Two main subunits of PSI, PsaA and PsaB, are closely related proteins involved in the
binding of the vital electron transfer cofactors P, Acc, A, A, and F. PsaA and PsaB are both
integral membrane proteins of 730 to 750
amino acids that contain 11
transmembrane segments. A 4Fe-4S|[4Fe-4S] iron-sulfur cluster called F is
coordinated by four
cysteines; two cysteines are provided each by PsaA and PsaB. The two cysteines in each are proximal and located in a
loop between the ninth and tenth transmembrane segments. A
leucine zipper motif seems to be present
downstream of the cysteines and could contribute to dimerisation of PsaA/PsaB. The terminal electron acceptors F and F, also [4Fe-4S] iron-sulfur clusters, are located in a 9-kDa protein called PsaC that binds to the PsaA/PsaB core near F.
Photon Photoexcitation of the pigment molecules in the antenna complex induces electron and energy transfer. These pigment molecules transmit the
resonance energy from photons when they become photoexcited. Antenna molecules can absorb all
wavelengths of light within the
visible spectrum. The number of these pigment molecules varies from organism to organism. For instance, the
cyanobacterium Synechococcus elongatus (
Thermosynechococcus elongatus) has about 100 chlorophylls and 20 carotenoids, whereas
spinach chloroplasts have around 200 chlorophylls and 50 carotenoids.
P700 reaction center The P700 reaction center is composed of modified
chlorophyll a that best absorbs light at a wavelength of 700
nm. P700 receives energy from antenna molecules and uses the energy from each photon to raise an electron to a higher energy level (P700*). These electrons are moved in pairs in an
oxidation/reduction process from P700* to electron acceptors, leaving behind P700. The pair of P700* - P700 has an
electric potential of about −1.2
volts. The reaction center is made of two chlorophyll molecules and is therefore referred to as a
dimer.
Phylloquinone A
phylloquinone, sometimes called vitamin K, is the next early electron acceptor in PSI. It oxidizes A in order to receive the electron and in turn is re-oxidized by F, from which the electron is passed to F and F. The reduction of Fx appears to be the rate-limiting step. In one model, F passes an electron to F, which passes it on to F to reach the ferredoxin. Fd moves to carry an electron either to a lone thylakoid or to an
enzyme that reduces .
FNR may also accept an electron from NADPH by binding to it. == Ycf4 protein domain ==