Evidence map›Paper›PMID 41316230›Full record

ArticleMicrobial cell factories2025

Novel transcription factor regulating cellulase expression and growth improvement in cellulolytic fungi.

Chunying Li, Shijia Dong, Mingjuan Cui, Shanhao Zhou, Min Zhang, Yunfei Gao, Yixin Sun, Xiaomei Hu

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Article in Microbial cell factories, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chunying Li *School of Geography and Tourism, Harbin University, Harbin, 150086, China.
Shijia Dong *School of Geography and Tourism, Harbin University, Harbin, 150086, China.
Mingjuan CuiCollege of Life Science, Northeast Agricultural University, Harbin, 150030, China.
Shanhao ZhouCollege of Life Science, Northeast Agricultural University, Harbin, 150030, China.
Min ZhangCollege of Life Science, Northeast Agricultural University, Harbin, 150030, China.
Yunfei GaoHeilongjiang Academy of Agricultural Sciences, Harbin, 150086, China.
Yixin SunCollege of Life Science, Linyi University, Linyi, 27600, China. sunyixin1006@163.com.
Xiaomei HuCollege of Life Science, Northeast Agricultural University, Harbin, 150030, China. xmhu@neau.edu.cn.

Funding

Heilongjiang Province Key Research and Development Plan project grant number GA23B015Natural Science Foundation of Heilongjiang Province of China No. YQ2022C027
6 · The paper itself

Abstract

backgroundTalaromyces sp., as powerful cellulolytic fungi, display a nearly complete enzymatic system, which exhibits a complex regulatory system involving multiple transcription factors to control the expression of cellulase genes. However, there are fewer studies on the transcriptional regulatory factors of cellulase expression in Talaromyces sp. This study provides a basis for in-depth analysis of the transcription regulatory mechanism of Talaromyces endophyticus for cellulase expression, offering new ways for the preparation of fermented sugars using straw resources to produce high value-added products and biofuels.

resultsIn this study, a novel transcription factor was investigated for T. endophyticus NEAU-6 which was a high cellulase-producing strain. Results revealed that TeSrdA was nuclear protein, which was stably expressed in the nucleus. TeSrdA deletion caused a remarkable increase of the activities of FPase (121.1%), CMCase (36.6%), pNPCase (97.0%), β-glucosidase (75.1%) and Xylanase (98.4%). Microscopic analysis showed that ΔTeSrdA strains increased the length of the hyphae and the number of branching. Notably, TeSrdA deletion could accelerated the microbial growth, which was unlike most studies in which deletion of transcription factor led to the reduction of cell growth. Quantitative reverse transcription polymerase chain reaction (RT-qPCR) analyses revealed that the expression of eg7A, cbh6A, bgl3A, xyl11A genes was up-regulated obviously in the ΔTeSrdA strain. Through Electrophoretic mobility shift assays (EMSA), we further discovered that the transcription factor TeSrdA regulated the transcription of eg7A, cbh6A, cbh6B, bgl3A, xyl11A and xyl11B by directly binding to the promoters of these enzyme genes, thereby repressing the cellulase production.

conclusionsTeSrdA plays an important role by increasing hyphal branching, accelerating strain growth, and promoting cellulase and hemicellulase production. The novel transcription factor TeSrdA is of great significance for studying the transcriptional regulatory network related to enzyme production and growth of strains in Talaromyces sp.

Indexed as

CellulaseFungal ProteinsTalaromycesTranscription FactorsGene Expression Regulation, FungalPromoter Regions, GeneticCellulaseFungal ProteinsTranscription FactorsCellulase expressionCellulolytic fungiTalaromyces sp.Transcription factor

Identifiers

PMID41316230
PMCPMC12765306

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.