Engineering strain for efficiently expressing MccJ25 and fermentation process of engineering strain
A high-efficiency expression and engineering strain technology, applied in fermentation, genetic engineering, bacteria and other directions, can solve the problem of low expression of MicrocinJ25, and achieve the effect of high-efficiency expression and simple post-processing purification process.
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[0031] Further detailed explanation through specific implementation mode below:
[0032] Part 1: Construction of engineering strains highly expressing Microcin J25
[0033] The engineering strain is constructed by the following method: respectively carry out gene manipulation on mcjABCD to become one direction, and share a promoter T7 in Escherichia coli, and clone it in the vector pBR322 to realize high-efficiency expression in Escherichia coli, and the expression amount is 2.4g / L;
[0034] At the same time, error-prone PCR was used for directional evolution, and mcjABCD was mutated, and the amino acid sequence was changed. When expressed in Escherichia coli, the expression amount and antibacterial activity of the product increased significantly, and the expression amount was 4.1g / L; Expression, sharing a promoter PslpA, cloned in the pLEM415 vector, the expression level is 2.3g / L.
[0035] The construction process of the engineering strain is described in detail below.
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