Loading…

Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita

In this study, the 3,4-dihydroxybenzoic acid (3,4-DHBA) from Terminalia nigrovenulosa bark (TNB) was purified and its in vitro nematicidal activity was investigated against Meloidogyne incognita. The purification of 3,4-DHBA used a silica gel column and Sephadex LH-20 chromatography combined with th...

Full description

Saved in:
Bibliographic Details
Published in:Microbial pathogenesis 2013-06, Vol.59-60, p.52-59
Main Authors: Nguyen, Dang-Minh-Chanh, Seo, Dong-Jun, Kim, Kil-Yong, Park, Ro-Dong, Kim, Dong-Hyun, Han, Yeon-Soo, Kim, Tae-Hwan, Jung, Woo-Jin
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93
cites cdi_FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93
container_end_page 59
container_issue
container_start_page 52
container_title Microbial pathogenesis
container_volume 59-60
creator Nguyen, Dang-Minh-Chanh
Seo, Dong-Jun
Kim, Kil-Yong
Park, Ro-Dong
Kim, Dong-Hyun
Han, Yeon-Soo
Kim, Tae-Hwan
Jung, Woo-Jin
description In this study, the 3,4-dihydroxybenzoic acid (3,4-DHBA) from Terminalia nigrovenulosa bark (TNB) was purified and its in vitro nematicidal activity was investigated against Meloidogyne incognita. The purification of 3,4-DHBA used a silica gel column and Sephadex LH-20 chromatography combined with thin-layer chromatography and high performance liquid chromatography. Structural identification of the 3,4-DHBA was conducted using 1H nuclear magnetic resonance (NMR), 13C NMR, and liquid chromatography time-of-flight mass spectrometry. Nematicidal activity bioassays revealed that 3,4-DHBA treatment resulted in 33.3, 47.5, 72.5 and 94.2% J2 mortality at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively after 12 h incubation. J2 mortality was increased significantly (P 
doi_str_mv 10.1016/j.micpath.2013.04.005
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1352281523</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S088240101300051X</els_id><sourcerecordid>1352281523</sourcerecordid><originalsourceid>FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93</originalsourceid><addsrcrecordid>eNqFkMFu1DAQhi0EotvCIwA-ciBhbMfZ5ISqCgpSgQPt2XLsSTpLEi92siLw8qTahSunuXzzzz8fYy8E5AJE-XaXD-T2drrPJQiVQ5ED6EdsI6AuMyGhesw2UFUyK0DAGTtPaQcAdaHqp-xMqhLUVm037PcXHOxEjrztuXUTHWhaeGi5elNknu4XH8PPpcHxVyC3AuT5fo7UEnrexjDwW4wDjbYny0fqYjjgOPchWd7Y-J3bztKYJv4Z-0A-dMuInEYXupEm-4w9aW2f8PlpXrC7D-9vrz5mN1-vP11d3mROg5wyXbVK-gptWbZFjQqcqxohW6fLcn1DgsMavdWqLGSpbb3VWiEUvgRoXIu1umCvj7n7GH7MmCYzUHLY93bEMCcjlJayElqqFdVH1MWQUsTW7CMNNi5GgHnwbnbm5N08eDdQmNX7uvfydGJuBvT_tv6KXoFXR6C1wdguUjJ339aEtaSQWm7FSrw7EriqOBBGkxzh6NBTRDcZH-g_Jf4AJtGh5A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1352281523</pqid></control><display><type>article</type><title>Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita</title><source>ScienceDirect Freedom Collection</source><creator>Nguyen, Dang-Minh-Chanh ; Seo, Dong-Jun ; Kim, Kil-Yong ; Park, Ro-Dong ; Kim, Dong-Hyun ; Han, Yeon-Soo ; Kim, Tae-Hwan ; Jung, Woo-Jin</creator><creatorcontrib>Nguyen, Dang-Minh-Chanh ; Seo, Dong-Jun ; Kim, Kil-Yong ; Park, Ro-Dong ; Kim, Dong-Hyun ; Han, Yeon-Soo ; Kim, Tae-Hwan ; Jung, Woo-Jin</creatorcontrib><description>In this study, the 3,4-dihydroxybenzoic acid (3,4-DHBA) from Terminalia nigrovenulosa bark (TNB) was purified and its in vitro nematicidal activity was investigated against Meloidogyne incognita. The purification of 3,4-DHBA used a silica gel column and Sephadex LH-20 chromatography combined with thin-layer chromatography and high performance liquid chromatography. Structural identification of the 3,4-DHBA was conducted using 1H nuclear magnetic resonance (NMR), 13C NMR, and liquid chromatography time-of-flight mass spectrometry. Nematicidal activity bioassays revealed that 3,4-DHBA treatment resulted in 33.3, 47.5, 72.5 and 94.2% J2 mortality at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively after 12 h incubation. J2 mortality was increased significantly (P &lt; 0.0001) with increasing incubation time in the range of 54.2–94.2% from 3 to 9 h after incubation with 3,4-DHBA (1.0 mg/ml), but with no significant difference observed where the incubation time was increased from 9 to 12 h. The 3,4-DHBA treatment resulted in 33.3, 65.0, 76.7 and 85.0% hatch inhibition at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively, 3 days after incubation. Changes in the shape of the eggs were determined after incubation for 1 day with a 3,4-DHBA concentration of 1.0 mg/ml. •Terminalia nigrovenulosa extracts showed high nematicidal activity against Meloidogyne incognita.•Ethyl acetate fraction of TNB demonstrated the highest nematicidal activity.•3,4-DHBA purified from TNB possess the high nematicidal activity against M. incognita.•Changes in the shape of the eggs were determined after incubation with a 3,4-DHBA.</description><identifier>ISSN: 0882-4010</identifier><identifier>EISSN: 1096-1208</identifier><identifier>DOI: 10.1016/j.micpath.2013.04.005</identifier><identifier>PMID: 23603737</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Anthelmintics - isolation &amp; purification ; Anthelmintics - pharmacology ; bark ; bioassays ; Biological Assay ; Chromatography, Gel ; Chromatography, High Pressure Liquid ; Chromatography, Thin Layer ; Egg morphology ; eggs ; Fluorescence staining ; high performance liquid chromatography ; Hydroxybenzoates - isolation &amp; purification ; Hydroxybenzoates - pharmacology ; Magnetic Resonance Spectroscopy ; mass spectrometry ; Meloidogyne incognita ; mortality ; Nematicidal compound ; nematicidal properties ; nuclear magnetic resonance spectroscopy ; Plant Bark - chemistry ; Plant extract ; silica gel ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Survival Analysis ; Terminalia ; Terminalia - chemistry ; thin layer chromatography ; Tylenchoidea - drug effects ; Tylenchoidea - physiology ; Zygote - drug effects</subject><ispartof>Microbial pathogenesis, 2013-06, Vol.59-60, p.52-59</ispartof><rights>2013 The authors</rights><rights>Copyright © 2013 The authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93</citedby><cites>FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23603737$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nguyen, Dang-Minh-Chanh</creatorcontrib><creatorcontrib>Seo, Dong-Jun</creatorcontrib><creatorcontrib>Kim, Kil-Yong</creatorcontrib><creatorcontrib>Park, Ro-Dong</creatorcontrib><creatorcontrib>Kim, Dong-Hyun</creatorcontrib><creatorcontrib>Han, Yeon-Soo</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</creatorcontrib><creatorcontrib>Jung, Woo-Jin</creatorcontrib><title>Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita</title><title>Microbial pathogenesis</title><addtitle>Microb Pathog</addtitle><description>In this study, the 3,4-dihydroxybenzoic acid (3,4-DHBA) from Terminalia nigrovenulosa bark (TNB) was purified and its in vitro nematicidal activity was investigated against Meloidogyne incognita. The purification of 3,4-DHBA used a silica gel column and Sephadex LH-20 chromatography combined with thin-layer chromatography and high performance liquid chromatography. Structural identification of the 3,4-DHBA was conducted using 1H nuclear magnetic resonance (NMR), 13C NMR, and liquid chromatography time-of-flight mass spectrometry. Nematicidal activity bioassays revealed that 3,4-DHBA treatment resulted in 33.3, 47.5, 72.5 and 94.2% J2 mortality at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively after 12 h incubation. J2 mortality was increased significantly (P &lt; 0.0001) with increasing incubation time in the range of 54.2–94.2% from 3 to 9 h after incubation with 3,4-DHBA (1.0 mg/ml), but with no significant difference observed where the incubation time was increased from 9 to 12 h. The 3,4-DHBA treatment resulted in 33.3, 65.0, 76.7 and 85.0% hatch inhibition at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively, 3 days after incubation. Changes in the shape of the eggs were determined after incubation for 1 day with a 3,4-DHBA concentration of 1.0 mg/ml. •Terminalia nigrovenulosa extracts showed high nematicidal activity against Meloidogyne incognita.•Ethyl acetate fraction of TNB demonstrated the highest nematicidal activity.•3,4-DHBA purified from TNB possess the high nematicidal activity against M. incognita.•Changes in the shape of the eggs were determined after incubation with a 3,4-DHBA.</description><subject>Animals</subject><subject>Anthelmintics - isolation &amp; purification</subject><subject>Anthelmintics - pharmacology</subject><subject>bark</subject><subject>bioassays</subject><subject>Biological Assay</subject><subject>Chromatography, Gel</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Chromatography, Thin Layer</subject><subject>Egg morphology</subject><subject>eggs</subject><subject>Fluorescence staining</subject><subject>high performance liquid chromatography</subject><subject>Hydroxybenzoates - isolation &amp; purification</subject><subject>Hydroxybenzoates - pharmacology</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>mass spectrometry</subject><subject>Meloidogyne incognita</subject><subject>mortality</subject><subject>Nematicidal compound</subject><subject>nematicidal properties</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Plant Bark - chemistry</subject><subject>Plant extract</subject><subject>silica gel</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Survival Analysis</subject><subject>Terminalia</subject><subject>Terminalia - chemistry</subject><subject>thin layer chromatography</subject><subject>Tylenchoidea - drug effects</subject><subject>Tylenchoidea - physiology</subject><subject>Zygote - drug effects</subject><issn>0882-4010</issn><issn>1096-1208</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkMFu1DAQhi0EotvCIwA-ciBhbMfZ5ISqCgpSgQPt2XLsSTpLEi92siLw8qTahSunuXzzzz8fYy8E5AJE-XaXD-T2drrPJQiVQ5ED6EdsI6AuMyGhesw2UFUyK0DAGTtPaQcAdaHqp-xMqhLUVm037PcXHOxEjrztuXUTHWhaeGi5elNknu4XH8PPpcHxVyC3AuT5fo7UEnrexjDwW4wDjbYny0fqYjjgOPchWd7Y-J3bztKYJv4Z-0A-dMuInEYXupEm-4w9aW2f8PlpXrC7D-9vrz5mN1-vP11d3mROg5wyXbVK-gptWbZFjQqcqxohW6fLcn1DgsMavdWqLGSpbb3VWiEUvgRoXIu1umCvj7n7GH7MmCYzUHLY93bEMCcjlJayElqqFdVH1MWQUsTW7CMNNi5GgHnwbnbm5N08eDdQmNX7uvfydGJuBvT_tv6KXoFXR6C1wdguUjJ339aEtaSQWm7FSrw7EriqOBBGkxzh6NBTRDcZH-g_Jf4AJtGh5A</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Nguyen, Dang-Minh-Chanh</creator><creator>Seo, Dong-Jun</creator><creator>Kim, Kil-Yong</creator><creator>Park, Ro-Dong</creator><creator>Kim, Dong-Hyun</creator><creator>Han, Yeon-Soo</creator><creator>Kim, Tae-Hwan</creator><creator>Jung, Woo-Jin</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><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>20130601</creationdate><title>Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita</title><author>Nguyen, Dang-Minh-Chanh ; Seo, Dong-Jun ; Kim, Kil-Yong ; Park, Ro-Dong ; Kim, Dong-Hyun ; Han, Yeon-Soo ; Kim, Tae-Hwan ; Jung, Woo-Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anthelmintics - isolation &amp; purification</topic><topic>Anthelmintics - pharmacology</topic><topic>bark</topic><topic>bioassays</topic><topic>Biological Assay</topic><topic>Chromatography, Gel</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Chromatography, Thin Layer</topic><topic>Egg morphology</topic><topic>eggs</topic><topic>Fluorescence staining</topic><topic>high performance liquid chromatography</topic><topic>Hydroxybenzoates - isolation &amp; purification</topic><topic>Hydroxybenzoates - pharmacology</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>mass spectrometry</topic><topic>Meloidogyne incognita</topic><topic>mortality</topic><topic>Nematicidal compound</topic><topic>nematicidal properties</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Plant Bark - chemistry</topic><topic>Plant extract</topic><topic>silica gel</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Survival Analysis</topic><topic>Terminalia</topic><topic>Terminalia - chemistry</topic><topic>thin layer chromatography</topic><topic>Tylenchoidea - drug effects</topic><topic>Tylenchoidea - physiology</topic><topic>Zygote - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nguyen, Dang-Minh-Chanh</creatorcontrib><creatorcontrib>Seo, Dong-Jun</creatorcontrib><creatorcontrib>Kim, Kil-Yong</creatorcontrib><creatorcontrib>Park, Ro-Dong</creatorcontrib><creatorcontrib>Kim, Dong-Hyun</creatorcontrib><creatorcontrib>Han, Yeon-Soo</creatorcontrib><creatorcontrib>Kim, Tae-Hwan</creatorcontrib><creatorcontrib>Jung, Woo-Jin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</collection><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>Microbial pathogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nguyen, Dang-Minh-Chanh</au><au>Seo, Dong-Jun</au><au>Kim, Kil-Yong</au><au>Park, Ro-Dong</au><au>Kim, Dong-Hyun</au><au>Han, Yeon-Soo</au><au>Kim, Tae-Hwan</au><au>Jung, Woo-Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita</atitle><jtitle>Microbial pathogenesis</jtitle><addtitle>Microb Pathog</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>59-60</volume><spage>52</spage><epage>59</epage><pages>52-59</pages><issn>0882-4010</issn><eissn>1096-1208</eissn><abstract>In this study, the 3,4-dihydroxybenzoic acid (3,4-DHBA) from Terminalia nigrovenulosa bark (TNB) was purified and its in vitro nematicidal activity was investigated against Meloidogyne incognita. The purification of 3,4-DHBA used a silica gel column and Sephadex LH-20 chromatography combined with thin-layer chromatography and high performance liquid chromatography. Structural identification of the 3,4-DHBA was conducted using 1H nuclear magnetic resonance (NMR), 13C NMR, and liquid chromatography time-of-flight mass spectrometry. Nematicidal activity bioassays revealed that 3,4-DHBA treatment resulted in 33.3, 47.5, 72.5 and 94.2% J2 mortality at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively after 12 h incubation. J2 mortality was increased significantly (P &lt; 0.0001) with increasing incubation time in the range of 54.2–94.2% from 3 to 9 h after incubation with 3,4-DHBA (1.0 mg/ml), but with no significant difference observed where the incubation time was increased from 9 to 12 h. The 3,4-DHBA treatment resulted in 33.3, 65.0, 76.7 and 85.0% hatch inhibition at 0.125, 0.25, 0.5 and 1.0 mg/ml, respectively, 3 days after incubation. Changes in the shape of the eggs were determined after incubation for 1 day with a 3,4-DHBA concentration of 1.0 mg/ml. •Terminalia nigrovenulosa extracts showed high nematicidal activity against Meloidogyne incognita.•Ethyl acetate fraction of TNB demonstrated the highest nematicidal activity.•3,4-DHBA purified from TNB possess the high nematicidal activity against M. incognita.•Changes in the shape of the eggs were determined after incubation with a 3,4-DHBA.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>23603737</pmid><doi>10.1016/j.micpath.2013.04.005</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0882-4010
ispartof Microbial pathogenesis, 2013-06, Vol.59-60, p.52-59
issn 0882-4010
1096-1208
language eng
recordid cdi_proquest_miscellaneous_1352281523
source ScienceDirect Freedom Collection
subjects Animals
Anthelmintics - isolation & purification
Anthelmintics - pharmacology
bark
bioassays
Biological Assay
Chromatography, Gel
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Egg morphology
eggs
Fluorescence staining
high performance liquid chromatography
Hydroxybenzoates - isolation & purification
Hydroxybenzoates - pharmacology
Magnetic Resonance Spectroscopy
mass spectrometry
Meloidogyne incognita
mortality
Nematicidal compound
nematicidal properties
nuclear magnetic resonance spectroscopy
Plant Bark - chemistry
Plant extract
silica gel
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Survival Analysis
Terminalia
Terminalia - chemistry
thin layer chromatography
Tylenchoidea - drug effects
Tylenchoidea - physiology
Zygote - drug effects
title Nematicidal activity of 3,4-dihydroxybenzoic acid purified from Terminalia nigrovenulosa bark against Meloidogyne incognita
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T02%3A51%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Nematicidal%20activity%20of%203,4-dihydroxybenzoic%20acid%20purified%20from%20Terminalia%20nigrovenulosa%20bark%20against%20Meloidogyne%20incognita&rft.jtitle=Microbial%20pathogenesis&rft.au=Nguyen,%20Dang-Minh-Chanh&rft.date=2013-06-01&rft.volume=59-60&rft.spage=52&rft.epage=59&rft.pages=52-59&rft.issn=0882-4010&rft.eissn=1096-1208&rft_id=info:doi/10.1016/j.micpath.2013.04.005&rft_dat=%3Cproquest_cross%3E1352281523%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c502t-58f32d8ea66f49e30cc8b12fc56660320ce9eda5364265a97553e04d600bcfe93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1352281523&rft_id=info:pmid/23603737&rfr_iscdi=true