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To study structure-function relationships in the D1 protein of Synechocystis 6803, mutated constructs can be introduced either into the psbA2 gene [R. J. Debus, B. A. Barry, I. Sithole, G. T. Babcock, and L. McIntosh, Biochemistry 27, 9071 (1988); P. Mäenpää, T. Kallio, P. Mulo, G. Salih, E.-M. Aro, E. Tyystjärvi, and C. Jansson, Plant Mol. Biol. 22, 1 (1993); N. Ohad and J. Hirschberg, Plant Cell 4, 273 (1992); G. Salih, R. Wiklund, T. Tyystjärvi, P. Mäenpää, C. Gerez, and C. Jansson, Photosynth. Res. 49, 131 (1996)] or into the psbA3 gene [J. G. Metz, P. J. Nixon, M. Rogner, G. W. Brudvig, and B. A. Diner, Biochemistry 28, 6960 (1989)]. Although perhaps not of primary concern in studies on psbA gene regulation, keep in mind that, since psbA2 is by far the most predominantly expressed psbA gene in the wild-type strain of Synechocystis 6803 [A. Mohamed, J. Eriksson, H. D. Osiewacz, and C. Jansson, Mol. Gen. Genet. 238, 161 (1993)], a control strain with psbA3 as the only active psbA gene might not necessarily always exhibit the same phenotype as the wild type.
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0027583397
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To study structure-function relationships in the D1 protein of Synechocystis 6803, mutated constructs can be introduced either into the psbA2 gene [R. J. Debus, B. A. Barry, I. Sithole, G. T. Babcock, and L. McIntosh, Biochemistry 27, 9071 (1988); P. Mäenpää, T. Kallio, P. Mulo, G. Salih, E.-M. Aro, E. Tyystjärvi, and C. Jansson, Plant Mol. Biol. 22, 1 (1993); N. Ohad and J. Hirschberg, Plant Cell 4, 273 (1992); G. Salih, R. Wiklund, T. Tyystjärvi, P. Mäenpää, C. Gerez, and C. Jansson, Photosynth. Res. 49, 131 (1996)] or into the psbA3 gene [J. G. Metz, P. J. Nixon, M. Rogner, G. W. Brudvig, and B. A. Diner, Biochemistry 28, 6960 (1989)]. Although perhaps not of primary concern in studies on psbA gene regulation, keep in mind that, since psbA2 is by far the most predominantly expressed psbA gene in the wild-type strain of Synechocystis 6803 [A. Mohamed, J. Eriksson, H. D. Osiewacz, and C. Jansson, Mol. Gen. Genet. 238, 161 (1993)], a control strain with psbA3 as the only active psbA gene might not necessarily always exhibit the same phenotype as the wild type.
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To study structure-function relationships in the D1 protein of Synechocystis 6803, mutated constructs can be introduced either into the psbA2 gene [R. J. Debus, B. A. Barry, I. Sithole, G. T. Babcock, and L. McIntosh, Biochemistry 27, 9071 (1988); P. Mäenpää, T. Kallio, P. Mulo, G. Salih, E.-M. Aro, E. Tyystjärvi, and C. Jansson, Plant Mol. Biol. 22, 1 (1993); N. Ohad and J. Hirschberg, Plant Cell 4, 273 (1992); G. Salih, R. Wiklund, T. Tyystjärvi, P. Mäenpää, C. Gerez, and C. Jansson, Photosynth. Res. 49, 131 (1996)] or into the psbA3 gene [J. G. Metz, P. J. Nixon, M. Rogner, G. W. Brudvig, and B. A. Diner, Biochemistry 28, 6960 (1989)]. Although perhaps not of primary concern in studies on psbA gene regulation, keep in mind that, since psbA2 is by far the most predominantly expressed psbA gene in the wild-type strain of Synechocystis 6803 [A. Mohamed, J. Eriksson, H. D. Osiewacz, and C. Jansson, Mol. Gen. Genet. 238, 161 (1993)], a control strain with psbA3 as the only active psbA gene might not necessarily always exhibit the same phenotype as the wild type.
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To study structure-function relationships in the D1 protein of Synechocystis 6803, mutated constructs can be introduced either into the psbA2 gene [R. J. Debus, B. A. Barry, I. Sithole, G. T. Babcock, and L. McIntosh, Biochemistry 27, 9071 (1988); P. Mäenpää, T. Kallio, P. Mulo, G. Salih, E.-M. Aro, E. Tyystjärvi, and C. Jansson, Plant Mol. Biol. 22, 1 (1993); N. Ohad and J. Hirschberg, Plant Cell 4, 273 (1992); G. Salih, R. Wiklund, T. Tyystjärvi, P. Mäenpää, C. Gerez, and C. Jansson, Photosynth. Res. 49, 131 (1996)] or into the psbA3 gene [J. G. Metz, P. J. Nixon, M. Rogner, G. W. Brudvig, and B. A. Diner, Biochemistry 28, 6960 (1989)]. Although perhaps not of primary concern in studies on psbA gene regulation, keep in mind that, since psbA2 is by far the most predominantly expressed psbA gene in the wild-type strain of Synechocystis 6803 [A. Mohamed, J. Eriksson, H. D. Osiewacz, and C. Jansson, Mol. Gen. Genet. 238, 161 (1993)], a control strain with psbA3 as the only active psbA gene might not necessarily always exhibit the same phenotype as the wild type.
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To study structure-function relationships in the D1 protein of Synechocystis 6803, mutated constructs can be introduced either into the psbA2 gene [R. J. Debus, B. A. Barry, I. Sithole, G. T. Babcock, and L. McIntosh, Biochemistry 27, 9071 (1988); P. Mäenpää, T. Kallio, P. Mulo, G. Salih, E.-M. Aro, E. Tyystjärvi, and C. Jansson, Plant Mol. Biol. 22, 1 (1993); N. Ohad and J. Hirschberg, Plant Cell 4, 273 (1992); G. Salih, R. Wiklund, T. Tyystjärvi, P. Mäenpää, C. Gerez, and C. Jansson, Photosynth. Res. 49, 131 (1996)] or into the psbA3 gene [J. G. Metz, P. J. Nixon, M. Rogner, G. W. Brudvig, and B. A. Diner, Biochemistry 28, 6960 (1989)]. Although perhaps not of primary concern in studies on psbA gene regulation, keep in mind that, since psbA2 is by far the most predominantly expressed psbA gene in the wild-type strain of Synechocystis 6803 [A. Mohamed, J. Eriksson, H. D. Osiewacz, and C. Jansson, Mol. Gen. Genet. 238, 161 (1993)], a control strain with psbA3 as the only active psbA gene might not necessarily always exhibit the same phenotype as the wild type.
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