Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Esterase and application thereof

An esterase and reaction technology, applied in the field of industrial microorganisms, can solve problems such as cloning and expression to genes

Active Publication Date: 2016-05-18
卓虹超源生物科技(郑州)有限公司
View PDF1 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It has been reported that Bacillus also has ferulic esterase activity (DetectionofferulicacidesteraseproductionbyBacillusspp.andlactobacilli.ApplMicrobiolBiotechnol, 1998, 50:257-260), but the relevant gene has not been cloned and expressed from Bacillus

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
  • Esterase and application thereof
  • Esterase and application thereof
  • Esterase and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] This example is the cloning of the esterase gene of the present invention and the construction of Escherichia coli engineering bacteria.

[0022] 1. Extraction of BacillusamyloliquefaciensATCC23350DNA

[0023] The Bacillus amyloliquefaciens ATCC23350 bacterial strain was cultivated in LB medium for 12 hours, centrifuged at 12000r / min for 10 minutes to obtain the thallus, and the bacterial genome DNA extraction kit (TaKaRa company) was used to extract the Bacillus amyloliquefaciens ATCC23350 bacterial genome total DNA according to its operation, and put it in the refrigerator for later use.

[0024] 2. Competent preparation of Escherichia coli

[0025] (1) Inoculate E. coli DH5α and BL21(DE3) into 250 mL shake flasks containing 20 mL of LB medium, respectively, and culture overnight at 37° C. and 200 rpm / min.

[0026] (2) Inoculate in 50 mL LB medium according to 1% inoculum amount, and culture at 37°C until OD600 is about 0.6 (about 2-3 hours).

[0027] (3) Transfer t...

Embodiment 2

[0055] This example is the induced expression and separation and purification of the esterase of the present invention.

[0056] 1. Add 500μl recombinant bacteria (BL21 Escherichia coli) solution to a 50ml shake flask. Cultivate at 37°C for 2.5h, and stand at 15°C for 0.5h. Then add 20 μl IPTG, cold induction culture at 15°C for 24h. The fermented broth obtained from fermentation was centrifuged to obtain bacterial cells, the bacterial cells were redissolved in disodium hydrogen phosphate-sodium dihydrogen phosphate buffer solution (20mmol / L, pH7.0), crushed by an ultrasonic breaker, and the supernatant was collected by centrifugation to obtain crude enzyme liquid.

[0057] 2. Use the AKTAavant150 protein purification system to purify the crude enzyme liquid obtained in step 1 with a nickel column. The elution method is: put the four pipelines A1, A2, B1, and B2 into water, and set the flow rate of systemflow to 20ml / min. Exhaust. Then set systemflow1ml / min, flowpath (colum...

Embodiment 3

[0059] This example shows the optimum temperature and temperature stability of the esterase of the present invention. As shown in Table 1, methyl ferulate is used as a substrate, and the substrate and a phosphate buffer solution with a pH of 6.0 are tested in a water bath for 1 h at a temperature of 25-60° C. to determine the enzyme activity of the enzyme. The optimum reaction temperature is 30°C. The esterase of the present invention was treated at 30, 40, 50, and 60°C for 1 hour, and it was found that there was basically no loss of enzyme activity under the conditions of 30 and 40°C. When the temperature reached 50°C, the enzyme activity remained after 1 hour. It was 40% at the beginning, and when the temperature was higher than 60°C, the enzyme was completely inactivated after 2 hours.

[0060] The impact of table 1 temperature on esterase activity

[0061]

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 relates to an esterase gene and the cloning and expression and application thereof and belongs to the field of bioengineering. The substrate characteristic of the esterase gene is disclosed. The esterase is wide in application range and high in industrial application value.

Description

technical field [0001] The invention clones and expresses an esterase, discloses its nucleotide sequence, amino acid sequence, enzymatic property and application, and belongs to the field of industrial microorganisms. Background technique [0002] Ferulic acid esterase (Feruloylesterases, FAEs), also known as cinnamic acid esterase, is a carboxylesterase that can hydrolyze the ester bond in ferulic acid methyl ester, oligosaccharide esterase and polysaccharide ferulic acid ester , an enzyme that releases free ferulic acid. It can cut off the polysaccharide-polysaccharide and polysaccharide-lignin crosslinks in the cell wall, which is beneficial to the degradation of polysaccharides in the cell wall material and the release of lignin, so it has broad application prospects in the food, feed and paper industries. In the food industry, esterase is used to degrade the ferulic acid ester bond in the plant cell wall to obtain free ferulic acid with medicinal value and health care ...

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): C12N9/18C12N15/55
CPCC12N9/18C12Y301/01073Y02P60/87
Inventor 蔡宇杰王小梅陈佳君白亚军郑晓晖
Owner 卓虹超源生物科技(郑州)有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
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