Method for producing glucose oxidase

A glucose oxidase and glucose technology, applied in the field of glucose oxidase production, can solve the problems of low efficiency of protein secretion and expression, easy loss of expression plasmids, etc.

Inactive Publication Date: 2018-05-25
福建力多利生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] (Saccharomyces cerevisiae) Low protein secretion and expres

Method used

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  • Method for producing glucose oxidase
  • Method for producing glucose oxidase
  • Method for producing glucose oxidase

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] Embodiment 1, construct recombinant bacteria

[0068] 1. Construction of recombinant bacteria X33 / pPIC9K-GOD

[0069] 1. Construct the recombinant plasmid pPIC9K-GOD. According to the sequencing results, the structure of the recombinant plasmid pPIC9K-GOD is described as follows: a double-stranded DNA molecule shown in sequence 2 of the sequence table is inserted between the EcoRI and NotI restriction sites of the pPIC9K vector. The DNA molecule shown in sequence 2 of the sequence listing is a GOD gene, which encodes the GOD protein shown in sequence 1 of the sequence listing. Extracellular expression of foreign proteins.

[0070] 2. The recombinant plasmid pPIC9K-GOD was linearized with the restriction endonuclease BglII, and then introduced into Pichia pastoris X33 to obtain the recombinant strain, which was named X33 / pPIC9K-GOD.

[0071] 2. Construction of recombinant bacteria X33 / pPIC9K-GOD / pPICZ-PDI

[0072] 1. Construct the recombinant plasmid pPICZ-PDI. Acco...

Embodiment 2

[0083] Embodiment 2, detect the ability of recombinant bacteria to produce glucose oxidase

[0084] The test strains are: recombinant bacteria X33 / pPIC9K-GOD, recombinant bacteria X33 / pPIC9K-GOD / pPICZ-PDI, recombinant bacteria X33 / pPIC9K-GOD / pPICZ-BiP, recombinant bacteria X33 / pPIC9K-GOD / pPICZ-BiP-PDI, Recombinant bacteria X33 / pPIC9K, recombinant bacteria X33 / pPIC9K / pPICZ or Pichia pastoris X33.

[0085] 1. Take the test strain and culture it with shaking at 30°C and 220rpm for 24 hours to obtain seed liquid.

[0086] 2. Inoculate 1 volume part of the seed solution obtained in step 1 into 99 volume parts of BMGY medium, and culture at 30°C and 220 rpm until OD 600nm The value is 10.

[0087] 3. Inoculate 10 parts by volume of the system obtained in step 2 into 90 parts by volume of BSM medium, and culture with shaking at 30° C. and 500 rpm. During the cultivation process, samples were taken every 12 hours, centrifuged at 10,000 rpm for 10 min at 4° C., and the supernatant w...

Embodiment 3

[0100] Embodiment 3, the large-scale production of glucose oxidase by fermenter using recombinant bacteria

[0101] The recombinant bacteria X33 / pPIC9K-GOD / pPICZ-BiP-PDI were inoculated into fermentors equipped with BSM medium (initial OD 600nm =1-2), cultured at 30°C. Stage 2 is carried out after stage 1 is completed, and stage 1 and stage 2 are carried out consecutively.

[0102] Phase 1: During the cultivation process, the pH of the system is controlled by adding 28% concentrated ammonia water to 5.0, and the dissolved oxygen of the system is controlled to be above 20% by adjusting the stirring speed and ventilation; when the glycerol in the BSM medium is exhausted, the dissolved oxygen rises , start to add feeding liquid A at a rate of 18.15 mL per liter of system per hour (feeding liquid A is an aqueous solution containing 1.2% PTM1 and 50 g / 100 ml glycerol by volume fraction), OD 600nm Stop feeding when it is 150-200, and continue to cultivate for 30 minutes to 2 hours...

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Abstract

The invention discloses a method for producing glucose oxidase. The invention firstly provides a recombinant bacterium, which is obtained by introducing a coding gene of glucose oxidase and a coding gene of a molecular chaperone into a starting bacterium. The molecular chaperone can be concretely protein disulfide isomerase and/or tuberculosis immune globulin. The invention also discloses the method for producing the glucose oxidase. The method comprises the following steps of culturing the recombinant bacterium to obtain the glucose oxidase. The invention also discloses application of the molecular chaperone in promoting microbial expression glucose oxidase. The method for producing the glucose oxidase provided by the invention has significance on secretory expression and industrial production of the enhanced glucose oxidase.

Description

technical field [0001] The invention belongs to the field of biotechnology, and in particular relates to a method for producing glucose oxidase. Background technique [0002] Glucose oxidase (Glucose oxidase, GOD) is an oxidase mainly produced by molds, which can oxidize glucose to glucuronic acid, and at the same time use molecular oxygen as an electron acceptor to generate hydrogen peroxide, so it is widely used in food, Industries such as medicine, feed and industrial production. [0003] At present, the level of glucose oxidase produced in China is low, and the purity of enzyme preparations is generally low. It still needs to rely heavily on imports every year, and the market price remains high. [0004] The Pichia pastoris expression system is a methanolotrophic yeast expression system that has developed rapidly since 1980, and nearly 500 foreign proteins have been successfully expressed in this system so far. It not only overcomes the shortcomings of the prokaryotic ...

Claims

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Application Information

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IPC IPC(8): C12N1/19C12N9/04C12R1/84
CPCC07K14/47C12N9/0006C12N9/90C12Y101/03004C12Y503/04001
Inventor 胡美荣陈榕陈飞牟庆璇陶勇
Owner 福建力多利生物科技有限公司
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