PoplarV1, Main, Exploration, bibRecord, 003E52

Cell suspension cultures of Populus tremula x P. tremuloides exhibit a high level of cellulose synthase gene expression that coincides with increased in vitro cellulose synthase activity.

Identifieur interne : 003E52 ( Main/Exploration ); précédent : 003E51; suivant : 003E53

Cell suspension cultures of Populus tremula x P. tremuloides exhibit a high level of cellulose synthase gene expression that coincides with increased in vitro cellulose synthase activity.

Auteurs : Anna B. Ohlsson [Suède] ; Soraya Djerbi ; Anders Winzell ; Laurence Bessueille ; Veronika St Ldal ; Xinguo Li ; Kristina Blomqvist ; Vincent Bulone ; Tuula T. Teeri ; Torkel Berglund

Source :

Protoplasma [ 0033-183X ] ; 2006.

RBID : pubmed:16838081

Descripteurs français

English descriptors

KwdEn :
- Benzenesulfonates (metabolism), Cells, Cultured (MeSH), Cellulase (metabolism), Cellulose (metabolism), Gene Expression Regulation, Enzymologic (genetics), Gene Expression Regulation, Plant (genetics), Glucosyltransferases (genetics), Glucosyltransferases (metabolism), Hybridization, Genetic (MeSH), Plant Proteins (genetics), Plant Proteins (metabolism), Populus (cytology), Populus (genetics), Populus (metabolism), RNA, Messenger (genetics), RNA, Messenger (metabolism), Reverse Transcriptase Polymerase Chain Reaction (MeSH), beta-Glucans (metabolism).
MESH :
- chemical , genetics : Glucosyltransferases, Plant Proteins, RNA, Messenger.
- chemical , metabolism : Benzenesulfonates, Cellulase, Cellulose, Glucosyltransferases, Plant Proteins, RNA, Messenger, beta-Glucans.
- cytology : Populus.
- genetics : Gene Expression Regulation, Enzymologic, Gene Expression Regulation, Plant, Populus.
- metabolism : Populus.
- Cells, Cultured, Hybridization, Genetic, Reverse Transcriptase Polymerase Chain Reaction.

Abstract

Compared to wood, cell suspension cultures provide convenient model systems to study many different cellular processes in plants. Here we have established cell suspension cultures of Populus tremula L. x P. tremuloides Michx. and characterized them by determining the enzymatic activities and/or mRNA expression levels of selected cell wall-specific proteins at the different stages of growth. While enzymes and proteins typically associated with primary cell wall synthesis and expansion were detected in the exponential growth phase of the cultures, the late stationary phase showed high expression of the secondary-cell-wall-associated cellulose synthase genes. Interestingly, detergent extracts of membranes from aging cell suspension cultures exhibited high levels of in vitro cellulose synthesis. The estimated ratio of cellulose to callose was as high as 50 : 50, as opposed to the ratio of 30 : 70 so far achieved with membrane preparations extracted from other systems. The increased cellulose synthase activity was also evidenced by higher levels of Calcofluor white binding in the cell material from the stationary-phase cultures. The ease of handling cell suspension cultures and the improved capacity for in vitro cellulose synthesis suggest that these cultures offer a new basis for studying the mechanism of cellulose biosynthesis.

DOI: 10.1007/s00709-006-0156-4
PubMed: 16838081

Affiliations:

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

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Le document en format XML

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<term>Cellulose (metabolism)</term>
<term>Gene Expression Regulation, Enzymologic (genetics)</term>
<term>Gene Expression Regulation, Plant (genetics)</term>
<term>Glucosyltransferases (genetics)</term>
<term>Glucosyltransferases (metabolism)</term>
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<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Populus (cytology)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
<term>RNA, Messenger (genetics)</term>
<term>RNA, Messenger (metabolism)</term>
<term>Reverse Transcriptase Polymerase Chain Reaction (MeSH)</term>
<term>beta-Glucans (metabolism)</term>
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<term>ARN messager (métabolisme)</term>
<term>Benzènesulfonates (métabolisme)</term>
<term>Cellulase (métabolisme)</term>
<term>Cellules cultivées (MeSH)</term>
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<term>Glucosyltransferases (métabolisme)</term>
<term>Hybridation génétique (MeSH)</term>
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<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>RT-PCR (MeSH)</term>
<term>Régulation de l'expression des gènes codant pour des enzymes (génétique)</term>
<term>Régulation de l'expression des gènes végétaux (génétique)</term>
<term>bêta-Glucanes (métabolisme)</term>
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<term>Plant Proteins</term>
<term>RNA, Messenger</term>
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<term>Cellulose</term>
<term>Glucosyltransferases</term>
<term>Plant Proteins</term>
<term>RNA, Messenger</term>
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<term>Glucosyltransferases</term>
<term>Populus</term>
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<term>Régulation de l'expression des gènes codant pour des enzymes</term>
<term>Régulation de l'expression des gènes végétaux</term>
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<term>bêta-Glucanes</term>
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<term>Hybridization, Genetic</term>
<term>Reverse Transcriptase Polymerase Chain Reaction</term>
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<front><div type="abstract" xml:lang="en">Compared to wood, cell suspension cultures provide convenient model systems to study many different cellular processes in plants. Here we have established cell suspension cultures of Populus tremula L. x P. tremuloides Michx. and characterized them by determining the enzymatic activities and/or mRNA expression levels of selected cell wall-specific proteins at the different stages of growth. While enzymes and proteins typically associated with primary cell wall synthesis and expansion were detected in the exponential growth phase of the cultures, the late stationary phase showed high expression of the secondary-cell-wall-associated cellulose synthase genes. Interestingly, detergent extracts of membranes from aging cell suspension cultures exhibited high levels of in vitro cellulose synthesis. The estimated ratio of cellulose to callose was as high as 50 : 50, as opposed to the ratio of 30 : 70 so far achieved with membrane preparations extracted from other systems. The increased cellulose synthase activity was also evidenced by higher levels of Calcofluor white binding in the cell material from the stationary-phase cultures. The ease of handling cell suspension cultures and the improved capacity for in vitro cellulose synthesis suggest that these cultures offer a new basis for studying the mechanism of cellulose biosynthesis.</div>
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<Abstract><AbstractText>Compared to wood, cell suspension cultures provide convenient model systems to study many different cellular processes in plants. Here we have established cell suspension cultures of Populus tremula L. x P. tremuloides Michx. and characterized them by determining the enzymatic activities and/or mRNA expression levels of selected cell wall-specific proteins at the different stages of growth. While enzymes and proteins typically associated with primary cell wall synthesis and expansion were detected in the exponential growth phase of the cultures, the late stationary phase showed high expression of the secondary-cell-wall-associated cellulose synthase genes. Interestingly, detergent extracts of membranes from aging cell suspension cultures exhibited high levels of in vitro cellulose synthesis. The estimated ratio of cellulose to callose was as high as 50 : 50, as opposed to the ratio of 30 : 70 so far achieved with membrane preparations extracted from other systems. The increased cellulose synthase activity was also evidenced by higher levels of Calcofluor white binding in the cell material from the stationary-phase cultures. The ease of handling cell suspension cultures and the improved capacity for in vitro cellulose synthesis suggest that these cultures offer a new basis for studying the mechanism of cellulose biosynthesis.</AbstractText>
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Cell suspension cultures of Populus tremula x P. tremuloides exhibit a high level of cellulose synthase gene expression that coincides with increased in vitro cellulose synthase activity.

Cell suspension cultures of Populus tremula x P. tremuloides exhibit a high level of cellulose synthase gene expression that coincides with increased in vitro cellulose synthase activity.

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