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Genetic engineering of shikonin biosynthesis hairy root cultures of Lithospermum erythrorhizon transformed with the bacterial ubiC gene
The biosynthetic pathway to 4-hydroxybenzoate (4HB), a precursor of the naphthoquinone pigment shikonin, was modified in Lithospermum erythrorhizon hairy root cultures by introduction of the bacterial gene ubiC. This gene of Escherichia coli encodes chorismate pyruvate-lyase (CPL), an enzyme that co...
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Published in: | Plant molecular biology 1999-03, Vol.39 (4), p.683-693 |
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description | The biosynthetic pathway to 4-hydroxybenzoate (4HB), a precursor of the naphthoquinone pigment shikonin, was modified in Lithospermum erythrorhizon hairy root cultures by introduction of the bacterial gene ubiC. This gene of Escherichia coli encodes chorismate pyruvate-lyase (CPL), an enzyme that converts chorismate into 4HB and is not normally present in plants. The ubiC gene was fused to the sequence for a chloroplast transit peptide and placed under control of a constitutive plant promoter. This construct was introduced into L. erythrorhizon by Agrobacterium rhizogenes-mediated transformation. The resulting hairy root cultures showed high CPL activity. 4HB produced by the CPL reaction was utilized for shikonin biosynthesis, as shown by in vivo inhibition of the native pathway to 4HB with 2-aminoindan-2-phosphonic acid (AIP), an inhibitor of phenylalanine ammonia-lyase. A feeding experiment with [1,7-13C2]shikimate showed that in the absence of AIP the artificially introduced CPL reaction contributed ca. 20% of the overall 4HB biosynthesis in the transgenic cultures. ubiC transformation did not lead to a statistically significant increase of shikonin formation, but to a 5-fold increase of the accumulation of menisdaurin, a nitrile glucoside which is presumably related to aromatic amino acid metabolism. |
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This gene of Escherichia coli encodes chorismate pyruvate-lyase (CPL), an enzyme that converts chorismate into 4HB and is not normally present in plants. The ubiC gene was fused to the sequence for a chloroplast transit peptide and placed under control of a constitutive plant promoter. This construct was introduced into L. erythrorhizon by Agrobacterium rhizogenes-mediated transformation. The resulting hairy root cultures showed high CPL activity. 4HB produced by the CPL reaction was utilized for shikonin biosynthesis, as shown by in vivo inhibition of the native pathway to 4HB with 2-aminoindan-2-phosphonic acid (AIP), an inhibitor of phenylalanine ammonia-lyase. A feeding experiment with [1,7-13C2]shikimate showed that in the absence of AIP the artificially introduced CPL reaction contributed ca. 20% of the overall 4HB biosynthesis in the transgenic cultures. ubiC transformation did not lead to a statistically significant increase of shikonin formation, but to a 5-fold increase of the accumulation of menisdaurin, a nitrile glucoside which is presumably related to aromatic amino acid metabolism.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1023/A:1006185806390</identifier><identifier>PMID: 10350083</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>4-hydroxybenzoate ; Amino acids ; Bacteria ; benzoates (esters) ; Biosynthesis ; carboxy-lyases ; Cell Line, Transformed ; chorismate pyruvate-lyase ; derivatives ; E coli ; enzyme activity ; Escherichia coli ; Escherichia coli - enzymology ; Escherichia coli - genetics ; gene transfer ; genes ; Genetic engineering ; Genetic Engineering - methods ; genetic transformation ; Genetic Vectors ; glucosides ; Kinetics ; Lithospermum erythrorhizon ; menisdaurin ; naphthoquinone ; Naphthoquinones - metabolism ; Oxo-Acid-Lyases - genetics ; Oxo-Acid-Lyases - metabolism ; pigments ; Plant Roots - metabolism ; Plants - metabolism ; plasmid vectors ; Recombinant Proteins - metabolism ; Rhizobium - genetics ; Rhizobium rhizogenes ; roots ; Shikimic Acid - metabolism ; tissue culture ; Transfection ; transgenic plants</subject><ispartof>Plant molecular biology, 1999-03, Vol.39 (4), p.683-693</ispartof><rights>Kluwer Academic Publishers 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-78ca878af7d832a473736a9074dd82bb9f733536ba17869adaf58e15145e5b393</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10350083$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sommer, S</creatorcontrib><creatorcontrib>Kohle, A</creatorcontrib><creatorcontrib>Yazaki, K</creatorcontrib><creatorcontrib>Shimomura, K</creatorcontrib><creatorcontrib>Bechthold, A</creatorcontrib><creatorcontrib>Heide, L</creatorcontrib><title>Genetic engineering of shikonin biosynthesis hairy root cultures of Lithospermum erythrorhizon transformed with the bacterial ubiC gene</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>The biosynthetic pathway to 4-hydroxybenzoate (4HB), a precursor of the naphthoquinone pigment shikonin, was modified in Lithospermum erythrorhizon hairy root cultures by introduction of the bacterial gene ubiC. This gene of Escherichia coli encodes chorismate pyruvate-lyase (CPL), an enzyme that converts chorismate into 4HB and is not normally present in plants. The ubiC gene was fused to the sequence for a chloroplast transit peptide and placed under control of a constitutive plant promoter. This construct was introduced into L. erythrorhizon by Agrobacterium rhizogenes-mediated transformation. The resulting hairy root cultures showed high CPL activity. 4HB produced by the CPL reaction was utilized for shikonin biosynthesis, as shown by in vivo inhibition of the native pathway to 4HB with 2-aminoindan-2-phosphonic acid (AIP), an inhibitor of phenylalanine ammonia-lyase. A feeding experiment with [1,7-13C2]shikimate showed that in the absence of AIP the artificially introduced CPL reaction contributed ca. 20% of the overall 4HB biosynthesis in the transgenic cultures. ubiC transformation did not lead to a statistically significant increase of shikonin formation, but to a 5-fold increase of the accumulation of menisdaurin, a nitrile glucoside which is presumably related to aromatic amino acid metabolism.</description><subject>4-hydroxybenzoate</subject><subject>Amino acids</subject><subject>Bacteria</subject><subject>benzoates (esters)</subject><subject>Biosynthesis</subject><subject>carboxy-lyases</subject><subject>Cell Line, Transformed</subject><subject>chorismate pyruvate-lyase</subject><subject>derivatives</subject><subject>E coli</subject><subject>enzyme activity</subject><subject>Escherichia coli</subject><subject>Escherichia coli - enzymology</subject><subject>Escherichia coli - genetics</subject><subject>gene transfer</subject><subject>genes</subject><subject>Genetic engineering</subject><subject>Genetic Engineering - methods</subject><subject>genetic transformation</subject><subject>Genetic Vectors</subject><subject>glucosides</subject><subject>Kinetics</subject><subject>Lithospermum erythrorhizon</subject><subject>menisdaurin</subject><subject>naphthoquinone</subject><subject>Naphthoquinones - metabolism</subject><subject>Oxo-Acid-Lyases - genetics</subject><subject>Oxo-Acid-Lyases - metabolism</subject><subject>pigments</subject><subject>Plant Roots - metabolism</subject><subject>Plants - metabolism</subject><subject>plasmid vectors</subject><subject>Recombinant Proteins - metabolism</subject><subject>Rhizobium - genetics</subject><subject>Rhizobium rhizogenes</subject><subject>roots</subject><subject>Shikimic Acid - metabolism</subject><subject>tissue culture</subject><subject>Transfection</subject><subject>transgenic plants</subject><issn>0167-4412</issn><issn>1573-5028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqF0U1v1DAQBmALgei2cOYGFgdugXEm_uJWraAgrdRD6TlyEmfjktiL7aha_kD_dl21vXDhNJdH8_EOIe8YfGZQ45fzrwxAMMUVCNTwgmwYl1hxqNVLsgEmZNU0rD4hpyndABSM4jU5YYAcQOGG3F1Yb7PrqfV7562Nzu9pGGma3O_gnaedC-no82STS3QyLh5pDCHTfp3zGm16wDuXp5AONi7rQm085imGOLm_wdMcjU9jiIsd6G1htHSinelzmWRmunZuS_dlhTfk1WjmZN8-1TNy_f3br-2Pand58XN7vqt6RJ4rqXqjpDKjHBTWppEoURgNshkGVXedHmVxKDrDpBLaDGbkyjLOGm55hxrPyKfHvocY_qw25XZxqbfzbLwNa2qFlvoh0v9CJmsFWjQFfvwH3oQ1-nJEK2WZi6igoPdPaO1KFO0husXEY_v8iAI-PILRhNbso0vt9VUNDKHWrBGC4T2ufJVy</recordid><startdate>19990301</startdate><enddate>19990301</enddate><creator>Sommer, S</creator><creator>Kohle, A</creator><creator>Yazaki, K</creator><creator>Shimomura, K</creator><creator>Bechthold, A</creator><creator>Heide, L</creator><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>19990301</creationdate><title>Genetic engineering of shikonin biosynthesis hairy root cultures of Lithospermum erythrorhizon transformed with the bacterial ubiC gene</title><author>Sommer, S ; Kohle, A ; Yazaki, K ; Shimomura, K ; Bechthold, A ; Heide, L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-78ca878af7d832a473736a9074dd82bb9f733536ba17869adaf58e15145e5b393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>4-hydroxybenzoate</topic><topic>Amino acids</topic><topic>Bacteria</topic><topic>benzoates (esters)</topic><topic>Biosynthesis</topic><topic>carboxy-lyases</topic><topic>Cell Line, Transformed</topic><topic>chorismate pyruvate-lyase</topic><topic>derivatives</topic><topic>E coli</topic><topic>enzyme activity</topic><topic>Escherichia coli</topic><topic>Escherichia coli - enzymology</topic><topic>Escherichia coli - genetics</topic><topic>gene transfer</topic><topic>genes</topic><topic>Genetic engineering</topic><topic>Genetic Engineering - methods</topic><topic>genetic transformation</topic><topic>Genetic Vectors</topic><topic>glucosides</topic><topic>Kinetics</topic><topic>Lithospermum erythrorhizon</topic><topic>menisdaurin</topic><topic>naphthoquinone</topic><topic>Naphthoquinones - metabolism</topic><topic>Oxo-Acid-Lyases - genetics</topic><topic>Oxo-Acid-Lyases - metabolism</topic><topic>pigments</topic><topic>Plant Roots - metabolism</topic><topic>Plants - metabolism</topic><topic>plasmid vectors</topic><topic>Recombinant Proteins - metabolism</topic><topic>Rhizobium - genetics</topic><topic>Rhizobium rhizogenes</topic><topic>roots</topic><topic>Shikimic Acid - metabolism</topic><topic>tissue culture</topic><topic>Transfection</topic><topic>transgenic plants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sommer, S</creatorcontrib><creatorcontrib>Kohle, A</creatorcontrib><creatorcontrib>Yazaki, K</creatorcontrib><creatorcontrib>Shimomura, K</creatorcontrib><creatorcontrib>Bechthold, A</creatorcontrib><creatorcontrib>Heide, L</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</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>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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Plant molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sommer, S</au><au>Kohle, A</au><au>Yazaki, K</au><au>Shimomura, K</au><au>Bechthold, A</au><au>Heide, L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic engineering of shikonin biosynthesis hairy root cultures of Lithospermum erythrorhizon transformed with the bacterial ubiC gene</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>1999-03-01</date><risdate>1999</risdate><volume>39</volume><issue>4</issue><spage>683</spage><epage>693</epage><pages>683-693</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>The biosynthetic pathway to 4-hydroxybenzoate (4HB), a precursor of the naphthoquinone pigment shikonin, was modified in Lithospermum erythrorhizon hairy root cultures by introduction of the bacterial gene ubiC. This gene of Escherichia coli encodes chorismate pyruvate-lyase (CPL), an enzyme that converts chorismate into 4HB and is not normally present in plants. The ubiC gene was fused to the sequence for a chloroplast transit peptide and placed under control of a constitutive plant promoter. This construct was introduced into L. erythrorhizon by Agrobacterium rhizogenes-mediated transformation. The resulting hairy root cultures showed high CPL activity. 4HB produced by the CPL reaction was utilized for shikonin biosynthesis, as shown by in vivo inhibition of the native pathway to 4HB with 2-aminoindan-2-phosphonic acid (AIP), an inhibitor of phenylalanine ammonia-lyase. A feeding experiment with [1,7-13C2]shikimate showed that in the absence of AIP the artificially introduced CPL reaction contributed ca. 20% of the overall 4HB biosynthesis in the transgenic cultures. ubiC transformation did not lead to a statistically significant increase of shikonin formation, but to a 5-fold increase of the accumulation of menisdaurin, a nitrile glucoside which is presumably related to aromatic amino acid metabolism.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>10350083</pmid><doi>10.1023/A:1006185806390</doi><tpages>11</tpages></addata></record> |
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subjects | 4-hydroxybenzoate Amino acids Bacteria benzoates (esters) Biosynthesis carboxy-lyases Cell Line, Transformed chorismate pyruvate-lyase derivatives E coli enzyme activity Escherichia coli Escherichia coli - enzymology Escherichia coli - genetics gene transfer genes Genetic engineering Genetic Engineering - methods genetic transformation Genetic Vectors glucosides Kinetics Lithospermum erythrorhizon menisdaurin naphthoquinone Naphthoquinones - metabolism Oxo-Acid-Lyases - genetics Oxo-Acid-Lyases - metabolism pigments Plant Roots - metabolism Plants - metabolism plasmid vectors Recombinant Proteins - metabolism Rhizobium - genetics Rhizobium rhizogenes roots Shikimic Acid - metabolism tissue culture Transfection transgenic plants |
title | Genetic engineering of shikonin biosynthesis hairy root cultures of Lithospermum erythrorhizon transformed with the bacterial ubiC gene |
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