High-resolution imaging of the microbial cell surface.
Identifieur interne : 000160 ( Main/Exploration ); précédent : 000159; suivant : 000161High-resolution imaging of the microbial cell surface.
Auteurs : Ki Woo Kim [Corée du Sud]Source :
- Journal of microbiology (Seoul, Korea) [ 1976-3794 ] ; 2016.
Descripteurs français
- KwdFr :
- Bactéries (composition chimique), Bactéries (ultrastructure), Bactériophages (composition chimique), Bactériophages (ultrastructure), Champignons (composition chimique), Champignons (ultrastructure), Membrane cellulaire (composition chimique), Membrane cellulaire (ultrastructure), Microscopie à force atomique (méthodes), Microscopie électronique à balayage (méthodes), Microscopie électronique à transmission (méthodes), Paroi cellulaire (MeSH), Spores fongiques (composition chimique), Spores fongiques (ultrastructure).
- MESH :
- composition chimique : Bactéries, Bactériophages, Champignons, Membrane cellulaire, Spores fongiques.
- méthodes : Microscopie à force atomique, Microscopie électronique à balayage, Microscopie électronique à transmission.
- ultrastructure : Bactéries, Bactériophages, Champignons, Membrane cellulaire, Paroi cellulaire, Spores fongiques.
English descriptors
- KwdEn :
- Bacteria (chemistry), Bacteria (ultrastructure), Bacteriophages (chemistry), Bacteriophages (ultrastructure), Cell Membrane (chemistry), Cell Membrane (ultrastructure), Cell Wall (MeSH), Fungi (chemistry), Fungi (ultrastructure), Microscopy, Atomic Force (methods), Microscopy, Electron, Scanning (methods), Microscopy, Electron, Transmission (methods), Spores, Fungal (chemistry), Spores, Fungal (ultrastructure).
- MESH :
- chemistry : Bacteria, Bacteriophages, Cell Membrane, Fungi, Spores, Fungal.
- methods : Microscopy, Atomic Force, Microscopy, Electron, Scanning, Microscopy, Electron, Transmission.
- ultrastructure : Bacteria, Bacteriophages, Cell Membrane, Fungi, Spores, Fungal.
- Cell Wall.
Abstract
Microorganisms, or microbes, can function as threatening pathogens that cause disease in humans, animals, and plants; however, they also act as litter decomposers in natural ecosystems. As the outermost barrier and interface with the environment, the microbial cell surface is crucial for cell-to-cell communication and is a potential target of chemotherapeutic agents. Surface ultrastructures of microbial cells have typically been observed using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Owing to its characteristics of low-temperature specimen preparation and superb resolution (down to 1 nm), cryo-field emission SEM has revealed paired rodlets, referred to as hydrophobins, on the cell walls of bacteria and fungi. Recent technological advances in AFM have enabled high-speed live cell imaging in liquid at the nanoscale level, leading to clear visualization of cell-drug interactions. Platinum-carbon replicas from freeze-fractured fungal spores have been observed using transmission electron microscopy, revealing hydrophobins with varying dimensions. In addition, AFM has been used to resolve bacteriophages in their free state and during infection of bacterial cells. Various microscopy techniques with enhanced spatial resolution, imaging speed, and versatile specimen preparation are being used to document cellular structures and events, thus addressing unanswered biological questions.
DOI: 10.1007/s12275-016-6348-5
PubMed: 27796933
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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37224</wicri:regionArea><wicri:noRegion>37224</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2016">2016</date><idno type="RBID">pubmed:27796933</idno><idno type="pmid">27796933</idno><idno type="doi">10.1007/s12275-016-6348-5</idno><idno type="wicri:Area/Main/Corpus">000152</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000152</idno><idno type="wicri:Area/Main/Curation">000152</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000152</idno><idno type="wicri:Area/Main/Exploration">000152</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">High-resolution imaging of the microbial cell surface.</title><author><name sortKey="Kim, Ki Woo" sort="Kim, Ki Woo" uniqKey="Kim K" first="Ki Woo" last="Kim">Ki Woo Kim</name><affiliation wicri:level="1"><nlm:affiliation>School of Ecology and Environmental System, Kyungpook National University, Sangju, 37224, Republic of Korea. kiwoo@knu.ac.kr.</nlm:affiliation><country xml:lang="fr">Corée du Sud</country><wicri:regionArea>School of Ecology and Environmental System, Kyungpook National University, Sangju, 37224</wicri:regionArea><wicri:noRegion>37224</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:affiliation>Tree Diagnostic Center, Kyungpook National University, Sangju, 37224, Republic of Korea. kiwoo@knu.ac.kr.</nlm:affiliation><country xml:lang="fr">Corée du Sud</country><wicri:regionArea>Tree Diagnostic Center, Kyungpook National University, Sangju, 37224</wicri:regionArea><wicri:noRegion>37224</wicri:noRegion></affiliation></author></analytic><series><title level="j">Journal of microbiology (Seoul, Korea)</title><idno type="eISSN">1976-3794</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacteria (chemistry)</term><term>Bacteria (ultrastructure)</term><term>Bacteriophages (chemistry)</term><term>Bacteriophages (ultrastructure)</term><term>Cell Membrane (chemistry)</term><term>Cell Membrane (ultrastructure)</term><term>Cell Wall (MeSH)</term><term>Fungi (chemistry)</term><term>Fungi (ultrastructure)</term><term>Microscopy, Atomic Force (methods)</term><term>Microscopy, Electron, Scanning (methods)</term><term>Microscopy, Electron, Transmission (methods)</term><term>Spores, Fungal (chemistry)</term><term>Spores, Fungal (ultrastructure)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bactéries (composition chimique)</term><term>Bactéries (ultrastructure)</term><term>Bactériophages (composition chimique)</term><term>Bactériophages (ultrastructure)</term><term>Champignons (composition chimique)</term><term>Champignons (ultrastructure)</term><term>Membrane cellulaire (composition chimique)</term><term>Membrane cellulaire (ultrastructure)</term><term>Microscopie à force atomique (méthodes)</term><term>Microscopie électronique à balayage (méthodes)</term><term>Microscopie électronique à transmission (méthodes)</term><term>Paroi cellulaire (MeSH)</term><term>Spores fongiques (composition chimique)</term><term>Spores fongiques (ultrastructure)</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Bacteria</term><term>Bacteriophages</term><term>Cell Membrane</term><term>Fungi</term><term>Spores, Fungal</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Bactéries</term><term>Bactériophages</term><term>Champignons</term><term>Membrane cellulaire</term><term>Spores fongiques</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Microscopy, Atomic Force</term><term>Microscopy, Electron, Scanning</term><term>Microscopy, Electron, Transmission</term></keywords><keywords scheme="MESH" qualifier="méthodes" xml:lang="fr"><term>Microscopie à force atomique</term><term>Microscopie électronique à balayage</term><term>Microscopie électronique à transmission</term></keywords><keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>Bacteria</term><term>Bacteriophages</term><term>Cell Membrane</term><term>Fungi</term><term>Spores, Fungal</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Cell Wall</term></keywords><keywords scheme="MESH" qualifier="ultrastructure" xml:lang="fr"><term>Bactéries</term><term>Bactériophages</term><term>Champignons</term><term>Membrane cellulaire</term><term>Paroi cellulaire</term><term>Spores fongiques</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Microorganisms, or microbes, can function as threatening pathogens that cause disease in humans, animals, and plants; however, they also act as litter decomposers in natural ecosystems. As the outermost barrier and interface with the environment, the microbial cell surface is crucial for cell-to-cell communication and is a potential target of chemotherapeutic agents. Surface ultrastructures of microbial cells have typically been observed using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Owing to its characteristics of low-temperature specimen preparation and superb resolution (down to 1 nm), cryo-field emission SEM has revealed paired rodlets, referred to as hydrophobins, on the cell walls of bacteria and fungi. Recent technological advances in AFM have enabled high-speed live cell imaging in liquid at the nanoscale level, leading to clear visualization of cell-drug interactions. Platinum-carbon replicas from freeze-fractured fungal spores have been observed using transmission electron microscopy, revealing hydrophobins with varying dimensions. In addition, AFM has been used to resolve bacteriophages in their free state and during infection of bacterial cells. Various microscopy techniques with enhanced spatial resolution, imaging speed, and versatile specimen preparation are being used to document cellular structures and events, thus addressing unanswered biological questions.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27796933</PMID><DateCompleted><Year>2017</Year><Month>02</Month><Day>08</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1976-3794</ISSN><JournalIssue CitedMedium="Internet"><Volume>54</Volume><Issue>11</Issue><PubDate><Year>2016</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Journal of microbiology (Seoul, Korea)</Title><ISOAbbreviation>J Microbiol</ISOAbbreviation></Journal><ArticleTitle>High-resolution imaging of the microbial cell surface.</ArticleTitle><Pagination><MedlinePgn>703-708</MedlinePgn></Pagination><Abstract><AbstractText>Microorganisms, or microbes, can function as threatening pathogens that cause disease in humans, animals, and plants; however, they also act as litter decomposers in natural ecosystems. As the outermost barrier and interface with the environment, the microbial cell surface is crucial for cell-to-cell communication and is a potential target of chemotherapeutic agents. Surface ultrastructures of microbial cells have typically been observed using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Owing to its characteristics of low-temperature specimen preparation and superb resolution (down to 1 nm), cryo-field emission SEM has revealed paired rodlets, referred to as hydrophobins, on the cell walls of bacteria and fungi. Recent technological advances in AFM have enabled high-speed live cell imaging in liquid at the nanoscale level, leading to clear visualization of cell-drug interactions. Platinum-carbon replicas from freeze-fractured fungal spores have been observed using transmission electron microscopy, revealing hydrophobins with varying dimensions. In addition, AFM has been used to resolve bacteriophages in their free state and during infection of bacterial cells. Various microscopy techniques with enhanced spatial resolution, imaging speed, and versatile specimen preparation are being used to document cellular structures and events, thus addressing unanswered biological questions.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kim</LastName><ForeName>Ki Woo</ForeName><Initials>KW</Initials><AffiliationInfo><Affiliation>School of Ecology and Environmental System, Kyungpook National University, Sangju, 37224, Republic of Korea. kiwoo@knu.ac.kr.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Tree Diagnostic Center, Kyungpook National University, Sangju, 37224, Republic of Korea. kiwoo@knu.ac.kr.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate 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