A heavy metal-binding protein gene derived from high-temperature resistant bacteria and its anti-heavy metal application
A protein-binding and anti-heavy metal technology, applied in the field of genetic breeding, can solve the problems of destroying soil structure, secondary pollution, and high cost
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Embodiment 1
[0035] Artificial Synthesis of Heavy Metal Binding Protein TtHMBP Gene of Thermostable Bacteria
[0036] According to the gene sequence of the thermostable bacteria TtHMBP registered in Genbank, the gene synthesis method [NucleicAcids Research, 2004, 32, e98] was used to design the coding region of the synthetic gene according to the following principles without changing the amino acid sequence encoded by the gene: (1) Optimize gene codons to improve gene translation efficiency. (2) Eliminate the recognition sites of commonly used restriction endonucleases inside the gene to facilitate the construction of expression cassettes. (3) Eliminate inverted repeat sequences, stem-loop structures and transcription termination signals, balance GC / AT within genes, and improve RNA stability. (4) Make the gene-encoded protein conform to the N-terminal principle (Tobias1991) to improve the stability of the translated protein. (5) The design increases the free energy at the 5' end of the g...
Embodiment 2
[0040] Construction of TtHMBP Agrobacterium Binary Vector
[0041] The positive clone of the artificially synthesized TtHMBP gene above was amplified by PCR with primers, then added BamHI and Sac I cutting points at the head and tail respectively, and double-digested with Bam HI+Sac I, and the recovered DNA fragments were connected with the corresponding enzyme-cut vectors and digested with enzymes. The correct binary vector was obtained after identification and sequencing (see figure 1 ).
Embodiment 3
[0043] Transformation of Agrobacterium by electroporation
[0044] 1) Preparation of Agrobacterium GV3101 competent, the method refers to MicroPulserTM Electroporation Apparatus Operating Instructions and Application Guide (BIO-RAD Company) ((Rainerie et al., Bio. Tech., 1990, 8: 33-38).
[0045] 2) Take 50 μL of LGV3101 competent cells, add 1 μL of DNA, and transfer to a 0.2 cm electric shock cup for transformation (400Ω, 2.5KV, 25 μf). Add 1 mL of LB medium containing 1% mannitol to recover the culture for 2 hours (28° C., 250 rpm). Take 10 μL and 100 μL respectively and apply on LB plates (rifampicin 50 μg / mL, gentamicin 50 μg / mL, chloramphenicol 100 μg / mL).
[0046] 3) Pick several clones, extract the Agrobacterium plasmid by alkaline method, identify by enzyme digestion, and detect by PCR.
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