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Method for improving soluble expression of microbial transglutaminase in escherichia coli

A technology of transglutaminase and Escherichia coli, applied in the field of genetic engineering, can solve problems such as insolubility, and achieve the effects of improving soluble expression and obvious expression effect

Inactive Publication Date: 2014-10-08
ANHUI BBCA FERMENTATION TECH ENG RES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, this system also has shortcomings, such as the expressed foreign protein often exists in the form of insoluble non-functional inclusion bodies

Method used

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  • Method for improving soluble expression of microbial transglutaminase in escherichia coli
  • Method for improving soluble expression of microbial transglutaminase in escherichia coli
  • Method for improving soluble expression of microbial transglutaminase in escherichia coli

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] The construction method of embodiment 1 plasmid pET-MTG

[0027] 1.1 PCR amplification of MTG gene

[0028] Using 1 μg of Streptoverticillium mobaraense genomic DNA as a PCR template, primer 1: 5′-TAAAAACATATGGACTCCGACGACAGGGTCAC-3′ and primer 2: 5′-TAAAAACTCGAGTTACGGCCAGCCCTGCTTTACC-3′ were designed for PCR amplification. The PCR reaction was carried out in a total volume of 50 μl, and the reaction conditions were: denaturation at 94°C for 5 min; denaturation at 94°C for 50 s, annealing at 58°C for 1 min, extension at 72°C for 2 min, and a total of 30 cycles; finally, extension at 72°C for 10 min.

[0029] 1.2 Construction of MTG expression plasmid

[0030] Gel recovery PCR amplified products were digested with NdeI and XhoI, and the digested fragments were recovered, ligated with the pET-22b vector that was also digested with NdeI and XhoI (ligated at 16°C for 16 hours), and transformed into E. coli DH5α competent cells , select positive clones, extract the plasmids...

Embodiment 2

[0031] The construction method of embodiment 2 plasmid pA-GESP

[0032] 2.1 Sticky-end PCR technique to amplify artificial operons containing molecular chaperones

[0033] According to the sequence of the upstream and downstream genes of the amplified artificial operon (GenBank ID: NC_010473.1), two pairs of primers were designed, primer 3: 5′-CATGGCAGCTAAAGACGTAAAATTC-3′ and primer 4: 5′-GTTAAGCTTTTGCTTTCGCTACAGT-3′, and primers 5: 5′-GCAGCTAAAGACGTAAAATTCGGTA-3′ and primer 6: 5′-TCGAGTTAAGCTTTTGCTTTCGCTA-3′, use primers 3 and 4, primers 5 and 6, respectively, perform PCR amplification in two tubes simultaneously, add 3 μl of plasmid E. coli Genomic DNA was used as a template. The PCR reaction was carried out in a total volume of 50 μl, and the reaction conditions were: denaturation at 94°C for 30 s; annealing at 55°C for 30 s, and extension at 72°C for 4 min, a total of 30 cycles.

[0034] Recover the PCR amplification product, measure the A260 value, mix the two PCR produc...

Embodiment 3

[0037] Co-transformation of embodiment 3 molecular chaperone and MTG

[0038] Co-transform Escherichia coli (Rosetta DE3) with pET-MTG and pA-GESP plasmids, and use the co-transformation of pET-MTG and pACYC plasmids as a control. The co-transformed bacterial solution contains 25 μg / ml ampicillin and 25 μg / ml chloramphenicol Plates resistant to two kinds of antibiotics were cultured upside down in a 37°C incubator for 12 hours. Pick a single colony and inoculate it in 10ml of LB liquid medium containing two antibiotics, 25μg / ml ampicillin and 25μg / ml chloramphenicol, culture overnight at 37°C with shaking at 220r / min; turn at 1:100 Into 100ml of LB medium, when OD 600 At about 0.6, add IPTG with a final concentration of 0.4mmol / L, induce at 28°C for 12h, centrifuge at 5000×g for 10min to collect the bacteria, add about 1ml of lysis buffer (100mmol / L sodium phosphate buffer, containing 300mmol / L NaCl and 10mmol / L imidazole, pH 8.0) sonicated at 300W power, 3s each time, 9s i...

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Abstract

The invention provides a method for improving soluble expression of microbial transglutaminase (MTG) in escherichia coli. According to the method, two plasmids, pET-MTG and pA-GESP are co-transformed into escherichia coli DE3, and microbial transglutaminase is solubly expressed in an induced supernantant. The pET system is utilized for efficiently expressing MTG, and also a molecular chaperone co-expression system is established, so that the solubility of a MTG expression product is improved, and results show that the method helps to improve the soluble expression of MTG in escherichia coli with obvious expression effect, and establishes a good base for industrialized production in future.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular to a method for improving the soluble expression of microbial transglutaminase in Escherichia coli. Background technique [0002] Microbial transglutaminase (MTG) is a transferase that catalyzes the transfer of the γ-acyl group of glutamine in a polypeptide chain to the amino group of another substrate to form a γ-glutamyl compound. At present, MTG has been widely used in the food industry. Transglutaminase exists widely in many animal tissues, but its industrial production is very difficult due to its low content, difficult separation, poor thermal stability and dependence on calcium ions. At present, MTG has been widely used in the food industry. Transglutaminase exists widely in many animal tissues, but its industrial production is very difficult due to its low content, difficult separation, poor thermal stability, and dependence on calcium ions. [0003] The expression syst...

Claims

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Application Information

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IPC IPC(8): C12N9/10C12N15/66C12N1/21C12R1/19
CPCC12N9/1044C12N15/70C12Y203/02013
Inventor 李荣杰徐斌常珠侠许鹏
Owner ANHUI BBCA FERMENTATION TECH ENG RES
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