Molecular Electronics of the Dionaea muscipula trap

Abstract

Transmission of electrical charge between a lobe and the midrib causes closure of the trap and induces an electrical signal propagating between a lobe and a midrib. The Venus flytrap can accumulate small subthreshold charges, and when the threshold value is reached, the trap closes. The cumulative character of electrical stimuli points to the existence of short-term electrical memory in the Venus flytrap. We investigated the electrical properties of the upper leaf of the Venus flytrap and proposed the equivalent electrical circuit in agreement with the experimental data.

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Signaling and memory play fundamental roles in plant responses.1–9 The existence of different forms of plant memory is well known.7 Depending on the duration of memory retention, there are three types of memory in plants: sensory memory, short term memory and long term memory.2,7,10 Learning and memory, usually associated with brain or neuronal activity, have been observed recently in the amoeba Physarum polycephalum, a unicellular organism.11 It is well-established that cells receive, interpret and adjust to environment.4,10,12,13 Plants are intelligent organisms and capable of functions such as learning, plasticity and memory.10 Some plants exhibit clues of an electrical memory as well.1,2,7

We found that Venus flytrap has a short term electrical memory.1,2,7 Rapid closure of the carnivorous plant Dionaea muscipula Ellis (Venus flytrap) has been attracting the attention of researchers and as a result its mechanism has been widely investigated. When an insect touches the trigger hairs, these mechanosensors generate an electrical signal that acts as an action potential, which activates the trap closing.

The reason why plants have developed pathways for electrical signal transmission most probably lies in the necessity to respond rapidly to environmental stress factors. Different environmental stimuli evoke specific responses in living cells, which have the capacity to transmit a signal to the responding region. In contrast to chemical signals such as hormones, electrical signals are able to rapidly transmit information over long distances with speed up to 270 m/s.14 Electrical potentials have been measured at the tissue and whole plant levels.4 In terms of electrophysiology, Venus flytrap responses can be considered in three stages: (i) stimulus perception, (ii) signal transmission and (iii) induction of response (Fig. 1).

Recently, we investigated the biologically closed electrical circuits in the upper leaf of the Venus flytrap and proposed the equivalent electrical circuit of the trap (Fig. 1, Box 2).1 It is often convenient to represent the real electrical and electrochemical properties of biointerfaces with idealized equivalent electrical circuit models consisting of discrete electrical components.

Using the charge injection method,2 it was evident that the application of an electrical stimulus between the midrib (positive potential) and a lobe (negative potential) causes Venus flytrap to close the trap without any mechanical stimulation. Application of a single 14 µC electrical charge from a capacitor causes trap closure and induces an electrical signal propagating between the lobes and the midrib. The Venus flytrap can accumulate and sum small charges, and when the threshold value is reached, the trap closes. A summation of stimuli is demonstrated through the repetitive application of smaller charges. The capacitor discharges exponentially with time, so although a 14 µC charge was applied, not all of this charge was accumulated to assist in closing the trap. As soon as 9.01 µC charge is transmitted between a lobe and midrib from the capacitor, the trap begins to close at room temperature. It was shown that voltage-gated ion channels have a time-dependent “molecular” memory phenomenon with profound implication on the biophysical properties of voltage-gated ion channels.15

Biologically closed electrical circuits operate over large distances in biological tissues. The activation of such circuit can lead to various physiological and biophysical responses. Action potentials play an important role in triggering photosynthetic responses in plants.16–20 The equivalent electrical circuit of photosynthesis is shown on Figure 1 (Box 3).

It is common knowledge that the leaves of the Venus flytrap actively employ turgor pressure and hydrodynamic flow for fast movement and catching insects. In these processes the upper and lower surfaces of the leaf behave quite differently. During the trap closing, the loss of turgor by parenchyma lying beneath the upper epidermis, accompanied by the active expansion of the tissues of the lower layers of parenchyma near the under epidermis, closes the trap. The cells on the inner face of the trap jettison their cargo of water, shrink and allow the trap lobe to fold over. The cells of the lower epidermis expand rapidly, folding the trap lobe over. These anatomical features constitute the basis of the new hydroelastic curvature model.21

There are many different biologically closed electrical circuits in plants (Fig. 1): photosynthetic electrical circuits (Box 3), plasma membrane electrical circuits responsible for receptor, action and resting potentials (Box 1), the electrical starter of a hydroelastic trap closing in Dionaea muscipula Ellis (Box 2), and others.

Abbreviations

Cm	=	membrane capacitance
Rm	=	membrane resistance
PS	=	photosystem
PQ pool	=	plastoquinone pool
D	=	diode as a model of a voltage gated ion channel
S	=	electrical charge or voltage sensor
P	=	ATP dependent H+ pump

Figures and Tables

Figure 1 Biologically closed electrical circuits in Venus flytrap. Abbreviations: C_m, membrane capacitance; R_m, membrane resistance; PS, photosystem; PQ pool, plastoquinone pool; D, diode as a model of a voltage gated ion channel; S, electrical charge or voltage sensor; P, ATP dependent H⁺ pump.

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