High-Level Bio-Based Production of Coproporphyrin in Escherichia coli

Bahareh Arab, Adam W. Westbrook, Murray Moo-Young, Yilan Liu, C. P. Chou
{"title":"High-Level Bio-Based Production of Coproporphyrin in Escherichia coli","authors":"Bahareh Arab, Adam W. Westbrook, Murray Moo-Young, Yilan Liu, C. P. Chou","doi":"10.3390/fermentation10050250","DOIUrl":null,"url":null,"abstract":"This study reports on the development of effective strain engineering strategies for the high-level bio-based production of coproporphyrin (CP), a porphyrin pigment compound with various applications, using Escherichia coli as a production host. Our approach involves heterologous implementation of the Shemin/C4 pathway in an E. coli host strain with an enlarged intracellular pool of succinyl-CoA. To regulate the expression of the key pathway genes, including hemA/B/D/E/Y, we employed a plasmid system comprising two operons regulated by strong trc and gracmax promoters, respectively. Using the engineered E. coli strains for bioreactor cultivation under aerobic conditions with glycerol as the carbon source, we produced up to 353 mg/L CP with minimal byproduct formation. The overproduced CP was secreted extracellularly, posing minimal physiological toxicity and impact on the producing cells. To date, targeted bio-based production of CP by E. coli has yet to be reported. In addition to the demonstration of high-level bio-based production of CP, our study underscores the importance of identifying key enzymatic reactions limiting the overall metabolite production for developing differential expression strategies for pathway modulation and even optimization. This investigation paves the way for the development of effective metabolic engineering strategies based on targeted manipulation of key enzymes to customize engineered strains for effective large-scale bio-based production.","PeriodicalId":12379,"journal":{"name":"Fermentation","volume":" 20","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fermentation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/fermentation10050250","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This study reports on the development of effective strain engineering strategies for the high-level bio-based production of coproporphyrin (CP), a porphyrin pigment compound with various applications, using Escherichia coli as a production host. Our approach involves heterologous implementation of the Shemin/C4 pathway in an E. coli host strain with an enlarged intracellular pool of succinyl-CoA. To regulate the expression of the key pathway genes, including hemA/B/D/E/Y, we employed a plasmid system comprising two operons regulated by strong trc and gracmax promoters, respectively. Using the engineered E. coli strains for bioreactor cultivation under aerobic conditions with glycerol as the carbon source, we produced up to 353 mg/L CP with minimal byproduct formation. The overproduced CP was secreted extracellularly, posing minimal physiological toxicity and impact on the producing cells. To date, targeted bio-based production of CP by E. coli has yet to be reported. In addition to the demonstration of high-level bio-based production of CP, our study underscores the importance of identifying key enzymatic reactions limiting the overall metabolite production for developing differential expression strategies for pathway modulation and even optimization. This investigation paves the way for the development of effective metabolic engineering strategies based on targeted manipulation of key enzymes to customize engineered strains for effective large-scale bio-based production.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在大肠杆菌中以生物为基础生产高级铜卟啉
本研究报告了利用大肠杆菌作为生产宿主,开发有效的菌株工程策略,以生物为基础生产共卟啉(CP)--一种具有多种用途的卟啉色素化合物。我们的方法涉及在大肠杆菌宿主菌株中异源实施 Shemin/C4 通路,该菌株细胞内的琥珀酰-CoA 池扩大。为了调控包括 hemA/B/D/E/Y 在内的关键途径基因的表达,我们采用了一种质粒系统,该系统包含两个操作子,分别由强 trc 和 gracmax 启动子调控。在有氧条件下,以甘油为碳源,利用工程化的大肠杆菌菌株进行生物反应器培养,我们生产出了高达 353 mg/L 的氯化石蜡,且副产物形成极少。过量生产的氯化石蜡被分泌到细胞外,对生产细胞的生理毒性和影响极小。迄今为止,大肠杆菌以生物为基础定向生产氯化石蜡的研究尚未见报道。除了展示高水平的以生物为基础的氯化石蜡生产,我们的研究还强调了识别限制整体代谢物生产的关键酶促反应的重要性,以便开发用于调节甚至优化通路的差异化表达策略。这项研究为开发有效的代谢工程策略铺平了道路,这些策略基于对关键酶的有针对性操作,以定制工程菌株,从而实现有效的大规模生物基生产。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Primary Metabolites and Microbial Diversity in Commercial Kombucha Products Black Tea Kombucha Consumption: Effect on Cardiometabolic Parameters and Diet Quality of Individuals with and without Obesity Chia Seed Mucilage as a Functional Ingredient to Improve Quality of Goat Milk Yoghurt: Effects on Rheology, Texture, Microstructure and Sensory Properties Biohydrogen Production from Methane-Derived Biomass of Methanotroph and Microalgae by Clostridium Characterization of the Gamma-Aminobutyric Acid (GABA) Biosynthetic Gene Cluster in High GABA-Producing Enterococcus avium G-15
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1