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An efficient Agrobacterium-mediated system based on the pyrG auxotrophic marker for recombinant expression in the filamentous fungus Penicillium rubens

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Abstract

Objectives

This work aimed to construct a versatile, effective, and food-grade Agrobacterium tumefaciens-mediated transformation (ATMT) system for recombinant expression in the filamentous fungus Penicillium rubens (also known as Pencillium chrysogenum).

Results

In this study, the wild-type P. chrysogenum VTCC 31172 strain was re-classified as P. rubens by a multilocus sequencing analysis. Further, the pyrG gene required for uridine/uracil biosynthesis was successfully deleted in the VTCC 31172 strain by homologous recombination to generate a stable uridine/uracil auxotrophic mutant (ΔpyrG). The growth of the P. rubens ΔpyrG strain could be restored by uridine/uracil supplementation, and a new ATMT system based on the uridine/uracil auxotrophic mechanism was established for this strain. The optimal ATMT efficiency could reach 1750 transformants for 106 spores (equivalent to 0.18%). In addition, supplementation of uridine/uracil at the concentrations of 0.005–0.02% during the co-cultivation process significantly promoted transformation efficiency. Especially, we demonstrated that the pyrG marker and the amyB promoter from the koji mold Aspergillus oryzae were fully functional in P. rubens ΔpyrG. Expression of the DsRed reporter gene under the regulation of the A. oryzae amyB promoter lighted up the mycelium of P. rubens with a robust red signal under fluorescence microscopy. Furthermore, genomic integration of multiple copies of the Aspergillus fumigatus phyA gene under the control of the amyB promoter significantly enhanced phytase activity in P. rubens.

Conclusions

The ATMT system developed in our work provides a safe genetic platform for producing recombinant products in P. rubens without using drug resistance markers.

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Data availability

The datasets generated during the current study are available from the corresponding author upon reasonable request.

References

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Acknowledgements

The authors thank members of the National Key Laboratory of Enzyme and Protein Technology (KLEPT) for technical assistance and helpful discussion.

Funding

This work was supported by Vietnam National University, Hanoi (VNU) through grant number TXTCN.21.29. 

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Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by HDT, TXV, HHV, GTN, MTT, HTTT, HTTP, NTHL, and VTT. The first draft of the manuscript was written by VTT, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Van-Tuan Tran.

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The authors have no relevant financial or non-financial interests to disclose.

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This article does not contain any study with human participants performed by any of the authors.

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Tran, VT., Thai, HD., Vu, T.X. et al. An efficient Agrobacterium-mediated system based on the pyrG auxotrophic marker for recombinant expression in the filamentous fungus Penicillium rubens. Biotechnol Lett 45, 689–702 (2023). https://doi.org/10.1007/s10529-023-03374-y

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  • DOI: https://doi.org/10.1007/s10529-023-03374-y

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