4.7 Article

Development of a flow cytometry-based plating-free system for strain engineering in industrial fungi

期刊

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 106, 期 2, 页码 713-727

出版社

SPRINGER
DOI: 10.1007/s00253-021-11733-w

关键词

Myceliophthora thermophila; Aspergillus niger; Plating-free; Flow cytometry; Glucoamylase; CRISPR-Cas9

资金

  1. National Key Research & Developmental Program of China [2018YFA0900500]
  2. National Natural Science Foundation of China [31771386, 31972878, 31972879]
  3. Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project [TSBICIP-KJGG-006]
  4. Youth Innovation Promotion Association of the Chinese Academy of Sciences [2019180]
  5. National Major Science and Technology Projects of China [2018YFA0900500]

向作者/读者索取更多资源

Recent research has developed a flow cytometry-based plating-free system for screening and isolating transformed protoplasts in industrial fungi. This system combines genetic engineering, flow cytometry, and colony sorting techniques to generate hyperproducing strains with significantly increased protein secretion levels. Overall, this system provides a convenient and efficient tool for strain engineering in fungal biotechnology, facilitating improvements in filamentous fungal strains for industrial applications.
Recent technical advances regarding filamentous fungi have accelerated the engineering of fungal-based production and benefited basic science. However, challenges still remain and limit the speed of fungal applications. For example, high-throughput technologies tailored to filamentous fungi are not yet commonly available for genetic modification. The currently used fungal genetic manipulations are time-consuming and laborious. Here, we developed a flow cytometry-based plating-free system to directly screen and isolate the transformed protoplasts in industrial fungi Myceliophthora thermophila and Aspergillus niger. This system combines genetic engineering via the 2A peptide and the CRISPR-Cas9 system, strain screening by flow cytometry, and direct sorting of colonies for deep-well-plate incubation and phenotypic analysis while avoiding culturing transformed protoplasts in plates, colony picking, conidiation, and cultivation. As a proof of concept, we successfully applied this system to generate the glucoamylase-hyperproducing strains MtYM6 and AnLM3 in M. thermophila and A. niger, respectively. Notably, the protein secretion level and enzyme activities in MtYM6 were 17.3- and 25.1-fold higher than in the host strain. Overall, these findings suggest that the flow cytometry-based plating-free system can be a convenient and efficient tool for strain engineering in fungal biotechnology. We expect this system to facilitate improvements of filamentous fungal strains for industrial applications.

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