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小GTP酶Rab7参与对碳饥饿的应激适应,以确保里氏木霉中诱导的纤维素酶生物合成。

Small GTPase Rab7 is involved in stress adaptation to carbon starvation to ensure the induced cellulase biosynthesis in Trichoderma reesei.

作者信息

Liu Lin, Wang Zhixing, Fang Yu, Yang Renfei, Pu Yi, Meng Xiangfeng, Liu Weifeng

机构信息

State Key Laboratory of Microbial Technology, Microbiology Technology Institute, Shandong University, No. 72 Binhai Road, Qingdao, 266237, People's Republic of China.

出版信息

Biotechnol Biofuels Bioprod. 2024 Apr 20;17(1):55. doi: 10.1186/s13068-024-02504-6.

DOI:10.1186/s13068-024-02504-6
PMID:38643207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11032611/
Abstract

BACKGROUND

The saprophytic filamentous fungus Trichoderma reesei represents one of the most prolific cellulase producers. The bulk production of lignocellulolytic enzymes by T. reesei not only relies on the efficient transcription of cellulase genes but also their efficient secretion after being translated. However, little attention has been paid to the functional roles of the involved secretory pathway in the high-level production of cellulases in T. reesei. Rab GTPases are key regulators in coordinating various vesicle trafficking associated with the eukaryotic secretory pathway. Specifically, Rab7 is a representative GTPase regulating the transition of the early endosome to the late endosome followed by its fusion to the vacuole as well as homotypic vacuole fusion. Although crosstalk between the endosomal/vacuolar pathway and the secretion pathway has been reported, the functional role of Rab7 in cellulase production in T. reesei remains unknown.

RESULTS

A TrRab7 was identified and characterized in T. reesei. TrRab7 was shown to play important roles in T. reesei vegetative growth and vacuole morphology. Whereas knock-down of Trrab7 significantly compromised the induced production of T. reesei cellulases, overexpression of the key transcriptional activator, Xyr1, restored the production of cellulases in the Trrab7 knock-down strain (Ptcu-rab7) on glucose, indicating that the observed defective cellulase biosynthesis results from the compromised cellulase gene transcription. Down-regulation of Trrab7 was also found to make T. reesei more sensitive to various stresses including carbon starvation. Interestingly, overexpression of Snf1, a serine/threonine protein kinase known as an energetic sensor, partially restored the cellulase production of Ptcu-rab7 on Avicel, implicating that TrRab7 is involved in an energetic adaptation to carbon starvation which contributes to the successful cellulase gene expression when T. reesei is transferred from glucose to cellulose.

CONCLUSIONS

TrRab7 was shown to play important roles in T. reesei development and a stress response to carbon starvation resulting from nutrient shift. This adaptation may allow T. reesei to successfully initiate the inducing process leading to efficient cellulase production. The present study provides useful insights into the functional involvement of the endosomal/vacuolar pathway in T. reesei development and hydrolytic enzyme production.

摘要

背景

腐生丝状真菌里氏木霉是最丰富的纤维素酶生产者之一。里氏木霉大量生产木质纤维素酶不仅依赖于纤维素酶基因的有效转录,还依赖于其翻译后的有效分泌。然而,在里氏木霉中,参与分泌途径在纤维素酶高水平生产中的功能作用却很少受到关注。Rab GTP酶是协调与真核生物分泌途径相关的各种囊泡运输的关键调节因子。具体而言,Rab7是一种代表性的GTP酶,它调节早期内体向晚期内体的转变,随后晚期内体与液泡融合以及同型液泡融合。尽管已经报道了内体/液泡途径与分泌途径之间的相互作用,但Rab7在里氏木霉纤维素酶生产中的功能作用仍然未知。

结果

在里氏木霉中鉴定并表征了TrRab7。结果表明,TrRab7在里氏木霉的营养生长和液泡形态中发挥重要作用。虽然敲低Trrab7显著损害了里氏木霉纤维素酶的诱导产生,但关键转录激活因子Xyr1的过表达恢复了Trrab7敲低菌株(Ptcu-rab7)在葡萄糖上纤维素酶的产生,这表明观察到的纤维素酶生物合成缺陷是由于纤维素酶基因转录受损所致。还发现敲低Trrab7会使里氏木霉对包括碳饥饿在内的各种胁迫更加敏感。有趣的是,丝氨酸/苏氨酸蛋白激酶Snf1(一种已知的能量传感器)的过表达部分恢复了Ptcu-rab7在微晶纤维素上的纤维素酶产生,这意味着TrRab7参与了对碳饥饿的能量适应,当里氏木霉从葡萄糖转移到纤维素时,这种适应有助于成功地表达纤维素酶基因。

结论

结果表明,TrRab7在里氏木霉的发育以及对营养转移导致的碳饥饿的应激反应中发挥重要作用。这种适应可能使里氏木霉成功启动诱导过程,从而高效生产纤维素酶。本研究为内体/液泡途径在里氏木霉发育和水解酶生产中的功能参与提供了有用的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/e756fce99eb6/13068_2024_2504_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/0e242a67debf/13068_2024_2504_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/a40da5b0c8ee/13068_2024_2504_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/e756fce99eb6/13068_2024_2504_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/dae27f168bfe/13068_2024_2504_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/f95f02fa3f3b/13068_2024_2504_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/9d1755089a1b/13068_2024_2504_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/5fbc982d801e/13068_2024_2504_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/bc10b27872e8/13068_2024_2504_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/0e242a67debf/13068_2024_2504_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/a40da5b0c8ee/13068_2024_2504_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/11032611/e756fce99eb6/13068_2024_2504_Fig8_HTML.jpg

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