Lipoxygenase pathway in model bryophytes: 12-oxo-9(13),15-phytodienoic acid is a predominant oxylipin in Physcomitrella patens

The model moss Physcomitrella patens and liverwort Marchantia polymorpha possess all enzymatic machinery responsible for the initial stages of jasmonate pathway, including the active 13(S)-lipoxygenase, allene oxide synthase (AOS) and allene oxide cyclase (AOC). At the same time, the jasmonic acid i...

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Veröffentlicht in:Phytochemistry (Oxford) 2020-12, Vol.180, p.112533-112533, Article 112533
Hauptverfasser: Mukhtarova, Lucia S., Lantsova, Natalia V., Khairutdinov, Bulat I., Grechkin, Alexander N.
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creator Mukhtarova, Lucia S.
Lantsova, Natalia V.
Khairutdinov, Bulat I.
Grechkin, Alexander N.
description The model moss Physcomitrella patens and liverwort Marchantia polymorpha possess all enzymatic machinery responsible for the initial stages of jasmonate pathway, including the active 13(S)-lipoxygenase, allene oxide synthase (AOS) and allene oxide cyclase (AOC). At the same time, the jasmonic acid is missing from both P. patens and M. polymorpha. Our GC-MS profiling of oxylipins of P. patens gametophores and M. polymorpha tissues revealed some distinctive peculiarities. The 15(Z)-cis-12-oxo-10,15-phytodienoic acid (12-OPDA) was the major oxylipin in M. polymorpha. In contrast, the 12-OPDA was only a minor constituent in P. patens, while another cyclopentenone 1 was the predominant oxylipin. Product 1 was identified by its MS, 1H-NMR, 1H–1H–COSY, HSQC and HMBC data as 15(Z)-12-oxo-9(13),15-phytodienoic acid, i.e., the iso-12-OPDA. The corresponding C16 homologue, 2,3-dinor-iso-12-OPDA (2), have also been detected as a minor component in P. patens and a prominent product in M. polymorpha. Besides, the 2,3-dinor-cis-12-OPDA (3) was also present in M. polymorpha. Apparently, the malfunction of cyclopentenone reduction by the 12-OPDA reductase in P. patens and (to a lesser extent) in M. polymorpha leads to the isomerization of 12-OPDA and formation of specific cyclopentenones 1 and 2, which are uncommon in flowering plants. [Display omitted] •Oxylipin profiles of Physcomitrella patens and Marchantia polymorpha were studied.•The iso-12-OPDA is a predominant oxylipin in P. patens.•Dinor-iso-12-OPDA is prominent in both P. patens and M. polymorpha.•M. polymorpha possesses 12-OPDA and dinor-12-OPDA.•Unusual cyclopentenone metabolism is related to jasmonate loss in Bryophyta.
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At the same time, the jasmonic acid is missing from both P. patens and M. polymorpha. Our GC-MS profiling of oxylipins of P. patens gametophores and M. polymorpha tissues revealed some distinctive peculiarities. The 15(Z)-cis-12-oxo-10,15-phytodienoic acid (12-OPDA) was the major oxylipin in M. polymorpha. In contrast, the 12-OPDA was only a minor constituent in P. patens, while another cyclopentenone 1 was the predominant oxylipin. Product 1 was identified by its MS, 1H-NMR, 1H–1H–COSY, HSQC and HMBC data as 15(Z)-12-oxo-9(13),15-phytodienoic acid, i.e., the iso-12-OPDA. The corresponding C16 homologue, 2,3-dinor-iso-12-OPDA (2), have also been detected as a minor component in P. patens and a prominent product in M. polymorpha. Besides, the 2,3-dinor-cis-12-OPDA (3) was also present in M. polymorpha. Apparently, the malfunction of cyclopentenone reduction by the 12-OPDA reductase in P. patens and (to a lesser extent) in M. polymorpha leads to the isomerization of 12-OPDA and formation of specific cyclopentenones 1 and 2, which are uncommon in flowering plants. [Display omitted] •Oxylipin profiles of Physcomitrella patens and Marchantia polymorpha were studied.•The iso-12-OPDA is a predominant oxylipin in P. patens.•Dinor-iso-12-OPDA is prominent in both P. patens and M. polymorpha.•M. polymorpha possesses 12-OPDA and dinor-12-OPDA.•Unusual cyclopentenone metabolism is related to jasmonate loss in Bryophyta.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2020.112533</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Allene oxide synthase ; cis-12-Oxo-phytodienoic acid ; Cyclopentenones ; Dinor-cis-12-oxo-phytodienoic acid ; Dinor-iso-12-oxo-phytodienoic acid ; iso-12-Oxo-phytodienoic acid ; Marchantia polymorpha (Marchantiaceae) ; Oxylipins ; Physcomitrella patens (Funariaceae)</subject><ispartof>Phytochemistry (Oxford), 2020-12, Vol.180, p.112533-112533, Article 112533</ispartof><rights>2020 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-565e64d0b78f8f900fac8b04e502bb2fdceee31fa228acfef11195c258bd70e53</citedby><cites>FETCH-LOGICAL-c414t-565e64d0b78f8f900fac8b04e502bb2fdceee31fa228acfef11195c258bd70e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.phytochem.2020.112533$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids></links><search><creatorcontrib>Mukhtarova, Lucia S.</creatorcontrib><creatorcontrib>Lantsova, Natalia V.</creatorcontrib><creatorcontrib>Khairutdinov, Bulat I.</creatorcontrib><creatorcontrib>Grechkin, Alexander N.</creatorcontrib><title>Lipoxygenase pathway in model bryophytes: 12-oxo-9(13),15-phytodienoic acid is a predominant oxylipin in Physcomitrella patens</title><title>Phytochemistry (Oxford)</title><description>The model moss Physcomitrella patens and liverwort Marchantia polymorpha possess all enzymatic machinery responsible for the initial stages of jasmonate pathway, including the active 13(S)-lipoxygenase, allene oxide synthase (AOS) and allene oxide cyclase (AOC). At the same time, the jasmonic acid is missing from both P. patens and M. polymorpha. Our GC-MS profiling of oxylipins of P. patens gametophores and M. polymorpha tissues revealed some distinctive peculiarities. The 15(Z)-cis-12-oxo-10,15-phytodienoic acid (12-OPDA) was the major oxylipin in M. polymorpha. In contrast, the 12-OPDA was only a minor constituent in P. patens, while another cyclopentenone 1 was the predominant oxylipin. Product 1 was identified by its MS, 1H-NMR, 1H–1H–COSY, HSQC and HMBC data as 15(Z)-12-oxo-9(13),15-phytodienoic acid, i.e., the iso-12-OPDA. The corresponding C16 homologue, 2,3-dinor-iso-12-OPDA (2), have also been detected as a minor component in P. patens and a prominent product in M. polymorpha. Besides, the 2,3-dinor-cis-12-OPDA (3) was also present in M. polymorpha. Apparently, the malfunction of cyclopentenone reduction by the 12-OPDA reductase in P. patens and (to a lesser extent) in M. polymorpha leads to the isomerization of 12-OPDA and formation of specific cyclopentenones 1 and 2, which are uncommon in flowering plants. [Display omitted] •Oxylipin profiles of Physcomitrella patens and Marchantia polymorpha were studied.•The iso-12-OPDA is a predominant oxylipin in P. patens.•Dinor-iso-12-OPDA is prominent in both P. patens and M. polymorpha.•M. polymorpha possesses 12-OPDA and dinor-12-OPDA.•Unusual cyclopentenone metabolism is related to jasmonate loss in Bryophyta.</description><subject>Allene oxide synthase</subject><subject>cis-12-Oxo-phytodienoic acid</subject><subject>Cyclopentenones</subject><subject>Dinor-cis-12-oxo-phytodienoic acid</subject><subject>Dinor-iso-12-oxo-phytodienoic acid</subject><subject>iso-12-Oxo-phytodienoic acid</subject><subject>Marchantia polymorpha (Marchantiaceae)</subject><subject>Oxylipins</subject><subject>Physcomitrella patens (Funariaceae)</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMFu1DAQhi0EEkvpM9THViLbGSdOsr1VVaGVVioHOFuOPWa9SuJgp9BceHYcFnFFsmTJM_P944-xC4QtAtbXx-10WOZgDjRsBYj8ikKW5Su2wbYpi7IBeM02ACUWu0qIt-xdSkcAkLKuN-zX3k_hZflGo07EJz0ffuqF-5EPwVLPu7iEFU_phqMowksodpdYXn1AWfyJtZ7G4A3XxlvuE9d8imTD4Ec9zjyTez9lWj6fD0syuTBH6nu9RtGY3rM3TveJzv_eZ-zrx_svdw_F_unT493tvjAVVnMha0l1ZaFrWte6HYDTpu2gIgmi64SzhohKdFqIVhtHDhF30gjZdrYBkuUZuzxxpxi-P1Oa1eCTWRcZKTwnJSqJbVWjELm1ObWaGFKK5NQU_aDjohDUalwd1T_jajWuTsbz5O1pkvJPfniKKpmsx5D1kcysbPD_ZfwGNNCQVA</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Mukhtarova, Lucia S.</creator><creator>Lantsova, Natalia V.</creator><creator>Khairutdinov, Bulat I.</creator><creator>Grechkin, Alexander N.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202012</creationdate><title>Lipoxygenase pathway in model bryophytes: 12-oxo-9(13),15-phytodienoic acid is a predominant oxylipin in Physcomitrella patens</title><author>Mukhtarova, Lucia S. ; Lantsova, Natalia V. ; Khairutdinov, Bulat I. ; Grechkin, Alexander N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-565e64d0b78f8f900fac8b04e502bb2fdceee31fa228acfef11195c258bd70e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Allene oxide synthase</topic><topic>cis-12-Oxo-phytodienoic acid</topic><topic>Cyclopentenones</topic><topic>Dinor-cis-12-oxo-phytodienoic acid</topic><topic>Dinor-iso-12-oxo-phytodienoic acid</topic><topic>iso-12-Oxo-phytodienoic acid</topic><topic>Marchantia polymorpha (Marchantiaceae)</topic><topic>Oxylipins</topic><topic>Physcomitrella patens (Funariaceae)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukhtarova, Lucia S.</creatorcontrib><creatorcontrib>Lantsova, Natalia V.</creatorcontrib><creatorcontrib>Khairutdinov, Bulat I.</creatorcontrib><creatorcontrib>Grechkin, Alexander N.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukhtarova, Lucia S.</au><au>Lantsova, Natalia V.</au><au>Khairutdinov, Bulat I.</au><au>Grechkin, Alexander N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lipoxygenase pathway in model bryophytes: 12-oxo-9(13),15-phytodienoic acid is a predominant oxylipin in Physcomitrella patens</atitle><jtitle>Phytochemistry (Oxford)</jtitle><date>2020-12</date><risdate>2020</risdate><volume>180</volume><spage>112533</spage><epage>112533</epage><pages>112533-112533</pages><artnum>112533</artnum><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>The model moss Physcomitrella patens and liverwort Marchantia polymorpha possess all enzymatic machinery responsible for the initial stages of jasmonate pathway, including the active 13(S)-lipoxygenase, allene oxide synthase (AOS) and allene oxide cyclase (AOC). At the same time, the jasmonic acid is missing from both P. patens and M. polymorpha. Our GC-MS profiling of oxylipins of P. patens gametophores and M. polymorpha tissues revealed some distinctive peculiarities. The 15(Z)-cis-12-oxo-10,15-phytodienoic acid (12-OPDA) was the major oxylipin in M. polymorpha. In contrast, the 12-OPDA was only a minor constituent in P. patens, while another cyclopentenone 1 was the predominant oxylipin. Product 1 was identified by its MS, 1H-NMR, 1H–1H–COSY, HSQC and HMBC data as 15(Z)-12-oxo-9(13),15-phytodienoic acid, i.e., the iso-12-OPDA. The corresponding C16 homologue, 2,3-dinor-iso-12-OPDA (2), have also been detected as a minor component in P. patens and a prominent product in M. polymorpha. Besides, the 2,3-dinor-cis-12-OPDA (3) was also present in M. polymorpha. Apparently, the malfunction of cyclopentenone reduction by the 12-OPDA reductase in P. patens and (to a lesser extent) in M. polymorpha leads to the isomerization of 12-OPDA and formation of specific cyclopentenones 1 and 2, which are uncommon in flowering plants. [Display omitted] •Oxylipin profiles of Physcomitrella patens and Marchantia polymorpha were studied.•The iso-12-OPDA is a predominant oxylipin in P. patens.•Dinor-iso-12-OPDA is prominent in both P. patens and M. polymorpha.•M. polymorpha possesses 12-OPDA and dinor-12-OPDA.•Unusual cyclopentenone metabolism is related to jasmonate loss in Bryophyta.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.phytochem.2020.112533</doi><tpages>1</tpages></addata></record>
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subjects Allene oxide synthase
cis-12-Oxo-phytodienoic acid
Cyclopentenones
Dinor-cis-12-oxo-phytodienoic acid
Dinor-iso-12-oxo-phytodienoic acid
iso-12-Oxo-phytodienoic acid
Marchantia polymorpha (Marchantiaceae)
Oxylipins
Physcomitrella patens (Funariaceae)
title Lipoxygenase pathway in model bryophytes: 12-oxo-9(13),15-phytodienoic acid is a predominant oxylipin in Physcomitrella patens
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