Recruitment of a foreign quinone into the A(1) site of photosystem I - Invivo replacement of plastoquinone-9 by media-supplemented naphthoquinones inphylloquinone biosynthetic pathway mutants of synechocystis sp PCC 6803

Interruption of the phylloquinone (PhQ) biosynthetic pathway by interposon mutagenesis of the menA and menB genes in Synechocystis sp. PCC 6803 result s in plastoquinone-9 (PQ-9) occupying the A, site and functioning in electr on transfer from Ao to the FeS clusters in photosystem (PS) I (Johnson, T. W., Shen, G., Zybailov, B., Kolling, D., Reategui, R., Beauparlant, S., Vas siliev, I. R., Bryant, D. A., Jones, A. D., Golbeck, J. H., and Chitnis, P. R. (2000) J. Biol. Chem. 275, 8523-8530. We report here the isolation of m enB26, a strain of the menB mutant that grows in high light by virtue of a higher PS I to PS II ratio. PhQ can be reincorporated into the A, site of t he menB26 mutant strain by supplementing the growth medium with authentic P hQ. The reincorporation of PhQ also occurs in cells that have been treated with protein synthesis inhibitors, consistent with a displacement of PQ-9 f rom the A, site by mass action. The doubling time of the menB26 mutant cell s, but not the menA mutant cells, approaches the wild type when the growth medium is supplemented with naphthoquinone (NQ) derivatives such as 2-CO2H- 1,4-NQ and 2-CH3-1,4-NQ. Since PhQ replaces PQ-9 in the supplemented menB26 mutant cells, but not in the menA mutant cells, the phytyl tail accompanie s the incorporation of these quinones into the A, site. Studies with menB26 mutant cells and perdeuterated 2-CH3-1,4-NQ shows that phytylation occurs at position 3 of the NQ ring because the deuterated 2-methyl group remains intact. Therefore, the specificity of the phytyltransferase enzyme is selec tive with respect to the group present at ring positions 2 and 3. Supplemen ting the growth medium of menB26 mutant cells with 1,4-NQ also leads to its incorporation into the A, site, but typically without either the phytyl ta il or the methyl group. These findings open the possibility of biologically incorporating novel quinones into the A, site by supplementing the growth medium of menB26 mutant cells.