A comparative fluorescence kinetics study of Photosystem I monomers and trimers from Synechocystis PCC 6803

1996 ◽  
Vol 49 (3) ◽  
pp. 263-268 ◽  
Author(s):  
Sandra Turconi ◽  
Jochen Kruip ◽  
Gerd Schweitzer ◽  
Matthias R�gner ◽  
Alfred R. Holzwarth
2003 ◽  
Vol 1607 (1) ◽  
pp. 1-4 ◽  
Author(s):  
Roman Kouřil ◽  
Nataliya Yeremenko ◽  
Sandrine D'Haene ◽  
Alevtyna E. Yakushevska ◽  
Wilko Keegstra ◽  
...  

1994 ◽  
Vol 1184 (2-3) ◽  
pp. 235-241 ◽  
Author(s):  
Manuel Hervás ◽  
JoséM. Ortega ◽  
JoséA. Navarro ◽  
Miguel A. De la Rosa ◽  
Hervé Bottin

2008 ◽  
Vol 147 (3) ◽  
pp. 1239-1250 ◽  
Author(s):  
Qiang Wang ◽  
Saowarath Jantaro ◽  
Bingshe Lu ◽  
Waqar Majeed ◽  
Marian Bailey ◽  
...  

1996 ◽  
Vol 51 (3-4) ◽  
pp. 195-199 ◽  
Author(s):  
Petra Jekow ◽  
Wolf-Dieter Schubert ◽  
Petra Fromme ◽  
Jochen Kruip ◽  
Parag R. Chitnis ◽  
...  

Abstract Photosystem I monomers from wildtype cells of Synechocystis PCC 6803 and from a mu­ tant deficient in the psaL gene were crystallized. PsaL encodes for the hydrophobic subunit L, which has been proposed to constitute the trimerization domain in the PS I trimer. The absence of subunit L facilitated crystallization of the PS I monomer. The unit cell dimensions and the space group for the crystals from this preparation could be determined to be a = b = 132 Å , c -525 Å, α = β = 90°, y = 120°, the space group is P61 or P65. The results show the potential of using specifically designed deletion mutants of an integral membrane protein for the systematic improvement of crystal structure data.


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