Selection of glucose-assimilating variants of Acinetobacter calcoaceticus LMD 79.41 in chemostat culture
Glucose metabolism has been studied in two strains of Acinetobacter calcoaceticus. Strain LMD 82.3, was able to grow on glucose and possessed glucose dehydrogenase (EC 1.1.99.17). Glucose oxidation by whole cells was stimulated by PQQ, the prosthetic group of glucose dehydrogenase. PQQ not only incr...
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Veröffentlicht in: | Antonie van Leeuwenhoek 1989-01, Vol.55 (1), p.39-52 |
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description | Glucose metabolism has been studied in two strains of Acinetobacter calcoaceticus. Strain LMD 82.3, was able to grow on glucose and possessed glucose dehydrogenase (EC 1.1.99.17). Glucose oxidation by whole cells was stimulated by PQQ, the prosthetic group of glucose dehydrogenase. PQQ not only increased the rate of glucose oxidation and gluconic acid production but also shortened the lag phase for growth on glucose. Strain LMD 79.41 also possessed glucose dehydrogenase but was unable to grow on glucose. Batch cultures and carbon-limited chemostat cultures growing on acetate in the presence of glucose oxidized the sugar to gluconic acid, which was not further metabolized. However, after prolonged cultivation on mixtures of acetate and glucose, carbon-limited chemostat cultures suddenly acquired the capacity to utilize gluconate. This phenomenon was accompanied by the appearance of gluconate kinase and a repression of isocitrate lyase synthesis. In contrast to the starter culture, cells from chemostats which had been fully adapted to gluconate utilization, were able to utilize glucose as a sole carbon and energy source in liquid and solid media. |
doi_str_mv | 10.1007/BF02309618 |
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J ; ROUWENHORST, R. J ; VAN DIJKEN, J. P ; KUENEN, J. G</creator><creatorcontrib>VAN SCHIE, B. J ; ROUWENHORST, R. J ; VAN DIJKEN, J. P ; KUENEN, J. G</creatorcontrib><description>Glucose metabolism has been studied in two strains of Acinetobacter calcoaceticus. Strain LMD 82.3, was able to grow on glucose and possessed glucose dehydrogenase (EC 1.1.99.17). Glucose oxidation by whole cells was stimulated by PQQ, the prosthetic group of glucose dehydrogenase. PQQ not only increased the rate of glucose oxidation and gluconic acid production but also shortened the lag phase for growth on glucose. Strain LMD 79.41 also possessed glucose dehydrogenase but was unable to grow on glucose. Batch cultures and carbon-limited chemostat cultures growing on acetate in the presence of glucose oxidized the sugar to gluconic acid, which was not further metabolized. However, after prolonged cultivation on mixtures of acetate and glucose, carbon-limited chemostat cultures suddenly acquired the capacity to utilize gluconate. This phenomenon was accompanied by the appearance of gluconate kinase and a repression of isocitrate lyase synthesis. In contrast to the starter culture, cells from chemostats which had been fully adapted to gluconate utilization, were able to utilize glucose as a sole carbon and energy source in liquid and solid media.</description><identifier>ISSN: 0003-6072</identifier><identifier>EISSN: 1572-9699</identifier><identifier>DOI: 10.1007/BF02309618</identifier><identifier>PMID: 2545167</identifier><identifier>CODEN: ANLEDR</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Acetates - metabolism ; Acinetobacter - enzymology ; Acinetobacter - growth & development ; Acinetobacter - metabolism ; assimilation ; Bacteriology ; Biological and medical sciences ; continuous culture ; Culture Media ; Fundamental and applied biological sciences. Psychology ; Gluconates - metabolism ; glucose ; Glucose - metabolism ; Glucose 1-Dehydrogenase ; glucose dehydrogenase (pyrroloquinoline-quinone) ; Glucose Dehydrogenases - analysis ; Metabolism. Enzymes ; Microbiology ; Oxidation-Reduction ; Phosphotransferases (Alcohol Group Acceptor) ; Phosphotransferases - analysis</subject><ispartof>Antonie van Leeuwenhoek, 1989-01, Vol.55 (1), p.39-52</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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=7218734$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2545167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VAN SCHIE, B. J</creatorcontrib><creatorcontrib>ROUWENHORST, R. J</creatorcontrib><creatorcontrib>VAN DIJKEN, J. P</creatorcontrib><creatorcontrib>KUENEN, J. G</creatorcontrib><title>Selection of glucose-assimilating variants of Acinetobacter calcoaceticus LMD 79.41 in chemostat culture</title><title>Antonie van Leeuwenhoek</title><addtitle>Antonie Van Leeuwenhoek</addtitle><description>Glucose metabolism has been studied in two strains of Acinetobacter calcoaceticus. Strain LMD 82.3, was able to grow on glucose and possessed glucose dehydrogenase (EC 1.1.99.17). Glucose oxidation by whole cells was stimulated by PQQ, the prosthetic group of glucose dehydrogenase. PQQ not only increased the rate of glucose oxidation and gluconic acid production but also shortened the lag phase for growth on glucose. Strain LMD 79.41 also possessed glucose dehydrogenase but was unable to grow on glucose. Batch cultures and carbon-limited chemostat cultures growing on acetate in the presence of glucose oxidized the sugar to gluconic acid, which was not further metabolized. However, after prolonged cultivation on mixtures of acetate and glucose, carbon-limited chemostat cultures suddenly acquired the capacity to utilize gluconate. This phenomenon was accompanied by the appearance of gluconate kinase and a repression of isocitrate lyase synthesis. In contrast to the starter culture, cells from chemostats which had been fully adapted to gluconate utilization, were able to utilize glucose as a sole carbon and energy source in liquid and solid media.</description><subject>Acetates - metabolism</subject><subject>Acinetobacter - enzymology</subject><subject>Acinetobacter - growth & development</subject><subject>Acinetobacter - metabolism</subject><subject>assimilation</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>continuous culture</subject><subject>Culture Media</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gluconates - metabolism</subject><subject>glucose</subject><subject>Glucose - metabolism</subject><subject>Glucose 1-Dehydrogenase</subject><subject>glucose dehydrogenase (pyrroloquinoline-quinone)</subject><subject>Glucose Dehydrogenases - analysis</subject><subject>Metabolism. Enzymes</subject><subject>Microbiology</subject><subject>Oxidation-Reduction</subject><subject>Phosphotransferases (Alcohol Group Acceptor)</subject><subject>Phosphotransferases - analysis</subject><issn>0003-6072</issn><issn>1572-9699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0DtPwzAUBWALgUopLOxIHhBbil-x47EUCkhFDMAc3bg3rVEeJXaQ-PcEEbEyXV2dT2c4hJxzNueMmeubFROSWc2zAzLlqRGJ1dYekiljTCaaGXFMTkJ4H16rMzMhE5GqlGszJbsXrNBF3za0Lem26l0bMIEQfO0riL7Z0k_oPDQx_ICF8w3GtgAXsaMOKteCw-hdH-j66ZYaO1ec-oa6HdZtiBCp66vYd3hKjkqoAp6Nd0beVnevy4dk_Xz_uFysk73QOiaWpVIoViAToNNSK1kym2nYWCwLlTm0ijsjgYtSWFsUslSZ3mhAppQyAuWMXP327rv2o8cQ89oHh1UFDbZ9yI1lxqQq-xfyVCpmdDrAixH2RY2bfN_5GrqvfNxwyC_HHMKwSNlB43z4Y0bwzEglvwHqY36u</recordid><startdate>19890101</startdate><enddate>19890101</enddate><creator>VAN SCHIE, B. J</creator><creator>ROUWENHORST, R. J</creator><creator>VAN DIJKEN, J. P</creator><creator>KUENEN, J. G</creator><general>Springer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19890101</creationdate><title>Selection of glucose-assimilating variants of Acinetobacter calcoaceticus LMD 79.41 in chemostat culture</title><author>VAN SCHIE, B. J ; ROUWENHORST, R. J ; VAN DIJKEN, J. P ; KUENEN, J. G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-9053240be02a65f643f0986ad9efb48ce941c73a12f299bb3f486d6ae044472e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Acetates - metabolism</topic><topic>Acinetobacter - enzymology</topic><topic>Acinetobacter - growth & development</topic><topic>Acinetobacter - metabolism</topic><topic>assimilation</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>continuous culture</topic><topic>Culture Media</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gluconates - metabolism</topic><topic>glucose</topic><topic>Glucose - metabolism</topic><topic>Glucose 1-Dehydrogenase</topic><topic>glucose dehydrogenase (pyrroloquinoline-quinone)</topic><topic>Glucose Dehydrogenases - analysis</topic><topic>Metabolism. Enzymes</topic><topic>Microbiology</topic><topic>Oxidation-Reduction</topic><topic>Phosphotransferases (Alcohol Group Acceptor)</topic><topic>Phosphotransferases - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VAN SCHIE, B. J</creatorcontrib><creatorcontrib>ROUWENHORST, R. J</creatorcontrib><creatorcontrib>VAN DIJKEN, J. P</creatorcontrib><creatorcontrib>KUENEN, J. 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G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selection of glucose-assimilating variants of Acinetobacter calcoaceticus LMD 79.41 in chemostat culture</atitle><jtitle>Antonie van Leeuwenhoek</jtitle><addtitle>Antonie Van Leeuwenhoek</addtitle><date>1989-01-01</date><risdate>1989</risdate><volume>55</volume><issue>1</issue><spage>39</spage><epage>52</epage><pages>39-52</pages><issn>0003-6072</issn><eissn>1572-9699</eissn><coden>ANLEDR</coden><abstract>Glucose metabolism has been studied in two strains of Acinetobacter calcoaceticus. Strain LMD 82.3, was able to grow on glucose and possessed glucose dehydrogenase (EC 1.1.99.17). Glucose oxidation by whole cells was stimulated by PQQ, the prosthetic group of glucose dehydrogenase. PQQ not only increased the rate of glucose oxidation and gluconic acid production but also shortened the lag phase for growth on glucose. Strain LMD 79.41 also possessed glucose dehydrogenase but was unable to grow on glucose. Batch cultures and carbon-limited chemostat cultures growing on acetate in the presence of glucose oxidized the sugar to gluconic acid, which was not further metabolized. However, after prolonged cultivation on mixtures of acetate and glucose, carbon-limited chemostat cultures suddenly acquired the capacity to utilize gluconate. This phenomenon was accompanied by the appearance of gluconate kinase and a repression of isocitrate lyase synthesis. In contrast to the starter culture, cells from chemostats which had been fully adapted to gluconate utilization, were able to utilize glucose as a sole carbon and energy source in liquid and solid media.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>2545167</pmid><doi>10.1007/BF02309618</doi><tpages>14</tpages></addata></record> |
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subjects | Acetates - metabolism Acinetobacter - enzymology Acinetobacter - growth & development Acinetobacter - metabolism assimilation Bacteriology Biological and medical sciences continuous culture Culture Media Fundamental and applied biological sciences. Psychology Gluconates - metabolism glucose Glucose - metabolism Glucose 1-Dehydrogenase glucose dehydrogenase (pyrroloquinoline-quinone) Glucose Dehydrogenases - analysis Metabolism. Enzymes Microbiology Oxidation-Reduction Phosphotransferases (Alcohol Group Acceptor) Phosphotransferases - analysis |
title | Selection of glucose-assimilating variants of Acinetobacter calcoaceticus LMD 79.41 in chemostat culture |
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