Photosystem

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  1. either of the two functionally distinct but cooperating systems, designated photosystem I (abbr.: PSI) and photosystem II (abbr.: PSII), between which are distributed the various molecules that effect the light reactions of photosynthesis; photosystems are located in the thylakoid membranes of the chloroplasts of higher plants and green algae or in the free thylakoid membranes of cyanobacteria. Photosystem I consists of a transmembrane multisubunit complex, of about 10 subunits in all, consisting of a heterodimer complex of PsaA and PsaB which binds P700, together with the chlorophyll acceptor A0, the phylloquinone acceptor A1, and Fx, a 4Fe — 4S centre. PsaC, which is bound to this complex, contains two additional 4Fe — 4S centres required for ferredoxin reduction. PsaC of pea is similar to bacterial-type 4Fe — 4S ferredoxins. Other subunits are involved in binding soluble ferredoxin, ferredoxin-NADP oxidoreductase and regulation of electron flow. Approximately 100 chlorophyll a molecules are bound to the minimal heterodimer unit. Photosystem II is formed from a heterodimer of the D1 and D2 proteins which bind P680, together with the pheophytin acceptor, two plastoquinone acceptors Qa and Qb, and a non-heme iron atom. The minimal purified unit contains about six chlorophyll a molecules. Cytochrome b559 is always associated with PSII. A large number of other subunits including light-harvesting chlorophyll-protein complexes, proteins involved in stabilizing the Mn complex, and regulatory subunits are required to form a functional photosystem II.
  2. any functionally analogous but simpler single photosystem present in photosynthetic bacteria. That from Rhodopseudomonas viridis contains three hydrophobic subunits, a special pair of bacteriochlorophyll b (the reaction-centre bacteriochlorophyll P960), two molecules of bacteriopheophytin b(see bacteriopheophytin), a bound iron atom and one molecule each of ubiquinone and a menaquinone. There are four heme c-type cytochromes in this case (but not in all). The complete structure has been determined by X-ray crystallography. See also photosynthetic reaction centre.

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Photosystems (ancient Greek: photos = light and systema = assembly) are functional and structural units of protein complexes involved in photosynthesis that together carry out the primary photochemistry of photosynthesis: the absorption of light and the transfer of energy and electrons. They are found in the thylakoid membranes of plants, algae and cyanobacteria (in plants and algae these are located in the chloroplasts), or in the cytoplasmic membrane of photosynthetic bacteria.

Contents

Reaction centers

At the heart of a photosystem lies the Reaction Center, which is an enzyme that uses light to reduce molecules. In a photosystem, this Reaction Center is surrounded by light-harvesting complexes that enhance the absorption of light and transfer the energy to the Reaction Centers. Light-Harvesting and Reaction Center complexes are membrane protein complexes that are made of several protein-subunits and contain numerous cofactors. In the photosynthetic membranes, reaction centers provide the driving force for the bioenergetic electron and proton transfer chain. When light is absorbed by a reaction center (either directly or passed by neighbouring pigment-antennae), a series of oxido-reduction reactions is initiated, leading to the reduction of a terminal acceptor. Two families of reaction centers in photosystems exist: type I reaction centers (such as photosystem I (P700) in chloroplasts and in green-sulphur bacteria) and type II reaction centers (such as photosystem II (P680) in chloroplasts and in non-sulphur purple bacteria). Each photosystem can be identified by the wavelength of light to which it is most reactive (700 and 680 nanometers, respectively for PSI and PSII in chloroplasts), the amount and type of light-harvesting complexes present and the type of terminal electron acceptor used. Type I photosystems use ferredoxin-like iron-sulfur cluster proteins as terminal electron acceptors, while type II photosystems ultimately shuttle electrons to a quinone terminal electron acceptor. One has to note that both reaction center types are present in chloroplasts and cyanobacteria, working together to form a unique photosynthetic chain able to extract electrons from water, creating oxygen as a byproduct.

Structure

A reaction center comprises several (>10 or >11) protein subunits, providing a scaffold for a series of cofactors. The latter can be pigments (like chlorophyll, pheophytin, carotenoids), quinones, or iron-sulfur clusters.

Relationship between Photosystems I and II

For oxygenic photosynthesis, both photosystems I and II are required. Oxygenic photosynthesis can be performed by plants and cyanobacteria; cyanobacteria are believed to be the progenitors of the photosystem-containing chloroplasts of eukaryotes. Photosynthetic bacteria that cannot produce oxygen have a single photosystem called BRC, bacterial reaction center.

The photosystem I was named "I" since it was discovered before photosystem II, but this does not represent the order of the electron flow.

When photosystem II absorbs light, electrons in the reaction-center chlorophyll are excited to a higher energy level and are trapped by the primary electron acceptors. To replenish the deficit of electrons, electrons are extracted from water by a cluster of four Manganese ions in photosystem II and supplied to the chlorophyll via a redox-active tyrosine.

Photoexcited electrons travel through the cytochrome b6f complex to photosystem I via an electron transport chain set in the thylakoid membrane. This energy fall is harnessed, (the whole process termed chemiosmosis), to transport hydrogen (H+) through the membrane, to the lumen, to provide a proton-motive force to generate ATP. The protons are transported by the plastoquinone. If electrons only pass through once, the process is termed noncyclic photophosphorylation.

When the electron reaches photosystem I, it fills the electron deficit of the reaction-center chlorophyll of photosystem I. The deficit is due to photo-excitation of electrons that are again trapped in an electron acceptor molecule, this time that of photosystem I.

ATP is generated when the ATP synthase transports the protons present in the lumen to the stroma, through the membrane. The electrons may either continue to go through cyclic electron transport around PS I or pass, via ferredoxin, to the enzyme NADP+ reductase. Electrons and hydrogen ions are added to NADP+ to form NADPH. This reducing agent is transported to the Calvin cycle to react with glycerate 3-phosphate, along with ATP to form glyceraldehyde 3-phosphate, the basic building-block from which plants can make a variety of substances.

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