Dissection of the Hydrogen Metabolism of the Enterobacterium Trabulsiella guamensis: Identification of a Formate-Dependent and Essential Formate Hydrogenlyase Complex Exhibiting Phylogenetic Similarity to Complex I.
Trabulsiella guamensis is a non-pathogenic enterobacterium that was isolated from a vacuum cleaner on the island of Guam. It has one H2-oxidizing Hyd-2-type hydrogenase (Hyd), and encodes a H2-evolving Hyd that is most similar to the uncharacterized Escherichia coli formate hydrogenlyase (FHL-2Ec) complex. The FHL-2Tg complex is predicted to have 5 membrane-integral and between 4-5 cytoplasmic subunits. We could show that FHL-2Tg complex catalyses the disproportionation of formate to CO2 and H2. FHL-2Tg has an activity similar to the E. coli FHL-1Ec complex in H2-evolution from formate, but the complex appears more labile upon cell lysis. Cloning of the entire 13 kbp FHL-2Tg operon in the heterologous E. coli host has now enabled us to prove FHL-2Tg activity unambiguously and allowed us to characterize the FHL-2Tg complex biochemically. Although the formate dehydrogenase (FdhH) gene fdhF is not encoded in the operon, the FdhH is part of the complex and FHL-2Tg activity was dependent on the presence of E. coli FdhH. Also, in contrast to E. coli, T. guamensis can ferment the alternative carbon source cellobiose, and we further investigated the participation of both the H2-oxidizing Hyd-2Tg and the H2-forming FHL-2Tg under these conditions. ImportanceBiological H2-production presents an attractive alternative for fossil fuels. But in order to compete with conventional H2-production methods, the process requires our understanding on the molecular level. FHL complexes are efficient H2-producers and the prototype FHL-1Ec complex in E. coli is well studied. This paper presents the first biochemical characterisation of an FHL-2-type complex. The data presented here will enable us to solve the long-standing mystery of the FHL-2Ec complex, allow a first biochemical characterisation of T. guamensiss fermentative metabolism and establish this enterobacterium as model organism for FHL-dependent energy conservation.