Photosynthesis Photosynthesis refers to the biological process that photosynthetic cells use to synthesize organic compounds from inorganic starting materials using sunlight. What has been primarily implicated as exhibiting non-trivial quantum behaviors is the
light reaction stage of photosynthesis. In this stage, photons are absorbed by the membrane-bound
photosystems. Photosystems contain two major domains, the
light-harvesting complex (antennae) and the
reaction center. These antennae vary among organisms. For example, bacteria use circular aggregates of chlorophyll pigments, while plants use membrane-embedded protein and chlorophyll complexes. Regardless, photons are first captured by the antennae and passed on to the reaction-center complex. Various pigment-protein complexes, such as the
FMO complex in green sulfur bacteria, are responsible for transferring energy from antennae to reaction site. The photon-driven excitation of the reaction-center complex mediates the oxidation and the reduction of the primary electron acceptor, a component of the reaction-center complex. Much like the
electron transport chain of the mitochondria, a linear series of oxidations and reductions drives proton (H+) pumping across the thylakoid membrane, the development of a
proton motive force, and energetic coupling to the synthesis of
ATP. Previous understandings of electron-excitation transference (EET) from light-harvesting antennae to the reaction center have relied on the Förster theory of incoherent EET, postulating weak electron coupling between
chromophores and incoherent hopping from one to another. This theory has largely been disproven by
FT electron spectroscopy experiments that show electron absorption and transfer with an efficiency of above 99%, which cannot be explained by classical mechanical models. Instead, as early as 1938, scientists theorized that quantum coherence was the mechanism for excitation-energy transfer. Indeed, the structure and nature of the photosystem places it in the quantum realm, with EET ranging from the femto- to nanosecond scale, covering sub-nanometer to nanometer distances. The effects of quantum coherence on EET in photosynthesis are best understood through state and process coherence. State coherence refers to the extent of individual superpositions of ground and excited states for quantum entities, such as
excitons. Process coherence, on the other hand, refers to the degree of coupling between multiple quantum entities and their evolution as either dominated by unitary or dissipative parts, which compete with one another. Both of these types of coherence are implicated in photosynthetic EET, where a exciton is coherently delocalized over several chromophores. This delocalization allows for the system to simultaneously explore several energy paths and use constructive and destructive interference to guide the path of the exciton's wave packet. It is presumed that natural selection has favored the most efficient path to the reaction center. Experimentally, the interaction between the different frequency wave packets, made possible by long-lived coherence, will produce
quantum beats. While quantum photosynthesis is still an emerging field, there have been many experimental results that support the quantum-coherence understanding of photosynthetic EET. A 2007 study claimed the identification of electronic
quantum coherence at −196 °C (77 K). Another theoretical study from 2010 provided evidence that quantum coherence lives as long as 300 femtoseconds at biologically relevant temperatures (4 °C or 277 K). In that same year, experiments conducted on photosynthetic cryptophyte algae using two-dimensional photon echo spectroscopy yielded further confirmation for long-term quantum coherence. These studies suggest that, through evolution, nature has developed a way of protecting quantum coherence to enhance the efficiency of photosynthesis. However, critical follow-up studies question the interpretation of these results. Single-molecule spectroscopy now shows the quantum characteristics of photosynthesis without the interference of static disorder, and some studies use this method to assign reported signatures of electronic quantum coherence to nuclear dynamics occurring in chromophores. A number of proposals emerged to explain unexpectedly long coherence. According to one proposal, if each site within the complex feels its own environmental noise, the electron will not remain in any local minimum due to both quantum coherence and its
thermal environment, but proceed to the reaction site via
quantum walks. Another proposal is that the rate of quantum coherence and electron
tunneling create an energy sink that moves the electron to the reaction site quickly. Other work suggested that geometric symmetries in the complex may favor efficient energy transfer to the reaction center, mirroring perfect state transfer in quantum networks. Furthermore, experiments with artificial dye molecules cast doubts on the interpretation that quantum effects last any longer than one hundred femtoseconds. In 2017, the first control experiment with the original FMO protein under ambient conditions confirmed that electronic quantum effects are washed out within 60 femtoseconds, while the overall exciton transfer takes a time on the order of a few picoseconds. In 2020 a review based on a wide collection of control experiments and theory concluded that the proposed quantum effects as long lived electronic coherences in the FMO system does not hold. Instead, research investigating transport dynamics suggests that interactions between electronic and vibrational modes of excitation in FMO complexes require a semi-classical, semi-quantum explanation for the transfer of exciton energy. In other words, while quantum coherence dominates in the short-term, a classical description is most accurate to describe long-term behavior of the excitons. Another process in photosynthesis that has almost 100% efficiency is
charge transfer, again suggesting that quantum mechanical phenomena are at play. This high degree of efficiency is largely attributed to the quantum tunnelling of electrons in the ETC and of protons in the proton motive gradient. Indeed, electron tunneling has already been demonstrated in certain elements of the ETC including
NADH:ubiquinone oxidoreductase(Complex I) and
CoQH2-cytochrome c reductase (Complex III). In quantum mechanics, both electrons and protons are quantum entities that exhibit
wave-particle duality, exhibiting both particle and wave-like properties depending on the method of experimental observation. Quantum tunneling is a direct consequence of this
wave-like nature of quantum entities that permits the passing-through of a potential energy barrier that would otherwise restrict the entity. Moreover, it depends on the shape and size of a potential barrier relative to the incoming energy of a particle. Because the incoming particle is defined by its wave function, its tunneling probability is dependent upon the potential barrier's shape in an exponential way. For example, if the barrier is relatively wide, the incoming particle's probability to tunnel will decrease. The potential barrier, in some sense, can come in the form of an actual biomaterial barrier. The inner mitochondria membrane which houses the various components of the ETC is on the order of 7.5 nm thick. In order to transfer particles, the membrane of the mitochondria must have the correct density of phospholipids to conduct a relevant charge distribution that attracts the particle in question. For instance, for a greater density of phospholipids, the membrane contributes to a greater conductance of protons. He showed that the molecular solitons are able to preserve their shape through nonlinear interaction of
amide I excitons and
phonon deformations inside the lattice of
hydrogen-bonded
peptide groups. In 1979, Davydov published his complete textbook on quantum biology entitled "Biology and Quantum Mechanics" featuring quantum dynamics of
proteins,
cell membranes,
bioenergetics,
muscle contraction, and
electron transport in
biomolecules. == Information encoding ==