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Absence of PsaC subunit allows assembly of photosystem I core but prevents the binding of PsaD and PsaE inSynechocystissp. PCC6803

✍ Scribed by Jianping Yu; Lawrence B. Smart; Yean-Sung Jung; John Golbeck; Lee McIntosh


Book ID
104620717
Publisher
Springer
Year
1995
Tongue
English
Weight
984 KB
Volume
29
Category
Article
ISSN
0167-4412

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✦ Synopsis


In photosystem I (PSI) of oxygenic photosynthetic organisms thepsaC polypeptide, encoded by thepsaC gene, provides the ligands for two [4Fe-4S] clusters, FA and FB. Unlike other cyanobacteria, two different psaC genes have been reported in the cyanobacterium Synechocystis 6803, one (copy 1) with a deduced amino acid sequence identical to that of tobacco and another (copy 2) with a deduced amino acid sequence similar to those reported for other cyanobacteria. Insertion of a gene encoding kanamycin resistance into copy 2 resulted in a photosynthesis-deficient strain, CDK25, lacking the PsaC, PsaD and PsaE polypeptides in isolated thylakoid membranes, while the PsaA/PsaB and PsaF subunits were found. Growth of the mutant cells was indistinguishable from that of wild-type cells under light-activated heterotrophic growth (LAHG). A reversible P700 + signal was detected by EPR spectroscopy in the isolated thylakoids during illumination at low temperature. Under these conditions, the E P R signals attributed to FA and F B were absent in the mutant strain, but a reversible F x signal was present with broad resonances at g = 2.079, 1.903, and 1.784. Addition of PsaC and PsaD proteins to the thylakoids gave rise to resonances at g = 2.046, 1.936, 1.922, and 1.880; these values are characteristic of an interaction-type spectrum of F2 and Fff. In room-temperature optical spectroscopic analysis, addition of PsaC and PsaD to the thylakoids also restored a 30 ms kinetic transient which is characteristic of the P700 + [FA/FB]-backreaction. Expression of copy 1 was not detected in cells grown under L A H G and under mixotrophic conditions. These results demonstrate that copy 2 encodes the PsaC polypeptide in PSI in Synechocystis 6803, while copy 1 is not involved in PSI; that the PsaC polypeptide is necessary for stable assembly of PsaD and PsaE into PSI complex in vivo; and that PsaC, PsaD and PsaE are not needed for assembly of PsaA-PsaB dimer and electron transport from P700 to Fx.


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