Group of amino acid sequences capable of improving activity and stability of SOD and application thereof
An amino acid and stability technology, which is applied to a group of amino acid sequences that can improve the activity and stability of SOD and its application fields, and can solve the problems of limited raw materials, difficult operation, and difficulty in meeting the needs of industrialization
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Embodiment 1
[0093] A clone of the complete sequence gene (sodM1) encoding Fe / Mn-SOD of M1 was constructed, and a clone of the DNA sequence (sodAM1) encoding the domain sodA of SODM1 was constructed, and the optimal activity and stability of the expressed protein were determined.
[0094] 1. Extraction of total DNA from Paenibacillus polymyxa M1
[0095] In this example, Paenibacillus isolated from oil well formation water in Dagang Oilfield, Tianjin, China Paenibacillus polymyxa For M1, take 3 mL of fresh culture cultured overnight, collect the cells by centrifugation, suspend the cells in 250 μL of 50 mM Tris buffer (pH8.0), add 10 μL of 0.4M EDTA (pH8.0), mix well and then incubate at 37 °C After 20min, add 30μL 20mg / L lysozyme, mix well and keep warm at 37℃ for another 20min, then add 5μL 20mg / L proteinase K, mix gently, then add 20μL 10% SDS, keep warm at 50℃ until the solution is clear, use Equal volume of phenol: chloroform: isoamyl alcohol extraction twice, chloroform: isoamyl al...
Embodiment 2
[0123] build code B. subtilis Mn-SOD full sequence gene of BSn5 (sod-BSn5 ), and construct the DNA sequence encoding the domain sodA of SOD-BSn5 (sodA-BSn5) clone, and finally construct the complete sequence gene encoding recombinant SOD (N-terminal sequence of SOD-GTNG_2215 and SODA of B. subtilis BSn5 recombined into recombinant SOD) ( sod- combinant ) clones. And the enzyme activity and thermal stability of the expressed protein were measured.
[0124] 1. B. subtilis Extraction of BSn5 total DNA
[0125] In this example, 3 mL of the fresh culture cultured overnight was collected, and the cells were collected by centrifugation. The cells were suspended in 250 μL of 50 mMTris buffer (pH8.0), added with 10 μL of 0.4M EDTA (pH8.0), and mixed Incubate at 37°C for 20min, then add 30μL 20mg / L lysozyme, mix well and then incubate at 37°C for 20min, then add 5μL 20mg / L proteinase K, mix gently, then add 20μL 10% SDS, keep warm at 50°C until solution For clarification, u...
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