Polypeptides of photosystem II and their role in oxygen evolution
- 1 January 1985
- journal article
- Published by Springer Nature in Photosynthesis Research
- Vol. 7 (2) , 97-114
- https://doi.org/10.1007/bf00037001
Abstract
The linear, four-step oxidation of water to molecular oxygen by photosystem II requires cooperation between redox reactions driven by light and a set of redox reactions involving the S-states within the oxygen-evolving complex. The oxygenevolving complex is a highly ordered structure in which a number of polypeptides interact with one another to provide the appropriate environment for productive binding of cofactors such as manganese, chloride and calcium, as well as for productive electron transfer within the photoact. A number of recent advances in the knowledge of the polypeptide structure of photosystem II has revealed a correlation between primary photochemical events and a ‘core’ complex of five hydrophobic polypeptides which provide binding sites for chlorophyll a, pheophytin a, the reaction center chlorophyll (P680), and its immediate donor, denoted Z. Although the ‘core’ complex of photosystem II is photochemically active, it does not possess the capacity to evolve oxygen. A second set of polypeptides, which are water-soluble, have been discovered to be associated with photosystem II; these polypeptides are now proposed to be the structural elements of a special domain which promotes the activities of the loosely-bound cofactors (manganese, chloride, calcium) that participate in oxygen evolution activity. Two of these proteins (whose molecular weights are 23 and 17 kDa) can be released from photosystem II without concurrent loss of functional manganese; studies on these proteins and on the membranes from which they have been removed indicate that the 23 and 17 kDa species from part of the structure which promotes retention of chloride and calcium within the oxygen-evolving complex. A third water-soluble polypeptide of molecular weight 33 kDa is held to the photosystem II ‘core’ complex by a series of forces which in some circumstances may include ligation to manganese. The 33 kDa protein has been studied in some detail and appears to promote the formation of the environment which is required for optimal participation by manganese in the oxygen evolving reaction. This minireview describes the polypeptides of photosystem II, places an emphasis on the current state of knowledge concerning these species, and discusses current areas of uncertainty concerning these important polypeptides.Keywords
This publication has 65 references indexed in Scilit:
- A photoactive Photosystem-II reaction-center complex lacking a chlorophyll-binding 40 kilodalton subunit from the thermophilic cyanobacterium Synechococcus sp.Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1984
- Characterization of the Photosystem II Reaction Center Polypeptide (CP47)Published by Springer Nature ,1984
- Evidence that CP 47 (CPa-1) is the Reaction Centre of Photosystem IIPublished by Springer Nature ,1984
- ELECTRON TRANSPORT ACTIVITY AND POLYPEPTIDE COMPOSITION OF THE ISOLATED PHOTOSYSTEM II COMPLEXPublished by Elsevier ,1983
- IDENTIFICATION OF PHOTOSYSTEM II-THYLAKOID PROTEINS THROUGH MUTATIONAL ANALYSIS WITH CHLAMYDOMONAS AND SCENEDESMUS PHENOTYPESPublished by Elsevier ,1983
- BIOCHEMICAL PROPERTIES OF THE ENIGMATIC CHLOROPLAST CYTOCHROME b-559: PARTIAL AMINO ACID SEQUENCE OF A PURIFIED b-559 POLYPEPTIDE AND STUDIES ON THE IDENTITY OF THE Mr = 9,000 PHOSPHOPROTEINPublished by Elsevier ,1983
- POSSIBLE ROLE OF CYTOCHROME b559 IN PHOTOSYSTEM IIPublished by Elsevier ,1983
- STRUCTURE AND INHIBITION OF COMPONENTS ON THE OXIDIZING SIDE OF PHOTOSYSTEM IIPublished by Elsevier ,1983
- PHOTOSYSTEM II REACTION CENTER COMPLEX PURIFIED FROM HIGHER PLANTSPublished by Elsevier ,1983
- Oxygen Evolution in Photosynthesis**Supported in part by grants from the Atomic Energy Commission, Contract # AT(II-1)-3326 and the National Science Foundation, Contract # NSF-C705.Published by Elsevier ,1975