Strain 30AT (T = type strain), which was isolated from an anaerobic bioreactor fed on waste from a potato starch factory in De Krim, The Netherlands, is a nonmotile, gram-positive, anaerobic, rod-shaped organism that is able to degrade various amino acids, including alanine, leucine, isoleucine, valine, serine, and threonine. Acetate is required as an electron acceptor for the utilization of alanine, valine, leucine, and isoleucine. Other growth substrates, including pyruvate, a-ketobutyrate, a-ketoisocaproate, cu-keto-3-methylvalerate, a-ketoisovalerate, and peptone, are intermediates in amino acid catabolism. Strain 30AT utilizes neither the branched-chain amino acids nor alanine via interspecies hydrogen transfer with methanogenic and sulfatereducing bacteria or via the Stickland reaction with proline or glycine as an electron acceptor. No growth occurs with the following electron acceptors: fumarate, nitrate, nitrite, sulfite, sulfate, and oxygen. Yeast extract is required for growth. Sugars are not degraded. The optimal temperature and optimal pH for growth are 39 to 43°C and 6.4 to 7.6, respectively. The results of a 16s rRNA sequence analysis phylogenetically placed strain 30AT in Clostridium group I (genus Clostridium sensu stricto), where it forms a new and distinct line of descent.In most investigations of anaerobic degradation of amino acids the workers have focused on fermentation by Clostridium species (1,3,9,10,17,27,28). Studies performed with species of several other genera (viz., the genera Peptostreptococcus [4, 421, Campylobacter [22, 311, Acidaminobacter [39], Megasphaera [41], Eubacterium [12, 451, and SeZenomonas [15,32]), most of which are members of the low-G+C-content Clostridium subphylum of the gram-positive bacteria, have also contributed to our knowledge of anaerobic metabolism of amino acids.Several workers have reported that in addition to the usual end products produced during fermentation of amino acids (i.e., carbon dioxide, volatile fatty acids, and ammonia), hydrogen is formed (3,4,15,39,(42)(43)(44). The importance of hydrogen consumption in interspecies hydrogen transfer during the degradation of amino acids has been investigated during the last decade (30,33,34,35,39,45). The first step in the degradation of several amino acids (e.g., the branched-chain amino acids) is invariably an oxidative deamination that is usually followed by an oxidative decarboxylation of the resulting keto acid (1). Oxidative deaminations are always endergonic under standard conditions and therefore depend on the removal of the electrons produced in this step (35). It is known that these reactions are also possible through the Stickland reaction (43,44) in addition to interspecies hydrogen transfer. In previous studies of the importance of interspecies hydrogen transfer for amino acid degradation in anaerobic mixed cultures, researchers obtained preliminary evidence that there are fermentative organisms that use acetate as an electron sink (33). In this paper we describe the properties of strain 3...