“…In fermentation processes where cell growth and/or product formation is inhibited by high substrate concentration or by the accumulation of a byproduct, substrate is intermittently fed to the culture system in order to maintain the substrate concentration below a certain level for enhancement of biological and metabolic activity. The feeding of substrate solution is often controlled by means of DO-stat (Mori et al, 1979;Yano et al, 1978) or pH-stat methods (Suzuki et al, 1990;Yamane et al, 1996), or by monitoring the glucose concentration with an on-line glucose analyzer when glucose is used as substrate (Kim et al, 1994;Luli et al, 1987). However, in the culture system of A. eutrophus with acetic acid as carbon source, it was very difficult to control the acetate concentration in the fermenter by a substrate feeding strategy because the optimum acetate concentration for cell growth is in a very narrow range around 1.0 g и dm −3 , and a slight increase or a slight decrease in acetate concentration will seriously suppress the cell growth.…”