ADP-ribosylation factor GTPase-activating proteins in lignocellulose utilization of Trichoderma guizhouense NJAU4742 的 ADP-ribosylation factor GTPase-activating proteins 的不同作用

IF 6.1 1区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tuo Li, Qin Wang, Yang Liu, Jiaguo Wang, Han Zhu, Linhua Cao, Dongyang Liu, Qirong Shen
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引用次数: 0

摘要

丝状真菌降解木质纤维素的能力一直归功于其高效的 CAZymes 系统,该系统在生物能源开发中具有更广泛的应用。ADP-ribosylation factor GTPase-activating proteins(Arf-GAPs)是真菌形态发生中的关键蛋白,但对其在木质纤维素利用中的调控机制缺乏全面的研究。在此,研究人员在贵州毛霉(Trichoderma guizhouense NJAU4742)中鉴定了Arf-GAPs在S. cerevisiae中的直向同源物(TgGlo3和TgGcs1)。结果表明,过量表达 Tggcs1(OE-Tggcs1)会提高木质纤维素的利用率,而增加 Tgglo3(OE-Tgglo3)的表达则会引起相反的反应。以稻草为唯一碳源进行发酵的第四天,野生型菌株(WT)的内切葡聚糖酶、纤维素水解酶、木聚糖酶和滤纸活性分别达到 8.20 U mL-1、4.42 U mL-1、14.10 U mL-1 和 3.56 U mL-1。与 WT 相比,OE-Tggcs1 的四种酶活性分别提高了 7.93%、6.11%、9.08% 和 12.92%,而 OE-Tgglo3 的四种酶活性则有不同程度的降低。在营养生长过程中,OE-Tgglo3 导致以稀疏和收缩为特征的菌丝形态,而 OE-Tggcs1 则导致液泡体积显著增加。此外,OE-Tggcs1 表现出更高的葡萄糖和纤维生物糖运输效率,从而维持了强大的细胞代谢率。进一步的研究发现,Tgglo3 和 Tggcs1 对类达能素 GTPase 基因(Tggtp)的转录水平进行了不同的调节,从而引起了不同的氧化还原状态和细胞凋亡反应,从而协调了细胞对木质纤维素利用的反应。总之,这些发现强调了 TgArf-GAPs 在木质纤维素利用过程中作为关键调控因子的重要性,并为它们对下游靶标的不同调控提供了初步见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Divergent roles of ADP-ribosylation factor GTPase-activating proteins in lignocellulose utilization of Trichoderma guizhouense NJAU4742

Background

The ability of lignocellulose degradation for filamentous fungi is always attributed to their efficient CAZymes system with broader applications in bioenergy development. ADP-ribosylation factor GTPase-activating proteins (Arf-GAPs), pivotal in fungal morphogenesis, lack comprehensive studies on their regulatory mechanisms in lignocellulose utilization.

Results

Here, the orthologs (TgGlo3 and TgGcs1) of Arf-GAPs in S. cerevisiae were characterized in Trichoderma guizhouense NJAU4742. The results indicated that overexpression of Tggcs1 (OE-Tggcs1) enhanced the lignocellulose utilization, whereas increased expression of Tgglo3 (OE-Tgglo3) elicited antithetical responses. On the fourth day of fermentation with rice straw as the sole carbon source, the activities of endoglucanase, cellobiohydrolase, xylanase, and filter paper of the wild-type strain (WT) reached 8.20 U mL−1, 4.42 U mL−1, 14.10 U mL−1, and 3.56 U mL−1, respectively. Compared to WT, the four enzymes activities of OE-Tggcs1 increased by 7.93%, 6.11%, 9.08%, and 12.92%, respectively, while those decreased to varying degrees of OE-Tgglo3. During the nutritional growth, OE-Tgglo3 resulted in the hyphal morphology characterized by sparsity and constriction, while OE-Tggcs1 led to a notable increase in vacuole volume. In addition, OE-Tggcs1 exhibited higher transport efficiencies for glucose and cellobiose thereby sustaining robust cellular metabolic rates. Further investigations revealed that Tgglo3 and Tggcs1 differentially regulated the transcription level of a dynamin-like GTPase gene (Tggtp), eliciting distinct redox states and apoptotic reaction, thus orchestrating the cellular response to lignocellulose utilization.

Conclusions

Overall, these findings underscored the significance of TgArf-GAPs as pivotal regulators in lignocellulose utilization and provided initial insights into their differential modulation of downstream targets.

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来源期刊
Biotechnology for Biofuels
Biotechnology for Biofuels 工程技术-生物工程与应用微生物
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审稿时长
2.7 months
期刊介绍: Biotechnology for Biofuels is an open access peer-reviewed journal featuring high-quality studies describing technological and operational advances in the production of biofuels, chemicals and other bioproducts. The journal emphasizes understanding and advancing the application of biotechnology and synergistic operations to improve plants and biological conversion systems for the biological production of these products from biomass, intermediates derived from biomass, or CO2, as well as upstream or downstream operations that are integral to biological conversion of biomass. Biotechnology for Biofuels focuses on the following areas: • Development of terrestrial plant feedstocks • Development of algal feedstocks • Biomass pretreatment, fractionation and extraction for biological conversion • Enzyme engineering, production and analysis • Bacterial genetics, physiology and metabolic engineering • Fungal/yeast genetics, physiology and metabolic engineering • Fermentation, biocatalytic conversion and reaction dynamics • Biological production of chemicals and bioproducts from biomass • Anaerobic digestion, biohydrogen and bioelectricity • Bioprocess integration, techno-economic analysis, modelling and policy • Life cycle assessment and environmental impact analysis
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