Phytase mutant

A technology of mutants and acid enzymes, applied in hydrolytic enzymes, plant genetic improvement, botanical equipment and methods, etc., can solve problems such as poor thermal stability, waste of phosphorus sources, pollution of the environment by high phosphorus feces, etc., and achieve improved heat resistance , Strong heat resistance effect

Pending Publication Date: 2021-11-26
QINGDAO VLAND BIOTECH GRP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, phosphorus in the form of phytate phosphorus is difficult to be utilized due to the lack of enzymes that can decompose phytic acid in monogastric animals, and its utilization rate is only 0% to 40%, which causes many problems: first, it causes waste of phosphorus On the one hand, the phosphorus source in the feed cannot be effectively utilized; on the other hand, in order to meet the demand of animals for phosphorus, inorganic phosphorus must be added to the feed, which increases the cost of feed; secondly, the formation of high-phosphorus feces pollutes the environment
Bacteria

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Example 1 Screening of heat-resistant mutants

[0046] The applicant mutated 10 sites (W46E, Q62W, G70E, A73P, T114H, N137V, D142R, S146E, R159Y, Y255D), to obtain the phytase mutant APPA-M0, its amino acid sequence is SEQ ID NO: 3, and a coding nucleotide sequence synthesized with reference to this sequence is SEQ ID NO: 4. Compared with phytase APPA, the heat resistance of mutant APPA-M0 was significantly improved. After being treated at 75°C for 5 minutes, the residual enzyme activity of phytase APPA was less than 10%, while the residual enzyme activity of mutant APPA-M0 was higher than that of phytase APPA. at 85%.

[0047] In order to further improve the heat resistance of the phytase mutant APPA-M0, the applicant analyzed the protein structure of its gene. Domain 1 is formed, and the remaining 124 amino acid residues in the middle form domain 2. The conserved sequence and active center are located in domain 1. On the premise of not destroying the protein seconda...

Embodiment 2

[0058] Example 2 Expression of phytase mutants in Pichia pastoris

[0059] According to the coding preference of Pichia pastoris, the APPA-M0 gene sequence SEQ ID NO: 4 and the mutant gene sequence were optimized and synthesized, and EcoRI and NotI were added to the 5' and 3' ends of the synthetic sequence respectively. enzyme cutting site.

[0060] 2.1 Construction of expression vector

[0061] The gene sequences of the synthesized APPA-M0 and the mutant were digested with EcoRI and NotI respectively, and then ligated with the pPIC-9K vector after the same digestion at 16°C overnight, and transformed into Escherichia coli DH5a, and spread on LB+Amp Plate, cultured upside down at 37°C, after transformants appear, perform colony PCR (reaction system: template-picked single clone, rTaqDNA polymerase 0.5ul, 10×Buffer 2.0μL, dNTPs (2.5mM) 2.0μL, 5'AOX primer (10M): 0.5 μL, 3’AOX Primer: 0.5 μL, ddH 2 O 14.5μL, reaction program: 95°C pre-denaturation for 5min, 30 cycles: 94°C fo...

Embodiment 3

[0079] Embodiment 3 Expression of phytase mutant in Trichoderma reesei

[0080] According to the codon preference of Trichoderma, the APPA-M0 gene sequence SEQ ID NO: 4 and the mutant gene sequence were optimized and synthesized, and KpnI and MluI were added to the 5' and 3' ends of the synthetic sequence respectively Two enzyme cutting sites.

[0081] 3.1 Construction of expression vector

[0082] The synthesized phytase gene fragment and pSC1G vector were digested with restriction endonucleases KpnI and MluI (Fermentas) respectively, and the digested products were purified using a gel purification kit, and separated with T4 DNA ligase (Fermentas). The above phytase gene was ligated with the digested product of pSC1G vector and transformed into Escherichia coli Trans5α (Transgen), selected with ampicillin, and the clone was verified by sequencing (Invitrogen). After the sequencing is correct, a recombinant plasmid containing the phytase gene is obtained.

[0083] 3.2 Const...

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Abstract

The invention relates to the field of biotechnology, in particular to a phytase mutant, a preparation method and application thereof, a DNA molecule for encoding the phytase mutant, a carrier and a host cell. The mutant provided by the invention comprises a substitution of an amino acid at at least one position selected from the group consisting of 36, 126, 211, 253, 258, 266. The heat resistance of the mutant is remarkably improved, so that the phytase can be widely applied to feeds.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a phytase mutant, its preparation method and application, a DNA molecule encoding the phytase mutant, a carrier, and a host cell. Background technique [0002] Phytase is a phosphatase that hydrolyzes phytic acid. It degrades phytate phosphorus (inositol hexaphosphate) into inositol and inorganic phosphate. This enzyme is divided into two classes: 3-phytase (EC. 3. 1. 3. 8) and 6-phytase (EC. 3. 1. 2. 6). Phytase widely exists in plants, animals and microorganisms, such as higher plants such as corn and wheat, prokaryotic microorganisms such as Bacillus subtilis, Pseudomonas, Lactobacillus, Escherichia coli, and eukaryotic microorganisms such as yeast, rhizopus, and Aspergillus . [0003] In the seeds of crops such as grains, beans and oilseeds, the basic storage form of phosphorus is phytate phosphorus, and its content is as high as 1% to 3%, which accounts for 60% to 80% of the ...

Claims

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Application Information

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IPC IPC(8): C12N9/16C12N15/55C12N15/80C12N15/81C12R1/885C12R1/84
CPCC12N9/16C12N15/80C12N15/815C12Y301/03008C12Y301/02006C12N15/81
Inventor 吴秀秀李馨培李瑞宋清清黄亦钧
Owner QINGDAO VLAND BIOTECH GRP
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