Metabolites involved in plant movement and ‘memory’: nyctinasty of legumes and trap movement in the Venus flytrap

2006 ◽  
Vol 23 (4) ◽  
pp. 548-557 ◽  
Author(s):  
Minoru Ueda ◽  
Yoko Nakamura
Keyword(s):  
2007 ◽  
Vol 79 (4) ◽  
pp. 519-527 ◽  
Author(s):  
Minoru Ueda ◽  
Yoko Nakamura ◽  
Masahiro Okada

The bioorganic basis of plant movement in two plant systems is described in this article: the circadian rhythmic leaf movement known as nyctinasty and trap movement in the Venus flytrap. The bioactive substances responsible for plant movement, the chemical mechanism of the rhythm, and studies on the key protein controlling nyctinasty are presented.The nyctinastic leaf movement is induced by a pair of leaf-movement factors, and one of each pair is a glucoside. There are two key proteins that are involved in the control of nyctinasty. One is β-glucosidase: a biological clock regulates the activity of β-glucosidase, which deactivates the glucoside-type leaf-movement factor, controlling the balance in the concentrations of the leaf-closing and -opening factors. The other is the specific receptor for each leaf-movement factor: the genuine target cell for each leaf-movement factor is confirmed to be a motor cell from leaflet pulvini, and the specific receptors that regulate the turgor of motor cells are localized in the membrane fraction. The article also discusses the isolation of the "memory" substance from the Venus flytrap and presents a mechanism for this action.


2020 ◽  
Vol 117 (27) ◽  
pp. 16035-16042 ◽  
Author(s):  
Renate Sachse ◽  
Anna Westermeier ◽  
Max Mylo ◽  
Joey Nadasdi ◽  
Manfred Bischoff ◽  
...  

The mechanical principles for fast snapping in the iconic Venus flytrap are not yet fully understood. In this study, we obtained time-resolved strain distributions via three-dimensional digital image correlation (DIC) for the outer and inner trap-lobe surfaces throughout the closing motion. In combination with finite element models, the various possible contributions of the trap tissue layers were investigated with respect to the trap’s movement behavior and the amount of strain required for snapping. Supported by in vivo experiments, we show that full trap turgescence is a mechanical–physiological prerequisite for successful (fast and geometrically correct) snapping, driven by differential tissue changes (swelling, shrinking, or no contribution). These are probably the result of the previous accumulation of internal hydrostatic pressure (prestress), which is released after trap triggering. Our research leads to an in-depth mechanical understanding of a complex plant movement incorporating various actuation principles.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anne Fabricant ◽  
Geoffrey Z. Iwata ◽  
Sönke Scherzer ◽  
Lykourgos Bougas ◽  
Katharina Rolfs ◽  
...  

AbstractUpon stimulation, plants elicit electrical signals that can travel within a cellular network analogous to the animal nervous system. It is well-known that in the human brain, voltage changes in certain regions result from concerted electrical activity which, in the form of action potentials (APs), travels within nerve-cell arrays. Electro- and magnetophysiological techniques like electroencephalography, magnetoencephalography, and magnetic resonance imaging are used to record this activity and to diagnose disorders. Here we demonstrate that APs in a multicellular plant system produce measurable magnetic fields. Using atomic optically pumped magnetometers, biomagnetism associated with electrical activity in the carnivorous Venus flytrap, Dionaea muscipula, was recorded. Action potentials were induced by heat stimulation and detected both electrically and magnetically. Furthermore, the thermal properties of ion channels underlying the AP were studied. Beyond proof of principle, our findings pave the way to understanding the molecular basis of biomagnetism in living plants. In the future, magnetometry may be used to study long-distance electrical signaling in a variety of plant species, and to develop noninvasive diagnostics of plant stress and disease.


Science ◽  
1961 ◽  
Vol 133 (3456) ◽  
pp. 878-879 ◽  
Author(s):  
J. R. Di Palma ◽  
R. Mohl ◽  
W. Best

PLoS ONE ◽  
2015 ◽  
Vol 10 (4) ◽  
pp. e0123887 ◽  
Author(s):  
Michael Krogh Jensen ◽  
Josef Korbinian Vogt ◽  
Simon Bressendorff ◽  
Andaine Seguin-Orlando ◽  
Morten Petersen ◽  
...  

2009 ◽  
Vol 9 (1) ◽  
pp. 67 ◽  
Author(s):  
Jianhua Cao ◽  
Siluo Huang ◽  
Ji Qian ◽  
Jinlin Huang ◽  
Li Jin ◽  
...  

Plant Biology ◽  
2017 ◽  
Vol 19 (6) ◽  
pp. 886-895 ◽  
Author(s):  
J. Kruse ◽  
P. Gao ◽  
M. Eibelmeier ◽  
S. Alfarraj ◽  
H. Rennenberg

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