Chloroplast-expressed human epidermal growth factor (hEGF) protein and preparation method thereof
An epidermal growth factor and chloroplast expression technology, applied in the field of genetic engineering, can solve the problems of undetectable, poor expression level of exogenous protein, and no fusion GUS gene EGF expression, etc.
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Embodiment 1
[0031] The construction of the tobacco chloroplast expression vector pWYP23404 (EGF) of embodiment 1 epidermal growth factor
[0032] 1) The nucleotide sequence of the human epidermal growth factor (human Epidermal growth factor, hEGF) gene in the NCBI database is optimally designed using modern bioinformatics technology. Under the premise of keeping the amino acid sequence unchanged, Gene Designer was used to replace all codons of the coding gene with the optimal coding method of tobacco chloroplast codons, and the modified gene sequence was passed through DNAMAN7.0 and Vector NTI10 .0 software analyzes the enzyme cutting site information therein, and changes the coding codon of the 35th amino acid Ile of the epidermal growth factor coding gene from the first optimal codon TAT to the second optimal codon TAC to eliminate EcoR I As for the enzyme cutting site, the nucleotide sequence of the modified human epidermal growth factor (human Epidermal growth factor, EGF) gene is sho...
Embodiment 2
[0036] Embodiment 2: Tobacco chloroplast transformation and homogenization screening of EGF gene
[0037] The gold powder was coated with vector pWYP23404 for gene gun bombardment. For specific operations, please refer to the patented human basic fibroblast growth factor, tobacco chloroplast expression vector and production method (application number: 201510310239.3, application date: 2015-06-08, publication number: CN104946656A).
[0038] A. Tobacco explant preparation
[0039] Tobacco seeds soaked in 70% ethanol for 30sec, shake gently during the period; carefully discard the ethanol, add 0.1% HgCl 2 , shake gently for 2min; carefully discard HgCl 2 Solution, rinse with sterile water 3 times, 1 min each time. After the last rinsing, leave a small amount of water, suspend the seeds, pour them on several layers of sterile filter paper, blot the water, and carefully inoculate the seeds on 1 / 2 MSO medium with tweezers. The cycle was cultured in a culture room with light 16h / ...
Embodiment 3
[0089] Example 3 In vivo detection of protein label green fluorescent protein GFP
[0090] For the whole plant fluorescence analysis of transgenic materials, please refer to the patent for a human basic fibroblast growth factor, tobacco chloroplast expression vector and production method (application number: 201510310239.3, application date: 2015-06-08, publication number: CN104946656A).
[0091] Fluorescent detection of the GFP tag at the N-terminus of the target protein expressed in the transgenic plants. Under 365nm ultraviolet light, the transgenic plants emitted strong green fluorescence in the dark room, indicating that the green fluorescent protein was expressed in large quantities, while the control plants showed auto-red fluorescence ( image 3 ).
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