Engineering All-Round Cellulase for Bioethanol Production

IF 3.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Minghui Wang, Haiyang Cui, Chenlei Gu, Anni Li, Jie Qiao, Ulrich Schwaneberg, Lihui Zhang, Junnan Wei*, Xiujuan Li* and He Huang, 
{"title":"Engineering All-Round Cellulase for Bioethanol Production","authors":"Minghui Wang,&nbsp;Haiyang Cui,&nbsp;Chenlei Gu,&nbsp;Anni Li,&nbsp;Jie Qiao,&nbsp;Ulrich Schwaneberg,&nbsp;Lihui Zhang,&nbsp;Junnan Wei*,&nbsp;Xiujuan Li* and He Huang,&nbsp;","doi":"10.1021/acssynbio.3c00289","DOIUrl":null,"url":null,"abstract":"<p >One strategy to decrease both the consumption of crude oil and environmental damage is through the production of bioethanol from biomass. Cellulolytic enzyme stability and enzymatic hydrolysis play important roles in the bioethanol process. However, the gradually increased ethanol concentration often reduces enzyme activity and leads to inactivation, thereby limiting the final ethanol yield. Herein, we employed an optimized Two-Gene Recombination Process (2GenReP) approach to evolve the exemplary cellulase CBHI for practical bioethanol fermentation. Two all-round CBHI variants (named as R2 and R4) were obtained with simultaneously improved ethanol resistance, organic solvent inhibitor tolerance, and enzymolysis stability in simultaneous saccharification and fermentation (SSF). Notably, CBHI R4 had a 7.0- to 34.5-fold enhanced catalytic efficiency (<i>k</i><sub>cat</sub>/<i>K</i><sub>M</sub>) in the presence/absence of ethanol. Employing the evolved CBHI R2 and R4 in the 1G bioethanol process resulted in up to 10.27% (6.7 g/L) improved ethanol yield (ethanol concentration) than non-cellulase, which was far more beyond than other optimization strategies. Besides bioenergy fields, this transferable protein engineering routine holds the potential to generate all-round enzymes that meet the requirement in biotransformation and bioenergy fields.</p>","PeriodicalId":26,"journal":{"name":"ACS Synthetic Biology","volume":"12 7","pages":"2187–2197"},"PeriodicalIF":3.7000,"publicationDate":"2023-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssynbio.3c00289","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 2

Abstract

One strategy to decrease both the consumption of crude oil and environmental damage is through the production of bioethanol from biomass. Cellulolytic enzyme stability and enzymatic hydrolysis play important roles in the bioethanol process. However, the gradually increased ethanol concentration often reduces enzyme activity and leads to inactivation, thereby limiting the final ethanol yield. Herein, we employed an optimized Two-Gene Recombination Process (2GenReP) approach to evolve the exemplary cellulase CBHI for practical bioethanol fermentation. Two all-round CBHI variants (named as R2 and R4) were obtained with simultaneously improved ethanol resistance, organic solvent inhibitor tolerance, and enzymolysis stability in simultaneous saccharification and fermentation (SSF). Notably, CBHI R4 had a 7.0- to 34.5-fold enhanced catalytic efficiency (kcat/KM) in the presence/absence of ethanol. Employing the evolved CBHI R2 and R4 in the 1G bioethanol process resulted in up to 10.27% (6.7 g/L) improved ethanol yield (ethanol concentration) than non-cellulase, which was far more beyond than other optimization strategies. Besides bioenergy fields, this transferable protein engineering routine holds the potential to generate all-round enzymes that meet the requirement in biotransformation and bioenergy fields.

Abstract Image

用于生物乙醇生产的工程全纤维素酶
减少原油消耗和环境破坏的一个策略是从生物质中生产生物乙醇。纤维素酶的稳定性和酶解在生物乙醇生产过程中起着重要的作用。然而,逐渐增加的乙醇浓度往往会降低酶的活性并导致失活,从而限制了最终的乙醇产量。在此,我们采用优化的双基因重组过程(2GenReP)方法来进化示范性纤维素酶CBHI,用于实际的生物乙醇发酵。获得了两种全面的cbi变体(命名为R2和R4),同时具有提高的乙醇抗性,有机溶剂抑制剂耐受性和同时糖化发酵(SSF)的酶解稳定性。值得注意的是,在乙醇存在/不存在的情况下,cbi R4的催化效率(kcat/KM)提高了7.0- 34.5倍。采用改进的cbbi R2和R4在1G生物乙醇工艺中,乙醇产量(乙醇浓度)比非纤维素酶提高了10.27% (6.7 g/L),这远远超过了其他优化策略。除了生物能源领域,这种可转移的蛋白质工程程序还具有产生满足生物转化和生物能源领域需求的全方位酶的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信