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Construction of reductive pathway in Saccharomyces cerevisiae for effective succinic acid fermentation at low pH value
•Metabolic engineering was developed to improve succinate production in yeast.•Reductive pathway was efficient for improving succinate yield.•Succinate production was improved by the deletion of GPD1.•Succinate yield was regulated by urea and biotin levels.•Succinic acid could be effectively produce...
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Published in: | Bioresource technology 2014-03, Vol.156, p.232-239 |
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description | •Metabolic engineering was developed to improve succinate production in yeast.•Reductive pathway was efficient for improving succinate yield.•Succinate production was improved by the deletion of GPD1.•Succinate yield was regulated by urea and biotin levels.•Succinic acid could be effectively produced at pH 3.8 in batch bioreactor.
Succinic acid is an important precursor for the synthesis of high-value-added products. Saccharomyces cerevisiae is a suitable platform for succinic acid production because of its high tolerance towards acidity. In this study, a modified pathway for succinate production was established and investigated in S. cerevisiae. The engineered strain could produce up to 6.17±0.34g/L of succinate through the constructed pathway. The succinate titer was further improved to 8.09±0.28g/L by the deletion of GPD1 and even higher to 9.98±0.23g/L with a yield of 0.32mol/mol glucose through regulation of biotin and urea levels. Under optimal supplemental CO2 conditions in a bioreactor, the engineered strain produced 12.97±0.42g/L succinate with a yield of 0.21mol/mol glucose at pH 3.8. These results demonstrated that the proposed engineering strategy was efficient for succinic acid production at low pH value. |
doi_str_mv | 10.1016/j.biortech.2014.01.053 |
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Succinic acid is an important precursor for the synthesis of high-value-added products. Saccharomyces cerevisiae is a suitable platform for succinic acid production because of its high tolerance towards acidity. In this study, a modified pathway for succinate production was established and investigated in S. cerevisiae. The engineered strain could produce up to 6.17±0.34g/L of succinate through the constructed pathway. The succinate titer was further improved to 8.09±0.28g/L by the deletion of GPD1 and even higher to 9.98±0.23g/L with a yield of 0.32mol/mol glucose through regulation of biotin and urea levels. Under optimal supplemental CO2 conditions in a bioreactor, the engineered strain produced 12.97±0.42g/L succinate with a yield of 0.21mol/mol glucose at pH 3.8. These results demonstrated that the proposed engineering strategy was efficient for succinic acid production at low pH value.</description><identifier>ISSN: 0960-8524</identifier><identifier>EISSN: 1873-2976</identifier><identifier>DOI: 10.1016/j.biortech.2014.01.053</identifier><identifier>PMID: 24508660</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Bioreactors ; Bioreactors - microbiology ; Biotechnology ; Biotin - pharmacology ; Calcium Carbonate - pharmacology ; Construction ; Enzyme Assays ; Fermentation - drug effects ; Fundamental and applied biological sciences. Psychology ; Gene Deletion ; Glucose ; Glucose - metabolism ; Glycerol-3-Phosphate Dehydrogenase (NAD+) - genetics ; Hydrogen-Ion Concentration ; Low pH ; Metabolic Engineering - methods ; Metabolic Networks and Pathways - drug effects ; Methods. Procedures. Technologies ; Microbial engineering. Fermentation and microbial culture technology ; Oxidation-Reduction - drug effects ; Pathways ; Reducing power ; Reductive pathway ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - drug effects ; Saccharomyces cerevisiae - enzymology ; Saccharomyces cerevisiae - growth & development ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins - genetics ; Strain ; Succinic acid ; Succinic Acid - metabolism ; Urea - pharmacology</subject><ispartof>Bioresource technology, 2014-03, Vol.156, p.232-239</ispartof><rights>2014 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-994311ee2f37aa0eac7443716ac7c1acb5aadd2fe8cf81111abed7efab86caa53</citedby><cites>FETCH-LOGICAL-c497t-994311ee2f37aa0eac7443716ac7c1acb5aadd2fe8cf81111abed7efab86caa53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28417724$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24508660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yan, Daojiang</creatorcontrib><creatorcontrib>Wang, Caixia</creatorcontrib><creatorcontrib>Zhou, Jiemin</creatorcontrib><creatorcontrib>Liu, Yilan</creatorcontrib><creatorcontrib>Yang, Maohua</creatorcontrib><creatorcontrib>Xing, Jianmin</creatorcontrib><title>Construction of reductive pathway in Saccharomyces cerevisiae for effective succinic acid fermentation at low pH value</title><title>Bioresource technology</title><addtitle>Bioresour Technol</addtitle><description>•Metabolic engineering was developed to improve succinate production in yeast.•Reductive pathway was efficient for improving succinate yield.•Succinate production was improved by the deletion of GPD1.•Succinate yield was regulated by urea and biotin levels.•Succinic acid could be effectively produced at pH 3.8 in batch bioreactor.
Succinic acid is an important precursor for the synthesis of high-value-added products. Saccharomyces cerevisiae is a suitable platform for succinic acid production because of its high tolerance towards acidity. In this study, a modified pathway for succinate production was established and investigated in S. cerevisiae. The engineered strain could produce up to 6.17±0.34g/L of succinate through the constructed pathway. The succinate titer was further improved to 8.09±0.28g/L by the deletion of GPD1 and even higher to 9.98±0.23g/L with a yield of 0.32mol/mol glucose through regulation of biotin and urea levels. Under optimal supplemental CO2 conditions in a bioreactor, the engineered strain produced 12.97±0.42g/L succinate with a yield of 0.21mol/mol glucose at pH 3.8. These results demonstrated that the proposed engineering strategy was efficient for succinic acid production at low pH value.</description><subject>Biological and medical sciences</subject><subject>Bioreactors</subject><subject>Bioreactors - microbiology</subject><subject>Biotechnology</subject><subject>Biotin - pharmacology</subject><subject>Calcium Carbonate - pharmacology</subject><subject>Construction</subject><subject>Enzyme Assays</subject><subject>Fermentation - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Deletion</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Glycerol-3-Phosphate Dehydrogenase (NAD+) - genetics</subject><subject>Hydrogen-Ion Concentration</subject><subject>Low pH</subject><subject>Metabolic Engineering - methods</subject><subject>Metabolic Networks and Pathways - drug effects</subject><subject>Methods. Procedures. Technologies</subject><subject>Microbial engineering. Fermentation and microbial culture technology</subject><subject>Oxidation-Reduction - drug effects</subject><subject>Pathways</subject><subject>Reducing power</subject><subject>Reductive pathway</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - drug effects</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - growth & development</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Strain</subject><subject>Succinic acid</subject><subject>Succinic Acid - metabolism</subject><subject>Urea - pharmacology</subject><issn>0960-8524</issn><issn>1873-2976</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkcGO0zAQhi0EYkvhFVa-IHFJsBMndm6gamGRVuIAnK3JZKy6SuJiJ1n17UlpF47gy9jS949H8zF2K0UuhazfH_LWhzgR7vNCSJULmYuqfMY20ugyKxpdP2cb0dQiM1WhbtirlA5CiFLq4iW7KVQlTF2LDVt2YUxTnHHyYeTB8Ujd-bEQP8K0f4QT9yP_Boh7iGE4ISWOFGnxyQNxFyIn5-iSSDOiHz1yQN9xR3GgcYLfnWHifXjkx3u-QD_Ta_bCQZ_ozbVu2Y9Pd99399nD189fdh8fMlSNnrKmUaWURIUrNYAgQK1UqWW9XlACthVA1xWODDoj1wMtdZoctKZGgKrcsneXvscYfs6UJjv4hNT3MFKYk5VVqYxoZP0_qDSFKoU8o_UFxRhSiuTsMfoB4slKYc967ME-6bFnPVZIu-pZg7fXP-Z2oO5P7MnHCry9ApAQehdhRJ_-ckZJrdcptuzDhaN1eYunaBN6GpE6H1cZtgv-X7P8Amk5tHs</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Yan, Daojiang</creator><creator>Wang, Caixia</creator><creator>Zhou, Jiemin</creator><creator>Liu, Yilan</creator><creator>Yang, Maohua</creator><creator>Xing, Jianmin</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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><scope>7SU</scope><scope>7TB</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20140301</creationdate><title>Construction of reductive pathway in Saccharomyces cerevisiae for effective succinic acid fermentation at low pH value</title><author>Yan, Daojiang ; Wang, Caixia ; Zhou, Jiemin ; Liu, Yilan ; Yang, Maohua ; Xing, Jianmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-994311ee2f37aa0eac7443716ac7c1acb5aadd2fe8cf81111abed7efab86caa53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Biological and medical sciences</topic><topic>Bioreactors</topic><topic>Bioreactors - microbiology</topic><topic>Biotechnology</topic><topic>Biotin - pharmacology</topic><topic>Calcium Carbonate - pharmacology</topic><topic>Construction</topic><topic>Enzyme Assays</topic><topic>Fermentation - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Deletion</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Glycerol-3-Phosphate Dehydrogenase (NAD+) - genetics</topic><topic>Hydrogen-Ion Concentration</topic><topic>Low pH</topic><topic>Metabolic Engineering - methods</topic><topic>Metabolic Networks and Pathways - drug effects</topic><topic>Methods. Procedures. Technologies</topic><topic>Microbial engineering. Fermentation and microbial culture technology</topic><topic>Oxidation-Reduction - drug effects</topic><topic>Pathways</topic><topic>Reducing power</topic><topic>Reductive pathway</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - drug effects</topic><topic>Saccharomyces cerevisiae - enzymology</topic><topic>Saccharomyces cerevisiae - growth & development</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Strain</topic><topic>Succinic acid</topic><topic>Succinic Acid - metabolism</topic><topic>Urea - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yan, Daojiang</creatorcontrib><creatorcontrib>Wang, Caixia</creatorcontrib><creatorcontrib>Zhou, Jiemin</creatorcontrib><creatorcontrib>Liu, Yilan</creatorcontrib><creatorcontrib>Yang, Maohua</creatorcontrib><creatorcontrib>Xing, Jianmin</creatorcontrib><collection>Pascal-Francis</collection><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><collection>Environmental Engineering Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Bioresource technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yan, Daojiang</au><au>Wang, Caixia</au><au>Zhou, Jiemin</au><au>Liu, Yilan</au><au>Yang, Maohua</au><au>Xing, Jianmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of reductive pathway in Saccharomyces cerevisiae for effective succinic acid fermentation at low pH value</atitle><jtitle>Bioresource technology</jtitle><addtitle>Bioresour Technol</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>156</volume><spage>232</spage><epage>239</epage><pages>232-239</pages><issn>0960-8524</issn><eissn>1873-2976</eissn><abstract>•Metabolic engineering was developed to improve succinate production in yeast.•Reductive pathway was efficient for improving succinate yield.•Succinate production was improved by the deletion of GPD1.•Succinate yield was regulated by urea and biotin levels.•Succinic acid could be effectively produced at pH 3.8 in batch bioreactor.
Succinic acid is an important precursor for the synthesis of high-value-added products. Saccharomyces cerevisiae is a suitable platform for succinic acid production because of its high tolerance towards acidity. In this study, a modified pathway for succinate production was established and investigated in S. cerevisiae. The engineered strain could produce up to 6.17±0.34g/L of succinate through the constructed pathway. The succinate titer was further improved to 8.09±0.28g/L by the deletion of GPD1 and even higher to 9.98±0.23g/L with a yield of 0.32mol/mol glucose through regulation of biotin and urea levels. Under optimal supplemental CO2 conditions in a bioreactor, the engineered strain produced 12.97±0.42g/L succinate with a yield of 0.21mol/mol glucose at pH 3.8. These results demonstrated that the proposed engineering strategy was efficient for succinic acid production at low pH value.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>24508660</pmid><doi>10.1016/j.biortech.2014.01.053</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Bioreactors Bioreactors - microbiology Biotechnology Biotin - pharmacology Calcium Carbonate - pharmacology Construction Enzyme Assays Fermentation - drug effects Fundamental and applied biological sciences. Psychology Gene Deletion Glucose Glucose - metabolism Glycerol-3-Phosphate Dehydrogenase (NAD+) - genetics Hydrogen-Ion Concentration Low pH Metabolic Engineering - methods Metabolic Networks and Pathways - drug effects Methods. Procedures. Technologies Microbial engineering. Fermentation and microbial culture technology Oxidation-Reduction - drug effects Pathways Reducing power Reductive pathway Saccharomyces cerevisiae Saccharomyces cerevisiae - drug effects Saccharomyces cerevisiae - enzymology Saccharomyces cerevisiae - growth & development Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins - genetics Strain Succinic acid Succinic Acid - metabolism Urea - pharmacology |
title | Construction of reductive pathway in Saccharomyces cerevisiae for effective succinic acid fermentation at low pH value |
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