The nature of the buffer species used in the drying process is importa
nt when lyophilized enzyme preparations are suspended in organic media
. The activity of subtilisin Carlsberg in a transesterification reacti
on was found to vary depending on the nature of the buffer used. It wa
s postulated that the large excess of salt present in the dried powder
could be affecting enzymatic activity by alterations to the microscop
ic structure of the powder. To establish if this were true, microscopi
c changes were eliminated by covalently immobilising the enzyme onto a
macroporous polymer support so that the counter-ions could be exchang
ed by washing with dilute salt solutions. It was found that in the imm
obilised samples no significant effects of salt ions were noted. This
was the case even when salt ions were in considerable excess of that n
eeded to balance protein charges. Hence the activity variations noted
in freeze-dried powders are probably due to changes to the microscopic
structure, rather than to molecular scale interactions. Similarly the
previously observed activating effect of crown ether solutions on fre
eze-dried powders is not repeated on an immobilised preparation sugges
ting that this too may be due to a microscopic effect on the powder.