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Construction of T7-Like Expression System in Pseudomonas putida KT2440 to Enhance the Heterologous Expression Level.

ABSTRACT: Pseudomonas putida KT2440 has become an attractive chassis for heterologous expression with the development of effective genetic manipulation tools. Improving the level of transcriptional regulation is particularly important for extending the potential of P. putida KT2440 in heterologous expression. Although many strategies have been applied to enhance the heterologous expression level in P. putida KT2440, it was still at a relatively low level. Herein we constructed a T7-like expression system in P. putida KT2440, mimicking the pET expression system in Escherichia coli, which consisted of T7-like RNA polymerase (MmP1) integrated strain and the corresponding expression vector for the heterologous expression enhancement. With the optimization of the insertion site and the copy number of RNA polymerase (RNAP), the relative fluorescence intensity (RFI) of the super-folder green fluorescent protein (sfGFP) was improved by 1.4-fold in MmP1 RNAP integrated strain. The induction point and IPTG concentration were also optimized. This strategy was extended to the gene-reduced strain EM42 and the expression of sfGFP was improved by 2.1-fold. The optimal RNAP integration site was also used for introducing T7 RNAP in P. putida KT2440 and the expression level was enhanced, indicating the generality of the integration site for the T7 expression system. Compared to other inducible expression systems in KT2440, the heterologous expression level of the Mmp1 system and T7 system were more than 2.5 times higher. Furthermore, the 3.6-fold enhanced expression level of a difficult-to-express nicotinate dehydrogenase from Comamonas testosteroni JA1 verified the efficiency of the T7-like expression system in P. putida KT2440. Taken together, we constructed and optimized the T7-like and T7 expression system in P. putida, thus providing a set of applicable chassis and corresponding plasmids to improve recombinant expression level, expecting to be used for difficult-to-express proteins.

SUBMITTER: Liang T

PROVIDER: S-EPMC8322953 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Tripartite efflux systems transport antimicrobial agents, toxic metabolites, and siderophores from Gram-negative cells into the environment. For example, the main siderophore pyoverdine of the soil bacterium Pseudomonas putida KT2440 is secreted into the environment via the PvdRT-OpmQ and MdtABC-OpmB systems. Here, we looked for efflux systems that might be involved in the secretion of pyoverdine in addition to the latter two systems. Screening of different efflux systems revealed that parX (encoding the periplasmic adapter protein of the ParXY system) is of particular importance for bacterial growth under iron limitation. Further analysis showed that the deletion of parX impairs the production and secretion of pyoverdine, causing the observed growth effect. The effects were dependent on the presence of other tripartite efflux systems and the conditions of iron limitation. The results suggest that ParXY not only plays a role in antibiotic resistance, as shown previously, but also influences the secretion of siderophores in a network of overlapping activities of different tripartite efflux systems.IMPORTANCEGram-negative bacteria from the Pseudomonas group are survivors in various environmental niches. For example, the bacteria secrete siderophores to capture ferric ions under deficiency conditions. Tripartite efflux systems are involved in the secretion of siderophores, which are also important for antibiotic resistance. For one of these efflux systems, the resistance-nodulation-cell division transporter ParXY from the model organism Pseudomonas putida KT2440, we show that it influences the secretion of the siderophore pyoverdine in addition to its already known involvement in antibiotic resistance. Phenotypically, its role in pyoverdine secretion is only apparent when other pyoverdine secretion systems are inactive. The results confirm that the different tripartite efflux systems have overlapping substrate specificities and can at least partially functionally substitute for each other, especially in important physiological activities such as supplying the cell with iron ions. This fact must be taken into account when developing specific inhibitors for tripartite efflux systems.

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Construction of T7-Like Expression System in Pseudomonas putida KT2440 to Enhance the Heterologous Expression Level.

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