Bacillus licheniformis ZL-1 and application thereof

A ZL-1, address technology, applied in applications, bacteria, biochemical equipment and methods, etc., can solve the problems of less keratin degrading bacteria, difficult biological treatment technology, backwardness and other problems, achieve strong temperature tolerance, shorten fermentation The effect of time and craftsmanship is simple

Active Publication Date: 2018-05-08
广州王道生物科技有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The research on the screening and application of feather keratin-degrading bacteria in my country lags behind foreign countries. There are not many high-efficiency strains isolated and screened, and most of them are fungi and actinomycetes, and most of these reported keratin-degrading bacteria grow in normal temperature environment. keratin-degrading bacteria under high temperature conditions (above 45°C)
Since the optimum reaction temperature of keratinase is generally between 40°C and 60°C, the compost temperature in the composting fermentation using feathers as raw materials is generally above 50°C, which brings great difficulties to conventional biological treatment techniques.

Method used

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  • Bacillus licheniformis ZL-1 and application thereof
  • Bacillus licheniformis ZL-1 and application thereof
  • Bacillus licheniformis ZL-1 and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] The isolation of embodiment 1 bacillus licheniformis (Bacillus licheniformis) ZL-1

[0032] The chicken feathers are taken from the chicken farm of Guangdong Wenshi Food Group Co., Ltd., and the edible fungus residues are taken from Guangzhou Wangdao Biotechnology Co., Ltd., mixed and put into an open solid fermentation tank, keeping the temperature in the tank at 45°C, and waiting for the feathers to decompose Finally, the fermentation residue was collected, dried in the shade, and stored at 4°C for later use.

[0033] Take 10g of the above sample and put it into a conical flask (with glass beads) filled with 90mL sterile water, shake it at 180rpm for 30min, let it stand for 10min, take the upper layer and dilute it 10 times, and make 10 -4 、10 -5 、10 -6 Take 0.1 mL of the diluted solution and spread it evenly on the NA medium plate, and place the inverted plate in a 45°C incubator for 2 days. Make 3 parallel purification plates for each strain with different colony...

Embodiment 2

[0037] The biological character and physiological biochemical and molecular identification of embodiment 2 bacillus licheniformis (Bacillus licheniformis) ZL-1

[0038] S1. Morphological characteristics

[0039] After Bacillus licheniformis (Bacillus licheniformis) ZL-1 was cultured on NA medium for 24 hours, the colonies were rough, opaque, tree-rooted with irregular edges, easy to pick, and the diameter of the colonies was 15mm. The bacteria were single, in pairs or Arranged in chains; Gram staining is positive; spores are oval, mesotopic and capsulated.

[0040] S2. Physiological and biochemical characteristics: through physiological and biochemical determination, contact enzyme, V-P experiment of Bacillus licheniformis (Bacillus licheniformis) ZL-1 of the present invention, anaerobic growth, nitrate reduction, starch hydrolysis, casein hydrolysis, gelatin hydrolysis, cellulose Decomposition and other tests are all positive, and indole, lecithinase, tyrosine hydrolysis, ph...

Embodiment 3

[0055] Example 3 Bacillus licheniformis (Bacillus licheniformis) ZL-1 Fermentation and Degradation of Pure Feathers to Produce Compound Amino Acid Solution and Determination of Related Indexes

[0056] (1) Pretreatment of feather raw materials: crush the feathers with a pulverizer to form fluffy flocs. Then mix the flocculent feathers with water at a mass ratio of 1:40, adjust the pH to 10, and heat for 180s under the condition of microwave energy of 700W.

[0057] (2) Bacillus licheniformis (Bacillus licheniformis) ZL-1 seed solution preparation: the Bacillus licheniformis (Bacillus licheniformis) ZL-1 screened in Example 1 was inoculated on the NA solid medium plate, and cultivated at 45°C for 24h to make it Activation: transfer the above-mentioned activated seeds to NB liquid seed medium, and cultivate them for 24 hours to the logarithmic growth phase.

[0058] (3) Mix the pretreated feathers with the inorganic salt solution at a mass ratio of 1:100, add 5wt% Bacillus lich...

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Abstract

The invention discloses Bacillus licheniformis ZL-1 and the application thereof. The Bacillus licheniformis ZL-1 is obtained by isolating and screening from a high-temperature stack of feathers combined with edible fungus residues, the Bacillus licheniformis ZL-1 is preserved at Guangdong Provincial Microorganism Culture Collection Center, with a preservation number of GDMCC No. 60284, the preservation address is 5th floor, Building 59, Compound, No. 100 Xianlie Middle Road, Guangzhou, China, and the preservation date is November 24, 2017. Experiments determine that the Bacillus licheniformisZL-1 can be cultured in a liquid culturing medium with pure feathers for three days, the keratinase activity of the Bacillus licheniformis ZL-1 reaches 52.14 U / ml, and the degradation rate of feathersreaches 90.15%. Further more, the Bacillus licheniformis ZL-1 has good tolerance to high temperature and salinity, can grow well at a temperature of 55 DEC G and is resistant to salinity of 14%, so that the Bacillus licheniformis ZL-1 is used for degrading the feathers, preparing compound amino acid solution, conducting high-temperature compost fermentation by using the feathers as raw materialsand preparing compound amino acid fertilizers and keratinase; the Bacillus licheniformis ZL-1 has good application prospects and market value.

Description

technical field [0001] The invention belongs to the technical field of microbes and their applications. More specifically, the invention relates to Bacillus licheniformis ZL-1 and its applications. Background technique [0002] Feathers are the waste left over from poultry processing. Worldwide, millions of tons of feather waste are produced every year, and nearly 700,000 tons of waste feathers are produced in my country every year. The problem of solid waste management has become poultry slaughtering. Business problems that need to be solved urgently. However, feather waste is a rich natural protein resource, its crude protein content is as high as 85%-90%, and it also contains vitamin B 12 and some unknown growth factors. Except for the significantly lower content of lysine and methionine in feather protein, the composition of other animal essential amino acids is slightly higher than that of fishmeal, which means that the production of compound amino acids by hydrolysis ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12P13/04C12N9/54C05F15/00C12R1/10
CPCC05F1/005C12N1/20C12N9/54C12P13/04C12N1/205C12R2001/10C05F5/00C05F11/08
Inventor 朱红惠谢小林周莲陈美标
Owner 广州王道生物科技有限公司
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