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ASGSB 2000 Annual Meeting Abstracts
[25]
CHANGES IN STATOCYTE STRUCTURE AND AMYLOPLAST STARCH IN ARABIDOPSIS THALIANA COLUMELLA CELLS AFTER GROWTH UNDER HYPERGRAVITY CONDITIONS. S.D. Hopkins1 and J.D. Smith2. 1Lockheed Martin Space Operations, Moffett Field CA, 2NASA Ames Research Center, Moffett Field CA.
The
purpose of this morphological study was to determine if amyloplast starch
content and size were reduced in Arabidopsis
root caps after growth in a hypergravity environment. During a past space
flight experiment it was shown that, in space and on a clinostat, statolith
mass in white clover (Trifolium repens) seedlings was dependent on the gravity environment; in an
under-stimulated environment (i. e. space
flight) it was shown that the volume of statocyte amyloplasts was increased
[Smith et. al., (1997) Plant J.
12:1361-1373]. With that in mind we propose the hypothesis that in an
over-stimulated environment (i. e.
hypergravity on a centrifuge) the statocyte amyloplast volume would decrease. Arabidopsis
seedlings were grown on vertical agar plates in an incubator at 25°C for
two days under constant illumination from fluorescent lights. After 48 hours
the fluorescent lights in the incubator were turned to the off position and
the experimental groups were taken to the NASA Ames 1 ft. diameter centrifuge
where they were subjected to either 2 g,
4 g or 8 g chronic
centrifugation at 25°C in total darkness. After 48 hours of exposure to
hypergravity the seedlings were chemically fixed, and the root caps were
excised and processed further for transmission electron microscopy. Negatives
of longitudinal root tip images were scanned and quantitative morphometrics
were completed using NIH Image. Initial observations have shown that the
overall root cap and the gross plant morphology remained unchanged by chronic
exposure to hypergravity. Preliminary morphometric analysis of columella cell
stories 2 and 3 for the 1 g and 8 g
samples showed no significant difference in amyloplast starch content;
however, the area fraction of amyloplast per cell was changed. Further
analysis is underway to substantiate these findings. Continuing
investi-gations will focus on vacuole, mitochondria and nucleus area fractions
as well as comparisons between cell story and statocyte development.
(This research was supported by NASA Ames Research Center.)
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