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A kind of alkalophilic bacillus ntt33c6d2 and its application

A technology of alkalophilic bacillus and strains, applied in the field of microorganisms, can solve problems such as low enzyme activity, achieve high production stability, avoid secondary pollution, and reduce production costs

Active Publication Date: 2019-12-13
曹军卫 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] From the current point of view, many biological degumming methods cannot be applied to industrial production, mainly because the enzyme activity is too low, and the raw hemp after enzyme degumming still contains more colloids, and its effect is only equivalent to that of the chemical degumming pretreatment process. Effect (Yu Chunhua, Feng Xinxing, Jia Changlan, etc. Ramie Fiber High Temperature-Enzyme Combined Degumming Technology [J]. Textile Journal, 2007, 28(6): 79-82. Cai Xia, Xiong Heping, Yan Li, etc. Ramie Microorganisms-Steam Explosive combined degumming technology [J]. Textile Journal, 2011, 32(7): 75-79.)

Method used

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  • A kind of alkalophilic bacillus ntt33c6d2 and its application
  • A kind of alkalophilic bacillus ntt33c6d2 and its application
  • A kind of alkalophilic bacillus ntt33c6d2 and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] A method for isolation and screening of alkalophilic bacillus NTT33C6D2, the steps of which are:

[0044] 1) Sample collection

[0045] Soil sampling was carried out from the Zhelimu League area of ​​Inner Mongolia Autonomous Region, China. Suspend 1g of the soil sample in sterile water, mix well, and put the supernatant into the glucose medium. The ingredients are: glucose 10g; peptone 5g; yeast extract 5g; K 2 HPO 4 1g; MgSO 4 ·7H 2 O 0.2g; Agar 18g; Water 1000mL; 2 CO 3 Adjust the pH to 10-11; incubate at 28°C for 24-48 hours.

[0046] 2) Separation and purification

[0047] Select a single colony in the above-mentioned medium and transfer it to the solid medium of locust bean gum, and its composition is: locust bean gum 10g, yeast extract 5g, peptone 5g, K 2 HPO 4 1g, MgSO 4 ·7H 2 O 0.1g, agar 18g, water 1000mL, with Na 2 CO 3 Adjust the pH to 10-11; incubate at 28°C for 24-36 hours, select the strains that produce a transparent circle around the colon...

Embodiment 2

[0069] A kind of application of alkalophilic bacillus NTT33C6D2 in ramie production, its steps are:

[0070] 1) Put the mutant strain NTT33C6D2 in locust bean gum liquid medium and activate it by culturing it at 37°C for 20-24 hours; then transfer it to the medium containing ramie, culture it with shaking at 37°C and 180rpm, and take samples at different times (every 4 hours) Observe its fiber dispersion situation, and measure residual glue rate (table 1), measure analysis method such as People's Republic of China " ramie chemical composition quantitative analysis method " (GB5889-86); Contain the substratum composition of ramie to be ramie 10g, (NH 4 ) 2 SO 4 1.5g, K 2 HPO 4 0.2g, MgSO 4 ·7H 2 O 0.25g, water 150mL, with Na 2 CO 3 Adjust the pH to 10-11, inoculate after sterilization.

[0071] Table 1 Degumming of ramie biodegumming residual gum rate

[0072]

[0073] 2) The mutant strain is used for biological degumming of ramie with burlap removed, and the degu...

Embodiment 3

[0075] A kind of application and effect evaluation of alkalophilic bacillus NTT33C6D2 in ramie production, its steps are:

[0076] 1) carry out biological degumming 6-8 hour to ramie according to the method described in step 1) in embodiment 2;

[0077] 2) After degumming, the ramie dispersed like cotton is washed once with water, and then boiled for 1-2 hours in a solution containing 0.3-0.5% NaOH and 0.1% mass concentration of sodium tripolyphosphate solution at 0.2Mpa;

[0078] 3) According to the general treatment method of chemical degumming (Ouyang Shu, Yao Gang, review and application of new technology of chemical degumming of ramie [J]. Ramie Textile Science and Technology, 1993,16(1):30-32.) Washing and beating , bleaching (available chlorine 0.5-0.8g / L), washing, pickling (pH2.5), washing, drying, after oiling, drying, drying, to obtain dry hemp. The quality standard shown, measuring analysis method such as People's Republic of China "ramie chemical composition quan...

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Abstract

The invention discloses an alkalophilic bacillus NTT33C6D2 and an application thereof. The strain has a deposit number of CCTCC M2016317, and has the ability of high-yield constitutive alkaline β-mannanase and is resistant to glucose metabolism repression; , the shape and size of 0.5 ~ 0.65 × 2.6 ~ 3.4μm, flagella lateral, motility, endospores are oval; aerobic, the colony is round, smooth surface, with concentric circles. Alkaliophilic Bacillus NTT33C6D2 can degumming ramie, the degumming cycle is short, the efficiency is high, the enzyme activity is stable, the treatment cost is low, the fiber quality is good, and the sewage treatment after degumming is extremely easy.

Description

technical field [0001] The invention belongs to the technical field of microorganisms, and in particular relates to an alkalophilic bacillus NTT33C6D2 which produces a constitutive alkaline β-mannanase resistant to glucose metabolism repression, and also relates to a method for separating and screening the alkalophilic bacillus NTT33C6D2, and also relates to the Application of strains in ramie degumming. Background technique [0002] Ramie is a nettle plant, the fiber content of which is more than 60%, second only to cotton. Its bast fibers are long and strong, and can replace cotton and flax to produce various products, so it is an important raw material for the textile industry. Yet ramie fiber adheres to a large amount of colloids, mainly pectin, hemicellulose, lignin etc., and its content can reach 24~45% according to the difference of ramie kind. Therefore, in order to obtain industrially available fibers, degumming must first be carried out. From the perspective of ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20D01C1/04C12R1/07
CPCC12N9/2491C12Y302/01025C12N1/205C12R2001/07D01C1/04
Inventor 曹军卫夏晨阳朱雨兰
Owner 曹军卫