![]() The three missing proteins could be detected immunologically in whole cells, but their levels were greatly reduced, and degradation products were also detected. These PS I complexes completely lacked the stromal subunits PsaC, PsaD, and PsaE but contained all membrane-intrinsic subunits. PS I levels were significantly lower than in the wild type (∼40%), but trimeric PS I complexes could be isolated from the rubA mutant. Fractionation studies suggest that RubA might transiently associate with PS I monomers, but no evidence for an association with PS I trimers or PS II was observed. RubA was present in thylakoid but not plasma membranes of cyanobacteria and in chloroplast thylakoids isolated from spinach and Chlamydomonas reinhardtii. Overproduction of the water-soluble rubredoxin domain in Escherichia coli led to a product with the absorption and EPR spectra of typical rubredoxins. RubA contains a domain of ∼50 amino acids with very high similarity to the rubredoxins of anaerobic bacteria and archaea, but it also contains a region of about 50 amino acids that is predicted to form a flexible hinge and a transmembrane α-helix at its C terminus. RubA and PS I electron transport activity were completely absent in the mutant, although PS II activity was ∼80% of the wild-type level. PCC 7002 produced a mutant unable to grow photoautotrophically. Inactivation of the rubA gene of Synechococcus sp. Inactivation of the slr2034 homolog produced a mutant with no detectable phenotype and wild-type photosystem (PS) II levels. PCC 6803 gene slr2034 and Arabidopsis thaliana HCF136, and the psbEFLJ operon, was cloned from the cyanobacterium Synechococcus sp. A 4.4-kb Hin dIII fragment, encoding an unusual rubredoxin (denoted RubA), a homolog of the Synechocystis sp. ![]()
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