Enzyme preparation that can be used for degumming of hemp and its bast degumming process of hemp
An enzyme preparation and bast technology, which is applied in the hemp bast degumming process and the field of enzyme preparations, can solve the problems of large degumming wastewater pollution, unstable quality, long degumming cycle, etc., and achieve short degumming time, rough culture conditions, and easy processing The effect of cost reduction
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Embodiment 1
[0030] The present invention can produce the strain of hemp bast degumming enzyme, the preservation number is CGMCC 14600, and the name is Dicardia chrysanthemum DC ( Dickeya chrysanthemi IBFC 2016), which was deposited in the China General Microorganism Collection Management Center on September 8, 2017.
[0031] The screening and identification method of the Dicardia chrysanthemum DC comprises the following steps:
[0032](1) Sampling and treatment: Take 10 g of the sludge sample from the retting pool, put it in a conical flask with an appropriate amount of glass beads, add 200 mL of sterile water, mix it at 180 rpm for 20 min, and filter it with multi-layer gauze to remove the residue Obtain a suspension.
[0033] (2) Enrichment screening: Mix 10 mL of suspension, 150 mL of tap water and 15 g of ramie bast, place in a Erlenmeyer flask, and ferment at 35°C with shaking at 180 rpm until the fibers are dispersed; take 10 mL of the fermentation broth, and 150 mL of tap water...
Embodiment 2
[0037] 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:
[0038] (1) Preparation of enzyme preparation:
[0039] S1. Inoculate the DC strain of Dicarpus chrysanthemum into 5 mL of broth medium for activation, shake or stir culture at 34°C for 10 h, and then add it to a Erlenmeyer flask containing 200 mL of sterile broth culture medium cultured at 34°C with 180 rpm for 7 h to obtain a bacterial suspension;
[0040] S2. Transfer 2% of the inoculum to a fermenter containing sterile broth medium, stir and ferment at 34°C at a speed of 180 rpm, and feed compressed air into it. The flow rate of the soup medium is 0.2m 3 / (m 3 h), maintain a pressure of 0.3 MPa in the...
Embodiment 3
[0051] 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:
[0052] (1) Preparation of enzyme preparation:
[0053] S1. Inoculate the DC strain of Dicardia chrysanthemum into 5 mL broth medium for activation, shake or stir culture at 34°C for 12 h, and then add it to a Erlenmeyer flask containing 200 mL sterile broth culture medium , cultured with stirring at 200 rpm for 8 h at 34°C to obtain a bacterial suspension;
[0054] S2. Transfer 2% of the inoculum to a fermenter containing sterile broth medium, stir and ferment at 34°C at a speed of 200 rpm, and feed compressed air into it. The flow rate of the soup medium is 0.3m 3 / (m 3 h), maintain a pressure of 0.5 MPa in the ferme...
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