Cloning, expression and application of eimeria tenella protein disulfide isomerase gene
A technology of disulfide isomerase and Eimeria, which can be used in applications, gene therapy, genetic engineering, etc., and can solve the problems of safety and price of drug-resistant insect strains.
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Embodiment 1
[0115] Cloning of a protein disulfide isomerase (EtPDI) gene from Eimeria tenella:
[0116] 1. Materials
[0117] (1) Experimental animals
[0118] Luoman's high-quality yellow-feathered chickens are purchased from Shanghai Huizhong Breeding Chicken Farm. After hatching, they are transported back to the laboratory for breeding. The cages, feed, and drinking water are strictly sterilized.
[0119] (2) Experimental strains
[0120] Eimeria tenella: sporulated oocysts of Eimeria tenella, number: CAAS 21111601, provided by Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences.
[0121] (3) Main reagents
[0122] Trizol and GeneRaceTM Kit were purchased from Invitrogen; TaKaRa Agarose Gel DNAPurification Kit was purchased from Dalian Bao Biological Engineering Co., Ltd.; Agarose and PGEM-T-easy vector were purchased from Promega; JM109 competent cells were purchased from Dalian Bao Biological Co., Ltd.; ampicillin , IPTG were purchased from Huamei Bio...
Embodiment 2
[0146] Expression of Eimeria tenella protein disulfide isomerase (EtPDI) gene in Escherichia coli
[0147] 1. Materials
[0148] (1) Main reagents
[0149] Restriction enzymes were purchased from Dalian Baobio Biotechnology Co., Ltd. T4 DNA ligase was purchased from Promega, and DNA Marker was purchased from Shanghai Meiji Biotechnology Co., Ltd.
[0150] (2) Plasmids and strains
[0151] The recombination cloning plasmid pGEM-T-EtPDI is the above cloning recombination plasmid. Plasmids pGEX-4T-2 and BL21(DE3) were provided by our Institute.
[0152] 2. Method
[0153] (1) Construction of recombinant expression plasmids:
[0154] With the identified correct recombinant plasmid pGEM-T-EtPDI, use the multiple cloning site of the cloning vector pGEM-T-easy and the expression vector pGEX-4T-2, select the appropriate enzyme to carry out double digestion (Bam H I and EcoR I) , BW1-E06 and pGEX-4T-2 fragments were recovered after enzyme digestion, and the recombinant expressio...
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