Skip Navigation

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (20)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hosokawa, M.
Right arrow Articles by Sato, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hosokawa, M.
Right arrow Articles by Sato, Y.
Agricola
Right arrow Articles by Hosokawa, M.
Right arrow Articles by Sato, Y.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Plant and Cell Physiology, 2001, Vol. 42, No. 9 959-968
© 2001 Oxford University Press

Progress of Lignification Mediated by Intercellular Transportation of Monolignols During Tracheary Element Differentiation of Isolated Zinnia Mesophyll Cells

Mami Hosokawa1, Shiro Suzuki2, Toshiaki Umezawa2 and Yasushi Sato1,3

1 Department of Biology and Earth Sciences, Faculty of Science, Ehime University, Matsuyama, 790-8577 Japan 2 Research Section of Lignin Chemistry, Wood Research Institute, Kyoto University, Uji, 611-0011 Japan

Tracheary element (TE) differentiation is a typical example of programmed cell death (PCD) in higher plants, and maturation of TEs is completed by degradation of all cell contents. However, lignification of TEs progresses even after PCD. We investigated how and whence monolignols are supplied to TEs which have undergone PCD during differentiation of isolated Zinnia mesophyll cells into TEs. Higher densities of cell culture induced greater lignification of TEs. Whereas the continuous exchanging of culture medium suppressed lignification of TEs, further addition of coniferyl alcohol into the exchanging medium reduced the suppression of lignification. Analysis of the culture medium by HPLC and GC-MS showed that coniferyl alcohol, coniferaldehyde, and sinapyl alcohol accumulated in TE inductive culture. The concentration of coniferyl alcohol peaked at the beginning of secondary wall thickening, decreased rapidly during secondary wall thickening, then increased again. These results indicated that lignification on TEs progresses by supply of monolignols from not only TEs themselves but also surrounding xylem parenchyma-like cells through medium in vitro.

3 Corresponding author: E-mail, ysato@sci.ehime-u.ac.jp; Fax, +81-89-927-9630.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J Exp BotHome page
K. Marjamaa, E. M. Kukkola, and K. V. Fagerstedt
The role of xylem class III peroxidases in lignification
J. Exp. Bot., February 1, 2009; 60(2): 367 - 376.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
M. Kaneda, K. H. Rensing, J. C.T. Wong, B. Banno, S. D. Mansfield, and A. L. Samuels
Tracking Monolignols during Wood Development in Lodgepole Pine
Plant Physiology, August 1, 2008; 147(4): 1750 - 1760.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
Y. Sato, T. Demura, K. Yamawaki, Y. Inoue, S. Sato, M. Sugiyama, and H. Fukuda
Isolation and Characterization of a Novel Peroxidase Gene ZPO-C Whose Expression and Function are Closely Associated with Lignification during Tracheary Element Differentiation
Plant Cell Physiol., April 1, 2006; 47(4): 493 - 503.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
E. Pesquet, P. Ranocha, S. Legay, C. Digonnet, O. Barbier, M. Pichon, and D. Goffner
Novel Markers of Xylogenesis in Zinnia Are Differentially Regulated by Auxin and Cytokinin
Plant Physiology, December 1, 2005; 139(4): 1821 - 1839.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
K. Ohashi-Ito, M. Kubo, T. Demura, and H. Fukuda
Class III Homeodomain Leucine-Zipper Proteins Regulate Xylem Cell Differentiation
Plant Cell Physiol., October 1, 2005; 46(10): 1646 - 1656.
[Abstract] [Full Text] [PDF]


Home page
Crop Sci.Home page
J. H. Grabber
How Do Lignin Composition, Structure, and Cross-Linking Affect Degradability? A Review of Cell Wall Model Studies
Crop Sci., March 28, 2005; 45(3): 820 - 831.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
N. Tokunaga, N. Sakakibara, T. Umezawa, Y. Ito, H. Fukuda, and Y. Sato
Involvement of Extracellular Dilignols in Lignification During Tracheary Element Differentiation of Isolated Zinnia Mesophyll Cells
Plant Cell Physiol., January 15, 2005; 46(1): 224 - 232.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
I. Nakanomyo, B. Kost, N.-H. Chua, and H. Fukuda
Preferential and Asymmetrical Accumulation of a Rac Small GTPase mRNA in Differentiating Xylem Cells of Zinnia elegans
Plant Cell Physiol., December 15, 2002; 43(12): 1484 - 1492.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
T. Demura, G. Tashiro, G. Horiguchi, N. Kishimoto, M. Kubo, N. Matsuoka, A. Minami, M. Nagata-Hiwatashi, K. Nakamura, Y. Okamura, et al.
Visualization by comprehensive microarray analysis of gene expression programs during transdifferentiation of mesophyll cells into xylem cells
PNAS, November 26, 2002; 99(24): 15794 - 15799.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
K. Ohashi-Ito, T. Demura, and H. Fukuda
Promotion of Transcript Accumulation of Novel Zinnia Immature Xylem-Specific HD-Zip III Homeobox Genes by Brassinosteroids
Plant Cell Physiol., October 15, 2002; 43(10): 1146 - 1153.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.