Phytotoxicity, uptake and metabolism of 1,4-dichlorobenzene by plant cells

1996 ◽  
Vol 15 (7) ◽  
pp. 1109-1114
Author(s):  
Kevin C. Jones ◽  
Min-Jian Wang ◽  
Maria Bokern ◽  
Christian Boehme ◽  
Hans Harms
Keyword(s):  
Plant Cells ◽  
Uptake And Metabolism

Parameters for growth measurement in suspension cultures of plant cells

1974 ◽  
Vol 52 (4) ◽  
pp. 903-912 ◽  
Author(s):  
Dyson Rose ◽  
S. M. Martin
Keyword(s):  
Stationary Phases ◽  
Plant Cells ◽  
Growth Period ◽  
Dry Weight ◽  
High Rate ◽  
Growth Phases ◽  
Batch Cultures ◽  
Growth Measurement ◽  
Large Increments ◽  
Uptake And Metabolism

Well-adapted cells, which had been initiated from root tissue of Ipomoea and of Daucus carota, were grown in 7.5-liter stirred-jar fermenters, and both the cells and media were analyzed for major components at intervals during the growth period. Controlled variables included the size of inoculum, the amount of sucrose, and the source and amount of nitrogen in the media.The data obtained indicate that there are two distinct growth phases in the development of batch cultures of these cell lines. The first, which we term "cytoplasmic growth phase," begins immediately upon addition of inoculum to fresh medium and is characterized by a high rate of nitrogen uptake and metabolism relative to the increase in cell dry weight. The second, or "maturation phase," is characterized by large increments in dry weight and total cell carbohydrate relative to the increments in cell nitrogen. It is suggested that the classical lag, log, and stationary phases of bacterial growth could apply only to the early hours of cytoplasmic growth, if indeed they are relevant at all.

PHYTOTOXICITY, UPTAKE AND METABOLISM OF 1,4-DICHLOROBENZENE BY PLANT CELLS

1996 ◽  
Vol 15 (7) ◽  
pp. 1109 ◽  
Author(s):  
Min-Jian Wang ◽  
Maria Bokern ◽  
Christian Boehme ◽  
Kevin C. Jones ◽  
Hans Harms
Keyword(s):  
Plant Cells ◽  
Uptake And Metabolism

SEM study of the morphological effects of kinetin and zeatin on the growth and development of the apical meristem in wheat

1995 ◽  
Vol 53 ◽  
pp. 978-979
Author(s):  
G. M. Hutchins ◽  
J. S. Gardner
Keyword(s):  
Growth And Development ◽  
Furfuryl Alcohol ◽  
Apical Meristem ◽  
Plant Cells ◽  
Triticum Aestivum L ◽  
Morphological Development ◽  
Naturally Occurring ◽  
Chinese Spring Wheat ◽  
Sem Study ◽  
Moist Environment

Cytokinins are plant hormones that play a large and incompletely understood role in the life-cycle of plants. The goal of this study was to determine what roles cytokinins play in the morphological development of wheat. To achieve any real success in altering the development and growth of wheat, the cytokinins must be applied directly to the apical meristem, or spike of the plant. It is in this region that the plant cells are actively undergoing mitosis. Kinetin and Zeatin were the two cytokinins chosen for this experiment. Kinetin is an artificial hormone that was originally extracted from old or heated DNA. Kinetin is easily made from the reaction of adenine and furfuryl alcohol. Zeatin is a naturally occurring hormone found in corn, wheat, and many other plants.Chinese Spring Wheat (Triticum aestivum L.) was used for this experiment. Prior to planting, the seeds were germinated in a moist environment for 72 hours.

Confocal microscopy of the cytoskeleton in living plant cells following microinjection of fluorescent probes

1993 ◽  
Vol 51 ◽  
pp. 130-131
Author(s):  
Ann Cleary
Keyword(s):  
Cell Division ◽  
Fluorescent Probes ◽  
Actin Filaments ◽  
Intracellular Transport ◽  
Cell Structure ◽  
Plant Cells ◽  
Cell Plate ◽  
Cell Cortex ◽  
Living Plant ◽  
Rhodamine Phalloidin

Microinjection of fluorescent probes into living plant cells reveals new aspects of cell structure and function. Microtubules and actin filaments are dynamic components of the cytoskeleton and are involved in cell growth, division and intracellular transport. To date, cytoskeletal probes used in microinjection studies have included rhodamine-phalloidin for labelling actin filaments and fluorescently labelled animal tubulin for incorporation into microtubules. From a recent study of Tradescantia stamen hair cells it appears that actin may have a role in defining the plane of cell division. Unlike microtubules, actin is present in the cell cortex and delimits the division site throughout mitosis. Herein, I shall describe actin, its arrangement and putative role in cell plate placement, in another material, living cells of Tradescantia leaf epidermis.The epidermis is peeled from the abaxial surface of young leaves usually without disruption to cytoplasmic streaming or cell division. The peel is stuck to the base of a well slide using 0.1% polyethylenimine and bathed in a solution of 1% mannitol +/− 1 mM probenecid.

Scanning electron microscopy of plant cells using a variable-pressure SEM and cryogenic techniques

1993 ◽  
Vol 51 ◽  
pp. 260-261
Author(s):  
M. Yamada ◽  
K. Ueda ◽  
K. Kuboki ◽  
H. Matsushima ◽  
S. Joens
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Saturated Vapor ◽  
Plant Cells ◽  
Variable Pressure ◽  
Specimen Preparation ◽  
Operating Pressure ◽  
Vapor Pressures ◽  
Low Temperature Microscopy ◽  
Scanning Electron

Use of variable Pressure SEMs is spreading among electron microscopists The variable Pressure SEM does not necessarily require specimen Preparation such as fixation, dehydration, coating, etc which have been required for conventional scanning electron microscopy. The variable Pressure SEM allows operating Pressure of 1˜270 Pa in specimen chamber It does not allow microscopy of water-containing specimens under a saturated vapor Pressure of water. Therefore, it may cause shrink or deformation of water-containing soft specimens such as plant cells due to evaporation of water. A solution to this Problem is to lower the specimen temperature and maintain saturated vapor Pressures of water at low as shown in Fig. 1 On this technique, there is a Published report of experiment to have sufficient signal to noise ratio for scondary electron imaging at a relatively long working distance using an environmental SEM. We report here a new low temperature microscopy of soft Plant cells using a variable Pressure SEM (Hitachi S-225ON).

Efficient initiation of translation at non-AUG triplets in plant cells.

1992 ◽  
Vol 2 (5) ◽  
pp. 809-813 ◽  
Author(s):  
K Gordon ◽  
J Futterer ◽  
T Hohn
Keyword(s):  
Plant Cells ◽  
Initiation Of Translation

Enrichment of vitronectin- and fibronectin-like proteins in NaCI-adapted plant cells and evidence for their involvement in plasma membrane-cell wall adhesion

1993 ◽  
Vol 3 (5) ◽  
pp. 637-646 ◽  
Author(s):  
Jian-Kang Zhu ◽  
Jun Shi ◽  
Utpal Singh ◽  
Sarah E. Wyatt ◽  
Ray A. Bressan ◽  
...  
Keyword(s):  
Cell Wall ◽  
Plasma Membrane ◽  
Plant Cells ◽  
Membrane Cell

Introduction of foreign DNA into walled plant cells via liposomes injected into the vacuole: a preliminary study

1990 ◽  
Vol 79 (1) ◽  
pp. 184-189
Author(s):  
W. J. Lucas ◽  
A. Lansing ◽  
J. R. de Wet ◽  
V. Walbot
Keyword(s):  
Plant Cells ◽  
Preliminary Study ◽  
Foreign Dna

Multi-walled Carbon Nanotubes Penetrate into Plant Cells and Affect the Growth of Onobrychis arenaria Seedlings

Acta Naturae ◽  
2011 ◽  
Vol 3 (1) ◽  
pp. 99-106 ◽  
Author(s):  
E A Smirnova ◽  
A A Gusev ◽  
O N Zaitseva ◽  
E M Lazareva ◽  
G E Onishchenko ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Plant Cells ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes
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