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Ultrahigh-throughput screening of Trichoderma reesei strains capable of carbon catabolite repression release and cellulase hyperproduction using a microfluidic droplet platform

ABSTRACT Trichoderma reesei is the most well-known cellulase producer in the biorefinery industry. Its cellulase biosynthesis is repressed by glucose via carbon catabolite repression (CCR), making CCR-releasing strains with cellulase hyperproduction desirable. Here, we employed a microfluidic drople...

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Published in:Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2023-10, Vol.87 (11), p.1393-1406
Main Authors: Luu, Xuan Chinh, Shida, Yosuke, Suzuki, Yoshiyuki, Kuwahara, Daiki, Fujimoto, Takeshi, Takahashi, Yuka, Sato, Naomi, Nakamura, Akihiro, Ogasawara, Wataru
Format: Article
Language:English
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Summary:ABSTRACT Trichoderma reesei is the most well-known cellulase producer in the biorefinery industry. Its cellulase biosynthesis is repressed by glucose via carbon catabolite repression (CCR), making CCR-releasing strains with cellulase hyperproduction desirable. Here, we employed a microfluidic droplet platform to culture and screen T. reesei mutants capable of CCR release and cellulase overproduction from extensive mutagenesis libraries. With 3 mutagenesis rounds, about 6.20 × 103 droplets were sorted from a population of 1.51 × 106 droplets in a period of 4.4 h; 76 recovery mutants were screened on flask fermentation, and 2 glucose uptake retarded mutants, MG-9-3 and MG-9-3-30, were eventually isolated. We also generated a hypercellulase producer, M-5, with CCR release via a single mutagenesis round. The hyphal morphology and molecular mechanisms in the mutants were analyzed. This versatile approach combined with a comprehensive understanding of CCR release mechanisms will provide innovative and effective strategies for low-cost cellulase production. Graphical Abstract Graphical Abstract A repeated high-throughput mutagenesis workflow for strain improvements of Trichoderma reesei using the droplet-based microfluidic platform
ISSN:1347-6947
1347-6947
DOI:10.1093/bbb/zbad108