Separating and purifying method and application of keratinase

A keratinase, separation and purification technology, applied in the field of separation and purification of keratinase, can solve problems such as reduced enzyme activity, and achieve the effects of high sample concentration, large sample loading, and short time consumption

Active Publication Date: 2016-08-03
BIOTECH RES CENT SHANDONG ACADEMY OF AGRI SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Keratinase from Bacillus brevibacillus sp.AS-S10-II in EDTA, SDS, TritonX-100, Tween20, H 2 o 2 keratinase still maintains a high enzyme activity, but the enzyme activity decreases to varying degrees after being incubated with different types of detergents (RaiKR, MukherjeeAK. BiochemEngJ.2011, 54:47-56); the optimum pH of keratinase fro

Method used

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  • Separating and purifying method and application of keratinase
  • Separating and purifying method and application of keratinase
  • Separating and purifying method and application of keratinase

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Experimental program
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Embodiment 1

[0034] The separation and purification method of embodiment 1 keratinase, concrete steps are as follows:

[0035] (1) Inoculate a single colony of Bacillus subtilis FJ-3-16 into LB liquid medium with an inoculation needle, and cultivate it at 30°C and 200rpm for 18h;

[0036] LB liquid medium (g L -1 ): peptone 10, yeast powder 5, NaCl10, pH7.5;

[0037] (2) Inoculate the logarithmic phase seed solution in the LB liquid medium into the FM3 medium according to the inoculation amount of 6% (volume ratio), and cultivate it at 30° C. for 72 hours at 200 rpm;

[0038] FM3 medium (g·L -1 ): corn flour 20, soybean flour 20, bran 10, KH 2 PO 4 1,K 2 HPO 4 3. CaCl 2 1, pH7.5;

[0039] (3) Use gauze to filter out the culture medium dregs after step (2), and centrifuge at 11000rpm for 15min to collect the crude enzyme solution;

[0040] (4) After the ammonium sulfate gradient precipitation with a mass fraction of 40-70% of the crude enzyme solution, use pH 10.0, 50mMTris-HCl buf...

Embodiment 2B

[0043] Embodiment 2B.subtilisFJ-3-16 strain identification

[0044] LB liquid medium (g / L): peptone 10.0, yeast powder 5.0, NaCl 10.0, pH 7.5. For transformant screening, add ampicillin (Amp) at a final concentration of 50 μg / mL to the culture medium.

[0045] LB solid medium (g / L): peptone 10.0, yeast powder 5.0, NaCl 10.0, agar 15.0, pH 7.5.

[0046] A single colony of the FJ-3-16 strain was inoculated in 5 mL of liquid LB medium and cultured overnight at 37°C. Take 1mL of the cultured bacterial solution, and extract the total bacterial DNA according to the instructions of the "Bitec Bacterial Genome Extraction Kit".

[0047] 16S universal primers 27F (5'-AGAGTTTGATCCTGGCTCAG-3') and 1492R (5'-ACGGCTACCTTGTTACGACTT-3') were designed. Using the bacterial genome as a template, according to the PCR system and procedures in the instruction manual of TaqDNA polymerase, PCR was used to obtain DNA fragments.

[0048] The PCR system is shown in Table 1, and the PCR program is sh...

Embodiment 3

[0055] The enzyme activity assay of embodiment 3 keratinase KerFJ

[0056] Take 1ml of the diluted crude enzyme solution and add 1ml of keratin substrate (TCI company, K0044) with a mass fraction of 2%, add 2ml of 0.4MTCA to terminate the reaction after reacting at 55°C for 1h, centrifuge at 11000rpm for 2min, take supernatant 1ml, add 5ml. .4MNa 2 CO 3 And 1ml of Folin reagent, after developing color at 40°C for 20min, colorimetric at 660nm, the absorbance value increased by 0.1 at 660nm per minute was defined as 1 enzyme activity unit (U).

[0057] Protein Concentration Determination

[0058] According to the instructions of "BCA Protein Concentration Determination Kit" (Beiyuntian Biotechnology), the B.subtilisFJ-3-16 fermentation broth obtained in the present invention has a total activity of keratinase in 1L of 73820.16U. Utilizing the purification method of the present invention, 16.59 mg of keratinase KerFJ pure enzyme can be harvested from 1LB.subtilisFJ-3-16 fermen...

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Abstract

The invention relates to a separating and purifying method and application of keratinase. The method comprises the steps that after crude enzyme liquid is precipitated with ammonium sulfate in a gradient mode, sediment is resuspended with a buffer solution, and dialysis is carried out; an ion exchange column is balanced with a buffer solution, sample feeding is carried out, and an enzyme activity peak is in a crossing peak; components with enzyme activity are collected, and dialysis is carried out with a buffer solution; the ion exchange column is balanced with a buffer solution, sample feeding is carried out, gradient elution is carried out with NaCl, and purified keratinase is obtained. 16.59 mg of pure enzymes of keratinase Ker FJ can be harvested through 1 L of fermentation broth, and the total enzyme activity is 2989 U. Obtained keratinase Ker FJ has a very good effect on livestock and poultry waste degradation, unhairing and a detergent additive.

Description

technical field [0001] The invention relates to a separation and purification method and application of keratinase, belonging to the field of biotechnology. Background technique [0002] The main component of poultry feathers, wool, animal fur, and hoof horns is keratin. Keratin is a hard protein with a dense and complex structure, which is difficult to be hydrolyzed by common proteases such as trypsin, pepsin and papain, and can only be hydrolyzed by proteases called "keratinase". Because keratinase can degrade keratin-rich feathers, wool, hooves, and hair, which are difficult for ordinary proteases to degrade, it is widely used in the treatment of tanning industry, textile industry and keratin waste. Existing commercially available keratinase enzyme preparations such as etc. are transformed from keratinase KerA (GuptaRetal., ApplMicrobiolBiotechnol.2013, 97:9931-9940). [0003] The poultry breeding, slaughtering, tanning and fur processing industries around the world b...

Claims

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Application Information

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IPC IPC(8): C12N9/54C12R1/125
CPCC12N9/54
Inventor 边斐岳寿松张晓玮朱耀霞马德源彭振英陈高毕玉平宣宁
Owner BIOTECH RES CENT SHANDONG ACADEMY OF AGRI SCI
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