It has been found that Ser-His could cleave bovine serum albumin (BSA), wit
h the most suitable pH around 6. 0. The kinds of buffers have different inf
luences on the cleavage activity. The phosphate buffer and BR buffer are th
e most effective. The hydroxyl group of the serine residue is the essential
functional group for the cleavage, while the amide bond, imidazole, and ca
rboxyl group of Ser-His increase the cleavage activity.