'Photosystems' (ancient
Greek: ''phos'' = light and ''systema'' = assembly) are
protein complexes involved in
photosynthesis. 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. A photosystem (or
Reaction Center) is an
enzyme which uses light to
reduce molecules. This
membrane protein complex is made of several subunits and contains 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 photosystems exist: type I reaction centers (like 'photosystem I (
P700)' in chloroplasts and in green-sulphur bacteria) and type II reaction centers (like '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), and the type of terminal electron acceptor. 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 centers types are present in chloroplasts and cyanobacteria, working together to form a unique photosynthetic chain able to extract electrons from water, evolving 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.
Because chlorophyll ''a'' can only absorb light of a narrow
wavelength, it works with the antenna pigments to gain energy from a larger part of the spectrum. The pigments absorb light of various wavelengths and pass along their gained energy to the reaction center chlorophyll. When the energy reaches the chlorophyll ''a'', it releases two
electrons into an
electron transport chain.
Though chlorophyll ''a'' normally has an optimal absorption wavelength of 660
nanometers, it associates with different proteins in each type of photosytem to slightly shift its optimal wavelength, producing two distinct photosystem types. Other proteins serve to support the structure and electron pathways in the photosystem.
Relationship between Photosystems I and II

Schematic drawing of photosystem I from higher plants
Historically photosystem I was named one 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-centre 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 (either through photolysis or enzymatic means) and supplied to the chlorophyll.
Photoexcited electrons travel though 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 provide a proton-motive force to generate ATP. 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-centre chlorophyll of photosystem I. The deficit is due to photo-excitation of electrons which are again trapped in an electron acceptor molecule, this time that of photosystem I.
These 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.
See also
★
Photosynthetic reaction centre
★
photosynthesis
★
chlorophyll
★
light reaction
★
photoinhibition
External links
★
Photosystems I + II: Imperial College, Barber Group
★
Photosystem I: Molecule of the Month in the Protein Data Bank
★
Photosystem II: Molecule of the Month in the Protein Data Bank
★
Photosystem II: ANU
★ - Calculated spatial positions of photosynthetic reaction centers and photosystems in membrane