Fig. 2 shows that the level of acetic acid varied from 0.8 g/L (St–Lr) to 1.5 g/L (Lr) and that of ethanol from only 0.2 g/L (St–Lr) to 0.4 g/L (Lr). Since S. thermophilus is a homofermentative bacterium, its fast metabolism was mainly responsible for the production of lactic acid, while the formations of acetic acid and ethanol have to be ascribed to the heterofermentative feature of L. rhamnosus. It is well known that, in a typical heterofermentative pathway, glucose from lactose hydrolysis, and in some microorganisms

even a portion of the remaining galactose moiety, are converted via phosphoketolase to glyceraldehydes 3-phosphate and acetyl-CoA, being the former converted to lactic acid and the latter reduced to ethanol by the NADH accumulated in the first part of the pathway ( Panobinostat datasheet Axelsson, 1998). Under oxidative conditions, such an excess reducing

power can be partially dissipated, and an appreciable amount of acetyl-P can Dasatinib be converted to acetic acid making the phosphoketolase pathway as efficient as the EMP one from the bioenergetic viewpoint ( Arsköld et al., 2008 and Zaunmüller et al., 2006). As the formation of acetic acid yields an additional equivalent of ATP ( Axelsson, 1998), it is less energy-consuming; therefore, the presence in the medium of additional hydrogen acceptors is needed to sustain its abundant production as in the present work. As we will see in the following, the concentration of acetoin from diacetyl reduction was too low to justify this production; thus, two possible explanations of such a partial dissipation of NADH could be the co-metabolization of citrate via pyruvate, with additional formation of lactic acid ( Axelsson, 1998), and the high NADH oxidase activity already detected and quantified in L. rhamnosus

by Jyoti et al. (2004) by metabolic flux analysis. In pure cultures, the productions of diacetyl and acetoin by L. rhamnosus (Lr) were 18 and 67% higher, respectively, when compared to those obtained with S. thermophilus (St). Ramos, Jordan, Cogan, and Santos (1994) demonstrated that in LABs the main route of diacetyl synthesis occurs via α-acetolactate, which is produced Amobarbital by the condensation of two pyruvate molecules catalyzed by the key enzyme α-acetolactate synthase. Once synthesized, α-acetolactate is unstable and is readily decarboxylated to acetoin by α-acetolactate decarboxylase, or by nonenzymatic oxidative decarboxylation to diacetyl, in the presence of oxygen. Besides that, acetoin can be synthesized from diacetyl by diacetyl reductase; so, the balance among the end-products of citrate fermentation will depend on the redox state of the cell. As S. thermophilus cannot metabolize citrate ( Chaves et al.