{"id":107,"date":"2025-03-10T12:32:38","date_gmt":"2025-03-10T19:32:38","guid":{"rendered":"https:\/\/labs.wsu.edu\/lange-lab\/?page_id=107"},"modified":"2025-03-12T14:00:13","modified_gmt":"2025-03-12T21:00:13","slug":"terpene-synthase-structure-function","status":"publish","type":"page","link":"https:\/\/labs.wsu.edu\/lange-lab\/terpene-synthase-structure-function\/","title":{"rendered":"Terpene Synthase Structure-Function"},"content":{"rendered":"\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>Project Goals<\/strong><\/td><td>Integrative approaches to tease out the determinants of product specificity in terpene synthases<\/td><\/tr><tr><td><strong>Funding<\/strong><\/td><td>Department of Energy &#8211; Energy Biosciences Program<\/td><\/tr><tr><td><strong>Collaborators<\/strong><\/td><td>Simone Raugei, Hoshin Kim &#8211; Pacific Northwest National Laboratory<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">Executive Summary<\/h2>\n\n\n\n<p class=\" wsu-font-size--medium\">Terpene synthases convert a prenyl diphosphate of a specific chain length to the first pathway-specific (often cyclic) intermediate in the biosynthesis of each class of terpenoids.&nbsp; While some terpene synthases are remarkably specific and generate only one product, others release a larger number of products from a common substrate, thus contributing to terpenoid chemical diversity. We are using data from&nbsp;sequence comparisons, crystal structures, and molecular dynamics simulations to develop an understanding of how specificity arises in terpene synthases. Based on these insights we are developing models with a longer term goal to be able to predict the function of terpene synthases.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Selected Recent Publications<\/h2>\n\n\n\n<p class=\" wsu-font-size--medium\">Srividya N., Kim H., Simone R., Lange B.M. (2024) Chemical diversity in angiosperms\u2212 monoterpene synthases control complex reactions that provide the precursors for ecologically and commercially important monoterpenoids. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1111\/tpj.16743\"><em>Plant J<\/em>. 119, 28-55<\/a>.<\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Lange B.M., Srividya N. (2023) Cannabis monoterpene synthases: evaluating structure\u2013function relationships. <a href=\"https:\/\/link.springer.com\/article\/10.1007\/s11101-023-09861-4\"><em>Phytochem. Rev<\/em>. 22, 449-465<\/a>.<\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Lange B.M., Srividya N., Lange I., Parrish A.N., Benzenberg L.R., Pandelova I., Vining K.J., W\u00fcst M. (2023) Biochemical basis for the formation of organ-specific volatile blends in mint. <a href=\"https:\/\/www.frontiersin.org\/journals\/plant-science\/articles\/10.3389\/fpls.2023.1125065\/full\"><em>Front. Plant Sci<\/em>. 14, 1125065<\/a>.<\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Kim H., Srividya N., Lange I., Huchala E.W., Ginovska B., Lange B.M., Raugei S. (2022) Determinants of selectivity for the formation of monocyclic and bicyclic products in monoterpene synthases. <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acscatal.2c01836\"><em>ACS Catal.<\/em> 12, 7453-7469<\/a>.<\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Srividya N., Lange I., Richter J.K., W\u00fcst M., Lange B.M. (2022). Selectivity of enzymes involved in the formation of opposite enantiomeric series of p-menthane monoterpenoids in peppermint and Japanese catnip.&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0168945221003150\"><em>Plant Sci.<\/em>&nbsp;314 , 111119<\/a>.&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0168945221003150\"><\/a><\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Srividya N., Lange I., Lange B.M. (2020) Determinants of enantiospecificity in limonene synthases.&nbsp;<em>Biochemistry&nbsp;<\/em>59, <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/32293167\/\">1661-1664<\/a>.&nbsp;<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/32293167\/\"><\/a><\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Lange B.M., Srividya N. (2019) Enzymology of monoterpene functionalization in glandular trichomes.&nbsp;<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/30624688\/\"><em>J. Exp. Bot.<\/em>, 70, 1095-1108<\/a>.<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/30624688\"><\/a><\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Srividya N., Lange I., Lange B.M. (2016) Generation and functional evaluation of designer monoterpene synthases.&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0076687916001257\"><em>Methods Enzymol.<\/em>&nbsp;576, 147-165<\/a>.&nbsp;<\/p>\n\n\n\n<p class=\" wsu-font-size--medium\">Srividya N., Davis E.M., Croteau R.B., Lange B.M. (2015) Functional analysis of (4S)-limonene synthase mutants reveals determinants of catalytic outcome in a model monoterpene synthase.&nbsp;<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/25733883\/\"><em>Proc. Natl. Acad. Sci. USA<\/em>&nbsp;112, 3332-3337<\/a>.&nbsp;<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25733883\"><\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Project Goals Integrative approaches to tease out the determinants of product specificity in terpene synthases Funding Department of Energy &#8211; Energy Biosciences Program Collaborators Simone Raugei, Hoshin Kim &#8211; Pacific Northwest National Laboratory Executive Summary Terpene synthases convert a prenyl diphosphate of a specific chain length to the first pathway-specific (often cyclic) intermediate in the [&hellip;]<\/p>\n","protected":false},"author":44101,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"categories":[],"tags":[],"wsuwp_university_location":[],"wsuwp_university_org":[],"_links":{"self":[{"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/pages\/107"}],"collection":[{"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/users\/44101"}],"replies":[{"embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/comments?post=107"}],"version-history":[{"count":10,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/pages\/107\/revisions"}],"predecessor-version":[{"id":205,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/pages\/107\/revisions\/205"}],"wp:attachment":[{"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/media?parent=107"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/categories?post=107"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/tags?post=107"},{"taxonomy":"wsuwp_university_location","embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/wsuwp_university_location?post=107"},{"taxonomy":"wsuwp_university_org","embeddable":true,"href":"https:\/\/labs.wsu.edu\/lange-lab\/wp-json\/wp\/v2\/wsuwp_university_org?post=107"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}