Biochemical characterization reveals the functional divergence of two tropinone reductases from Przewalskia tangutica
Przewalskia tangutica is a traditional medicinal plant from Tibet used for the analgesic effect from the tropane alkaloids (TAs) produced by the plant. Its roots have the highest yield of hyoscyamine in all plant species and so have been overharvested becoming an endangered medicinal plant species....
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Veröffentlicht in: | Biotechnology and applied biochemistry 2019-07, Vol.66 (4), p.597-606 |
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creator | Wu, Nianyang Jian, Dongqin Xiang, Min Chen, Min Lan, Xiaozhong Liao, Zhihua Liu, Xiaoqiang |
description | Przewalskia tangutica is a traditional medicinal plant from Tibet used for the analgesic effect from the tropane alkaloids (TAs) produced by the plant. Its roots have the highest yield of hyoscyamine in all plant species and so have been overharvested becoming an endangered medicinal plant species. Metabolic engineering is a good way to improve the yield of TAs in plants. In our study, two functionally distinct tropinone reductases genes, PtTRI and PtTRII, were cloned from P. tangutica and the functional divergence were characterized. The enzyme kinetics of PtTRI and PtTRII were investigated. The phylogenetic analysis classified them into different clades: PtTRI and PtTRII were in the clade of tropine‐forming reductase and pseudotropine‐forming reductase, respectively. We found PtTRI to be expressed in the roots but less in leaves, whereas PtTRII was expressed in the roots at higher levels than in the leaves. The kinetic parameters (Km, Vmax, and Kcat) were analyzed using purified recombinant enzymes at their optimum pH. Enzymatic analysis results showed that tropinone is a better substrate for PtTRII compared with PtTRI, suggesting that PtTRII might be a potential gene target for TA biosynthesis engineering. Compared with the reported TRIs, PtTRI exhibited a higher affinity for tropinone. |
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Its roots have the highest yield of hyoscyamine in all plant species and so have been overharvested becoming an endangered medicinal plant species. Metabolic engineering is a good way to improve the yield of TAs in plants. In our study, two functionally distinct tropinone reductases genes, PtTRI and PtTRII, were cloned from P. tangutica and the functional divergence were characterized. The enzyme kinetics of PtTRI and PtTRII were investigated. The phylogenetic analysis classified them into different clades: PtTRI and PtTRII were in the clade of tropine‐forming reductase and pseudotropine‐forming reductase, respectively. We found PtTRI to be expressed in the roots but less in leaves, whereas PtTRII was expressed in the roots at higher levels than in the leaves. The kinetic parameters (Km, Vmax, and Kcat) were analyzed using purified recombinant enzymes at their optimum pH. Enzymatic analysis results showed that tropinone is a better substrate for PtTRII compared with PtTRI, suggesting that PtTRII might be a potential gene target for TA biosynthesis engineering. Compared with the reported TRIs, PtTRI exhibited a higher affinity for tropinone.</description><identifier>ISSN: 0885-4513</identifier><identifier>EISSN: 1470-8744</identifier><identifier>DOI: 10.1002/bab.1760</identifier><identifier>PMID: 31051047</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Alcohol Oxidoreductases - chemistry ; Alcohol Oxidoreductases - genetics ; Alcohol Oxidoreductases - metabolism ; Alkaloids ; Biosynthesis ; Divergence ; Endangered plants ; Endangered species ; Enzyme kinetics ; Flowers & plants ; functional identification ; Herbal medicine ; Kinetics ; Leaves ; Medicinal plants ; Metabolic Engineering ; Phylogeny ; Plant species ; Przewalskia ; Przewalskia tangutica ; Reductase ; Reductases ; Roots ; Solanaceae - enzymology ; Substrates ; Tropane alkaloids ; tropinone reductase</subject><ispartof>Biotechnology and applied biochemistry, 2019-07, Vol.66 (4), p.597-606</ispartof><rights>2019 International Union of Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3490-dfd31d39c58f8aa53004d32cb8fe15d613953b3d0304b25a98b083bbfffb77ff3</citedby><cites>FETCH-LOGICAL-c3490-dfd31d39c58f8aa53004d32cb8fe15d613953b3d0304b25a98b083bbfffb77ff3</cites><orcidid>0000-0002-1283-4649 ; 0000-0002-3833-7405</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbab.1760$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbab.1760$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31051047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Nianyang</creatorcontrib><creatorcontrib>Jian, Dongqin</creatorcontrib><creatorcontrib>Xiang, Min</creatorcontrib><creatorcontrib>Chen, Min</creatorcontrib><creatorcontrib>Lan, Xiaozhong</creatorcontrib><creatorcontrib>Liao, Zhihua</creatorcontrib><creatorcontrib>Liu, Xiaoqiang</creatorcontrib><title>Biochemical characterization reveals the functional divergence of two tropinone reductases from Przewalskia tangutica</title><title>Biotechnology and applied biochemistry</title><addtitle>Biotechnol Appl Biochem</addtitle><description>Przewalskia tangutica is a traditional medicinal plant from Tibet used for the analgesic effect from the tropane alkaloids (TAs) produced by the plant. Its roots have the highest yield of hyoscyamine in all plant species and so have been overharvested becoming an endangered medicinal plant species. Metabolic engineering is a good way to improve the yield of TAs in plants. In our study, two functionally distinct tropinone reductases genes, PtTRI and PtTRII, were cloned from P. tangutica and the functional divergence were characterized. The enzyme kinetics of PtTRI and PtTRII were investigated. The phylogenetic analysis classified them into different clades: PtTRI and PtTRII were in the clade of tropine‐forming reductase and pseudotropine‐forming reductase, respectively. We found PtTRI to be expressed in the roots but less in leaves, whereas PtTRII was expressed in the roots at higher levels than in the leaves. The kinetic parameters (Km, Vmax, and Kcat) were analyzed using purified recombinant enzymes at their optimum pH. Enzymatic analysis results showed that tropinone is a better substrate for PtTRII compared with PtTRI, suggesting that PtTRII might be a potential gene target for TA biosynthesis engineering. Compared with the reported TRIs, PtTRI exhibited a higher affinity for tropinone.</description><subject>Alcohol Oxidoreductases - chemistry</subject><subject>Alcohol Oxidoreductases - genetics</subject><subject>Alcohol Oxidoreductases - metabolism</subject><subject>Alkaloids</subject><subject>Biosynthesis</subject><subject>Divergence</subject><subject>Endangered plants</subject><subject>Endangered species</subject><subject>Enzyme kinetics</subject><subject>Flowers & plants</subject><subject>functional identification</subject><subject>Herbal medicine</subject><subject>Kinetics</subject><subject>Leaves</subject><subject>Medicinal plants</subject><subject>Metabolic Engineering</subject><subject>Phylogeny</subject><subject>Plant species</subject><subject>Przewalskia</subject><subject>Przewalskia tangutica</subject><subject>Reductase</subject><subject>Reductases</subject><subject>Roots</subject><subject>Solanaceae - enzymology</subject><subject>Substrates</subject><subject>Tropane alkaloids</subject><subject>tropinone reductase</subject><issn>0885-4513</issn><issn>1470-8744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1rFEEQhhtRzBoFf4E0ePEysT-3e47Z4BcEzCE5D_1Rne04M71292RJfr29SVQQPBUUTz1F1YvQW0pOKCHsozX2hKo1eYZWVCjSaSXEc7QiWstOSMqP0KtSbgghWmn2Eh1xSiQlQq3QsonJbWGKzozYbU02rkKO96bGNOMMt2DGgusWcFhmd2g2zsdbyNcwO8Ap4LpPuOa0i3OaoY34xVVToOCQ04Qv8j3sm-NHNLia-XqpbdVr9CK0Hrx5qsfo6vOny7Ov3fn3L9_OTs87x0VPOh88p573TuqgjZGcEOE5c1YHoNKvKe8lt9wTToRl0vTaEs2tDSFYpULgx-jDo3eX088FSh2mWByMo5khLWVgjPVMMMXXDX3_D3qTltyuPVC9XFOqKPsrdDmVkiEMuxwnk-8GSoZDFEOLYjhE0dB3T8LFTuD_gL9_34DuEdjHEe7-Kxo2p5sH4S_g0ZQn</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Wu, Nianyang</creator><creator>Jian, Dongqin</creator><creator>Xiang, Min</creator><creator>Chen, Min</creator><creator>Lan, Xiaozhong</creator><creator>Liao, Zhihua</creator><creator>Liu, Xiaoqiang</creator><general>Wiley Subscription Services, 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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TB</scope><scope>7TK</scope><scope>7U5</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>L7M</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1283-4649</orcidid><orcidid>https://orcid.org/0000-0002-3833-7405</orcidid></search><sort><creationdate>201907</creationdate><title>Biochemical characterization reveals the functional divergence of two tropinone reductases from Przewalskia tangutica</title><author>Wu, Nianyang ; Jian, Dongqin ; Xiang, Min ; Chen, Min ; Lan, Xiaozhong ; Liao, Zhihua ; Liu, Xiaoqiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3490-dfd31d39c58f8aa53004d32cb8fe15d613953b3d0304b25a98b083bbfffb77ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alcohol Oxidoreductases - chemistry</topic><topic>Alcohol Oxidoreductases - genetics</topic><topic>Alcohol Oxidoreductases - metabolism</topic><topic>Alkaloids</topic><topic>Biosynthesis</topic><topic>Divergence</topic><topic>Endangered plants</topic><topic>Endangered species</topic><topic>Enzyme kinetics</topic><topic>Flowers & plants</topic><topic>functional identification</topic><topic>Herbal medicine</topic><topic>Kinetics</topic><topic>Leaves</topic><topic>Medicinal plants</topic><topic>Metabolic Engineering</topic><topic>Phylogeny</topic><topic>Plant species</topic><topic>Przewalskia</topic><topic>Przewalskia tangutica</topic><topic>Reductase</topic><topic>Reductases</topic><topic>Roots</topic><topic>Solanaceae - enzymology</topic><topic>Substrates</topic><topic>Tropane alkaloids</topic><topic>tropinone reductase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Nianyang</creatorcontrib><creatorcontrib>Jian, Dongqin</creatorcontrib><creatorcontrib>Xiang, Min</creatorcontrib><creatorcontrib>Chen, Min</creatorcontrib><creatorcontrib>Lan, Xiaozhong</creatorcontrib><creatorcontrib>Liao, Zhihua</creatorcontrib><creatorcontrib>Liu, Xiaoqiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology and applied biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Nianyang</au><au>Jian, Dongqin</au><au>Xiang, Min</au><au>Chen, Min</au><au>Lan, Xiaozhong</au><au>Liao, Zhihua</au><au>Liu, Xiaoqiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochemical characterization reveals the functional divergence of two tropinone reductases from Przewalskia tangutica</atitle><jtitle>Biotechnology and applied biochemistry</jtitle><addtitle>Biotechnol Appl Biochem</addtitle><date>2019-07</date><risdate>2019</risdate><volume>66</volume><issue>4</issue><spage>597</spage><epage>606</epage><pages>597-606</pages><issn>0885-4513</issn><eissn>1470-8744</eissn><abstract>Przewalskia tangutica is a traditional medicinal plant from Tibet used for the analgesic effect from the tropane alkaloids (TAs) produced by the plant. Its roots have the highest yield of hyoscyamine in all plant species and so have been overharvested becoming an endangered medicinal plant species. Metabolic engineering is a good way to improve the yield of TAs in plants. In our study, two functionally distinct tropinone reductases genes, PtTRI and PtTRII, were cloned from P. tangutica and the functional divergence were characterized. The enzyme kinetics of PtTRI and PtTRII were investigated. The phylogenetic analysis classified them into different clades: PtTRI and PtTRII were in the clade of tropine‐forming reductase and pseudotropine‐forming reductase, respectively. We found PtTRI to be expressed in the roots but less in leaves, whereas PtTRII was expressed in the roots at higher levels than in the leaves. The kinetic parameters (Km, Vmax, and Kcat) were analyzed using purified recombinant enzymes at their optimum pH. Enzymatic analysis results showed that tropinone is a better substrate for PtTRII compared with PtTRI, suggesting that PtTRII might be a potential gene target for TA biosynthesis engineering. Compared with the reported TRIs, PtTRI exhibited a higher affinity for tropinone.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31051047</pmid><doi>10.1002/bab.1760</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1283-4649</orcidid><orcidid>https://orcid.org/0000-0002-3833-7405</orcidid></addata></record> |
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subjects | Alcohol Oxidoreductases - chemistry Alcohol Oxidoreductases - genetics Alcohol Oxidoreductases - metabolism Alkaloids Biosynthesis Divergence Endangered plants Endangered species Enzyme kinetics Flowers & plants functional identification Herbal medicine Kinetics Leaves Medicinal plants Metabolic Engineering Phylogeny Plant species Przewalskia Przewalskia tangutica Reductase Reductases Roots Solanaceae - enzymology Substrates Tropane alkaloids tropinone reductase |
title | Biochemical characterization reveals the functional divergence of two tropinone reductases from Przewalskia tangutica |
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