Plant Physiol. Drug Metab Dispos
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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 Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Web of Science (16)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Babb, V. M.
Right arrow Articles by Haigler, C. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Babb, V. M.
Right arrow Articles by Haigler, C. H.
Agricola
Right arrow Articles by Babb, V. M.
Right arrow Articles by Haigler, C. H.

Plant Physiol, November 2001, Vol. 127, pp. 1234-1242

Sucrose Phosphate Synthase Activity Rises in Correlation with High-Rate Cellulose Synthesis in Three Heterotrophic Systems1

V. Michelle Babb and Candace H. Haigler*

Department of Biological Sciences, Texas Tech University, Lubbock, Texas 79409

Based on work with cotton fibers, a particulate form of sucrose (Suc) synthase was proposed to support secondary wall cellulose synthesis by degrading Suc to fructose and UDP-glucose. The model proposed that UDP-glucose was then channeled to cellulose synthase in the plasma membrane, and it implies that Suc availability in cellulose sink cells would affect the rate of cellulose synthesis. Therefore, if cellulose sink cells could synthesize Suc and/or had the capacity to recycle the fructose released by Suc synthase back to Suc, cellulose synthesis might be supported. The capacity of cellulose sink cells to synthesize Suc was tested by analyzing the Suc phosphate synthase (SPS) activity of three heterotrophic systems with cellulose-rich secondary walls. SPS is a primary regulator of the Suc synthesis rate in leaves and some Suc-storing, heterotrophic organs, but its activity has not been previously correlated with cellulose synthesis. Two systems analyzed, cultured mesophyll cells of Zinnia elegans L. var. Envy and etiolated hypocotyls of kidney beans (Phaseolus vulgaris), contained differentiating tracheary elements. Cotton (Gossypium hirsutum L. cv Acala SJ-1) fibers were also analyzed during primary and secondary wall synthesis. SPS activity rose in all three systems during periods of maximum cellulose deposition within secondary walls. The Z. elegans culture system was manipulated to establish a tight linkage between the timing of tracheary element differentiation and rising SPS activity and to show that SPS activity did not depend on the availability of starch for degradation. The significance of these findings in regard to directing metabolic flux toward cellulose will be discussed.


1 This work was supported by the Howard Hughes Medical Institute (through the Undergraduate Biological Sciences Education Program), by the Texas Advanced Research Program (grant no. 003644-095), and by Cotton Incorporated (Raleigh, NC).

* Corresponding author; e-mail candace.haigler{at}ttu.edu; fax 806-742-2963.

© 2001 American Society of Plant Physiologists



This article has been cited by other articles:


Home page
Crop Sci.Home page
S. Wang, G.-H. Zhao, Y.-H. Jia, and X.-M. Du
Cloning and Characterization of a CAP Gene Expressed in Gossypium arboreum Fuzzless Mutant
Crop Sci., November 24, 2008; 48(6): 2314 - 2320.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
T. Suzuki, K. Masaoka, M. Nishi, K. Nakamura, and S. Ishiguro
Identification of kaonashi Mutants Showing Abnormal Pollen Exine Structure in Arabidopsis thaliana
Plant Cell Physiol., October 1, 2008; 49(10): 1465 - 1477.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
A. C. Cumino, C. Marcozzi, R. Barreiro, and G. L. Salerno
Carbon Cycling in Anabaena sp. PCC 7120. Sucrose Synthesis in the Heterocysts and Possible Role in Nitrogen Fixation
Plant Physiology, March 1, 2007; 143(3): 1385 - 1397.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
N. Nakagawa and N. Sakurai
A Mutation in At-nMat1a, Which Encodes a Nuclear Gene Having High Similarity to Group II Intron Maturase, Causes Impaired Splicing of Mitochondrial NAD4 Transcript and Altered Carbon Metabolism in Arabidopsis thaliana
Plant Cell Physiol., June 1, 2006; 47(6): 772 - 783.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
H. Aspeborg, J. Schrader, P. M. Coutinho, M. Stam, A. Kallas, S. Djerbi, P. Nilsson, S. Denman, B. Amini, F. Sterky, et al.
Carbohydrate-Active Enzymes Involved in the Secondary Cell Wall Biogenesis in Hybrid Aspen
Plant Physiology, March 1, 2005; 137(3): 983 - 997.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 2001 by the American Society of Plant Biologists