Chemical imaging of poplar wood cell walls by confocal Raman microscopy.
Identifieur interne : 003E48 ( Main/Exploration ); précédent : 003E47; suivant : 003E49Chemical imaging of poplar wood cell walls by confocal Raman microscopy.
Auteurs : Notburga Gierlinger [Allemagne] ; Manfred SchwanningerSource :
- Plant physiology [ 0032-0889 ] ; 2006.
Descripteurs français
- KwdFr :
- MESH :
- analyse : Lignine.
- composition chimique : Paroi cellulaire, Populus.
- croissance et développement : Populus.
- cytologie : Populus.
- méthodes : Analyse spectrale Raman, Microscopie confocale.
- ultrastructure : Paroi cellulaire.
English descriptors
- KwdEn :
- MESH :
- chemical , analysis : Lignin.
- chemistry : Cell Wall, Populus.
- cytology : Populus.
- growth & development : Populus.
- methods : Microscopy, Confocal, Spectrum Analysis, Raman.
- ultrastructure : Cell Wall.
Abstract
Confocal Raman microscopy was used to illustrate changes of molecular composition in secondary plant cell wall tissues of poplar (Populus nigra x Populus deltoids) wood. Two-dimensional spectral maps were acquired and chemical images calculated by integrating the intensity of characteristic spectral bands. This enabled direct visualization of the spatial variation of the lignin content without any chemical treatment or staining of the cell wall. A small (0.5 microm) lignified border toward the lumen was observed in the gelatinous layer of poplar tension wood. The variable orientation of the cellulose was also characterized, leading to visualization of the S1 layer with dimensions smaller than 0.5 mum. Scanning Raman microscopy was thus shown to be a powerful, nondestructive tool for imaging changes in molecular cell wall organization with high spatial resolution.
DOI: 10.1104/pp.105.066993
PubMed: 16489138
PubMed Central: PMC1435827
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<front><div type="abstract" xml:lang="en">Confocal Raman microscopy was used to illustrate changes of molecular composition in secondary plant cell wall tissues of poplar (Populus nigra x Populus deltoids) wood. Two-dimensional spectral maps were acquired and chemical images calculated by integrating the intensity of characteristic spectral bands. This enabled direct visualization of the spatial variation of the lignin content without any chemical treatment or staining of the cell wall. A small (0.5 microm) lignified border toward the lumen was observed in the gelatinous layer of poplar tension wood. The variable orientation of the cellulose was also characterized, leading to visualization of the S1 layer with dimensions smaller than 0.5 mum. Scanning Raman microscopy was thus shown to be a powerful, nondestructive tool for imaging changes in molecular cell wall organization with high spatial resolution.</div>
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<Abstract><AbstractText>Confocal Raman microscopy was used to illustrate changes of molecular composition in secondary plant cell wall tissues of poplar (Populus nigra x Populus deltoids) wood. Two-dimensional spectral maps were acquired and chemical images calculated by integrating the intensity of characteristic spectral bands. This enabled direct visualization of the spatial variation of the lignin content without any chemical treatment or staining of the cell wall. A small (0.5 microm) lignified border toward the lumen was observed in the gelatinous layer of poplar tension wood. The variable orientation of the cellulose was also characterized, leading to visualization of the S1 layer with dimensions smaller than 0.5 mum. Scanning Raman microscopy was thus shown to be a powerful, nondestructive tool for imaging changes in molecular cell wall organization with high spatial resolution.</AbstractText>
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<ReferenceList><Reference><Citation>Appl Spectrosc. 2003 Jan;57(1):58-66</Citation>
<ArticleIdList><ArticleId IdType="pubmed">14610937</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochemistry. 2001 Jul;57(6):859-73</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11423137</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Spectrochim Acta A Mol Biomol Spectrosc. 1997 Nov;53A(13):2383-92</Citation>
<ArticleIdList><ArticleId IdType="pubmed">9477578</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Carbohydr Res. 2004 Feb 25;339(3):629-35</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15013400</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 1994 Dec;106(4):1623-1631</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12232436</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Phytochemistry. 2001 Jul;57(6):811-21</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11423133</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Biopolymers. 2004 May-Jun 5;74(1-2):151-6</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15137114</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 2001 Dec;127(4):1513-23</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11743096</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 1992 Dec;100(4):1940-7</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16653221</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Fresenius J Anal Chem. 2000 Mar-Apr;366(6-7):712-6</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11225782</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Science. 1985 Feb 8;227(4687):636-8</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17781824</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Planta. 1986 Nov;169(3):325-32</Citation>
<ArticleIdList><ArticleId IdType="pubmed">24232643</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Planta. 2004 Jun;219(2):338-45</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15067547</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Mol Biol. 2001 Sep;47(1-2):239-74</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11554475</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>C R Biol. 2004 Sep-Oct;327(9-10):889-901</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15587080</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Biol Rev Camb Philos Soc. 2004 May;79(2):461-72</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15191232</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
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