Hao Zhang , Hairui Tong , Qiang Yin , Yibin Qiu , Hong Xu , Sha Li
{"title":"利用工程大肠杆菌从菊芋中高效生产异托因","authors":"Hao Zhang , Hairui Tong , Qiang Yin , Yibin Qiu , Hong Xu , Sha Li","doi":"10.1016/j.biortech.2025.132589","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, a recombinant <em>Escherichia coli</em> strain was constructed to produce ectoine from Jerusalem artichoke through modular pathway engineering. First, a promoter-optimized ectoine synthesis module was integrated into the chromosome using multiple copies. Then, the introduction and expression of inulin hydrolase was optimized because inulin cannot be directly utilized. Subsequently, Fructose transport and phosphorylation, glycolysis, and oxaloacetate supply module were enhanced separately and in combination to improve ectoine production and substrate utilization. The strain ETC16 (co-expression of <em>gapA</em>, <em>ppc</em>, and <em>fruK</em>, Δ<em>iclR</em>) produced 6.51 g/L ectoine with 0.13 g/g inulin. Furthermore, the raw inulin extract and monosodium glutamate (MSG) residue were optimized for ectoine production. Finally, 35.60 g/L of ectoine with a yield of 0.36 g/g inulin was achieved in a 7.5 L fermenter. This study revealed a potential method of non-food fermentation to produce high-value products.</div></div>","PeriodicalId":258,"journal":{"name":"Bioresource Technology","volume":"431 ","pages":"Article 132589"},"PeriodicalIF":9.7000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient production of ectoine from Jerusalem artichoke using engineered Escherichia coli\",\"authors\":\"Hao Zhang , Hairui Tong , Qiang Yin , Yibin Qiu , Hong Xu , Sha Li\",\"doi\":\"10.1016/j.biortech.2025.132589\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, a recombinant <em>Escherichia coli</em> strain was constructed to produce ectoine from Jerusalem artichoke through modular pathway engineering. First, a promoter-optimized ectoine synthesis module was integrated into the chromosome using multiple copies. Then, the introduction and expression of inulin hydrolase was optimized because inulin cannot be directly utilized. Subsequently, Fructose transport and phosphorylation, glycolysis, and oxaloacetate supply module were enhanced separately and in combination to improve ectoine production and substrate utilization. The strain ETC16 (co-expression of <em>gapA</em>, <em>ppc</em>, and <em>fruK</em>, Δ<em>iclR</em>) produced 6.51 g/L ectoine with 0.13 g/g inulin. Furthermore, the raw inulin extract and monosodium glutamate (MSG) residue were optimized for ectoine production. Finally, 35.60 g/L of ectoine with a yield of 0.36 g/g inulin was achieved in a 7.5 L fermenter. This study revealed a potential method of non-food fermentation to produce high-value products.</div></div>\",\"PeriodicalId\":258,\"journal\":{\"name\":\"Bioresource Technology\",\"volume\":\"431 \",\"pages\":\"Article 132589\"},\"PeriodicalIF\":9.7000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioresource Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0960852425005553\",\"RegionNum\":1,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURAL ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioresource Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960852425005553","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURAL ENGINEERING","Score":null,"Total":0}
Efficient production of ectoine from Jerusalem artichoke using engineered Escherichia coli
In this study, a recombinant Escherichia coli strain was constructed to produce ectoine from Jerusalem artichoke through modular pathway engineering. First, a promoter-optimized ectoine synthesis module was integrated into the chromosome using multiple copies. Then, the introduction and expression of inulin hydrolase was optimized because inulin cannot be directly utilized. Subsequently, Fructose transport and phosphorylation, glycolysis, and oxaloacetate supply module were enhanced separately and in combination to improve ectoine production and substrate utilization. The strain ETC16 (co-expression of gapA, ppc, and fruK, ΔiclR) produced 6.51 g/L ectoine with 0.13 g/g inulin. Furthermore, the raw inulin extract and monosodium glutamate (MSG) residue were optimized for ectoine production. Finally, 35.60 g/L of ectoine with a yield of 0.36 g/g inulin was achieved in a 7.5 L fermenter. This study revealed a potential method of non-food fermentation to produce high-value products.
期刊介绍:
Bioresource Technology publishes original articles, review articles, case studies, and short communications covering the fundamentals, applications, and management of bioresource technology. The journal seeks to advance and disseminate knowledge across various areas related to biomass, biological waste treatment, bioenergy, biotransformations, bioresource systems analysis, and associated conversion or production technologies.
Topics include:
• Biofuels: liquid and gaseous biofuels production, modeling and economics
• Bioprocesses and bioproducts: biocatalysis and fermentations
• Biomass and feedstocks utilization: bioconversion of agro-industrial residues
• Environmental protection: biological waste treatment
• Thermochemical conversion of biomass: combustion, pyrolysis, gasification, catalysis.