Enzyme preparation for bast fiber degumming, and hemp bast degumming technology thereof
An enzyme preparation and bast technology, applied in the field of hemp bast degumming process and enzyme preparation, can solve the problems of large pollution of degumming wastewater, unstable quality, long degumming cycle, etc., and achieve rough culture conditions, wide application range, and processing. cost reduction effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] The strain of the present invention that can produce hemp bast degumming enzyme, the preservation number is CGMCC 14600, named as Dickeya chrysanthemi IBFC 2016, which was preserved in China's common microbial strains on September 08, 2017 Preservation Management Center.
[0033] The screening and identification method of the Dicardia chrysanthemum DC comprises the following steps:
[0034] (1) Sampling and treatment: Take 10 g of the sludge sample from the retting pool, place it in a conical flask with an appropriate amount of glass beads, add 200 mL of sterile water, mix at 180 rpm for 20 min, filter and remove the slag with multi-layer gauze to obtain a suspension.
[0035] (2) Enrichment screening: take 10mL of suspension, 150mL of tap water and 15g of ramie bast, mix them in a conical flask, and ferment at 35°C with shaking at 180rpm until the fibers are dispersed; take 10mL of the fermentation broth, 150mL of tap water, and 15g of cannabis Mix bast, place in coni...
Embodiment 2
[0039] The Dicardia chrysanthemum DC obtained in Example 1 was applied, and on October 12-20, 2016, the preparation of the enzyme preparation and the degumming technology of apocynum apocynum were carried out in the Chinese Academy of Agricultural Sciences' hemp processing enzyme preparation pilot workshop. Process such as figure 1 As shown, the specific steps include:
[0040] (1) Preparation of enzyme preparation:
[0041] S1. Inoculate the DC strain of Dicarpus chrysanthemum into 5mL broth medium for activation, shake or stir culture at 34°C for 10h, then add it to a Erlenmeyer flask containing 200mL sterile broth culture medium, and Stirring culture at 180rpm at 34°C for 7h to obtain bacterial suspension;
[0042] S2. transfer to the fermentor containing aseptic broth medium by 2% inoculum size, stir and ferment with the rotating speed of 180rpm at 34 ℃, and pass into compressed air wherein, compressed air is to containing aseptic broth The flow rate of the culture medi...
Embodiment 3
[0053] The Dicardia chrysanthemum DC obtained in Example 1 was applied, and on December 20-28, 2016, the preparation of enzyme preparations and the degumming of ramie were carried out in Hunan Lierkang Biological Company and Hanshou Ziyang Textile Raw Materials Co., Ltd. technology, the process of which is as figure 1 As shown, the specific steps include:
[0054] (1) Preparation of enzyme preparation:
[0055] S1. Inoculate the DC strain of Dicardia chrysanthemum into 5mL broth medium for activation, shake or stir culture at 34°C for 12h, then add it to a Erlenmeyer flask containing 200mL sterile broth culture medium, and Stirring culture at 200rpm at 34°C for 8h to obtain bacterial suspension;
[0056] S2. transfer to the fermenter containing aseptic broth medium by 2% inoculum size, stir and ferment with the rotating speed of 200rpm at 34 ℃, and pass into compressed air wherein, compressed air is to containing aseptic broth The flow rate of the culture medium is 0.3m 3 ...
PUM
Property | Measurement | Unit |
---|---|---|
height | aaaaa | aaaaa |
height | aaaaa | aaaaa |
height | aaaaa | aaaaa |
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