Shibata Nozomu, Kakeshita Hiroshi, Igarashi Kazuaki, Takimura Yasushi, Shida Yosuke, Ogasawara Wataru, Koda Tohru, Hasunuma Tomohisa, Kondo Akihiko
Biological Science Research, Kao Corporation, 1334 Minato, Wakayama, Wakayama, 640-8580, Japan.
Graduate School of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai, Nada-ku, Kobe, Hyogo, 657-8501, Japan.
Biotechnol Biofuels. 2021 Feb 8;14(1):39. doi: 10.1186/s13068-021-01887-0.
Trichoderma reesei is a filamentous fungus that is important as an industrial producer of cellulases and hemicellulases due to its high secretion of these enzymes and outstanding performance in industrial fermenters. However, the reduction of enzyme production caused by carbon catabolite repression (CCR) has long been a problem. Disruption of a typical transcriptional regulator, Cre1, does not sufficiently suppress this reduction in the presence of glucose.
We found that deletion of an α-tubulin (tubB) in T. reesei enhanced both the amount and rate of secretory protein production. Also, the tubulin-disrupted (ΔtubB) strain had high enzyme production and the same enzyme profile even if the strain was cultured in a glucose-containing medium. From transcriptome analysis, the ΔtubB strain exhibited upregulation of both cellulase and hemicellulase genes including some that were not originally induced by cellulose. Moreover, cellobiose transporter genes and the other sugar transporter genes were highly upregulated, and simultaneous uptake of glucose and cellobiose was also observed in the ΔtubB strain. These results suggested that the ΔtubB strain was released from CCR.
Trichoderma reesei α-tubulin is involved in the transcription of cellulase and hemicellulase genes, as well as in CCR. This is the first report of overcoming CCR by disrupting α-tubulin gene in T. reesei. The disruption of α-tubulin is a promising approach for creating next-generation enzyme-producing strains of T. reesei.
里氏木霉是一种丝状真菌,因其能高效分泌纤维素酶和半纤维素酶且在工业发酵罐中表现出色,作为这些酶的工业生产者具有重要意义。然而,长期以来,碳分解代谢物阻遏(CCR)导致的酶产量降低一直是个问题。破坏典型的转录调节因子Cre1,在有葡萄糖存在的情况下并不能充分抑制这种产量降低。
我们发现,敲除里氏木霉中的α-微管蛋白(tubB)可提高分泌蛋白的产量和分泌速率。此外,即使在含葡萄糖的培养基中培养,微管蛋白敲除(ΔtubB)菌株仍具有高产酶量且酶谱相同。通过转录组分析,ΔtubB菌株中纤维素酶和半纤维素酶基因均上调,包括一些原本不受纤维素诱导的基因。此外,纤维二糖转运蛋白基因和其他糖转运蛋白基因也高度上调,并且在ΔtubB菌株中还观察到葡萄糖和纤维二糖的同时摄取。这些结果表明,ΔtubB菌株摆脱了CCR。
里氏木霉α-微管蛋白参与纤维素酶和半纤维素酶基因的转录以及CCR过程。这是首次报道通过敲除里氏木霉中的α-微管蛋白基因来克服CCR。敲除α-微管蛋白是创建下一代里氏木霉产酶菌株的一种有前景的方法。