Funk C
Department of Biochemistry, Stockholm University, Sweden.
Plant Mol Biol. 2000 Dec;44(6):815-27. doi: 10.1023/a:1026764728846.
The psbX gene (sml0002) coding for a 4.1 kDa protein in Photosystem II of plants and cyanobacteria was deleted in both wild type and in a Photosystem I-less mutant of the cyanobacterium Synechocystis sp. PCC 6803. Polymerase chain reaction and sequencing analysis showed that the mutants had completely segregated. Deletion of the PsbX protein does not seem to influence growth rate, electron transport or water oxidation ability. Whereas a high light induction of the psbX mRNA could be observed in wild type, deletion of the gene did not lead to high light sensibility. Light saturation measurements and 77K fluorescence measurements indicated a minor disconnection of the antenna in the deletion mutant. Furthermore, fluorescence induction measurements as well as immuno-staining of the D1 protein showed that the amount of Photosystem II complexes in the mutants was reduced by 30%. Therefore, PsbX does not seem to be necessary for the Photosystem II electron transport, but directly or indirectly involved in the regulation of the amount of functionally active Photosystem II centres in Synechocystis sp. PCC 6803.
在植物和蓝细菌的光系统II中编码一种4.1 kDa蛋白质的psbX基因(sml0002),在蓝细菌集胞藻PCC 6803的野生型和无光系统I突变体中均被删除。聚合酶链反应和测序分析表明,突变体已完全分离。PsbX蛋白的缺失似乎不影响生长速率、电子传递或水氧化能力。虽然在野生型中可以观察到psbX mRNA的高光诱导,但该基因的缺失并未导致高光敏感性。光饱和测量和77K荧光测量表明,缺失突变体中天线存在轻微断开。此外,荧光诱导测量以及D1蛋白的免疫染色表明,突变体中光系统II复合物的数量减少了30%。因此,PsbX似乎不是光系统II电子传递所必需的,但直接或间接参与了集胞藻PCC 6803中功能活性光系统II中心数量的调节。