Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins
The production of biswasalexins A1 and A2 in sodium chloride and UV stressed salt cress plants, as well as their chemical syntheses and antifungal activity against four cruciferous pathogens is reported. Biswasalexins A1 and A2 are cruciferous phytoalexins whose formation in planta appears to result...
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creator | Pedras, M. Soledade C. Zheng, Qing-An Schatte, Gabriele Adio, Adewale M. |
description | The production of biswasalexins A1 and A2 in sodium chloride and UV stressed salt cress plants, as well as their chemical syntheses and antifungal activity against four cruciferous pathogens is reported. Biswasalexins A1 and A2 are cruciferous phytoalexins whose formation
in
planta appears to result from a photochemical reaction that might protect the plant from fungal pathogens and UV-radiation.
The production of phytoalexins in
Thellungiella halophila exposed to UV-radiation and NaCl was investigated over a period of 8
days. UV-radiation induced substantially larger quantities of wasalexins A and B than NaCl irrigation or CuCl
2 spray. Isolation of two metabolites and their chemical structure determination using X-ray diffraction analysis provided the phytoalexins biswasalexins A1 and A2, that resulted from head-to-tail photodimerization of wasalexin A. The production of biswasalexins A1 and A2 in stressed
T. halophila, as well as their chemical synthesis and antifungal activity are reported. Biswasalexins A1 and A2 (60
nmol/g and 15
nmol/g fresh wt, respectively, 2
days after UV elicitation) are cruciferous phytoalexins whose formation
in planta appears to result from a photochemical reaction, which might protect the plant from fungal attack and UV-radiation. |
doi_str_mv | 10.1016/j.phytochem.2009.09.008 |
format | Article |
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in
planta appears to result from a photochemical reaction that might protect the plant from fungal pathogens and UV-radiation.
The production of phytoalexins in
Thellungiella halophila exposed to UV-radiation and NaCl was investigated over a period of 8
days. UV-radiation induced substantially larger quantities of wasalexins A and B than NaCl irrigation or CuCl
2 spray. Isolation of two metabolites and their chemical structure determination using X-ray diffraction analysis provided the phytoalexins biswasalexins A1 and A2, that resulted from head-to-tail photodimerization of wasalexin A. The production of biswasalexins A1 and A2 in stressed
T. halophila, as well as their chemical synthesis and antifungal activity are reported. Biswasalexins A1 and A2 (60
nmol/g and 15
nmol/g fresh wt, respectively, 2
days after UV elicitation) are cruciferous phytoalexins whose formation
in planta appears to result from a photochemical reaction, which might protect the plant from fungal attack and UV-radiation.</description><identifier>ISSN: 0031-9422</identifier><identifier>EISSN: 1873-3700</identifier><identifier>DOI: 10.1016/j.phytochem.2009.09.008</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>antifungal properties ; Biological and medical sciences ; Brassinin ; Chemical constitution ; Crucifer ; Fundamental and applied biological sciences. Psychology ; Halophila ; indoles ; Photodimerization ; Phytoalexin ; phytoalexins ; plant pathogenic fungi ; Plant physiology and development ; Salt cress ; salt stress ; Sodium chloride stress ; Thellungiella ; Thellungiella halophila ; ultraviolet radiation ; UV-radiation ; wasalexins ; Wasalexins A and B</subject><ispartof>Phytochemistry (Oxford), 2009-12, Vol.70 (17), p.2010-2016</ispartof><rights>2009 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-f810ac37a3998c60adafdb78bae9474c85d483d3babbed1f226ff42b6cc0106e3</citedby><cites>FETCH-LOGICAL-c466t-f810ac37a3998c60adafdb78bae9474c85d483d3babbed1f226ff42b6cc0106e3</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.2009.09.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22337656$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Pedras, M. Soledade C.</creatorcontrib><creatorcontrib>Zheng, Qing-An</creatorcontrib><creatorcontrib>Schatte, Gabriele</creatorcontrib><creatorcontrib>Adio, Adewale M.</creatorcontrib><title>Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins</title><title>Phytochemistry (Oxford)</title><description>The production of biswasalexins A1 and A2 in sodium chloride and UV stressed salt cress plants, as well as their chemical syntheses and antifungal activity against four cruciferous pathogens is reported. Biswasalexins A1 and A2 are cruciferous phytoalexins whose formation
in
planta appears to result from a photochemical reaction that might protect the plant from fungal pathogens and UV-radiation.
The production of phytoalexins in
Thellungiella halophila exposed to UV-radiation and NaCl was investigated over a period of 8
days. UV-radiation induced substantially larger quantities of wasalexins A and B than NaCl irrigation or CuCl
2 spray. Isolation of two metabolites and their chemical structure determination using X-ray diffraction analysis provided the phytoalexins biswasalexins A1 and A2, that resulted from head-to-tail photodimerization of wasalexin A. The production of biswasalexins A1 and A2 in stressed
T. halophila, as well as their chemical synthesis and antifungal activity are reported. Biswasalexins A1 and A2 (60
nmol/g and 15
nmol/g fresh wt, respectively, 2
days after UV elicitation) are cruciferous phytoalexins whose formation
in planta appears to result from a photochemical reaction, which might protect the plant from fungal attack and UV-radiation.</description><subject>antifungal properties</subject><subject>Biological and medical sciences</subject><subject>Brassinin</subject><subject>Chemical constitution</subject><subject>Crucifer</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Halophila</subject><subject>indoles</subject><subject>Photodimerization</subject><subject>Phytoalexin</subject><subject>phytoalexins</subject><subject>plant pathogenic fungi</subject><subject>Plant physiology and development</subject><subject>Salt cress</subject><subject>salt stress</subject><subject>Sodium chloride stress</subject><subject>Thellungiella</subject><subject>Thellungiella halophila</subject><subject>ultraviolet radiation</subject><subject>UV-radiation</subject><subject>wasalexins</subject><subject>Wasalexins A and B</subject><issn>0031-9422</issn><issn>1873-3700</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkN1u1DAQhSMEEkvhGeobuMsytrNOcllV_EmVQKLLrTXxz2ZW2Xixsy3lCfrYdciqt0gjzVx8Z-bMKYpLDmsOXH3cr4_9wxRM7w5rAdCu54LmRbHiTS1LWQO8LFYAkpdtJcTr4k1KewDYbJRaFY8_-rCIyeDALB1cpL84URhZ8OweEw7uD42J0ci2v0qKES3h5Cy77d0wnMYd5YasxyEce8oTjnaG72iKge3c6GLGEzuN9PvkmIknQ97FcErsn_Hz_rfFK49Dcu_O_aLYfv50e_21vPn-5dv11U1pKqWm0jcc0MgaZds2RgFa9Larmw5dW9WVaTa2aqSVHXads9wLobyvRKeMAQ7KyYviw7L3GEP2kyZ9oGTmF0aXPWnBRaNE22awXkATQ0rReX2MdMD4oDnoOXm918_J6zl5PRc0Wfn-fAJTDtVHHA2lZ7kQUtZqozJ3uXAeg8ZdzMz2pwAugddcqRoycbUQLidyRy7qZMiNxlmKzkzaBvqvmyevC6y8</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Pedras, M. Soledade C.</creator><creator>Zheng, Qing-An</creator><creator>Schatte, Gabriele</creator><creator>Adio, Adewale M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>20091201</creationdate><title>Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins</title><author>Pedras, M. Soledade C. ; Zheng, Qing-An ; Schatte, Gabriele ; Adio, Adewale M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-f810ac37a3998c60adafdb78bae9474c85d483d3babbed1f226ff42b6cc0106e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>antifungal properties</topic><topic>Biological and medical sciences</topic><topic>Brassinin</topic><topic>Chemical constitution</topic><topic>Crucifer</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Halophila</topic><topic>indoles</topic><topic>Photodimerization</topic><topic>Phytoalexin</topic><topic>phytoalexins</topic><topic>plant pathogenic fungi</topic><topic>Plant physiology and development</topic><topic>Salt cress</topic><topic>salt stress</topic><topic>Sodium chloride stress</topic><topic>Thellungiella</topic><topic>Thellungiella halophila</topic><topic>ultraviolet radiation</topic><topic>UV-radiation</topic><topic>wasalexins</topic><topic>Wasalexins A and B</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pedras, M. Soledade C.</creatorcontrib><creatorcontrib>Zheng, Qing-An</creatorcontrib><creatorcontrib>Schatte, Gabriele</creatorcontrib><creatorcontrib>Adio, Adewale M.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Phytochemistry (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pedras, M. Soledade C.</au><au>Zheng, Qing-An</au><au>Schatte, Gabriele</au><au>Adio, Adewale M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins</atitle><jtitle>Phytochemistry (Oxford)</jtitle><date>2009-12-01</date><risdate>2009</risdate><volume>70</volume><issue>17</issue><spage>2010</spage><epage>2016</epage><pages>2010-2016</pages><issn>0031-9422</issn><eissn>1873-3700</eissn><abstract>The production of biswasalexins A1 and A2 in sodium chloride and UV stressed salt cress plants, as well as their chemical syntheses and antifungal activity against four cruciferous pathogens is reported. Biswasalexins A1 and A2 are cruciferous phytoalexins whose formation
in
planta appears to result from a photochemical reaction that might protect the plant from fungal pathogens and UV-radiation.
The production of phytoalexins in
Thellungiella halophila exposed to UV-radiation and NaCl was investigated over a period of 8
days. UV-radiation induced substantially larger quantities of wasalexins A and B than NaCl irrigation or CuCl
2 spray. Isolation of two metabolites and their chemical structure determination using X-ray diffraction analysis provided the phytoalexins biswasalexins A1 and A2, that resulted from head-to-tail photodimerization of wasalexin A. The production of biswasalexins A1 and A2 in stressed
T. halophila, as well as their chemical synthesis and antifungal activity are reported. Biswasalexins A1 and A2 (60
nmol/g and 15
nmol/g fresh wt, respectively, 2
days after UV elicitation) are cruciferous phytoalexins whose formation
in planta appears to result from a photochemical reaction, which might protect the plant from fungal attack and UV-radiation.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.phytochem.2009.09.008</doi><tpages>7</tpages></addata></record> |
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subjects | antifungal properties Biological and medical sciences Brassinin Chemical constitution Crucifer Fundamental and applied biological sciences. Psychology Halophila indoles Photodimerization Phytoalexin phytoalexins plant pathogenic fungi Plant physiology and development Salt cress salt stress Sodium chloride stress Thellungiella Thellungiella halophila ultraviolet radiation UV-radiation wasalexins Wasalexins A and B |
title | Photochemical dimerization of wasalexins in UV-irradiated Thellungiella halophila and in vitro generates unique cruciferous phytoalexins |
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