Serveur d'exploration sur le phanerochaete

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.

Identifieur interne : 000A88 ( Main/Exploration ); précédent : 000A87; suivant : 000A89

Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.

Auteurs : Y F Dufrêne [Belgique]

Source :

RBID : pubmed:10828004

Descripteurs français

English descriptors

Abstract

A new method is described for characterizing the physicochemical properties of native microbial cells by using atomic force microscopy (AFM) with chemically functionalized probes. Adhesion forces were measured, under deionized water, between probes and model substrata functionalized with alkanethiol self-assembled monolayers terminated with OH and CH(3) groups. These were found to be 6 +/- 2 nN (n = 1024), 0.9 +/- 0.4 nN, and approximately 0 nN, for CH(3)/CH(3), CH(3)/OH, and OH/OH surfaces, respectively, and were not significantly influenced by changes of ionic strength (0.1 M NaCl versus deionized water). This shows that functionalized probes are very sensitive to changes of surface hydrophobicity. Using OH- and CH(3)-terminated probes, patterns of rodlets, approximately 10 nm in diameter, were visualized, under physiological conditions, at the surface of spores of Phanerochaete chrysosporium. Multiple (1024) force-distance curves recorded over 500 x 500-nm areas at the spore surface, either in deionized water or in 0.1 M NaCl solutions, always showed no adhesion for both OH- and CH(3)-terminated probes. Control experiments indicated that the lack of adhesion is not due to transfer of cellular material onto the probe, but to the hydrophilic nature of the spore surface.

DOI: 10.1016/S0006-3495(00)76864-0
PubMed: 10828004
PubMed Central: PMC1300909


Affiliations:


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


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.</title>
<author>
<name sortKey="Dufrene, Y F" sort="Dufrene, Y F" uniqKey="Dufrene Y" first="Y F" last="Dufrêne">Y F Dufrêne</name>
<affiliation wicri:level="4">
<nlm:affiliation>Unité de Chimie des Interfaces, Université Catholique de Louvain, 1348 Louvain-la-Neuve, Belgium. dufrene@cifa.ucl.ac.be</nlm:affiliation>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Unité de Chimie des Interfaces, Université Catholique de Louvain, 1348 Louvain-la-Neuve</wicri:regionArea>
<orgName type="university">Université catholique de Louvain</orgName>
<placeName>
<settlement type="city">Louvain-la-Neuve</settlement>
<region type="region" nuts="1">Région wallonne</region>
<region type="province" nuts="1">Province du Brabant wallon</region>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2000">2000</date>
<idno type="RBID">pubmed:10828004</idno>
<idno type="pmid">10828004</idno>
<idno type="pmc">PMC1300909</idno>
<idno type="doi">10.1016/S0006-3495(00)76864-0</idno>
<idno type="wicri:Area/Main/Corpus">000A96</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000A96</idno>
<idno type="wicri:Area/Main/Curation">000A96</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000A96</idno>
<idno type="wicri:Area/Main/Exploration">000A96</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.</title>
<author>
<name sortKey="Dufrene, Y F" sort="Dufrene, Y F" uniqKey="Dufrene Y" first="Y F" last="Dufrêne">Y F Dufrêne</name>
<affiliation wicri:level="4">
<nlm:affiliation>Unité de Chimie des Interfaces, Université Catholique de Louvain, 1348 Louvain-la-Neuve, Belgium. dufrene@cifa.ucl.ac.be</nlm:affiliation>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Unité de Chimie des Interfaces, Université Catholique de Louvain, 1348 Louvain-la-Neuve</wicri:regionArea>
<orgName type="university">Université catholique de Louvain</orgName>
<placeName>
<settlement type="city">Louvain-la-Neuve</settlement>
<region type="region" nuts="1">Région wallonne</region>
<region type="province" nuts="1">Province du Brabant wallon</region>
</placeName>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Biophysical journal</title>
<idno type="ISSN">0006-3495</idno>
<imprint>
<date when="2000" type="published">2000</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Cell Adhesion (MeSH)</term>
<term>Indicators and Reagents (MeSH)</term>
<term>Microscopy, Atomic Force (methods)</term>
<term>Phanerochaete (physiology)</term>
<term>Phanerochaete (ultrastructure)</term>
<term>Reproducibility of Results (MeSH)</term>
<term>Spores, Fungal (physiology)</term>
<term>Spores, Fungal (ultrastructure)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adhérence cellulaire (MeSH)</term>
<term>Indicateurs et réactifs (MeSH)</term>
<term>Microscopie à force atomique (méthodes)</term>
<term>Phanerochaete (physiologie)</term>
<term>Phanerochaete (ultrastructure)</term>
<term>Reproductibilité des résultats (MeSH)</term>
<term>Spores fongiques (physiologie)</term>
<term>Spores fongiques (ultrastructure)</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en">
<term>Indicators and Reagents</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Microscopy, Atomic Force</term>
</keywords>
<keywords scheme="MESH" qualifier="méthodes" xml:lang="fr">
<term>Microscopie à force atomique</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Phanerochaete</term>
<term>Spores fongiques</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Phanerochaete</term>
<term>Spores, Fungal</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en">
<term>Phanerochaete</term>
<term>Spores, Fungal</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Cell Adhesion</term>
<term>Reproducibility of Results</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adhérence cellulaire</term>
<term>Indicateurs et réactifs</term>
<term>Phanerochaete</term>
<term>Reproductibilité des résultats</term>
<term>Spores fongiques</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A new method is described for characterizing the physicochemical properties of native microbial cells by using atomic force microscopy (AFM) with chemically functionalized probes. Adhesion forces were measured, under deionized water, between probes and model substrata functionalized with alkanethiol self-assembled monolayers terminated with OH and CH(3) groups. These were found to be 6 +/- 2 nN (n = 1024), 0.9 +/- 0.4 nN, and approximately 0 nN, for CH(3)/CH(3), CH(3)/OH, and OH/OH surfaces, respectively, and were not significantly influenced by changes of ionic strength (0.1 M NaCl versus deionized water). This shows that functionalized probes are very sensitive to changes of surface hydrophobicity. Using OH- and CH(3)-terminated probes, patterns of rodlets, approximately 10 nm in diameter, were visualized, under physiological conditions, at the surface of spores of Phanerochaete chrysosporium. Multiple (1024) force-distance curves recorded over 500 x 500-nm areas at the spore surface, either in deionized water or in 0.1 M NaCl solutions, always showed no adhesion for both OH- and CH(3)-terminated probes. Control experiments indicated that the lack of adhesion is not due to transfer of cellular material onto the probe, but to the hydrophilic nature of the spore surface.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">10828004</PMID>
<DateCompleted>
<Year>2000</Year>
<Month>07</Month>
<Day>10</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Print">
<Journal>
<ISSN IssnType="Print">0006-3495</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>78</Volume>
<Issue>6</Issue>
<PubDate>
<Year>2000</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Biophysical journal</Title>
<ISOAbbreviation>Biophys J</ISOAbbreviation>
</Journal>
<ArticleTitle>Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.</ArticleTitle>
<Pagination>
<MedlinePgn>3286-91</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText>A new method is described for characterizing the physicochemical properties of native microbial cells by using atomic force microscopy (AFM) with chemically functionalized probes. Adhesion forces were measured, under deionized water, between probes and model substrata functionalized with alkanethiol self-assembled monolayers terminated with OH and CH(3) groups. These were found to be 6 +/- 2 nN (n = 1024), 0.9 +/- 0.4 nN, and approximately 0 nN, for CH(3)/CH(3), CH(3)/OH, and OH/OH surfaces, respectively, and were not significantly influenced by changes of ionic strength (0.1 M NaCl versus deionized water). This shows that functionalized probes are very sensitive to changes of surface hydrophobicity. Using OH- and CH(3)-terminated probes, patterns of rodlets, approximately 10 nm in diameter, were visualized, under physiological conditions, at the surface of spores of Phanerochaete chrysosporium. Multiple (1024) force-distance curves recorded over 500 x 500-nm areas at the spore surface, either in deionized water or in 0.1 M NaCl solutions, always showed no adhesion for both OH- and CH(3)-terminated probes. Control experiments indicated that the lack of adhesion is not due to transfer of cellular material onto the probe, but to the hydrophilic nature of the spore surface.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Dufrêne</LastName>
<ForeName>Y F</ForeName>
<Initials>YF</Initials>
<AffiliationInfo>
<Affiliation>Unité de Chimie des Interfaces, Université Catholique de Louvain, 1348 Louvain-la-Neuve, Belgium. dufrene@cifa.ucl.ac.be</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>Biophys J</MedlineTA>
<NlmUniqueID>0370626</NlmUniqueID>
<ISSNLinking>0006-3495</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007202">Indicators and Reagents</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D002448" MajorTopicYN="N">Cell Adhesion</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007202" MajorTopicYN="N">Indicators and Reagents</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018625" MajorTopicYN="N">Microscopy, Atomic Force</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
<QualifierName UI="Q000648" MajorTopicYN="Y">ultrastructure</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015203" MajorTopicYN="N">Reproducibility of Results</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013172" MajorTopicYN="N">Spores, Fungal</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName>
<QualifierName UI="Q000648" MajorTopicYN="Y">ultrastructure</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2000</Year>
<Month>5</Month>
<Day>29</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2000</Year>
<Month>7</Month>
<Day>15</Day>
<Hour>11</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2000</Year>
<Month>5</Month>
<Day>29</Day>
<Hour>9</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">10828004</ArticleId>
<ArticleId IdType="pmc">PMC1300909</ArticleId>
<ArticleId IdType="pii">S0006-3495(00)76864-0</ArticleId>
<ArticleId IdType="doi">10.1016/S0006-3495(00)76864-0</ArticleId>
</ArticleIdList>
<ReferenceList>
<Reference>
<Citation>Biophys J. 1996 Jan;70(1):556-67</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">8770233</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biophys J. 1995 May;68(5):1678-80</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7612810</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Science. 1992 Sep 25;257(5078):1900-5</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">1411505</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biophys J. 1980 Sep;31(3):425-31</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7260296</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Science. 1994 Nov 4;266(5186):771-3</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7973628</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Bacteriol. 1993 Apr;175(7):1946-55</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">8458836</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biochemistry. 1985 Aug 13;24(17):4608-18</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">4063343</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biophys J. 1990 Dec;58(6):1473-80</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">2275963</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Bacteriol. 1993 Aug;175(16):5135-44</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">8349553</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Science. 1995 Apr 7;268(5207):92-4</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">7701347</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Can J Microbiol. 1994 May;40(5):412-6</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">8069785</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biophys J. 1990 Nov;58(5):1251-8</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">2291944</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Science. 1994 Sep 30;265(5181):2071-4</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17811409</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Nature. 1976 Feb 19;259(5544):601-3</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">1250410</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>Belgique</li>
</country>
<region>
<li>Province du Brabant wallon</li>
<li>Région wallonne</li>
</region>
<settlement>
<li>Louvain-la-Neuve</li>
</settlement>
<orgName>
<li>Université catholique de Louvain</li>
</orgName>
</list>
<tree>
<country name="Belgique">
<region name="Région wallonne">
<name sortKey="Dufrene, Y F" sort="Dufrene, Y F" uniqKey="Dufrene Y" first="Y F" last="Dufrêne">Y F Dufrêne</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/PhanerochaeteV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000A88 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000A88 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Bois
   |area=    PhanerochaeteV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:10828004
   |texte=   Direct characterization of the physicochemical properties of fungal spores using functionalized AFM probes.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:10828004" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a PhanerochaeteV1 

Wicri

This area was generated with Dilib version V0.6.37.
Data generation: Fri Nov 13 18:33:39 2020. Site generation: Fri Nov 13 18:35:20 2020