Method for separating and screening oligographic bacterium producing protease
A technology for separation, screening and production of protease, which is applied in the field of separation and screening of protease-producing strains, and can solve the problems of undiscovered reports on the physiological function of secreted protease.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2013-01-23
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
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Abstract
Description
Technical field:
[0001] The invention relates to a method for separating and screening protease-producing strains, in particular to a method for separating and screening protease-producing oligotrophic bacteria. Background technique:
[0002] Protease is the commercial enzyme with the largest production and sales volume in the world today. It is widely used in industries such as food, brewing, medicine, textile, leather, detergent and feed, and plays an important role in the development of the national economy. The enzymes are widely distributed in animals, plants and microorganisms. Due to the short production cycle and simple extraction process, microorganisms have increasingly become the main source of industrial enzyme preparations. There are many kinds of microorganisms that produce proteases, and the main microbial strains currently used in the industrial production of proteases are Bacillus. my country's protease research has made great progress in the past 20 years...
Examples
Embodiment 1
[0029] Preparation of medium:
[0030] Separation medium: slant / plate medium: (NH 4 ) 2 SO 4 0.5, KH 2 PO 4 1g, MgSO 4 0.2g, NaCl 5g, CaCO 3 5g, glucose (15mg carbon content per liter medium), 11g agar powder (not added to liquid medium); 1000ml distilled water, pH7.0-7.2;
[0031] Primary selection medium: gelatin medium: beef extract 3g, peptone 5g, gelatin 120g, pH7.0-7.2;
[0032] Multiple selection medium / shake flask medium: corn flour 20g, bean cake powder 15g, bran 20g, Na 2 HPO 4 0.3g, NaH 2 PO 4 0.2g, MgSO 4 0.2g, CaCl 2 0.2g, distilled water 1000ml, pH 7-7.2;
[0033] Sampling: Take a soil sample at 0-5cm from the Gurbantunggut Desert in Xinjiang and put it into a sampling bag for later use;
[0034] Isolation of bacterial strains: the sample was spread on the plate of the separation medium (inorganic nitrogen medium) by plate dilution separation method, and cultured at 37°C for 48 hours. After obtaining a single colony, it was purified by streak...