Online citations, reference lists, and bibliographies.
← Back to Search

Ethylene Biosynthesis During Aerenchyma Formation In Roots Of Maize Subjected To Mechanical Impedance And Hypoxia

C. He, S. Finlayson, M. Drew, Wayne R. Jordan, P. W. Morgan
Published 1996 · Biology, Medicine

Save to my Library
Download PDF
Analyze on Scholarcy
Share
Germinated maize (Zea mays L.) seedlings were enclosed in modified triaxial cells in an artificial substrate and exposed to oxygen deficiency stress (4% oxygen, hypoxia) or to mechanical resistance to elongation growth (mechanical impedance) achieved by external pressure on the artificial substrate, or to both hypoxia and impedance simultaneously. Compared with controls, seedlings that received either hypoxia or mechanical impedance exhibited increased rates of ethylene evolution, greater activities of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase, ACC oxidase, and cellulase, and more cell death and aerenchyma formation in the root cortex. Effects of hypoxia plus mechanical impedance were strongly synergistic on ethylene evolution and ACC synthase activity; cellulase activity, ACC oxidase activity, or aerenchyma formation did not exhibit this synergism. In addition, the lag between the onset of stress and increases in both ACC synthase activity and ethylene production was shortened by 2 to 3 h when mechanical impedance or impedance plus hypoxia was applied compared with hypoxia alone. The synergistic effects of hypoxia and mechanical impedance and the earlier responses to mechanical impedance than to hypoxia suggest that different mechanisms are involved in the promotive effects of these stresses on maize root ethylene biosynthesis.
This paper references
Ethylene in relation to 266 - 271 97 : 19 - 25 861 - 865 the response of roots to physical impedance
SJ Kays (1974)
10.1139/B88-294
The effect of mechanical impedance on ethylene production by maize roots
M. Whalen (1988)
A simple and sensitive assay for 1aminocyclopropane1carboxylic acid
JA DeGreef (1979)
10.1104/PP.97.1.19
Elicitor-induced ethylene biosynthesis in tomato cells: characterization and use as a bioassay for elicitor action.
G. Felix (1991)
10.1016/0031-9422(91)85241-Q
Complete recovery in vitro of ethylene-forming enzyme activity
P. Ververidis (1991)
10.1071/SR9850577
The effect of soil strength on germination and emergence of wheat (Triticum aestivum L. ) I
N. Collis-george (1985)
10.1073/PNAS.88.16.7021
Two genes encoding 1-aminocyclopropane-1-carboxylate synthase in zucchini (Cucurbita pepo) are clustered and similar but differentially regulated.
P. Huang (1991)
10.1104/pp.106.2.529
The Apparent Turnover of 1-Aminocyclopropane-1-Carboxylate Synthase in Tomato Cells Is Regulated by Protein Phosphorylation and Dephosphorylation
P. Spanu (1994)
10.1104/PP.93.4.1482
Inactivation of stress induced 1-aminocyclopropane carboxylate synthase in vivo differs from substrate-dependent inactivation in vitro.
P. Spanu (1990)
10.1111/J.1399-3054.1982.TB06313.X
Ethylene‐promoted formation of aerenchyma in seedling roots of Zea mays L. under aerated and non‐aerated conditions
H. Konings (1982)
10.1073/PNAS.92.5.1595
A mechanical strain-induced 1-aminocyclopropane-1-carboxylic acid synthase gene.
J. Botella (1995)
10.1046/J.1365-313X.1995.7040589.X
Characterization of a maize G-box binding factor that is induced by hypoxia.
N. de Vetten (1995)
10.1016/0003-2697(79)90123-4
A simple and sensitive assay for 1-aminocyclopropane-1-carboxylic acid.
M. C. Lizada (1979)
10.1016/S0176-1617(11)80456-6
Differential accumulation of transcripts of 1-aminocyclopropane-1-carboxylate synthase genes in tomato plants infected with Phytophthora infestans and in elicitor-treated tomato cell suspensions
P. Spanu (1993)
10.1111/J.1399-3054.1978.TB01543.X
Kinetic measurements of small ethylene changes in an open system designed for plant physiological studies
J. A. Greef (1978)
10.1104/PP.98.4.1342
Metabolism of 1-Aminocyclopropane-1-Carboxylic Acid in Etiolated Maize Seedlings Grown under Mechanical Impedance.
J. Sarquís (1992)
10.1104/pp.112.2.463
Transduction of an Ethylene Signal Is Required for Cell Death and Lysis in the Root Cortex of Maize during Aerenchyma Formation Induced by Hypoxia
C. He (1996)
10.1111/J.1399-3054.1988.TB06616.X
The influence of oxygen deficiency on ethylene synthesis, 1‐aminocyclopropane‐1‐carboxylic acid levels and aerenchyma formation in roots of Zea mays
B. Atwell (1988)
10.1104/pp.105.3.861
Induction of Enzymes Associated with Lysigenous Aerenchyma Formation in Roots of Zea mays during Hypoxia or Nitrogen Starvation
C. He (1994)
10.1111/J.1399-3054.1980.TB02661.X
Formation of aerenchyma in roots of Zea mays in aerated solutions, and its relation to nutrient supply
H. Konings (1980)
10.1111/J.1365-3040.1996.TB02064.X
Enhanced ethylene production by primary roots of Zea mays L. in response to sub-ambient partial pressures of oxygen
R. W. Brailsford (1992)
10.1104/pp.109.4.1435
Increased 1-Aminocyclopropane-1-Carboxylic Acid Oxidase Activity in Shoots of Flooded Tomato Plants Raises Ethylene Production to Physiologically Active Levels
P. English (1995)
10.1104/PP.91.1.266
Decreased Ethylene Biosynthesis, and Induction of Aerenchyma, by Nitrogen- or Phosphate-Starvation in Adventitious Roots of Zea mays L.
M. Drew (1989)
10.1104/PP.98.1.137
Enhanced Sensitivity to Ethylene in Nitrogen- or Phosphate-Starved Roots of Zea mays L. during Aerenchyma Formation.
C. He (1992)
10.1104/PP.96.4.1171
Ethylene Evolution from Maize (Zea mays L.) Seedling Roots and Shoots in Response to Mechanical Impedance.
J. Sarquís (1991)
10.1104/PP.94.4.1616
Does water deficit stress promote ethylene synthesis by intact plants?
P. W. Morgan (1990)
Ethylene in relation to 266271 97 : 19 - 25 861865 the response of roots to physical impedance
SJ Kays (1974)



This paper is referenced by
10.1046/J.1469-8137.2003.00907.X
Aerenchyma formation: Tansley review
D. Evans (2003)
Gas exchange in young plants of... GAS EXCHANGE IN YOUNG PLANTS OF Tabebuia aurea (Bignoniaceae Juss.) SUBJECTED TO FLOODING STRESS1
A. Oliveira (2016)
10.3389/fpls.2015.00497
Development of schizogenous intercellular spaces in plants
K. Ishizaki (2015)
10.1104/pp.107.115519
Genetic Dissection of Hormonal Responses in the Roots of Arabidopsis Grown under Continuous Mechanical Impedance1[W][OA]
T. Okamoto (2008)
10.1093/aobpla/plu043
Role of ethylene signalling in the formation of constitutive aerenchyma in primary roots of rice
Kenta Yukiyoshi (2014)
10.1111/ppl.12076
Hypoxia and bicarbonate could limit the expression of iron acquisition genes in Strategy I plants by affecting ethylene synthesis and signaling in different ways.
M. J. Garcia (2014)
10.1046/J.1365-3040.2001.00774.X
Rapid changes in cell wall pectic polysaccharides are closely associated with early stages of aerenchyma formation, a spatially localized form of programmed cell death in roots of maize ( Zea mays L.) promoted by ethylene
A. Gunawardena (2001)
10.1146/annurev.arplant.59.032607.092752
Flooding stress: acclimations and genetic diversity.
J. Bailey-Serres (2008)
10.1007/s11104-017-3533-1
Functional implications of root cortical senescence for soil resource capture
Hannah M. Schneider (2017)
10.1007/1-4020-4099-7_10
Acclimation to soil flooding - sensing and signal-transduction
E. Visser (2005)
10.1007/S11270-011-0772-2
Root Porosity Changes in Salix nigra Cuttings in Response to Copper and Ultraviolet-B Radiation Exposure
D. Baud (2011)
10.1590/S0100-84042007000100013
Respostas morfológicas em Guibourtia hymenifolia (Moric.) J. Leonard (Fabaceae) e Genipa americana L. (Rubiaceae), submetidas ao estresse por deficiência nutricional e alagamento do substrato
E. F. Santiago (2007)
10.1590/0102-33062014ABB0035
Anatomical and morphological modifications in response to flooding by six Cerrado tree species
Adilson Serafim de Oliveira (2015)
10.1007/s00468-012-0827-z
Antioxidative responses and morpho-anatomical adaptations to waterlogging in Sesbania virgata
J. D. Alves (2012)
10.1007/978-3-662-09784-7_6
Root Growth and Function in Relation to Soil Structure, Composition, and Strength
A. Bengough (2003)
Study of aerenchyma formation in maize roots under waterlogged conditions
I. Rajhi (2011)
10.1105/tpc.112.101790
Emerging Roots Alter Epidermal Cell Fate through Mechanical and Reactive Oxygen Species Signaling[C][W]
B. Steffens (2012)
10.1104/PP.121.2.429
Arabidopsis alcohol dehydrogenase expression in both shoots and roots is conditioned by root growth environment.
H. Chung (1999)
10.1139/B09-041
Ethylene and programmed cell death in plants
Christopher P. Trobacher (2009)
10.1186/1939-8433-5-2
Mechanisms for coping with submergence and waterlogging in rice
S. Nishiuchi (2011)
Regulation of the development of constitutive aerenchyma in Juncus effusus.
Hanneke van Leur (2000)
10.1111/pce.13061
Nitric oxide is essential for the development of aerenchyma in wheat roots under hypoxic stress.
Aakanksha Wany (2017)
10.1007/s11032-010-9532-z
Construction of intraspecific linkage maps, detection of a chromosome inversion, and mapping of QTL for constitutive root aerenchyma formation in the teosinte Zea nicaraguensis
Y. Mano (2010)
10.3389/fpls.2020.00696
Hydrogen Sulfide Alleviates Waterlogging-Induced Damage in Peach Seedlings via Enhancing Antioxidative System and Inhibiting Ethylene Synthesis
Yuansong Xiao (2020)
10.1079/9781845939953.0148
Flooding tolerance in plants
C. Pucciariello (2012)
10.1007/978-3-662-09784-7_8
Physiology, Biochemistry and Molecular Biology of Plant Root Systems Subjected to Flooding of the Soil
M. B. Jackson (2003)
10.1007/s11103-014-0227-4
Ectopic expression of CaRLK1 enhances hypoxia tolerance with increasing alanine production in Nicotiana spp.
D. J. Lee (2014)
10.1094/MPMI-21-1-0098
Maize 9-lipoxygenase ZmLOX3 controls development, root-specific expression of defense genes, and resistance to root-knot nematodes.
Xiquan Gao (2008)
10.1007/978-1-4939-2211-6_9
Small and Large G Proteins in Biotic and Abiotic Stress Responses in Plants
A. Pandey (2015)
10.5897/JSSEM11.152
Root and leaf changes in Salix nigra cuttings in response to increasing soil temperature
Donald R. Baud (2012)
10.1034/J.1399-3054.2000.110105.X
ACC oxidase is found in seedlings of two (Coniferales, Gnetales) of the four gymnosperm orders
E. Reynolds (2000)
10.1007/s10059-010-0086-z
Inhibition of biphasic ethylene production enhances tolerance to abiotic stress by reducing the accumulation of reactive oxygen species in Nicotiana tabacum
Soo Jin Wi (2010)
See more
Semantic Scholar Logo Some data provided by SemanticScholar