Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Rhizomucor miehei strain and application thereof in preparation of Beta-glucanase and chymosin

A technology of Rhizomucor miehei and dextranase, which is applied in the direction of biochemical equipment and methods, hydrolytic enzymes, fungi, etc., can solve the problems of long production cycle, low rennet level, high fermentation cost, etc., and achieve the production cycle Short, high enzyme production, low fermentation cost

Active Publication Date: 2015-04-22
CHINA AGRI UNIV
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the level of rennet production is generally low, the production cycle is long and the fermentation cost is high

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Rhizomucor miehei strain and application thereof in preparation of Beta-glucanase and chymosin
  • Rhizomucor miehei strain and application thereof in preparation of Beta-glucanase and chymosin
  • Rhizomucor miehei strain and application thereof in preparation of Beta-glucanase and chymosin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0052] Embodiment 1, isolation and identification of bacterial strain

[0053] 1. Isolation of strains

[0054] The Rhizomucor miehei CAU432 provided by the invention is screened from soil.

[0055] The preparation method of the separation medium: oat (0.18-0.3mm particle size powder) 20g, soybean peptone 10g, KH 2 PO 4 5g, MgSO 4 ·7H 2 O 0.3g, CaCl 2 0.3g, 20g agar, add water to 1L, natural pH.

[0056] The preparation method of the primary screening medium: oat (0.18-0.3mm particle size powder) 20g, soybean peptone 10g, KH 2 PO 4 5g, MgSO 4 ·7H 2 O 0.3g, CaCl 2 0.3g, Congo red 0.05g, agar 20g, add water to 1L, natural pH.

[0057] Preparation method of fermentation medium: oat (0.18-0.3mm particle size powder) 20g, soybean peptone 10g, KH 2 PO 4 5g, MgSO 4 ·7H 2 O 0.3g, CaCl 2 0.3g, add water to 1L, natural pH.

[0058] The fresh soil samples were diluted, spread on the separation medium, and cultivated in a constant temperature incubator at 50°C. Whe...

Embodiment 2

[0064] Example 2, Optimization of Conditions for the Preparation of β-Glucanase by Shake Flask Fermentation

[0065] 1. Screening of carbon source in fermentation medium

[0066]The preparation method of the fermentation medium in this step: carbon source 10g (0.45-0.9mm particle size range powder), peptone 10g, KH 2 PO 4 5g, MgSO 4 ·7H 2 O 0.3g, CaCl 2 0.3g, add water to 1L, natural pH. The following 15 carbon sources were used respectively: sugarcane husk, corn husk, corn stalk, oats, wheat bran, bagasse, corn cob, beer grains, rice husk, soluble starch, chitin, sorghum stalk, liquor distillers grains, bran and straw.

[0067] 1. Activation of strains

[0068] The preserved Rhizomucor miehei CAU432 was activated on the activation medium plate.

[0069] 2. Preparation of seed solution

[0070] The activated fresh strains were inoculated into the seed medium, and cultured on a reciprocating shaker in a constant temperature air bath at 50°C at 200 rpm for 24 hours to...

Embodiment 3

[0095] Example 3, Conditions for preparing β-glucanase by solid fermentation

[0096] 1. Screening of carbon source in solid fermentation medium

[0097] 1. Activation of strains

[0098] Same as step 1 of embodiment 2.

[0099] 2. Preparation of seed solution

[0100] Same as step 1 of embodiment 2.

[0101] 3. Solid fermentation to produce β-glucanase

[0102] Basic culture solution A: peptone 10g, KH 2 PO 4 5g, MgSO 4 ·7H 2 O 0.3g, CaCl 2 0.3g, add water to 1L, natural pH.

[0103] Take by weighing 5g carbon source (the powder of 0.18-0.3mm particle diameter range) in 250mL Erlenmeyer flask, pour into basal culture solution A, obtain solid fermentation medium (adjust the content of solid fermentation medium by the addition of basal culture solution A) The water content is 80%), stir evenly with a glass rod, and sterilize at 121°C for 20 minutes; inoculate 1mL of the seed liquid in step 2 after the solid fermentation medium is cooled, mix it and place it in a 50°...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
molecular weightaaaaaaaaaa
Login to View More

Abstract

The invention discloses a rhizomucor miehei strain and an application thereof to preparation of Beta-glucanase and chymosin. The rhizomucor miehei CAU432 disclosed by the invention has a preservation number of CGMCC (China General Microbiological Culture Collection Center) No.4967. The rhizomucor miehei CAU432 disclosed by the invention is good in heat resistance and strain stability, high in enzyme yield, low in fermentation cost (a used carbon source and a used nitrogen source are easy to buy and low in price), short in production peroid, suitable for being applied to the field of industrial production and better in industrial application prospect.

Description

technical field [0001] The invention relates to a strain of Rhizomucor miehei and its application in preparing β-glucanase and rennet. Background technique [0002] β-glucan (Glucan) is a polymeric polysaccharide formed from glucose as a monomer, widely present in the cell walls of plants and microorganisms. β-glucanase (Glucanase) is an important class of hydrolase, which acts on 1, 3 and 1, 4 glycosidic bonds of β-glucan; this enzyme can effectively decompose β in the endosperm cell wall of wheat and cereal plants - Dextran; in feed, it can reduce the content of non-starch polysaccharides (NSP) and its anti-nutritional factors, improve the absorption of nutrients by livestock and poultry, improve the growth rate and feed conversion efficiency of livestock and poultry; it can be used in beer brewing Reduce wort viscosity, improve filtration performance, increase malt dissolution rate, prevent beer turbidity, stabilize beer quality, etc. [0003] So far, research on fermen...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/14C12N9/24C12N9/64C12R1/645
Inventor 江正强唐艳斌崔健闫巧娟杨绍青
Owner CHINA AGRI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products