Method for analyzing degree of sugar-based oxidation of fish eggs through in-vitro model
A technology of oxidation degree and fish meat protein, which is applied in the direction of material inspection, food testing, etc., can solve problems such as multi-factor interference
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0054] To compare the degree of protein oxidation of sturgeon meat during vacuum low heat processing and atmospheric pressure low heat processing.
[0055] (1) Construction of in vitro model device
[0056] Use a constant temperature water bath, circulation pump, electric stirrer, three-necked flask, catheter, etc. to set up such as figure 1 device shown. The feeding pipe goes deep below the liquid level in the bottle, and the circulating pump conduit is higher than the liquid level in the bottle.
[0057] (2) Preparation of myofibrillar protein precipitate
[0058] 10 g of fish samples were defatted, chopped, put into a beater, added 100 mL of 50 mmol / L phosphate buffer (pH=7.0) containing 0.1 mol / L NaCl, beat and crushed for 1 min in an ice bath, and centrifuged at 8000 g for 10 min (4 ℃), remove the supernatant, wash twice to remove water-soluble protein; add 200mL 50mmol / L phosphate buffer (pH=7.0) containing 0.6mol / L NaCl and mix with the precipitate, extract at 4℃ for 1...
Embodiment 2
[0065] Analysis of protein glycosylation and anti-oxidation in sturgeon meat during vacuum low heat process.
[0066] (1) Construction of in vitro model device
[0067] Use a constant temperature water bath, circulation pump, electric stirrer, three-necked flask, catheter, etc. to set up such as figure 1 device shown. The feeding pipe goes deep below the liquid level in the bottle, and the circulating pump conduit is higher than the liquid level in the bottle.
[0068] (2) Preparation of myofibrillar protein freeze-dried powder
[0069] Remove the fat from 10g fish sample, chop it, put it into a beater, add 100mL of 50 mmol / L phosphate buffer (pH=7.0), beat and crush it in an ice bath for 1min, centrifuge at 8000g for 10min (4°C), and remove the supernatant , repeated washing 4 times to remove water-soluble protein; add 200mL 50mmol / L phosphate buffer (pH=7.0) containing 0.6mol / L NaCl and mix well with the precipitate, extract at 4°C for 12h, centrifuge at 8000g for 10min (...
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