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pH optimum for tobacco prenylcysteine α-carboxyl methyltransferase. Assays were performed in the presence of 200 μm AGGC or AGC using the following buffers at 100 mm: sodium acetate at pH 5.48, sodium acetate at pH 5.97, sodium acetate at pH 6.46, Hepes at pH 6.76, Hepes at pH 7.00, and Hepes at pH 7.61.
