The deacylation of Pen G was carried out by using recombinant E. coli in an
aqueous two-phase system consisting of polyethylene glycol and potassium p
hosphate solution, which partitions the cells to the bottom phase and the p
roducts to the top phase. Bioconversion and product separation were carried
out in the same reactor. Repeated batch conversion was employed ten times
and enzymic activity showed only a slight decline. When pure enzyme was use
d for bioconversion in an aqueous two-phase system, the decline was fast an
d bioconversion using whole cell penicillin acylase was better than that ob
tained using the pure acylase. (C) 1999 Elsevier Science Ireland Ltd. All r
ights reserved.