A kind of mutant type sus scrofa pig-derived trypsin and its coding gene as well as its acquisition method and application

A trypsin gene and trypsin technology, applied in the field of molecular enzymology and biology, can solve the problems of complicated analysis steps

Active Publication Date: 2018-10-26
TIANJIN UNIV
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  • Application Information

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Problems solved by technology

Denatured proteins are usually added with chemical reagents, adding additional steps, which complicates the analysis steps

Method used

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  • A kind of mutant type sus scrofa pig-derived trypsin and its coding gene as well as its acquisition method and application
  • A kind of mutant type sus scrofa pig-derived trypsin and its coding gene as well as its acquisition method and application
  • A kind of mutant type sus scrofa pig-derived trypsin and its coding gene as well as its acquisition method and application

Examples

Experimental program
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Effect test

Embodiment Construction

[0064] (1) Construction of wild-type Sus scrofa pig-derived trypsinogen expression vector

[0065] The constructed wild-type recombinant porcine trypsinogen expression vector pPIC9K-rpTry vector was synthesized from the whole gene of Beijing Jinweizhi Co., Ltd., as shown in figure 1 shown. Among them, the first 20 amino acids of the first 25 amino acids of the N-terminal zymogen activating peptide of the original gene were removed, and the remaining sequence of the N-terminal activating peptide was the enterokinase recognition site (DDDDK). The shortened Sus scrofa porcine zymogen sequence was digested with EcoRI and NotI and inserted into the corresponding single cloning site of pPIC9K.

[0066] (2) Quick-Change PCR technology to obtain mutant vector

[0067] According to the primer design principles of the TransGen Fast Mutagenesis System Kit, we designed mutation primers for the mutation N84S, as shown in Table 1-1. The polymerase for the PCR reaction was Phusion High-fi...

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Abstract

The invention relates to a mutant-type Sus scrofa swine trypsin and an encoding gene thereof as well as an acquisition method and an application. According to the invention, the original wild type Sus scrofa swine trypsin is subjected to mutation to obtain the mutant enzyme with heat stability obviously improved; the invention further provides the encoding gene for encoding the trypsin mutant, the amino acid sequence and a construction method of a trypsin yeast engineering bacteria, wherein the amino acid sequence is SEQ ID NO.1, and the protein DNA sequence in encoding is SEQ ID NO.2. The invention lays a foundation for the research, development and production of the protease through a bioanalysis method, and is beneficial for the early realization of the clean and low-energy biological tanning, and the bio-safe production of leather. With the strain for producing swine trypsin, the yield is relatively high, the process is relatively simple, and the industrial application is facilitated.

Description

technical field [0001] The invention relates to molecular enzymology and biotechnology, more specifically to a coding gene of a high-thermal stability and high-activity Sus scrofa pig-derived trypsin, a method for obtaining the enzyme, and an application thereof. Background technique [0002] Trypsin (EC.3.4.21.4) is a single-chain serine protease consisting of 223 amino acid residues, and its precursor trypsinogen contains a signal peptide of 15 amino acids, followed by a signal peptide of 8 amino acids Leader peptide, zymogen activation peptide. Trypsinogen is produced in the ribosomes of the rough endoplasmic reticulum in the pancreatic cells of vertebrate animals, transported by the Golgi apparatus, enters the pancreatic transport duct, and is finally released into the intestinal lumen, where it utilizes the duodenal intestine Enterokinase secreted by mucosal cells specifically recognizes the N-terminal short peptide chain DDDDK of the trypsinogen sequence, cuts the C-t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N9/76C12N15/57C12N15/10C12N15/81C12N1/19C12R1/84
CPCC12N9/6427C12Y304/21004
Inventor 黄鹤杜坤郭超刘冶
Owner TIANJIN UNIV
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