AbstractThe release of polypeptides from inside-out thylakoid vesicles and photosystem II by alkaline Tris treatment was reinvestigated, using SDS-polyacrylanude gel electrophoresis (PAGE) in the presence of urea, with highly increased resolution in the low molecular mass region. In addition to the 33-, 23-, and 16-kDa proteins of the oxygen-evolving complex, a 10-kDa polypeptide was released. This 10-kDa polypeptide is an entrinsic polypeptide located at the inner grana thylakoid surface and with a likely role in photosynthetic oxygen evolution
AbstractThe newly reported 9-kDa polypeptide in photosystem I [(1991) FEBS Lett. 280, 332–334) is an...
Biochemical techniques now exist to produce the oxygen-evolving complex of photosystem II (PSII) and...
AbstractThe release of both Mn and polypeptides as well as the inactivation of O2 evolution in C18:3...
AbstractThe release of polypeptides from inside-out thylakoid vesicles and photosystem II by alkalin...
AbstractTris-treatment of a highly active O2-evolving photosystem-II preparation induced release of ...
AbstractTreatment with 2.6 M urea of the Photosystem II particles depleted of two polypeptides of 24...
Removal of 23 and 17 kDa water-soluble polypeptides from PS II membranes causes a marked decrease in...
AbstractThe accumulation of the 33-, 23- and 16-kDa polypeptides of the oxygen-evolving complex has ...
AbstractTreatment with 3 M urea of the oxygen-evolving PS II core complex previously described [(198...
AbstractExposure of detergent-isolated preparations of the Photosystem II complex to 2 M NaCl releas...
The linear, four-step oxidation of water to molecular oxygen by photosystem II requires cooperation ...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/117036/1/feb20014579384813939.pd
AbstractRepeated extractions of spinach thylakoid membranes with a solution containing 50 mM sodium ...
AbstractDigitonin extracts of spinach thylakoid membranes obtained as 100000 × g supernatant have be...
AbstractTreatment of Photosystem II particles from spinach chloroplasts with Triton X-100 with 2.6 M...
AbstractThe newly reported 9-kDa polypeptide in photosystem I [(1991) FEBS Lett. 280, 332–334) is an...
Biochemical techniques now exist to produce the oxygen-evolving complex of photosystem II (PSII) and...
AbstractThe release of both Mn and polypeptides as well as the inactivation of O2 evolution in C18:3...
AbstractThe release of polypeptides from inside-out thylakoid vesicles and photosystem II by alkalin...
AbstractTris-treatment of a highly active O2-evolving photosystem-II preparation induced release of ...
AbstractTreatment with 2.6 M urea of the Photosystem II particles depleted of two polypeptides of 24...
Removal of 23 and 17 kDa water-soluble polypeptides from PS II membranes causes a marked decrease in...
AbstractThe accumulation of the 33-, 23- and 16-kDa polypeptides of the oxygen-evolving complex has ...
AbstractTreatment with 3 M urea of the oxygen-evolving PS II core complex previously described [(198...
AbstractExposure of detergent-isolated preparations of the Photosystem II complex to 2 M NaCl releas...
The linear, four-step oxidation of water to molecular oxygen by photosystem II requires cooperation ...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/117036/1/feb20014579384813939.pd
AbstractRepeated extractions of spinach thylakoid membranes with a solution containing 50 mM sodium ...
AbstractDigitonin extracts of spinach thylakoid membranes obtained as 100000 × g supernatant have be...
AbstractTreatment of Photosystem II particles from spinach chloroplasts with Triton X-100 with 2.6 M...
AbstractThe newly reported 9-kDa polypeptide in photosystem I [(1991) FEBS Lett. 280, 332–334) is an...
Biochemical techniques now exist to produce the oxygen-evolving complex of photosystem II (PSII) and...
AbstractThe release of both Mn and polypeptides as well as the inactivation of O2 evolution in C18:3...