome is used as a template, and RCLF and RCLR are used as primers to carry out PCR reaction. If a band of about 1000bp is obtained, it is determined as a positive Pichia genetically engineered bacterium.

[0027] Embodiment 4: Positive bacterial strain shakes flask fermentation

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

No PUM Login to View More

Abstract

The invention discloses a disulfide bond reinforced folding based lipase mutant with high heat stability and a construction method and application thereof, belonging to the technical field of enzyme engineering. With Rhizopus chinensis CCTCC M201021 lipase as a template, a disulfide bond is introduced into a lip hinge region of lipase, so as to obtain lipase mutant with high heat stability; compared with parent lipase, the lipase mutant has the advantage of improving Tm by 7 DEG C and has a wide application range.

Description

technical field [0001] The invention relates to a lipase mutant with improved thermostability, in particular to a lipase mutant with improved thermostability obtained by using molecular biology techniques, and belongs to the technical field of enzyme engineering. Background technique [0002] Lipase (EC 3.1.1.3) can not only catalyze the hydrolysis of oil, but also catalyze ester synthesis, transesterification, acid hydrolysis and other reactions in the non-aqueous phase. It is widely used in chemistry, food, pharmaceutical and detergent or bioenergy in industry. Microorganisms are an important source of lipase, and Rhizopus is an important producer of microbial lipase. Today, more than 30 Rhizopus lipases have been commercially produced. Most Rhizopus lipases have high 1,3-position selectivity, so they are often used in oil processing. However, oil processing usually needs to be carried out at a relatively high temperature, and Rhizopus lipase is a mesophilic lipase, and...

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 Patents(China)
IPC IPC(8): C12N9/20C12N15/55C12N15/81C12N1/19C12N1/21C12R1/845C12R1/84
Inventor 喻晓蔚徐岩
Owner 宁夏夏盛实业集团有限公司
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