Redox potential changes at 30 °C in anaerobic reconstituted skim-milk cultures of Streptococcus cremoris AM^ and AM 2 and Streptococcus lactis ML 8 have been investigated in batch cultures and continuous cultures maintained at constant pH by the addition of fresh medium. Str. lactis ML 8 was more strongly reducing than either Str. cremoris AM X or AM a . The positive E h values which can arise in dense continuous cultures of lactic streptococci are not likely to affect either the lactic acid formation or proteolytic activity of the resultant bacterial concentrate. An electrolytic reduction cell is described which allows variations in redox potential in cultures to be controlled simply and effectively.Oxidation-reduction potentials constitute one of a number of environmental factors which affect the growth of bacteria (Tabatabai & Walker, 1970). For many years investigations into this factor were primarily concerned with measuring the potentials achieved in culture medium during the growth cycle of microbial cells under anaerobic or aerobic conditions. It has been established that changes in the redox potential not only indicate the level of dissolved O 2 present in the culture medium (Tengerdy, 1961a; Wimpenny 1969a; Jacobs, 1970) but also cause varaitions in cell regulation by different groups of enzymes (Wimpenny, 19696) and alter the production of a number of fermentation products (Tengerdy, 19616).The purpose of the present investigation was to observe redox potential changes in batch cultures and in continuous cultures with controlled pH of single strains of lactic streptococci. Preliminary investigations indicated that for some strains of lactic streptococci, positive redox potentials were obtained under continuous culture conditions at optimum pH values for growth. It was necessary, therefore, to determine whether these redox potentials which may arise in continuous cultures of the lactic streptococci affect their ability to form lactic acid and to degrade protein, both of which activities are important in the manufacture and ripening of cheese. In addition, a simple method is described for the control of redox potential in continuous cultures.