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Selected phytotoxins and organic extracts from endophytic fungus Edenia gomezpompae as light reaction of photosynthesis inhibitors
Morphological variants of Edenia gomezpompae. Colony appearance on potato dextrose agar after 14days at 25°C. [Display omitted] •Organic extracts from morphological variants of E. gomezpompae possess phytotoxic activity.•Naphthoquinone spiroketals tested inhibited the ATP synthesis from water to MV....
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| Published in: | Journal of photochemistry and photobiology. B, Biology Biology, 2014-09, Vol.138, p.17-26 |
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| creator | Macías-Rubalcava, Martha Lydia Ruiz-Velasco Sobrino, María Emma Meléndez-González, Claudio King-Díaz, Beatriz Lotina-Hennsen, Blas |
| description | Morphological variants of Edenia gomezpompae. Colony appearance on potato dextrose agar after 14days at 25°C. [Display omitted]
•Organic extracts from morphological variants of E. gomezpompae possess phytotoxic activity.•Naphthoquinone spiroketals tested inhibited the ATP synthesis from water to MV.•All naphthoquinone spiroketals tested act as Hill reaction inhibitors.•Naphthoquinone spiroketals tested exhibited an effect on the PSII electron.•Site of inhibition was corroborated by fluorescence of the chlorophyll a of PSII.
In a search for natural herbicides, we investigated the action mechanism of the naphthoquinone spiroketals, isolated from the endophytic fungus Edenia gomezpompae: preussomerins EG1 (1) and EG4 (2), and palmarumycins CP17 (3), and CP2 (4) on the photosynthesis light reactions. The naphthoquinone spiroketals 1–4 inhibited the ATP synthesis in freshly lysed spinach thylakoids from water to MV, and they also inhibited the non-cyclic electron transport in the basal, phosphorylating and uncoupled conditions from water to MV. Therefore, they act as Hill reaction inhibitors. The results suggested that naphthoquinone spiroketals 1–4 have two interactions and inhibition site on the PSII electron transport chain. The first one involves the water splitting enzyme inhibition; and, the second on the acceptor site of PSII in a similar way that herbicide Diuron, studied by polaroghaphy and corroborated by fluorescence of the chlorophyll a of PSII. The culture medium and mycelium organic extracts from four morphological variants of E. gomezpompae were phytotoxic, and the culture medium extracts were more potent than mycelium extracts. They also act as Hill reaction inhibitors. |
| doi_str_mv | 10.1016/j.jphotobiol.2014.05.003 |
| format | article |
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•Organic extracts from morphological variants of E. gomezpompae possess phytotoxic activity.•Naphthoquinone spiroketals tested inhibited the ATP synthesis from water to MV.•All naphthoquinone spiroketals tested act as Hill reaction inhibitors.•Naphthoquinone spiroketals tested exhibited an effect on the PSII electron.•Site of inhibition was corroborated by fluorescence of the chlorophyll a of PSII.
In a search for natural herbicides, we investigated the action mechanism of the naphthoquinone spiroketals, isolated from the endophytic fungus Edenia gomezpompae: preussomerins EG1 (1) and EG4 (2), and palmarumycins CP17 (3), and CP2 (4) on the photosynthesis light reactions. The naphthoquinone spiroketals 1–4 inhibited the ATP synthesis in freshly lysed spinach thylakoids from water to MV, and they also inhibited the non-cyclic electron transport in the basal, phosphorylating and uncoupled conditions from water to MV. Therefore, they act as Hill reaction inhibitors. The results suggested that naphthoquinone spiroketals 1–4 have two interactions and inhibition site on the PSII electron transport chain. The first one involves the water splitting enzyme inhibition; and, the second on the acceptor site of PSII in a similar way that herbicide Diuron, studied by polaroghaphy and corroborated by fluorescence of the chlorophyll a of PSII. The culture medium and mycelium organic extracts from four morphological variants of E. gomezpompae were phytotoxic, and the culture medium extracts were more potent than mycelium extracts. They also act as Hill reaction inhibitors.</description><identifier>ISSN: 1011-1344</identifier><identifier>EISSN: 1873-2682</identifier><identifier>DOI: 10.1016/j.jphotobiol.2014.05.003</identifier><identifier>PMID: 24911268</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Ascomycota - chemistry ; Ascomycota - metabolism ; Chlorophyll - chemistry ; Diuron - toxicity ; Edenia gomezpompae ; Electron Transport - drug effects ; Electron Transport - radiation effects ; Endophytic fungi ; Epoxy Compounds - chemistry ; Epoxy Compounds - isolation & purification ; Epoxy Compounds - pharmacology ; Furans - chemistry ; Furans - isolation & purification ; Furans - pharmacology ; Herbicides - toxicity ; Heterocyclic Compounds, 4 or More Rings - chemistry ; Heterocyclic Compounds, 4 or More Rings - isolation & purification ; Heterocyclic Compounds, 4 or More Rings - pharmacology ; Hill reaction inhibitors ; Light ; Mycelium - chemistry ; Mycelium - metabolism ; Naphthoquinone spiroketals ; Naphthoquinones - chemistry ; Organic Chemicals - chemistry ; Palmarumycins ; Photosynthesis - drug effects ; Photosynthetic activities ; Photosystem II Protein Complex - antagonists & inhibitors ; Photosystem II Protein Complex - metabolism ; Phytotoxic compounds ; Preussomerins ; Spinacia oleracea - metabolism ; Spiro Compounds - chemistry ; Spiro Compounds - isolation & purification ; Spiro Compounds - pharmacology ; Thylakoids - metabolism</subject><ispartof>Journal of photochemistry and photobiology. B, Biology, 2014-09, Vol.138, p.17-26</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c374t-8804b966ea14f6c04af218f1ec5924629ca5c558b4b4be0a3143e99cce9fa13</citedby><cites>FETCH-LOGICAL-c374t-8804b966ea14f6c04af218f1ec5924629ca5c558b4b4be0a3143e99cce9fa13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24911268$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Macías-Rubalcava, Martha Lydia</creatorcontrib><creatorcontrib>Ruiz-Velasco Sobrino, María Emma</creatorcontrib><creatorcontrib>Meléndez-González, Claudio</creatorcontrib><creatorcontrib>King-Díaz, Beatriz</creatorcontrib><creatorcontrib>Lotina-Hennsen, Blas</creatorcontrib><title>Selected phytotoxins and organic extracts from endophytic fungus Edenia gomezpompae as light reaction of photosynthesis inhibitors</title><title>Journal of photochemistry and photobiology. B, Biology</title><addtitle>J Photochem Photobiol B</addtitle><description>Morphological variants of Edenia gomezpompae. Colony appearance on potato dextrose agar after 14days at 25°C. [Display omitted]
•Organic extracts from morphological variants of E. gomezpompae possess phytotoxic activity.•Naphthoquinone spiroketals tested inhibited the ATP synthesis from water to MV.•All naphthoquinone spiroketals tested act as Hill reaction inhibitors.•Naphthoquinone spiroketals tested exhibited an effect on the PSII electron.•Site of inhibition was corroborated by fluorescence of the chlorophyll a of PSII.
In a search for natural herbicides, we investigated the action mechanism of the naphthoquinone spiroketals, isolated from the endophytic fungus Edenia gomezpompae: preussomerins EG1 (1) and EG4 (2), and palmarumycins CP17 (3), and CP2 (4) on the photosynthesis light reactions. The naphthoquinone spiroketals 1–4 inhibited the ATP synthesis in freshly lysed spinach thylakoids from water to MV, and they also inhibited the non-cyclic electron transport in the basal, phosphorylating and uncoupled conditions from water to MV. Therefore, they act as Hill reaction inhibitors. The results suggested that naphthoquinone spiroketals 1–4 have two interactions and inhibition site on the PSII electron transport chain. The first one involves the water splitting enzyme inhibition; and, the second on the acceptor site of PSII in a similar way that herbicide Diuron, studied by polaroghaphy and corroborated by fluorescence of the chlorophyll a of PSII. The culture medium and mycelium organic extracts from four morphological variants of E. gomezpompae were phytotoxic, and the culture medium extracts were more potent than mycelium extracts. They also act as Hill reaction inhibitors.</description><subject>Ascomycota - chemistry</subject><subject>Ascomycota - metabolism</subject><subject>Chlorophyll - chemistry</subject><subject>Diuron - toxicity</subject><subject>Edenia gomezpompae</subject><subject>Electron Transport - drug effects</subject><subject>Electron Transport - radiation effects</subject><subject>Endophytic fungi</subject><subject>Epoxy Compounds - chemistry</subject><subject>Epoxy Compounds - isolation & purification</subject><subject>Epoxy Compounds - pharmacology</subject><subject>Furans - chemistry</subject><subject>Furans - isolation & purification</subject><subject>Furans - pharmacology</subject><subject>Herbicides - toxicity</subject><subject>Heterocyclic Compounds, 4 or More Rings - chemistry</subject><subject>Heterocyclic Compounds, 4 or More Rings - isolation & purification</subject><subject>Heterocyclic Compounds, 4 or More Rings - pharmacology</subject><subject>Hill reaction inhibitors</subject><subject>Light</subject><subject>Mycelium - chemistry</subject><subject>Mycelium - metabolism</subject><subject>Naphthoquinone spiroketals</subject><subject>Naphthoquinones - chemistry</subject><subject>Organic Chemicals - chemistry</subject><subject>Palmarumycins</subject><subject>Photosynthesis - drug effects</subject><subject>Photosynthetic activities</subject><subject>Photosystem II Protein Complex - antagonists & inhibitors</subject><subject>Photosystem II Protein Complex - metabolism</subject><subject>Phytotoxic compounds</subject><subject>Preussomerins</subject><subject>Spinacia oleracea - metabolism</subject><subject>Spiro Compounds - chemistry</subject><subject>Spiro Compounds - isolation & purification</subject><subject>Spiro Compounds - pharmacology</subject><subject>Thylakoids - metabolism</subject><issn>1011-1344</issn><issn>1873-2682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkU2P1SAUhhujccbRv2BYummHQ6GXLnUyfiSTuBj3hNLDLTctVKBmrsv55XK9oy6FBSQ87znwUFUEaAMUuutDc1inkMPgwtwwCryhoqG0fVZdgty1Neske172FKCGlvOL6lVKB1qG6HYvqwvGe4ACXVaP9zijyTiSdTrmUvLB-US0H0mIe-2dIfiQozY5ERvDQtCP4USWA7v5_ZbI7YjeabIPC_5cw7JqJDqR2e2nTCKWpAueBEt-XzgdfZ4wuUScn9zgcojpdfXC6jnhm6f1qrr_ePvt5nN99_XTl5v3d7VpdzzXUlI-9F2HGrjtDOXaMpAW0Iie8Y71RgsjhBx4mUh1C7zFvjcGe6uhvarenauuMXzfMGW1uGRwnrXHsCUFQkDLpGSioPKMmhhSimjVGt2i41EBVSf_6qD--Vcn_4oKVfyX6NunLtuw4Pg3-Ed4AT6cASwv_eEwqmQceoOji-Uf1Bjc_7v8AtPOoFw</recordid><startdate>20140905</startdate><enddate>20140905</enddate><creator>Macías-Rubalcava, Martha Lydia</creator><creator>Ruiz-Velasco Sobrino, María Emma</creator><creator>Meléndez-González, Claudio</creator><creator>King-Díaz, Beatriz</creator><creator>Lotina-Hennsen, Blas</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>20140905</creationdate><title>Selected phytotoxins and organic extracts from endophytic fungus Edenia gomezpompae as light reaction of photosynthesis inhibitors</title><author>Macías-Rubalcava, Martha Lydia ; Ruiz-Velasco Sobrino, María Emma ; Meléndez-González, Claudio ; King-Díaz, Beatriz ; Lotina-Hennsen, Blas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c374t-8804b966ea14f6c04af218f1ec5924629ca5c558b4b4be0a3143e99cce9fa13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Ascomycota - chemistry</topic><topic>Ascomycota - metabolism</topic><topic>Chlorophyll - chemistry</topic><topic>Diuron - toxicity</topic><topic>Edenia gomezpompae</topic><topic>Electron Transport - drug effects</topic><topic>Electron Transport - radiation effects</topic><topic>Endophytic fungi</topic><topic>Epoxy Compounds - chemistry</topic><topic>Epoxy Compounds - isolation & purification</topic><topic>Epoxy Compounds - pharmacology</topic><topic>Furans - chemistry</topic><topic>Furans - isolation & purification</topic><topic>Furans - pharmacology</topic><topic>Herbicides - toxicity</topic><topic>Heterocyclic Compounds, 4 or More Rings - chemistry</topic><topic>Heterocyclic Compounds, 4 or More Rings - isolation & purification</topic><topic>Heterocyclic Compounds, 4 or More Rings - pharmacology</topic><topic>Hill reaction inhibitors</topic><topic>Light</topic><topic>Mycelium - chemistry</topic><topic>Mycelium - metabolism</topic><topic>Naphthoquinone spiroketals</topic><topic>Naphthoquinones - chemistry</topic><topic>Organic Chemicals - chemistry</topic><topic>Palmarumycins</topic><topic>Photosynthesis - drug effects</topic><topic>Photosynthetic activities</topic><topic>Photosystem II Protein Complex - antagonists & inhibitors</topic><topic>Photosystem II Protein Complex - metabolism</topic><topic>Phytotoxic compounds</topic><topic>Preussomerins</topic><topic>Spinacia oleracea - metabolism</topic><topic>Spiro Compounds - chemistry</topic><topic>Spiro Compounds - isolation & purification</topic><topic>Spiro Compounds - pharmacology</topic><topic>Thylakoids - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Macías-Rubalcava, Martha Lydia</creatorcontrib><creatorcontrib>Ruiz-Velasco Sobrino, María Emma</creatorcontrib><creatorcontrib>Meléndez-González, Claudio</creatorcontrib><creatorcontrib>King-Díaz, Beatriz</creatorcontrib><creatorcontrib>Lotina-Hennsen, Blas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of photochemistry and photobiology. B, Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Macías-Rubalcava, Martha Lydia</au><au>Ruiz-Velasco Sobrino, María Emma</au><au>Meléndez-González, Claudio</au><au>King-Díaz, Beatriz</au><au>Lotina-Hennsen, Blas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selected phytotoxins and organic extracts from endophytic fungus Edenia gomezpompae as light reaction of photosynthesis inhibitors</atitle><jtitle>Journal of photochemistry and photobiology. B, Biology</jtitle><addtitle>J Photochem Photobiol B</addtitle><date>2014-09-05</date><risdate>2014</risdate><volume>138</volume><spage>17</spage><epage>26</epage><pages>17-26</pages><issn>1011-1344</issn><eissn>1873-2682</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>Morphological variants of Edenia gomezpompae. Colony appearance on potato dextrose agar after 14days at 25°C. [Display omitted]
•Organic extracts from morphological variants of E. gomezpompae possess phytotoxic activity.•Naphthoquinone spiroketals tested inhibited the ATP synthesis from water to MV.•All naphthoquinone spiroketals tested act as Hill reaction inhibitors.•Naphthoquinone spiroketals tested exhibited an effect on the PSII electron.•Site of inhibition was corroborated by fluorescence of the chlorophyll a of PSII.
In a search for natural herbicides, we investigated the action mechanism of the naphthoquinone spiroketals, isolated from the endophytic fungus Edenia gomezpompae: preussomerins EG1 (1) and EG4 (2), and palmarumycins CP17 (3), and CP2 (4) on the photosynthesis light reactions. The naphthoquinone spiroketals 1–4 inhibited the ATP synthesis in freshly lysed spinach thylakoids from water to MV, and they also inhibited the non-cyclic electron transport in the basal, phosphorylating and uncoupled conditions from water to MV. Therefore, they act as Hill reaction inhibitors. The results suggested that naphthoquinone spiroketals 1–4 have two interactions and inhibition site on the PSII electron transport chain. The first one involves the water splitting enzyme inhibition; and, the second on the acceptor site of PSII in a similar way that herbicide Diuron, studied by polaroghaphy and corroborated by fluorescence of the chlorophyll a of PSII. The culture medium and mycelium organic extracts from four morphological variants of E. gomezpompae were phytotoxic, and the culture medium extracts were more potent than mycelium extracts. They also act as Hill reaction inhibitors.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>24911268</pmid><doi>10.1016/j.jphotobiol.2014.05.003</doi><tpages>10</tpages></addata></record> |
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| source | ScienceDirect Freedom Collection 2022-2024 |
| subjects | Ascomycota - chemistry Ascomycota - metabolism Chlorophyll - chemistry Diuron - toxicity Edenia gomezpompae Electron Transport - drug effects Electron Transport - radiation effects Endophytic fungi Epoxy Compounds - chemistry Epoxy Compounds - isolation & purification Epoxy Compounds - pharmacology Furans - chemistry Furans - isolation & purification Furans - pharmacology Herbicides - toxicity Heterocyclic Compounds, 4 or More Rings - chemistry Heterocyclic Compounds, 4 or More Rings - isolation & purification Heterocyclic Compounds, 4 or More Rings - pharmacology Hill reaction inhibitors Light Mycelium - chemistry Mycelium - metabolism Naphthoquinone spiroketals Naphthoquinones - chemistry Organic Chemicals - chemistry Palmarumycins Photosynthesis - drug effects Photosynthetic activities Photosystem II Protein Complex - antagonists & inhibitors Photosystem II Protein Complex - metabolism Phytotoxic compounds Preussomerins Spinacia oleracea - metabolism Spiro Compounds - chemistry Spiro Compounds - isolation & purification Spiro Compounds - pharmacology Thylakoids - metabolism |
| title | Selected phytotoxins and organic extracts from endophytic fungus Edenia gomezpompae as light reaction of photosynthesis inhibitors |
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