The fermentative capacities of the acetogenic bacterium Peptostreptococcus productus U-1 (ATCC 35244) were examined. Although acetate was formed from all the substrates tested, additional products were produced in response to CO 2 limitation. Under CO 2 -limited conditions, fructose-dependent growth yielded high levels of lactate as a reduced end product; lactate was also produced under CO 2 -enriched conditions when fructose concentrations were elevated. In the absence of supplemental CO 2 , xylose-dependent growth yielded lactate and succinate as major reduced end products. Although supplemental CO 2 and acetogenesis stimulated cell yields on fructose, xylose-dependent cell yields were decreased in response to CO 2 and acetogenesis. In contrast, glycerol-dependent growth yielded high levels of ethanol in the absence of supplemental CO 2 , and pyruvate was subject to only acetogenic utilization independent of CO 2 . CO 2 pulsing during the growth of CO 2 -limited fructose cultures stopped lactate synthesis immediately, indicating that CO 2 -limited cells were nonetheless metabolically poised to respond quickly to exogenous CO 2 . Resting cells that were cultivated at the expense of fructose without supplemental CO 2 readily consumed fructose in the absence of exogenous CO 2 and formed only lactate. Although the specific activity of lactate dehydrogenase was not appreciably influenced by supplemental CO 2 during cultivation, cells cultivated on fructose under CO 2 -enriched conditions displayed minimal capacities to consume fructose in the absence of exogenous CO 2 . These results demonstrate that the utilization of alternative fermentations for the conservation of energy and growth of P. productus U-1 is augmented by the relative availability of CO 2 and growth substrate.Acetogenic bacteria utilize CO 2 as a terminal electron acceptor and synthesize acetate by the acetyl coenzyme A (acetyl-CoA) Wood/Ljungdahl pathway (12,16,35,36,44). The reduction of CO 2 to acetate is coupled to respiratory conservation of energy via either membranous electron transport or sodium pumping systems (11,27,33). Although supplemental CO 2 can be essential or greatly stimulatory to acetogenesis under certain conditions, acetogens can use other respiratory reductant sinks (15,17,18), including aromatic acrylate groups (2,22,32,40), fumarate (13, 31), dimethyl sulfoxide (3), and nitrate (20,37).In contrast to the numerous studies that have evaluated the respiratory capacities of acetogens, the fermentation capacities of this bacteriological group have been minimally examined. Indeed, although certain acetogens can form fermentative end products such as ethanol (8, 39), acetogens are commonly thought to route the reductant derived from glycolysis toward the respiration of CO 2 to acetate (12,16,44). The acetogenic sewage isolate Peptostreptococcus productus U-1 has been reported to form lactate (28). Although lactate production by P. productus U-1 has not been quantitatively examined, preliminary studies in our laboratory indicated th...