Merope Tsimilli-Michael

Photosynthetica covers wide range of photosynthesis research or research including photosynthetic parameters of both experimental and theoretical nature.

Photosynthetica covers wide range of photosynthesis research or research including photosynthetic parameters of both experimental and theoretical nature.

In this article, related to a talk given at the International Meeting “Photosynthesis Research for Sustainability — 2015”, we honor Dr. George C. Papageorgiou a highly respected scientist and an outstanding teacher and mentor. Praising him for these virtues, indispensable for research sustainability, we also bring to discussion aspects that undermine nowadays both education and research sustainability. We argue that these aspects are principally created by the predominant bureaucratic system, which, by favoring short-term utilitarian orientations and obeying “market laws”, jeopardizes university freedom and autonomy, and has turned to “measuring” scientific “production” and establishing accordingly designed funding policies and hiring/firing/promotion criteria, which lead to merit-chasing, grant-hunting, changes in publication practice, and suppression of heterodox ideas. Such system impedes research, creates antagonism, and drives the potentially creative researcher away from originality and discovery, and from the unique satisfaction and benefit that these bring.

Several models have been proposed for the energetic behavior of the photosynthetic apparatus and a variety of experimental techniques are nowadays available to determine parameters that can quantify this behavior. The Energy Flux Theory (EFT) developed by Strasser 35 years ago provides a straightforward way to formulate any possible energetic communication between any complex arrangement of interconnected pigment systems and any energy transduction by these systems. We here revisit the EFT, starting from the basic general definitions and equations and presenting applications in formulating the energy distribution in photosystem (PS) II units with variable connectivity, as originally derived, where certain simplifications were adopted. We then proceed to the derivation of equations for a PSII model of higher complexity, which corresponds, from the formalistic point of view, to the later formulated and now broadly accepted exciton–radical-pair model. We also compare the formulations derived with the EFT with those obtained, by different approaches, in the classic papers on energetic connectivity. Moreover, we apply the EFT for the evaluation of the excitation energy distribution between PSII and PSI and the distinction between state transitions and PSII to PSI excitation energy migration. Our analysis demonstrates that the EFT is a powerful approach for the formulation of any possible model, at any complexity level, even of models that may be proposed in the future, with the advantage that any possible energetic communication or energy transduction can be easily formulated mathematically by trivial algebraic equations. Moreover, the biophysical parameters introduced by the EFT and applicable for any possible model can be linked with obtainable experimental signals, provided that the theoretical resolution of the model does not go beyond the experimental resolution.

We investigated the dark-to-light transition in Synechococcus sp. PCC 7942 cells by a detailed analysis of fluorescence transients induced by strong red light. The transients, recorded with high data-acquisition, revealed all the steps of the fast (OJIP; 10⁻⁵–1 s) and slow phase (PSM(T); 1–10³ s), kinetically distinguished with precision. Focusing on the OJIP-rise, we show, for the first time, how the variable to initial fluorescence ratio and the relative height of J-level can serve as indexes of the plastoquinone redox poise and the established state in the dark; hence, differences among cyanobacteria can be recognised in a simple way. Applying intermittent illumination (20-s light pulses separated by 10-s dark intervals) to induce dark-to-light transition and analysing the individual transients, we establish a method by which we determine the fluorescence component not originating from photosystem (PS) II and we assess PSII dynamics during state 2 to state 1 transition. The development of photochemical and non-photochemical quenching is also discussed, as well as evidences favouring the mobile antenna model.