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MAP20, a Microtubule-Associated Protein in the Secondary Cell Walls of Hybrid Aspen, Is a Target of the Cellulose Synthesis Inhibitor 2,6-Dichlorobenzonitrile
KTH, Skolan för bioteknologi (BIO), Centra, Strategiskt Centrum för Biomimetiska Material, BioMime.
KTH, Skolan för bioteknologi (BIO), Centra, Strategiskt Centrum för Biomimetiska Material, BioMime.ORCID-id: 0000-0002-8576-4370
KTH, Skolan för bioteknologi (BIO), Centra, Strategiskt Centrum för Biomimetiska Material, BioMime.
Vise andre og tillknytning
2008 (engelsk)Inngår i: Plant Physiology, ISSN 0032-0889, E-ISSN 1532-2548, Vol. 148, nr 3, s. 1283-1294Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We have identified a gene, denoted PttMAP20, which is strongly up-regulated during secondary cell wall synthesis and tightly coregulated with the secondary wall-associated CESA genes in hybrid aspen (Populus tremula x tremuloides). Immunolocalization studies with affinity-purified antibodies specific for PttMAP20 revealed that the protein is found in all cell types in developing xylem and that it is most abundant in cells forming secondary cell walls. This PttMAP20 protein sequence contains a highly conserved TPX2 domain first identified in a microtubule-associated protein (MAP) in Xenopus laevis. Overexpression of PttMAP20 in Arabidopsis (Arabidopsis thaliana) leads to helical twisting of epidermal cells, frequently associated with MAPs. In addition, a PttMAP20-yellow fluorescent protein fusion protein expressed in tobacco (Nicotiana tabacum) leaves localizes to microtubules in leaf epidermal pavement cells. Recombinant PttMAP20 expressed in Escherichia coli also binds specifically to in vitro-assembled, taxol-stabilized bovine microtubules. Finally, the herbicide 2,6-dichlorobenzonitrile, which inhibits cellulose synthesis in plants, was found to bind specifically to PttMAP20. Together with the known function of cortical microtubules in orienting cellulose microfibrils, these observations suggest that PttMAP20 has a role in cellulose biosynthesis.

sted, utgiver, år, opplag, sider
2008. Vol. 148, nr 3, s. 1283-1294
Emneord [en]
carbohydrate-active enzymes, plant functional genomics, kinesin-like, protein, cortical microtubules, plasma-membrane, wood formation, arabidopsis-thaliana, conifer tracheids, angiosperm trees, urea solution
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-17951DOI: 10.1104/pp.108.121913ISI: 000260719500010PubMedID: 18805954Scopus ID: 2-s2.0-57749101097OAI: oai:DiVA.org:kth-17951DiVA, id: diva2:335996
Merknad

QC 20100525

Tilgjengelig fra: 2010-08-05 Laget: 2010-08-05 Sist oppdatert: 2022-12-07bibliografisk kontrollert
Inngår i avhandling
1. Functional genomics of wood degradation and biosynthesis
Åpne denne publikasjonen i ny fane eller vindu >>Functional genomics of wood degradation and biosynthesis
2005 (engelsk)Licentiatavhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Forest biotechnology is a fast emerging field of research. The application of biotechnological tools will enhance the quality of the forest products. The resultant value added and environmentally sustainable products are an absolute necessity in the future. The study of wood biosynthesis and degradation will result in enormous knowledge resources, which can be used for exploiting wood properties. This thesis addresses questions representing both wood degradation and biosynthesis.

The wood degrading fungus Phanerochaete chrysosporium is expression profiled with the microarray technology. The objective is to understand the expression pattern of the extracellular carbohydrate active enzymes (CAZymes) secreted by the organism. The data obtained increases our understanding of gene expression upon growth on cellulose.

Wood biosynthesis is studied with the model wood forming tree species, Populus. The plentiful data resources from the expression profiling during wood formation in Populus are used as the platform of this work. One of the wood specific genes, PttMAP20, previously with an unknown function is studied in this thesis. The immunolocalisation of PttMAP20 with specific antibodies is demonstrated. The putative microtubule-targeting domain of the protein is demonstrated microscopically and by using a biochemical binding assay.

sted, utgiver, år, opplag, sider
Stockholm: KTH, 2005. s. 42
Emneord
populus, xylogenesis, secondary cell wall, cellulose, hemicellulose, microarrays, transcript profiling
HSV kategori
Identifikatorer
urn:nbn:se:kth:diva-592 (URN)91-7178-250-8 (ISBN)
Presentation
2006-01-30, Sal FB54, AlbaNova, Roslagstullsbacken, Stockholm, 10:00
Opponent
Veileder
Merknad
QC 20101217Tilgjengelig fra: 2006-01-16 Laget: 2006-01-16 Sist oppdatert: 2022-06-26bibliografisk kontrollert

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Aspeborg, HenrikHober, SophiaDivne, ChristinaEzcurra, Inés

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Rajangam, Alex S.Aspeborg, HenrikGuerriero, GeaArvestad, LarsPansri, PodjamasBrown, Christian J. L.Hober, SophiaBlomqvist, KristinaDivne, ChristinaEzcurra, InésBulone, VincentTeeri, Tuula T.
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