“…The higher reduction state of glycerol needs excess of reducing equivalents, which can be accomplished by diverting NADH consuming pathway towards reduced or neutral end-products (ethanol or 1,3-PD) or via H 2 production (Heyndrickx et al, 1991). Research carried out using the Enterobacter and Clostridium with crude glycerol as substrate either produced ethanol (Ito et al, 2005;Jitrwung and Yargeau, 2011;Nwachukwu et al, 2012;Nwachukwu et al, 2013) or 1,3-propanediol (Zeng, 1996;Gonzalez-Pajuelo et al, 2004;Gonzalez-Pajuelo et al, 2005;Chatzifragkou et al, 2011;Szymanowska-Powałowska, 2014), which needs to be produced at higher concentration at the expense of media cost (Jitrwung and Yargeau, 2011). Additionally a co-culture of facultative (Enterobacter aerogenes) and strict anaerobe (Clostridium butyricum) can ensure high H 2 yield by using glucose as carbon source in the absence of expensive reducing agent (Yokoi et al, 1998;Phowan et al, 2010).…”