I have tested enzyme activity (b-galactosidase) with cation ions in different buffer and the results differ dramatically. For example, while I used MES buffer calcium acts as an activator but when I dissolved my enzyme in phosphate buffer calcium acts as an inhibitor.

is there any explanation besides I done something wrong?

Kindly ask for help and thank you for any answer.

More Aleksandra Rosińska's questions See All
Similar questions and discussions