Method for improving yield of cadaverine produced by utilizing microorganisms for saccharides fermentation
A technology of microorganisms and cadaverine, applied in the field of genetically engineered bacteria, can solve the problems of no knockout or weakened cadaverine production, and achieve the effects of preventing degradation, improving utilization rate, and reducing production costs
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Embodiment 1
[0032] A method for improving the production of cadaverine by microorganisms using sugar fermentation, in which the key regulatory sites for the synthesis of cadaverine by microorganisms are modified, for example, the key regulatory sites are the lysE site of the lysine transporter gene and / or the pgi site of the 6-phosphate glucose isomerase gene, or, the key regulatory site is a regulatory site that regulates the expression of the above-mentioned genes.
[0033] Preferably, the modification of the key regulatory sites for the synthesis of cadaverine by microorganisms is: knocking out the lysine transporter gene lysE and / or the glucose-6-phosphate isomerase gene pgi, and / or, by changing their promoters, ribosome binding sites, or genetic mutations to attenuate their expression or attenuate enzyme activity.
[0034] Preferably, the microorganism is Escherichia coli, Corynebacterium glutamicum, Haffney hive or their recombinant strains.
[0035] The method for improving the p...
Embodiment 2
[0057] A method for improving the production of cadaverine by microorganisms using sugar fermentation, by modifying key regulatory sites in the metabolic pathway of microorganisms to synthesize cadaverine.
[0058] Preferably, the key regulatory sites are the lysE site of the lysine transporter gene and the pgi site of the 6-phosphate glucose isomerase gene, or the regulatory sites of these two genes that regulate the gene expression of the above key regulatory sites point.
[0059] Preferably, the transformation is: knocking out the lysine transporter gene lysE and / or the glucose-6-phosphate isomerase gene pgi, and / or, by changing their promoters, ribosome binding sites or performing gene Mutations to attenuate their expression or attenuate enzyme activity.
[0060] Preferably, the microorganism is Escherichia coli, Corynebacterium glutamicum, Haffney hive or their recombinant strains.
[0061] The specific steps of the transformation are as follows:
[0062] By cloning th...
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