4.7 Article

Development of an efficient protein expression system in the thermophilic fungus Myceliophthora thermophila

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MICROBIAL CELL FACTORIES
卷 22, 期 1, 页码 -

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BMC
DOI: 10.1186/s12934-023-02245-5

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Myceliophthora thermophila; Protein expression; Promoter; 5'UTR; Signal peptide

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In this study, an efficient protein expression system was established in Myceliophthora thermophila, enabling high-level expression and secretion of various proteins. The system was stable and could be used for the production of different enzymes, expanding the biotechnological potential of M. thermophila.
Background Thermophilic fungus Myceliophthora thermophila has been widely used in industrial applications due to its ability to produce various enzymes. However, the lack of an efficient protein expression system has limited its biotechnological applications.Results In this study, using a laccase gene reporting system, we developed an efficient protein expression system in M. thermophila through the selection of strong constitutive promoters, 5'UTRs and signal peptides. The expression of the laccase was confirmed by enzyme activity assays. The results showed that the Mtpdc promoter (Ppdc) was able to drive high-level expression of the target protein in M. thermophila. Manipulation of the 5'UTR also has significant effects on protein expression and secretion. The best 5'UTR (NCA-7d) was identified. The transformant containing the laccase gene under the Mtpdc promoter, NCA-7d 5'UTR and its own signal peptide with the highest laccase activity (1708 U/L) was obtained. In addition, the expression system was stable and could be used for the production of various proteins, including homologous proteins like MtCbh-1, MtGh5-1, MtLPMO9B, and MtEpl1, as well as a glucoamylase from Trichoderma reesei.Conclusions An efficient protein expression system was established in M. thermophila for the production of various proteins. This study provides a valuable tool for protein production in M. thermophila and expands its potential for biotechnological applications.

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