PoplarV1, Main, Exploration, bibRecord, 002057

Separation and purification of bioactive botrallin and TMC-264 by a combination of HSCCC and semi-preparative HPLC from endophytic fungus Hyalodendriella sp. Ponipodef12.

Identifieur interne : 002057 ( Main/Exploration ); précédent : 002056; suivant : 002058

Separation and purification of bioactive botrallin and TMC-264 by a combination of HSCCC and semi-preparative HPLC from endophytic fungus Hyalodendriella sp. Ponipodef12.

Auteurs : Ziling Mao [République populaire de Chine] ; Ruiya Luo ; Haiyu Luo ; Jin Tian ; Hongwei Liu ; Yang Yue ; Mingan Wang ; Youliang Peng ; Ligang Zhou

Source :

World journal of microbiology & biotechnology [ 1573-0972 ] ; 2014.

RBID : pubmed:24898177

Descripteurs français

KwdFr :
- Anthelminthiques (isolement et purification), Anthelminthiques (pharmacologie), Antibactériens (isolement et purification), Antibactériens (pharmacologie), Anticholinestérasiques (isolement et purification), Anticholinestérasiques (pharmacologie), Ascomycota (composition chimique), Ascomycota (isolement et purification), Chromatographie en phase liquide (méthodes), Composés hétérocycliques 3 noyaux (isolement et purification), Composés hétérocycliques 3 noyaux (pharmacologie), Concentration inhibitrice 50 (MeSH), Endophytes (composition chimique), Endophytes (isolement et purification), Populus (microbiologie), Structure moléculaire (MeSH), Tests de sensibilité microbienne (MeSH).
MESH :
- composition chimique : Ascomycota, Endophytes.
- isolement et purification : Anthelminthiques, Antibactériens, Anticholinestérasiques, Ascomycota, Composés hétérocycliques 3 noyaux, Endophytes.
- microbiologie : Populus.
- méthodes : Chromatographie en phase liquide.
- pharmacologie : Anthelminthiques, Antibactériens, Anticholinestérasiques, Composés hétérocycliques 3 noyaux.
- Concentration inhibitrice 50, Structure moléculaire, Tests de sensibilité microbienne.

English descriptors

KwdEn :
- Anthelmintics (isolation & purification), Anthelmintics (pharmacology), Anti-Bacterial Agents (isolation & purification), Anti-Bacterial Agents (pharmacology), Ascomycota (chemistry), Ascomycota (isolation & purification), Cholinesterase Inhibitors (isolation & purification), Cholinesterase Inhibitors (pharmacology), Chromatography, Liquid (methods), Endophytes (chemistry), Endophytes (isolation & purification), Heterocyclic Compounds, 3-Ring (isolation & purification), Heterocyclic Compounds, 3-Ring (pharmacology), Inhibitory Concentration 50 (MeSH), Microbial Sensitivity Tests (MeSH), Molecular Structure (MeSH), Populus (microbiology).
MESH :
- chemical , isolation & purification : Anthelmintics, Anti-Bacterial Agents, Cholinesterase Inhibitors, Heterocyclic Compounds, 3-Ring.
- chemical , pharmacology : Anthelmintics, Anti-Bacterial Agents, Cholinesterase Inhibitors, Heterocyclic Compounds, 3-Ring.
- chemistry : Ascomycota, Endophytes.
- isolation & purification : Ascomycota, Endophytes.
- methods : Chromatography, Liquid.
- microbiology : Populus.
- Inhibitory Concentration 50, Microbial Sensitivity Tests, Molecular Structure.

Abstract

Two dibenzo-α-pyrones, botrallin (1) and TMC-264 (2) were preparatively separated from crude ethyl acetate extract of the endophytic fungus Hyalodendriella sp. Ponipodef12, which was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. using a combination of high-speed counter-current chromatography (HSCCC) and semi-preparative HPLC. Botrallin (1) with 74.73% of purity and TMC-264 (2) with 82.29% of purity were obtained through HSCCC by employing a solvent system containing n-hexane-ethyl acetate-methanol-water at a volume ratio of 1.2:1.0:0.9:1.0. It was the first time for TMC-264 (2) to be isolated from this fungus. TMC-264 (2) showed strong antimicrobial and antinematodal activity, and botrallin (1) exhibited moderate inhibitory activity on acetylcholinesterase.

DOI: 10.1007/s11274-014-1678-0
PubMed: 24898177

Affiliations:

République populaire de Chine

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 002151
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Le document en format XML

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<front><div type="abstract" xml:lang="en">Two dibenzo-α-pyrones, botrallin (1) and TMC-264 (2) were preparatively separated from crude ethyl acetate extract of the endophytic fungus Hyalodendriella sp. Ponipodef12, which was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. using a combination of high-speed counter-current chromatography (HSCCC) and semi-preparative HPLC. Botrallin (1) with 74.73% of purity and TMC-264 (2) with 82.29% of purity were obtained through HSCCC by employing a solvent system containing n-hexane-ethyl acetate-methanol-water at a volume ratio of 1.2:1.0:0.9:1.0. It was the first time for TMC-264 (2) to be isolated from this fungus. TMC-264 (2) showed strong antimicrobial and antinematodal activity, and botrallin (1) exhibited moderate inhibitory activity on acetylcholinesterase.</div>
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<Abstract><AbstractText>Two dibenzo-α-pyrones, botrallin (1) and TMC-264 (2) were preparatively separated from crude ethyl acetate extract of the endophytic fungus Hyalodendriella sp. Ponipodef12, which was isolated from the hybrid 'Neva' of Populus deltoides Marsh × P. nigra L. using a combination of high-speed counter-current chromatography (HSCCC) and semi-preparative HPLC. Botrallin (1) with 74.73% of purity and TMC-264 (2) with 82.29% of purity were obtained through HSCCC by employing a solvent system containing n-hexane-ethyl acetate-methanol-water at a volume ratio of 1.2:1.0:0.9:1.0. It was the first time for TMC-264 (2) to be isolated from this fungus. TMC-264 (2) showed strong antimicrobial and antinematodal activity, and botrallin (1) exhibited moderate inhibitory activity on acetylcholinesterase.</AbstractText>
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<ReferenceList><Reference><Citation>Mini Rev Med Chem. 2011 Feb;11(2):159-68</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21222580</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Antibiot (Tokyo). 2003 Jun;56(6):513-9</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12931859</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Molecules. 2012 Jul 10;17(7):8276-84</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22781440</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Molecules. 2013 Oct 16;18(10):12896-908</Citation>
<ArticleIdList><ArticleId IdType="pubmed">24135943</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2003 Apr 25;994(1-2):37-43</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12779217</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Microbes Infect. 2003 May;5(6):535-44</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12758283</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Nat Prod Res. 2013;27(11):1020-2</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22624991</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Mini Rev Med Chem. 2010 Sep;10 (10 ):977-89</Citation>
<ArticleIdList><ArticleId IdType="pubmed">20491650</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2005 Feb 18;1065(2):145-68</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15782961</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2009 May 29;1216(22):4668-72</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19394946</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Curr Top Med Chem. 2013;13(15):1864-78</Citation>
<ArticleIdList><ArticleId IdType="pubmed">23931437</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2010 Sep 3;1217(36):5687-92</Citation>
<ArticleIdList><ArticleId IdType="pubmed">20688334</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Org Lett. 2003 Apr 3;5(7):1083-5</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12659579</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Nat Prod Rep. 2011 Jul;28(7):1208-28</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21455524</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Curr Med Chem. 2012;19(18):2992-3030</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22489725</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Molecules. 2012 Sep 25;17(10):11303-14</Citation>
<ArticleIdList><ArticleId IdType="pubmed">23011274</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Molecules. 2014 Apr 22;19(4):5088-108</Citation>
<ArticleIdList><ArticleId IdType="pubmed">24759070</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Z Naturforsch C. 2005 Jan-Feb;60(1-2):11-21</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15787237</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Science. 2007 Sep 28;317(5846):1881-6</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17901324</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochem Anal. 2013 Feb;24(2):129-34</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22811209</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Ethnopharmacol. 2013 May 20;147(2):357-65</Citation>
<ArticleIdList><ArticleId IdType="pubmed">23541932</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Med Chem. 2008 Aug 14;51(15):4359-69</Citation>
<ArticleIdList><ArticleId IdType="pubmed">18570365</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2003 Feb 21;988(1):95-105</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12647824</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Chromatogr A. 2012 Feb 3;1223:53-63</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22227359</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Talanta. 2006 Mar 15;69(1):172-9</Citation>
<ArticleIdList><ArticleId IdType="pubmed">18970550</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochem Anal. 2009 Jan-Feb;20(1):77-81</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19003936</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Biochem Pharmacol. 1961 Jul;7:88-95</Citation>
<ArticleIdList><ArticleId IdType="pubmed">13726518</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>J Ethnopharmacol. 2004 Oct;94(2-3):279-81</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15325731</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
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Separation and purification of bioactive botrallin and TMC-264 by a combination of HSCCC and semi-preparative HPLC from endophytic fungus Hyalodendriella sp. Ponipodef12.

Separation and purification of bioactive botrallin and TMC-264 by a combination of HSCCC and semi-preparative HPLC from endophytic fungus Hyalodendriella sp. Ponipodef12.

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