Xinyao Lu , Xiaoqing Hao , Xinran Mao , Bin Zhuge , Hong Zong
{"title":"RNA解旋酶CgDBP4提高了产甘油假丝酵母和解脂耶氏菌对未解毒纤维素水解产物的耐受性和发酵性能","authors":"Xinyao Lu , Xiaoqing Hao , Xinran Mao , Bin Zhuge , Hong Zong","doi":"10.1016/j.bej.2025.109919","DOIUrl":null,"url":null,"abstract":"<div><div>RNA helicase functions in RNA transcription, translation, and degradation that promotes the assembly of mRNP, affecting the cell's sugar transport process, DNA repair, and cell cycle progression. This study employed the RNA helicase CgDBP4 from <em>Candida glycerinogenes</em> as a stress-resistant genetic element for both <em>C. glycerinogenes</em> and <em>Y. lipolytica</em>. CgDBP4 affected cell tolerance of <em>C glycerinogenes</em> to NaCl, high sugar, acetic acid, and heat stresses. Under 44 ℃, the ethanol production rate of <em>C. g-antiDBP4</em> (It is a recombinant strain that moderately upregulates the transcriptional level of <em>CgDBP4</em>) increased from 1.5 g·(L·h⁻¹) to 2.0 g·(L·h⁻¹). <em>CgTy3</em> is a retrotransposon rescued the cell growth of the <em>C. g-antiDBP4</em> under heat stress. The downregulation of <em>CgTy3</em> impaired the transcription of RNA polymerase III, genomic stability, protein processing, and the activation of heat-responsive genes, consequently influencing the ability of <em>CgDBP4</em> in cell tolerate to heat stress. <em>CgDBP4</em> also enhanced the resistance of <em>Y. lipolytica</em> Po1f to multiple stresses and improved lipid titer by 44.5 % in typical media. Besides, <em>Y. l‐CgDBP4</em> produced 38.1 mg/L of lipids under 34 ℃ and 49.1 mg/L of lipids in undetoxified cellulose hydrolysates.</div></div>","PeriodicalId":8766,"journal":{"name":"Biochemical Engineering Journal","volume":"225 ","pages":"Article 109919"},"PeriodicalIF":3.7000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"RNA helicase CgDBP4 improves tolerance and fermentation performance of Candida glycerinogenes and Yarrowia lipolytica from undetoxified cellulose hydrolysate\",\"authors\":\"Xinyao Lu , Xiaoqing Hao , Xinran Mao , Bin Zhuge , Hong Zong\",\"doi\":\"10.1016/j.bej.2025.109919\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>RNA helicase functions in RNA transcription, translation, and degradation that promotes the assembly of mRNP, affecting the cell's sugar transport process, DNA repair, and cell cycle progression. This study employed the RNA helicase CgDBP4 from <em>Candida glycerinogenes</em> as a stress-resistant genetic element for both <em>C. glycerinogenes</em> and <em>Y. lipolytica</em>. CgDBP4 affected cell tolerance of <em>C glycerinogenes</em> to NaCl, high sugar, acetic acid, and heat stresses. Under 44 ℃, the ethanol production rate of <em>C. g-antiDBP4</em> (It is a recombinant strain that moderately upregulates the transcriptional level of <em>CgDBP4</em>) increased from 1.5 g·(L·h⁻¹) to 2.0 g·(L·h⁻¹). <em>CgTy3</em> is a retrotransposon rescued the cell growth of the <em>C. g-antiDBP4</em> under heat stress. The downregulation of <em>CgTy3</em> impaired the transcription of RNA polymerase III, genomic stability, protein processing, and the activation of heat-responsive genes, consequently influencing the ability of <em>CgDBP4</em> in cell tolerate to heat stress. <em>CgDBP4</em> also enhanced the resistance of <em>Y. lipolytica</em> Po1f to multiple stresses and improved lipid titer by 44.5 % in typical media. Besides, <em>Y. l‐CgDBP4</em> produced 38.1 mg/L of lipids under 34 ℃ and 49.1 mg/L of lipids in undetoxified cellulose hydrolysates.</div></div>\",\"PeriodicalId\":8766,\"journal\":{\"name\":\"Biochemical Engineering Journal\",\"volume\":\"225 \",\"pages\":\"Article 109919\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-08-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1369703X25002931\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369703X25002931","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
RNA helicase CgDBP4 improves tolerance and fermentation performance of Candida glycerinogenes and Yarrowia lipolytica from undetoxified cellulose hydrolysate
RNA helicase functions in RNA transcription, translation, and degradation that promotes the assembly of mRNP, affecting the cell's sugar transport process, DNA repair, and cell cycle progression. This study employed the RNA helicase CgDBP4 from Candida glycerinogenes as a stress-resistant genetic element for both C. glycerinogenes and Y. lipolytica. CgDBP4 affected cell tolerance of C glycerinogenes to NaCl, high sugar, acetic acid, and heat stresses. Under 44 ℃, the ethanol production rate of C. g-antiDBP4 (It is a recombinant strain that moderately upregulates the transcriptional level of CgDBP4) increased from 1.5 g·(L·h⁻¹) to 2.0 g·(L·h⁻¹). CgTy3 is a retrotransposon rescued the cell growth of the C. g-antiDBP4 under heat stress. The downregulation of CgTy3 impaired the transcription of RNA polymerase III, genomic stability, protein processing, and the activation of heat-responsive genes, consequently influencing the ability of CgDBP4 in cell tolerate to heat stress. CgDBP4 also enhanced the resistance of Y. lipolytica Po1f to multiple stresses and improved lipid titer by 44.5 % in typical media. Besides, Y. l‐CgDBP4 produced 38.1 mg/L of lipids under 34 ℃ and 49.1 mg/L of lipids in undetoxified cellulose hydrolysates.
期刊介绍:
The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology.
The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields:
Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics
Biosensors and Biodevices including biofabrication and novel fuel cell development
Bioseparations including scale-up and protein refolding/renaturation
Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells
Bioreactor Systems including characterization, optimization and scale-up
Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization
Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals
Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release
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Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation
Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis
Protein Engineering including enzyme engineering and directed evolution.