Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites

To find new pesticides for agricultural use, 133 fungal strains were isolated from coastal marine habitats, from which 37 independent isolates were identified, belonging to 20 genera in nine orders, and the diversity of the isolated fungi were discussed. The phytotoxicity and anti-phytopathogenic fu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:RSC advances 2018-01, Vol.8 (66), p.37573-37580
Hauptverfasser: Huang, Rui-Huan, Gou, Jian-Yu, Zhao, Dong-Lin, Wang, Dan, Liu, Jing, Ma, Guo-Yong, Li, Yi-Qiang, Zhang, Cheng-Sheng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 37580
container_issue 66
container_start_page 37573
container_title RSC advances
container_volume 8
creator Huang, Rui-Huan
Gou, Jian-Yu
Zhao, Dong-Lin
Wang, Dan
Liu, Jing
Ma, Guo-Yong
Li, Yi-Qiang
Zhang, Cheng-Sheng
description To find new pesticides for agricultural use, 133 fungal strains were isolated from coastal marine habitats, from which 37 independent isolates were identified, belonging to 20 genera in nine orders, and the diversity of the isolated fungi were discussed. The phytotoxicity and anti-phytopathogenic fungal and bacterial activities of these 37 extracts, and two previously isolated fungal extracts were evaluated, displaying different levels of bioactivity. Based on the bioactive and chemical screening, an sp. (P8) strain, which showed prominent bioactivity and contained abundant secondary metabolites was selected for further chemical investigation; one new compound, a benzopyranone (1), and seven known compounds (2-8) were obtained. Their structures were determined by analysing extensive NMR spectroscopic data and ECD comparisons. Compounds 1, 2, and 6-8 showed obvious phytotoxicity, especially against amaranth, and compound 1 also showed potent antifungal activity toward . To the best of our knowledge, this is the first report of the phytotoxicity of marine-derived fungi and their secondary metabolites. These studies should provide the foundation for future research into the use of such fungal extracts to combat weeds and diseases in agriculture.
doi_str_mv 10.1039/c8ra08047j
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9089327</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2664807782</sourcerecordid><originalsourceid>FETCH-LOGICAL-c447t-5859f898922754caa29811641e3fe4fd0983781101e8282aeb83e7de50f193f23</originalsourceid><addsrcrecordid>eNpdkV1rHCEUhqW0NCHNTX9AGehNKUzj18zoTSEs_SSQUNprcZ3j7llmdavO0v33dZM0pBFEOT7n9dWXkNeMfmBU6AunkqWKymHzjJxyKvuW014_f7Q_Iec5b2gdfcd4z16SE9F1neq0OCV4sz6UWOIfdFgOjQ1jnQXb3bG8s2UdVxDQNdYV3GNByE30zdYmDNCOkHAPY-PnsMLb3rIGTE0GF8No06HZQrHLOGGB_Iq88HbKcH6_npFfnz_9XHxtr66_fFtcXrVOyqG0R19eaaU5HzrprOVaMdZLBsKD9CPVSgy1QhkorriFpRIwjNBRz7TwXJyRj3e6u3m5hdFBKMlOZpewuj6YaNH8fxJwbVZxbzRVWvChCry7F0jx9wy5mC1mB9NkA8Q5G973UtFhUMe73j5BN3FOoT7PcFY_mTHNZKXe31EuxZwT-AczjJpjiGahflzehvi9wm8e239A_0Um_gJZlJj9</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2135511914</pqid></control><display><type>article</type><title>Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Huang, Rui-Huan ; Gou, Jian-Yu ; Zhao, Dong-Lin ; Wang, Dan ; Liu, Jing ; Ma, Guo-Yong ; Li, Yi-Qiang ; Zhang, Cheng-Sheng</creator><creatorcontrib>Huang, Rui-Huan ; Gou, Jian-Yu ; Zhao, Dong-Lin ; Wang, Dan ; Liu, Jing ; Ma, Guo-Yong ; Li, Yi-Qiang ; Zhang, Cheng-Sheng</creatorcontrib><description>To find new pesticides for agricultural use, 133 fungal strains were isolated from coastal marine habitats, from which 37 independent isolates were identified, belonging to 20 genera in nine orders, and the diversity of the isolated fungi were discussed. The phytotoxicity and anti-phytopathogenic fungal and bacterial activities of these 37 extracts, and two previously isolated fungal extracts were evaluated, displaying different levels of bioactivity. Based on the bioactive and chemical screening, an sp. (P8) strain, which showed prominent bioactivity and contained abundant secondary metabolites was selected for further chemical investigation; one new compound, a benzopyranone (1), and seven known compounds (2-8) were obtained. Their structures were determined by analysing extensive NMR spectroscopic data and ECD comparisons. Compounds 1, 2, and 6-8 showed obvious phytotoxicity, especially against amaranth, and compound 1 also showed potent antifungal activity toward . To the best of our knowledge, this is the first report of the phytotoxicity of marine-derived fungi and their secondary metabolites. These studies should provide the foundation for future research into the use of such fungal extracts to combat weeds and diseases in agriculture.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c8ra08047j</identifier><identifier>PMID: 35558593</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Agrochemicals ; Amaranth ; Aquatic habitats ; Biochemistry ; Biological activity ; Chemistry ; Coastal ecology ; Fungi ; Fungicides ; Germination ; Metabolites ; NMR ; Nuclear magnetic resonance ; Organic chemistry ; Pesticides ; Phytotoxicity ; Tables</subject><ispartof>RSC advances, 2018-01, Vol.8 (66), p.37573-37580</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2018</rights><rights>This journal is © The Royal Society of Chemistry 2018 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-5859f898922754caa29811641e3fe4fd0983781101e8282aeb83e7de50f193f23</citedby><cites>FETCH-LOGICAL-c447t-5859f898922754caa29811641e3fe4fd0983781101e8282aeb83e7de50f193f23</cites><orcidid>0000-0002-6118-8479</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089327/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089327/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35558593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Rui-Huan</creatorcontrib><creatorcontrib>Gou, Jian-Yu</creatorcontrib><creatorcontrib>Zhao, Dong-Lin</creatorcontrib><creatorcontrib>Wang, Dan</creatorcontrib><creatorcontrib>Liu, Jing</creatorcontrib><creatorcontrib>Ma, Guo-Yong</creatorcontrib><creatorcontrib>Li, Yi-Qiang</creatorcontrib><creatorcontrib>Zhang, Cheng-Sheng</creatorcontrib><title>Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>To find new pesticides for agricultural use, 133 fungal strains were isolated from coastal marine habitats, from which 37 independent isolates were identified, belonging to 20 genera in nine orders, and the diversity of the isolated fungi were discussed. The phytotoxicity and anti-phytopathogenic fungal and bacterial activities of these 37 extracts, and two previously isolated fungal extracts were evaluated, displaying different levels of bioactivity. Based on the bioactive and chemical screening, an sp. (P8) strain, which showed prominent bioactivity and contained abundant secondary metabolites was selected for further chemical investigation; one new compound, a benzopyranone (1), and seven known compounds (2-8) were obtained. Their structures were determined by analysing extensive NMR spectroscopic data and ECD comparisons. Compounds 1, 2, and 6-8 showed obvious phytotoxicity, especially against amaranth, and compound 1 also showed potent antifungal activity toward . To the best of our knowledge, this is the first report of the phytotoxicity of marine-derived fungi and their secondary metabolites. These studies should provide the foundation for future research into the use of such fungal extracts to combat weeds and diseases in agriculture.</description><subject>Agrochemicals</subject><subject>Amaranth</subject><subject>Aquatic habitats</subject><subject>Biochemistry</subject><subject>Biological activity</subject><subject>Chemistry</subject><subject>Coastal ecology</subject><subject>Fungi</subject><subject>Fungicides</subject><subject>Germination</subject><subject>Metabolites</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Organic chemistry</subject><subject>Pesticides</subject><subject>Phytotoxicity</subject><subject>Tables</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkV1rHCEUhqW0NCHNTX9AGehNKUzj18zoTSEs_SSQUNprcZ3j7llmdavO0v33dZM0pBFEOT7n9dWXkNeMfmBU6AunkqWKymHzjJxyKvuW014_f7Q_Iec5b2gdfcd4z16SE9F1neq0OCV4sz6UWOIfdFgOjQ1jnQXb3bG8s2UdVxDQNdYV3GNByE30zdYmDNCOkHAPY-PnsMLb3rIGTE0GF8No06HZQrHLOGGB_Iq88HbKcH6_npFfnz_9XHxtr66_fFtcXrVOyqG0R19eaaU5HzrprOVaMdZLBsKD9CPVSgy1QhkorriFpRIwjNBRz7TwXJyRj3e6u3m5hdFBKMlOZpewuj6YaNH8fxJwbVZxbzRVWvChCry7F0jx9wy5mC1mB9NkA8Q5G973UtFhUMe73j5BN3FOoT7PcFY_mTHNZKXe31EuxZwT-AczjJpjiGahflzehvi9wm8e239A_0Um_gJZlJj9</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Huang, Rui-Huan</creator><creator>Gou, Jian-Yu</creator><creator>Zhao, Dong-Lin</creator><creator>Wang, Dan</creator><creator>Liu, Jing</creator><creator>Ma, Guo-Yong</creator><creator>Li, Yi-Qiang</creator><creator>Zhang, Cheng-Sheng</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6118-8479</orcidid></search><sort><creationdate>20180101</creationdate><title>Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites</title><author>Huang, Rui-Huan ; Gou, Jian-Yu ; Zhao, Dong-Lin ; Wang, Dan ; Liu, Jing ; Ma, Guo-Yong ; Li, Yi-Qiang ; Zhang, Cheng-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-5859f898922754caa29811641e3fe4fd0983781101e8282aeb83e7de50f193f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Agrochemicals</topic><topic>Amaranth</topic><topic>Aquatic habitats</topic><topic>Biochemistry</topic><topic>Biological activity</topic><topic>Chemistry</topic><topic>Coastal ecology</topic><topic>Fungi</topic><topic>Fungicides</topic><topic>Germination</topic><topic>Metabolites</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Organic chemistry</topic><topic>Pesticides</topic><topic>Phytotoxicity</topic><topic>Tables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Rui-Huan</creatorcontrib><creatorcontrib>Gou, Jian-Yu</creatorcontrib><creatorcontrib>Zhao, Dong-Lin</creatorcontrib><creatorcontrib>Wang, Dan</creatorcontrib><creatorcontrib>Liu, Jing</creatorcontrib><creatorcontrib>Ma, Guo-Yong</creatorcontrib><creatorcontrib>Li, Yi-Qiang</creatorcontrib><creatorcontrib>Zhang, Cheng-Sheng</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Rui-Huan</au><au>Gou, Jian-Yu</au><au>Zhao, Dong-Lin</au><au>Wang, Dan</au><au>Liu, Jing</au><au>Ma, Guo-Yong</au><au>Li, Yi-Qiang</au><au>Zhang, Cheng-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>8</volume><issue>66</issue><spage>37573</spage><epage>37580</epage><pages>37573-37580</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>To find new pesticides for agricultural use, 133 fungal strains were isolated from coastal marine habitats, from which 37 independent isolates were identified, belonging to 20 genera in nine orders, and the diversity of the isolated fungi were discussed. The phytotoxicity and anti-phytopathogenic fungal and bacterial activities of these 37 extracts, and two previously isolated fungal extracts were evaluated, displaying different levels of bioactivity. Based on the bioactive and chemical screening, an sp. (P8) strain, which showed prominent bioactivity and contained abundant secondary metabolites was selected for further chemical investigation; one new compound, a benzopyranone (1), and seven known compounds (2-8) were obtained. Their structures were determined by analysing extensive NMR spectroscopic data and ECD comparisons. Compounds 1, 2, and 6-8 showed obvious phytotoxicity, especially against amaranth, and compound 1 also showed potent antifungal activity toward . To the best of our knowledge, this is the first report of the phytotoxicity of marine-derived fungi and their secondary metabolites. These studies should provide the foundation for future research into the use of such fungal extracts to combat weeds and diseases in agriculture.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35558593</pmid><doi>10.1039/c8ra08047j</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6118-8479</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2046-2069
ispartof RSC advances, 2018-01, Vol.8 (66), p.37573-37580
issn 2046-2069
2046-2069
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9089327
source DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Agrochemicals
Amaranth
Aquatic habitats
Biochemistry
Biological activity
Chemistry
Coastal ecology
Fungi
Fungicides
Germination
Metabolites
NMR
Nuclear magnetic resonance
Organic chemistry
Pesticides
Phytotoxicity
Tables
title Phytotoxicity and anti-phytopathogenic activities of marine-derived fungi and their secondary metabolites
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T12%3A41%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phytotoxicity%20and%20anti-phytopathogenic%20activities%20of%20marine-derived%20fungi%20and%20their%20secondary%20metabolites&rft.jtitle=RSC%20advances&rft.au=Huang,%20Rui-Huan&rft.date=2018-01-01&rft.volume=8&rft.issue=66&rft.spage=37573&rft.epage=37580&rft.pages=37573-37580&rft.issn=2046-2069&rft.eissn=2046-2069&rft_id=info:doi/10.1039/c8ra08047j&rft_dat=%3Cproquest_pubme%3E2664807782%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2135511914&rft_id=info:pmid/35558593&rfr_iscdi=true