Metabolic engineering of Corynebacterium glutamicum for shikimate overproduction by growth-arrested cell reaction
Corynebacterium glutamicum with the ability to simultaneously utilize glucose/pentose mixed sugars was metabolically engineered to overproduce shikimate, a valuable hydroaromatic compound used as a starting material for the synthesis of the anti-influenza drug oseltamivir. To achieve this, the shiki...
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description | Corynebacterium glutamicum with the ability to simultaneously utilize glucose/pentose mixed sugars was metabolically engineered to overproduce shikimate, a valuable hydroaromatic compound used as a starting material for the synthesis of the anti-influenza drug oseltamivir. To achieve this, the shikimate kinase and other potential metabolic activities for the consumption of shikimate and its precursor dehydroshikimate were inactivated. Carbon flux toward shikimate synthesis was enhanced by overexpression of genes for the shikimate pathway and the non-oxidative pentose phosphate pathway. Subsequently, to improve the availability of the key aromatics precursor phosphoenolpyruvate (PEP) toward shikimate synthesis, the PEP: sugar phosphotransferase system (PTS) was inactivated and an endogenous myo-inositol transporter IolT1 and glucokinases were overexpressed. Unexpectedly, the resultant non-PTS strain accumulated 1,3-dihydroxyacetone (DHA) and glycerol as major byproducts. This observation and metabolome analysis identified glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-catalyzed reaction as a limiting step in glycolysis. Consistently, overexpression of GAPDH significantly stimulated both glucose consumption and shikimate production. Blockage of the DHA synthesis further improved shikimate yield. We applied an aerobic, growth-arrested and high-density cell reaction to the shikimate production by the resulting strain and notably achieved the highest shikimate titer (141g/l) and a yield (51% (mol/mol)) from glucose reported to date after 48h in minimal medium lacking nutrients required for cell growth. Moreover, comparable shikimate productivity could be attained through simultaneous utilization of glucose, xylose, and arabinose, enabling efficient shikimate production from lignocellulosic feedstocks. These findings demonstrate that C. glutamicum has significant potential for the production of shikimate and derived aromatic compounds.
•Engineered strain achieved the highest shikimate productivity reported to date.•141g/L of shikimate was produced from glucose at a yield of 51% after 48h.•A novel aerobic growth-arrested cell reaction developed for shikimate production.•Engineering of the sugar uptake route and glycolytic pathway enhanced productivity.•Shikimate overproduction through simultaneous utilization of mixed sugars. |
doi_str_mv | 10.1016/j.ymben.2016.08.005 |
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•Engineered strain achieved the highest shikimate productivity reported to date.•141g/L of shikimate was produced from glucose at a yield of 51% after 48h.•A novel aerobic growth-arrested cell reaction developed for shikimate production.•Engineering of the sugar uptake route and glycolytic pathway enhanced productivity.•Shikimate overproduction through simultaneous utilization of mixed sugars.</description><identifier>ISSN: 1096-7176</identifier><identifier>EISSN: 1096-7184</identifier><identifier>DOI: 10.1016/j.ymben.2016.08.005</identifier><identifier>PMID: 27553883</identifier><language>eng</language><publisher>Belgium: Elsevier Inc</publisher><subject>Cell Proliferation - physiology ; Corynebacterium glutamicum ; Corynebacterium glutamicum - cytology ; Corynebacterium glutamicum - physiology ; Escherichia coli - genetics ; Genetic Enhancement - methods ; Glucose - metabolism ; Metabolic engineering ; Metabolic Engineering - methods ; Metabolic Networks and Pathways - physiology ; Oseltamivir ; Pentoses - metabolism ; Phosphoenolpyruvate ; Phosphotransferases (Alcohol Group Acceptor) - genetics ; Phosphotransferases (Alcohol Group Acceptor) - metabolism ; Recombinant Proteins - genetics ; Recombinant Proteins - metabolism ; Shikimate pathway ; Shikimic acid ; Shikimic Acid - metabolism ; Sugars - metabolism ; Up-Regulation - physiology</subject><ispartof>Metabolic engineering, 2016-11, Vol.38, p.204-216</ispartof><rights>2016 International Metabolic Engineering Society</rights><rights>Copyright © 2016 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-66dcddfc2d361daa57261d7d726fa87c232bb5c39c7c8d024c65b43c01d116e43</citedby><cites>FETCH-LOGICAL-c425t-66dcddfc2d361daa57261d7d726fa87c232bb5c39c7c8d024c65b43c01d116e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ymben.2016.08.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27553883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kogure, Takahisa</creatorcontrib><creatorcontrib>Kubota, Takeshi</creatorcontrib><creatorcontrib>Suda, Masako</creatorcontrib><creatorcontrib>Hiraga, Kazumi</creatorcontrib><creatorcontrib>Inui, Masayuki</creatorcontrib><title>Metabolic engineering of Corynebacterium glutamicum for shikimate overproduction by growth-arrested cell reaction</title><title>Metabolic engineering</title><addtitle>Metab Eng</addtitle><description>Corynebacterium glutamicum with the ability to simultaneously utilize glucose/pentose mixed sugars was metabolically engineered to overproduce shikimate, a valuable hydroaromatic compound used as a starting material for the synthesis of the anti-influenza drug oseltamivir. To achieve this, the shikimate kinase and other potential metabolic activities for the consumption of shikimate and its precursor dehydroshikimate were inactivated. Carbon flux toward shikimate synthesis was enhanced by overexpression of genes for the shikimate pathway and the non-oxidative pentose phosphate pathway. Subsequently, to improve the availability of the key aromatics precursor phosphoenolpyruvate (PEP) toward shikimate synthesis, the PEP: sugar phosphotransferase system (PTS) was inactivated and an endogenous myo-inositol transporter IolT1 and glucokinases were overexpressed. Unexpectedly, the resultant non-PTS strain accumulated 1,3-dihydroxyacetone (DHA) and glycerol as major byproducts. This observation and metabolome analysis identified glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-catalyzed reaction as a limiting step in glycolysis. Consistently, overexpression of GAPDH significantly stimulated both glucose consumption and shikimate production. Blockage of the DHA synthesis further improved shikimate yield. We applied an aerobic, growth-arrested and high-density cell reaction to the shikimate production by the resulting strain and notably achieved the highest shikimate titer (141g/l) and a yield (51% (mol/mol)) from glucose reported to date after 48h in minimal medium lacking nutrients required for cell growth. Moreover, comparable shikimate productivity could be attained through simultaneous utilization of glucose, xylose, and arabinose, enabling efficient shikimate production from lignocellulosic feedstocks. These findings demonstrate that C. glutamicum has significant potential for the production of shikimate and derived aromatic compounds.
•Engineered strain achieved the highest shikimate productivity reported to date.•141g/L of shikimate was produced from glucose at a yield of 51% after 48h.•A novel aerobic growth-arrested cell reaction developed for shikimate production.•Engineering of the sugar uptake route and glycolytic pathway enhanced productivity.•Shikimate overproduction through simultaneous utilization of mixed sugars.</description><subject>Cell Proliferation - physiology</subject><subject>Corynebacterium glutamicum</subject><subject>Corynebacterium glutamicum - cytology</subject><subject>Corynebacterium glutamicum - physiology</subject><subject>Escherichia coli - genetics</subject><subject>Genetic Enhancement - methods</subject><subject>Glucose - metabolism</subject><subject>Metabolic engineering</subject><subject>Metabolic Engineering - methods</subject><subject>Metabolic Networks and Pathways - physiology</subject><subject>Oseltamivir</subject><subject>Pentoses - metabolism</subject><subject>Phosphoenolpyruvate</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - genetics</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - metabolism</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - metabolism</subject><subject>Shikimate pathway</subject><subject>Shikimic acid</subject><subject>Shikimic Acid - metabolism</subject><subject>Sugars - metabolism</subject><subject>Up-Regulation - physiology</subject><issn>1096-7176</issn><issn>1096-7184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtu2zAQRYmgQR5uvyBAwWU3UvmQKHnRRWGkDyBFNsmaoIYjm44kJiTlwH9f2k6z7OoOB3c4dw4hN5yVnHH1dVvuxw6nUuRHydqSsfqMXHG2VEXD2-rDe92oS3Id45YxzuslvyCXoqlr2bbyirz8wWQ6PzigOK3dhBjctKa-pysf9hN2BlJuzSNdD3Myo4Nc9j7QuHFPbjQJqd9heA7ezpCcn2i3p-vgX9OmMCFgTGgp4DDQgOZo-EjOezNE_PSmC_L44_Zh9au4u__5e_X9roBK1KlQyoK1PQgrFbfG1I3I2tgsvWkbEFJ0XQ1yCQ20lokKVN1VEhi3nCus5IJ8Of2bs73MOYgeXTwkMRP6OWreysxAKHmwypMVgo8xYK-fQ74t7DVn-sBab_WRtT6w1qzVmXWe-vy2YO5GtO8z_-Bmw7eTAfOZO4dBR3A4AVoXEJK23v13wV_8qpRG</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Kogure, Takahisa</creator><creator>Kubota, Takeshi</creator><creator>Suda, Masako</creator><creator>Hiraga, Kazumi</creator><creator>Inui, Masayuki</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201611</creationdate><title>Metabolic engineering of Corynebacterium glutamicum for shikimate overproduction by growth-arrested cell reaction</title><author>Kogure, Takahisa ; Kubota, Takeshi ; Suda, Masako ; Hiraga, Kazumi ; Inui, Masayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-66dcddfc2d361daa57261d7d726fa87c232bb5c39c7c8d024c65b43c01d116e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cell Proliferation - physiology</topic><topic>Corynebacterium glutamicum</topic><topic>Corynebacterium glutamicum - cytology</topic><topic>Corynebacterium glutamicum - physiology</topic><topic>Escherichia coli - genetics</topic><topic>Genetic Enhancement - methods</topic><topic>Glucose - metabolism</topic><topic>Metabolic engineering</topic><topic>Metabolic Engineering - methods</topic><topic>Metabolic Networks and Pathways - physiology</topic><topic>Oseltamivir</topic><topic>Pentoses - metabolism</topic><topic>Phosphoenolpyruvate</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - genetics</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - metabolism</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - metabolism</topic><topic>Shikimate pathway</topic><topic>Shikimic acid</topic><topic>Shikimic Acid - metabolism</topic><topic>Sugars - metabolism</topic><topic>Up-Regulation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kogure, Takahisa</creatorcontrib><creatorcontrib>Kubota, Takeshi</creatorcontrib><creatorcontrib>Suda, Masako</creatorcontrib><creatorcontrib>Hiraga, Kazumi</creatorcontrib><creatorcontrib>Inui, Masayuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolic engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kogure, Takahisa</au><au>Kubota, Takeshi</au><au>Suda, Masako</au><au>Hiraga, Kazumi</au><au>Inui, Masayuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic engineering of Corynebacterium glutamicum for shikimate overproduction by growth-arrested cell reaction</atitle><jtitle>Metabolic engineering</jtitle><addtitle>Metab Eng</addtitle><date>2016-11</date><risdate>2016</risdate><volume>38</volume><spage>204</spage><epage>216</epage><pages>204-216</pages><issn>1096-7176</issn><eissn>1096-7184</eissn><abstract>Corynebacterium glutamicum with the ability to simultaneously utilize glucose/pentose mixed sugars was metabolically engineered to overproduce shikimate, a valuable hydroaromatic compound used as a starting material for the synthesis of the anti-influenza drug oseltamivir. To achieve this, the shikimate kinase and other potential metabolic activities for the consumption of shikimate and its precursor dehydroshikimate were inactivated. Carbon flux toward shikimate synthesis was enhanced by overexpression of genes for the shikimate pathway and the non-oxidative pentose phosphate pathway. Subsequently, to improve the availability of the key aromatics precursor phosphoenolpyruvate (PEP) toward shikimate synthesis, the PEP: sugar phosphotransferase system (PTS) was inactivated and an endogenous myo-inositol transporter IolT1 and glucokinases were overexpressed. Unexpectedly, the resultant non-PTS strain accumulated 1,3-dihydroxyacetone (DHA) and glycerol as major byproducts. This observation and metabolome analysis identified glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-catalyzed reaction as a limiting step in glycolysis. Consistently, overexpression of GAPDH significantly stimulated both glucose consumption and shikimate production. Blockage of the DHA synthesis further improved shikimate yield. We applied an aerobic, growth-arrested and high-density cell reaction to the shikimate production by the resulting strain and notably achieved the highest shikimate titer (141g/l) and a yield (51% (mol/mol)) from glucose reported to date after 48h in minimal medium lacking nutrients required for cell growth. Moreover, comparable shikimate productivity could be attained through simultaneous utilization of glucose, xylose, and arabinose, enabling efficient shikimate production from lignocellulosic feedstocks. These findings demonstrate that C. glutamicum has significant potential for the production of shikimate and derived aromatic compounds.
•Engineered strain achieved the highest shikimate productivity reported to date.•141g/L of shikimate was produced from glucose at a yield of 51% after 48h.•A novel aerobic growth-arrested cell reaction developed for shikimate production.•Engineering of the sugar uptake route and glycolytic pathway enhanced productivity.•Shikimate overproduction through simultaneous utilization of mixed sugars.</abstract><cop>Belgium</cop><pub>Elsevier Inc</pub><pmid>27553883</pmid><doi>10.1016/j.ymben.2016.08.005</doi><tpages>13</tpages></addata></record> |
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subjects | Cell Proliferation - physiology Corynebacterium glutamicum Corynebacterium glutamicum - cytology Corynebacterium glutamicum - physiology Escherichia coli - genetics Genetic Enhancement - methods Glucose - metabolism Metabolic engineering Metabolic Engineering - methods Metabolic Networks and Pathways - physiology Oseltamivir Pentoses - metabolism Phosphoenolpyruvate Phosphotransferases (Alcohol Group Acceptor) - genetics Phosphotransferases (Alcohol Group Acceptor) - metabolism Recombinant Proteins - genetics Recombinant Proteins - metabolism Shikimate pathway Shikimic acid Shikimic Acid - metabolism Sugars - metabolism Up-Regulation - physiology |
title | Metabolic engineering of Corynebacterium glutamicum for shikimate overproduction by growth-arrested cell reaction |
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