Metabolic engineering of Saccharomyces cerevisiae for efficient production of pure L-(+)-lactic acid
We developed a metabolically engineered Saccharomyces cerevisiae, which produces optically pure L-lactic acid efficiently using cane juice-based medium. In this recombinant, the coding region of pyruvate decarboxylase (PDC)1 was completely deleted, and six copies of the bovine L-lactate dehydrogenas...
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Veröffentlicht in: | Applied biochemistry and biotechnology 2006, Vol.129-132 (1-3), p.795-807 |
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creator | Ishida, Nobuhiro Saitoh, Satoshi Ohnishi, Toru Tokuhiro, Kenro Nagamori, Eiji Kitamoto, Katsuhiko Takahashi, Haruo |
description | We developed a metabolically engineered Saccharomyces cerevisiae, which produces optically pure L-lactic acid efficiently using cane juice-based medium. In this recombinant, the coding region of pyruvate decarboxylase (PDC)1 was completely deleted, and six copies of the bovine L-lactate dehydrogenase (L-LDH) genes were introduced on the genome under the control of the PDC1 promoter. To confirm optically pure lactate production in low-cost medium, cane juice-based medium was used in fermentation with neutralizing conditions. L-lactate production reached 122 g/L, with 61% of sugar being transformed into L-lactate finally. The optical purity of this L-lactate, that affects the physical characteristics of poly-L-lactic acid, was extremely high, 99.9% or over. |
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In this recombinant, the coding region of pyruvate decarboxylase (PDC)1 was completely deleted, and six copies of the bovine L-lactate dehydrogenase (L-LDH) genes were introduced on the genome under the control of the PDC1 promoter. To confirm optically pure lactate production in low-cost medium, cane juice-based medium was used in fermentation with neutralizing conditions. L-lactate production reached 122 g/L, with 61% of sugar being transformed into L-lactate finally. The optical purity of this L-lactate, that affects the physical characteristics of poly-L-lactic acid, was extremely high, 99.9% or over.</description><identifier>ISSN: 0273-2289</identifier><identifier>EISSN: 0273-2289</identifier><identifier>EISSN: 1559-0291</identifier><identifier>DOI: 10.1385/abab:131:1:795</identifier><identifier>PMID: 16915689</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Animals ; Bacteria ; Cattle ; Cloning, Molecular - methods ; Feasibility Studies ; Fermentation ; Genetic Enhancement - methods ; L-Lactate Dehydrogenase - genetics ; L-Lactate Dehydrogenase - metabolism ; Lactic Acid - isolation & purification ; Lactic Acid - metabolism ; Microbiology ; Pilot Projects ; Promoter Regions, Genetic ; Protein Engineering - methods ; Pyruvate Decarboxylase - genetics ; Pyruvate Decarboxylase - metabolism ; Recombinant Proteins - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism</subject><ispartof>Applied biochemistry and biotechnology, 2006, Vol.129-132 (1-3), p.795-807</ispartof><rights>Humana Press Inc. 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-5052d9eb78db1064b882ebc185dda7679ea4a9905cd87fa4a08274d29ee89cd23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4022,27921,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16915689$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishida, Nobuhiro</creatorcontrib><creatorcontrib>Saitoh, Satoshi</creatorcontrib><creatorcontrib>Ohnishi, Toru</creatorcontrib><creatorcontrib>Tokuhiro, Kenro</creatorcontrib><creatorcontrib>Nagamori, Eiji</creatorcontrib><creatorcontrib>Kitamoto, Katsuhiko</creatorcontrib><creatorcontrib>Takahashi, Haruo</creatorcontrib><title>Metabolic engineering of Saccharomyces cerevisiae for efficient production of pure L-(+)-lactic acid</title><title>Applied biochemistry and biotechnology</title><addtitle>Appl Biochem Biotechnol</addtitle><description>We developed a metabolically engineered Saccharomyces cerevisiae, which produces optically pure L-lactic acid efficiently using cane juice-based medium. In this recombinant, the coding region of pyruvate decarboxylase (PDC)1 was completely deleted, and six copies of the bovine L-lactate dehydrogenase (L-LDH) genes were introduced on the genome under the control of the PDC1 promoter. To confirm optically pure lactate production in low-cost medium, cane juice-based medium was used in fermentation with neutralizing conditions. L-lactate production reached 122 g/L, with 61% of sugar being transformed into L-lactate finally. The optical purity of this L-lactate, that affects the physical characteristics of poly-L-lactic acid, was extremely high, 99.9% or over.</description><subject>Animals</subject><subject>Bacteria</subject><subject>Cattle</subject><subject>Cloning, Molecular - methods</subject><subject>Feasibility Studies</subject><subject>Fermentation</subject><subject>Genetic Enhancement - methods</subject><subject>L-Lactate Dehydrogenase - genetics</subject><subject>L-Lactate Dehydrogenase - metabolism</subject><subject>Lactic Acid - isolation & purification</subject><subject>Lactic Acid - metabolism</subject><subject>Microbiology</subject><subject>Pilot Projects</subject><subject>Promoter Regions, Genetic</subject><subject>Protein Engineering - methods</subject><subject>Pyruvate Decarboxylase - genetics</subject><subject>Pyruvate Decarboxylase - metabolism</subject><subject>Recombinant Proteins - metabolism</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - 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methods</topic><topic>Feasibility Studies</topic><topic>Fermentation</topic><topic>Genetic Enhancement - methods</topic><topic>L-Lactate Dehydrogenase - genetics</topic><topic>L-Lactate Dehydrogenase - metabolism</topic><topic>Lactic Acid - isolation & purification</topic><topic>Lactic Acid - metabolism</topic><topic>Microbiology</topic><topic>Pilot Projects</topic><topic>Promoter Regions, Genetic</topic><topic>Protein Engineering - methods</topic><topic>Pyruvate Decarboxylase - genetics</topic><topic>Pyruvate Decarboxylase - metabolism</topic><topic>Recombinant Proteins - metabolism</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishida, Nobuhiro</creatorcontrib><creatorcontrib>Saitoh, Satoshi</creatorcontrib><creatorcontrib>Ohnishi, Toru</creatorcontrib><creatorcontrib>Tokuhiro, Kenro</creatorcontrib><creatorcontrib>Nagamori, Eiji</creatorcontrib><creatorcontrib>Kitamoto, Katsuhiko</creatorcontrib><creatorcontrib>Takahashi, Haruo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - 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In this recombinant, the coding region of pyruvate decarboxylase (PDC)1 was completely deleted, and six copies of the bovine L-lactate dehydrogenase (L-LDH) genes were introduced on the genome under the control of the PDC1 promoter. To confirm optically pure lactate production in low-cost medium, cane juice-based medium was used in fermentation with neutralizing conditions. L-lactate production reached 122 g/L, with 61% of sugar being transformed into L-lactate finally. The optical purity of this L-lactate, that affects the physical characteristics of poly-L-lactic acid, was extremely high, 99.9% or over.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>16915689</pmid><doi>10.1385/abab:131:1:795</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Bacteria Cattle Cloning, Molecular - methods Feasibility Studies Fermentation Genetic Enhancement - methods L-Lactate Dehydrogenase - genetics L-Lactate Dehydrogenase - metabolism Lactic Acid - isolation & purification Lactic Acid - metabolism Microbiology Pilot Projects Promoter Regions, Genetic Protein Engineering - methods Pyruvate Decarboxylase - genetics Pyruvate Decarboxylase - metabolism Recombinant Proteins - metabolism Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism |
title | Metabolic engineering of Saccharomyces cerevisiae for efficient production of pure L-(+)-lactic acid |
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