Enzymic solution reco6ery
In each batch of each test conducted, 40 g of the
fermented medium was supplemented with 100 ml of an
acetate buffer 200 mM (pH 4.2). The mixture was
stirred for 1 h at 180 rpm and 32°C. The solid residue
was separated from the enzymic solution by filtration
through Whatman 40 filter paper