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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
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