Method for heterologous expression of epothilone
A technology of epothilone and heterologous expression, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problem of low epothilone expression efficiency and achieve the effect of increasing production
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Embodiment 1
[0071] Embodiment 1 Add precursor metabolic pathway pathway gene and tRNA to improve the output of epothilone
[0072] As analyzed previously, the DSM 7029 strain lacks a complete S-methylmalonyl-CoA synthesis pathway, and it lacks the PCC pathway and the mutase-isomerase pathway. Therefore, it is considered to increase the production of epothilone by supplementing the synthesis pathway of S-methylmalonyl-CoA, and the supplementary pathway diagram is shown in figure 1 shown. The method of operation is to first construct a plasmid containing the epo gene cluster and transfer it into the DSM 7029 strain, then construct a plasmid containing different supplementary pathway genes and / tRNA genes, and then transfer it into the above-mentioned DSM7029 strain containing the epo gene cluster to obtain Modified strains.
[0073]The construction process of plasmid 1 (containing the epo gene cluster) is as follows: the plasmids Cosmid 10 and Fosmid3B11 obtained by screening the So0157-2...
Embodiment 2
[0085] Embodiment 2The epo gene cluster is spliced again to add the promoter so as to improve the output of epothilone
[0086] After transcriptome sequencing of the strain MMR1 containing the epothilone gene cluster, it was found that the expression levels of each gene in the epothilone gene cluster were very low ( image 3 ), low-level gene expression may be another key factor restricting the production of epothilone.
[0087] In view of the above situation, in order to improve the expression efficiency of epothilone gene cluster in DSM7029, the six genes of epothilone gene cluster epoA, epoB, epoC, epoD, epoE and epoF were processed as follows by using Bxb1 integrase splicing technology. Figure 4 The resplicing shown. In front of each gene in the epothilone gene cluster, a promoter is added to increase the expression of each gene in the gene cluster. Attempt to increase epothilone production by adding a promoter.
[0088]Specifically, the plasmid pSB1A3 (derived from ...
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