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Expression of endo-1,4-β-glucanase (cel1) in Arabidopsis thaliana is associated with plant growth, xylem development and cell wall thickening
Year:
2006
Source of publication :
Plant Cell Reports
Authors :
Koltai, Hinanit
;
.
Volume :
25
Co-Authors:
Shani, Z., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Dekel, M., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel, Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Roiz, L., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Horowitz, M., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Kolosovski, N., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Lapidot, S., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Alkan, S., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Koltai, H., Department of Genomics, Volcani Center, P.O. Box 6, Bet Dagan 50250, Israel
Tsabary, G., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Goren, R., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Shoseyov, O., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Facilitators :
From page:
1067
To page:
1074
(
Total pages:
8
)
Abstract:
Arabidopsis thaliana CEL1 protein was detected in young expanding tissues. Immunostaining revealed that CEL1 accumulated mostly in xylem cells. The primary, as well as the secondary xylem showed considerable CEL1 staining. CEL1 was also observed in young epidermal cells, in which the thicker lateral and tangential walls stained more intensely than the inner walls. In newly formed cell walls, the lateral tangential walls were labeled more intensively than the inner walls. Cellulase activity was found to be significantly higher in growing tissue compared to mature parts of the plant. Cel1 expression concurrently with cellulase activity could be restored in detached matured leaves by sucrose treatment after 48 h in the culture medium. © 2006 Springer-Verlag.
Note:
Related Files :
arabidopsis
Arabidopsis thaliana
drug effect
Genetics
Growth, Development and Aging
Histology
metabolism
Plants
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More details
DOI :
10.1007/s00299-006-0167-9
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
21641
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:45
Scientific Publication
Expression of endo-1,4-β-glucanase (cel1) in Arabidopsis thaliana is associated with plant growth, xylem development and cell wall thickening
25
Shani, Z., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Dekel, M., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel, Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Roiz, L., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Horowitz, M., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Kolosovski, N., CBD-Technologies Ltd., Tamar Science Park, P.O. Box 199, Rehovot 76100, Israel
Lapidot, S., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Alkan, S., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Koltai, H., Department of Genomics, Volcani Center, P.O. Box 6, Bet Dagan 50250, Israel
Tsabary, G., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Goren, R., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Shoseyov, O., Robert Smith Institute of Plant Sciences and Genetics, Faculty of Agricultural, Food and Environmental Quality Sciences, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100, Israel
Expression of endo-1,4-β-glucanase (cel1) in Arabidopsis thaliana is associated with plant growth, xylem development and cell wall thickening
Arabidopsis thaliana CEL1 protein was detected in young expanding tissues. Immunostaining revealed that CEL1 accumulated mostly in xylem cells. The primary, as well as the secondary xylem showed considerable CEL1 staining. CEL1 was also observed in young epidermal cells, in which the thicker lateral and tangential walls stained more intensely than the inner walls. In newly formed cell walls, the lateral tangential walls were labeled more intensively than the inner walls. Cellulase activity was found to be significantly higher in growing tissue compared to mature parts of the plant. Cel1 expression concurrently with cellulase activity could be restored in detached matured leaves by sucrose treatment after 48 h in the culture medium. © 2006 Springer-Verlag.
Scientific Publication
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