Evidence of root zone hypoxia in Brassica rapa L. grown in microgravity

A series of experiments was conducted aboard the U.S. space shuttle and the Mir space station to evaluate microgravity-induced root zone hypoxia in rapid-cycling Brassica (Brassica rapa L.), using both root and foliar indicators of low-oxygen stress to the root zone. Root systems from two groups of...

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Veröffentlicht in:International journal of plant sciences 2001-03, Vol.162 (2), p.249-255
Hauptverfasser: Stout, S. C., Porterfield, D. M., Briarty, L. G., Kuang, A., Musgrave, M. E.
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container_end_page 255
container_issue 2
container_start_page 249
container_title International journal of plant sciences
container_volume 162
creator Stout, S. C.
Porterfield, D. M.
Briarty, L. G.
Kuang, A.
Musgrave, M. E.
description A series of experiments was conducted aboard the U.S. space shuttle and the Mir space station to evaluate microgravity-induced root zone hypoxia in rapid-cycling Brassica (Brassica rapa L.), using both root and foliar indicators of low-oxygen stress to the root zone. Root systems from two groups of plants 15 and 30 d after planting, grown in a phenolic foam nutrient delivery system on the shuttle (STS-87), were harvested and fixed for microscopy or frozen for enzyme assays immediately postflight or following a ground-based control. Activities of fermentative enzymes were measured as indicators of root zone hypoxia and metabolism. Following 16 d of microgravity, ADH (alcohol dehydrogenase) activity was increased in the spaceflight roots 47% and 475% in the 15-d-old and 30-d-old plants, respectively, relative to the ground control. Cytochemical localization showed ADH activity in only the root tips of the space-grown plants. Shoots from plants that were grown from seed in flight in a particulate medium on the Mir station were harvested at 13 d after planting and quick-frozen and stored in flight in a gaseous nitrogen freezer or chemically fixed in flight for subsequent microscopy. When compared to material from a high-fidelity ground control, concentrations of shoot sucrose and total soluble carbohydrate were significantly greater in the spaceflight treatment according to enzymatic carbohydrate analysis. Stereological analysis of micrographs of sections from leaf and cotyledon tissue fixed in flight and compared with ground controls indicated no changes in the volume of protoplast, cell wall, and intercellular space in parenchyma cells. Within the protoplasm, the volume occupied by starch was threefold higher in the spaceflight than in the ground control, with a concomitant decrease in vacuolar volume in the spaceflight treatment. Both induction of fermentative enzyme activity in roots and accumulation of carbohydrates in foliage have been repeatedly shown to occur in response to root zone oxygen deprivation. These results indicate that root zone hypoxia is a persistent challenge in spaceflight plant growth experiments and may be caused by microgravity-induced changes in fluid and gas distribution.
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Root systems from two groups of plants 15 and 30 d after planting, grown in a phenolic foam nutrient delivery system on the shuttle (STS-87), were harvested and fixed for microscopy or frozen for enzyme assays immediately postflight or following a ground-based control. Activities of fermentative enzymes were measured as indicators of root zone hypoxia and metabolism. Following 16 d of microgravity, ADH (alcohol dehydrogenase) activity was increased in the spaceflight roots 47% and 475% in the 15-d-old and 30-d-old plants, respectively, relative to the ground control. Cytochemical localization showed ADH activity in only the root tips of the space-grown plants. Shoots from plants that were grown from seed in flight in a particulate medium on the Mir station were harvested at 13 d after planting and quick-frozen and stored in flight in a gaseous nitrogen freezer or chemically fixed in flight for subsequent microscopy. When compared to material from a high-fidelity ground control, concentrations of shoot sucrose and total soluble carbohydrate were significantly greater in the spaceflight treatment according to enzymatic carbohydrate analysis. Stereological analysis of micrographs of sections from leaf and cotyledon tissue fixed in flight and compared with ground controls indicated no changes in the volume of protoplast, cell wall, and intercellular space in parenchyma cells. Within the protoplasm, the volume occupied by starch was threefold higher in the spaceflight than in the ground control, with a concomitant decrease in vacuolar volume in the spaceflight treatment. Both induction of fermentative enzyme activity in roots and accumulation of carbohydrates in foliage have been repeatedly shown to occur in response to root zone oxygen deprivation. These results indicate that root zone hypoxia is a persistent challenge in spaceflight plant growth experiments and may be caused by microgravity-induced changes in fluid and gas distribution.</abstract><cop>Legacy CDMS</cop><pub>The University of Chicago Press</pub><pmid>11725801</pmid><doi>10.1086/319585</doi><tpages>7</tpages></addata></record>
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subjects Alcohol Dehydrogenase - metabolism
Botany
Brassica - enzymology
Brassica - growth & development
Brassica - physiology
Brassica - ultrastructure
Carbohydrate Metabolism
Cell Hypoxia - physiology
Cell Wall
Cotyledon - growth & development
Cotyledon - physiology
Cotyledon - ultrastructure
Enzymes
Extracellular Space
Flowers & plants
Glucosephosphate Dehydrogenase - metabolism
Life Sciences (General)
Metabolism
Plant Leaves - growth & development
Plant Leaves - physiology
Plant Leaves - ultrastructure
Plant Roots - enzymology
Plant Roots - growth & development
Plant Roots - physiology
Plant Shoots - enzymology
Plant Shoots - growth & development
Plant Shoots - physiology
Protoplasts
Pyruvate Decarboxylase - metabolism
Space biology
Space Flight
Space life sciences
Weightlessness
title Evidence of root zone hypoxia in Brassica rapa L. grown in microgravity
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