The kinetic behavior of a typical Hill reaction catalyzed by thylakoids and using the oxidized form of 2,6-dichloroindophenol (DCPIPox) as the artificial clectron acceptor, is considered. Here, the light absorption process and the reduction of DCPlPox are autocatalytically coupled, leading to the occurrence of rnultiplc steady states with respect to either the acceptor concentration or the incident light intensity. Experimental evidence is prescntcd for both cases and the emergence of autocatalysis is discussed. The effect of the spatial arrangment on the global behavior of the system described is emphasized.Biocatalytic reactions have bcen studied almost enlerely from the viewpoint of their time-dependent behavior. Rcccntly, a more relevant and realistic approach has consisted of coupling purely catalytic functions with various phenomena intrinsically linked to space, such as diffusion, partition of metabolites, vectorial processes and convection. When autocatalytic reactions are considered, qualitatively different behavior of the system has been predicted theoretically, for example multistability and/or spatiotcniporal structure formation [I]. Experimental evidence of multistability for either ki nctic or electrochemical memory in diffusion-reaction coupled and reconstitutcd enzyme systems has been reported [2 -51. Nevertheless, in the framework of this spatiotemporal concept, littlc attention has been paid to radiation phenomena which, likc diffusion. are also essentially space-dependent and whose role is fundamental in numerous chemical and biochemical processes. A thorough theoretical analysis considcring a simple photodependent isomerization reaction in which one of the isomers absorbs light and restores this energy to the system in the form of heat, was published by Nitzan et al. 16, 71. Here, the light absorption process and the increase of the system's temperature become autocatalytically coupled, leading to the occurrence of multiple steady states and hysteresis. The latter predictions have been experimentally confirmed in the case of the N 0 2 / N 2 0 4 dissociation reaction [8] and more recently in the S03F/S206F2 system [9]. As far as we are aware, no experimental examination of the phenomena pertaining the biological photoreactions has been yet attemped.In the present work, chloroplast thylakoids are immobilized [lo-121 in an artificial membrane lying on the bottom of a reactor fed with DCPIPox as the electron acceptor. The DCPl Pox species adsorbs strongly within the range of illumi- Ahhrc~viutions. DCPIPox, oxidized form of the 2,6-dichloroindophenol. nation wavelengths. Under such conditions we show that thc association between the purely photoassisted reduction of the DCPIPox, and its absorption by light intensity in the range of 600 -800 nm, leads to the appearance of an autocatalytic effect in the rate of reaction. More precisely, the yield of the photoreaction first increases and then decreases. as the DCPIPox concentration increases. The coupling of this nonlinear reaction term with a tra...