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Stronger cellulose microfibrils network structure through the expression of cellulose-binding modules in plant primary cell walls
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Glykovetenskap.ORCID-id: 0000-0002-5541-7853
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Glykovetenskap.
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Glykovetenskap.ORCID-id: 0000-0001-9832-027X
(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
Nationell ämneskategori
Annan kemi
Identifikatorer
URN: urn:nbn:se:kth:diva-240966OAI: oai:DiVA.org:kth-240966DiVA, id: diva2:1275526
Anmärkning

QC 20190107

Tillgänglig från: 2019-01-07 Skapad: 2019-01-07 Senast uppdaterad: 2019-05-08Bibliografiskt granskad
Ingår i avhandling
1.
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2. Understanding and manipulating primary cell walls in plant cell suspension cultures
Öppna denna publikation i ny flik eller fönster >>Understanding and manipulating primary cell walls in plant cell suspension cultures
2019 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

The cell wall is required for many aspects of plant function and development. It is also an accessible and renewable resource utilized both in unrefined forms and as raw material for further development. Increased knowledge regarding cell wall structure and components will contribute to better utilization of plants and the resources they provide. In this thesis aspects of the primary cell wall of Populus trichocarpa and Nicotiana tabacum are explored.

In Publication I a method for isolation and biochemical characterization of plant glycosyltransferases using a spectrophotometric or a radiometric assay was optimized. The radiometric assay was applied in Publication II where the proteome of the plasmodesmata isolated from P. trichocarpa was analyzed. Proteins identified belonged to functional classes such as “transport”, “signalling” and “stress responses”. Plasmodesmata-enriched fractions had high levels of callose synthase activity under ion depleted conditions as well as with calcium present.

The second part of the thesis comprises the alteration of the cell wall of N. tabacum cells and A. thaliana plants through in vivo expression of a carbohydrate binding module (CBM) (Publication III). In tobacco this resulted in cell walls with loose ultrastructure containing an increased proportion of 1,4-β-glucans. The cell walls were more susceptible to saccharification, possibly due to changes in the structure of cellulose or xyloglucan. Arabidopsis plants showed increased saccharification after mild pretreatment, suggesting that heterologous expression of CBMs is a promising method for cell wall engineering. In Publication IV cellulose microfibrils (CMFs) and nanocrystals (CNCs) were extracted from the transgenic cells. CNC preparation resulted in higher yields and longer CNCs. Nanopapers prepared from the CMFs of the CBM line demonstrated enhanced strength and toughness. Thus, changes to the ordered regions of cellulose were suggested to take place due to CBM expression.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH Royal Institute of Technology, 2019. s. 82
Serie
TRITA-CBH-FOU ; 2
Nyckelord
Callose synthase, carbohydrate-binding module, cell wall engineering, cellulose microfibril, cellulose nanocrystal, glycosyltransferase, mass spectrometry, plasmodesmata, Populus, primary cell wall, radiometric assay, spectrophotometric assay
Nationell ämneskategori
Naturvetenskap
Forskningsämne
Bioteknologi
Identifikatorer
urn:nbn:se:kth:diva-251039 (URN)978-91-7873-074-2 (ISBN)
Disputation
2019-06-10, FA32, Roslagstullsbacken 21, AlbaNova, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning

QC 2019-05-08

Tillgänglig från: 2019-05-08 Skapad: 2019-05-08 Senast uppdaterad: 2019-05-08Bibliografiskt granskad

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Bulone, VincentZhou, Qi

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Leijon, FeliciaBulone, VincentZhou, Qi
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Glykovetenskap
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