Myxobacteria are Gram-negative soil bacteria that can form fruiting bodies under starvation conditions (1). These fruiting bodies are visible to the naked eye and can reach a tree-like complexity in some species. During the developmental process, a certain amount of vegetative cells differentiates into heat-and desiccation-resistant myxospores enabling the survival of the colony. The model organism to study this highly complex process is Myxococcus xanthus from which different extracellular signals and regulators have already been described that can be combined in a model likely reflecting the essential parts of the underlying regulatory network (2, 3). However, the biochemical changes that are involved in this process or appear as a result of it have been barely identified. That biochemical changes occur is evident from change in cell shape from vegetative rods to round myxospores with thick spore coats (4, 5) and high amounts of trehalose (6), which is proposed to act as a compatible solute. Furthermore, the pioneering work of White and co-workers (7-9) showed that several enzymes involved in increase of carbohydrate biosynthesis are induced during sporulation.Ten years ago, Downard and coworkers identified a mutant that was disrupted in the branched-chain keto acid dehydrogenase (Bkd) 2 complex, which resulted in a developmental phenotype forming almost no aggregates or spores under starvation conditions (10). The Bkd complex is involved in the degradation of the branched-chain amino acids leucine, valine, and isoleucine, with all three being essential amino acids for M. xanthus (11). The degradation products of these amino acids are isovaleryl-CoA, isobutyryl-CoA, and 2-methylbutyryl-CoA, respectively (12), which are used as starting units for iso-and anteiso-fatty acids and also for several secondary metabolites from different bacteria (e.g. avermectin from Streptomyces avermitilis (13) or myxothiazol (14), myxalamides (15), and aurafuron * This work was supported by Deutsche Forschungsgemeinschaft Grants Bo1834/3-1 and Bo1834/4-1 (to H. B. B.) and Schu984/6-1 (to S. S.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. □ S The on-line version of this article (available at http://www.jbc.org) contains supplemental text and references. 1 To whom correspondence should be addressed. Tel.: 49-681-302-5494; Fax:49-681-302-5473; E-mail: h.bode@mx.uni-saarland.de.2 The abbreviations used are: Bkd, branched-chain keto acid dehydrogenase; FA, fatty acid; SCFA, straight-chain fatty acid; FAME, fatty acid methyl ester; IVA, isovalerate;