Project Description

In the Beginning…

Over millennia, eukaryotic cells have evolved sophisticated organelles, which enabled them to partition their cytoplasmic contents into functional sectors (e.g. the nucleus for storage of genetic material). Such compartmentalisation allows greater efficiency of cellular processes, where each organelle is allocated a set of specific metabolic tasks. Some prokaryotes have also developed a method of forming intracellular subdivisions called bacterial microcompartments (BMCs) by expressing a set of proteins that ‘cage in’ a reaction pathway to make it more efficient. A wide range of metabolic pathways are isolated by BMCs, from carbon dioxide fixation pathways to organic compound degradation. Despite these varying functions, the proteinaceous BMC shells show considerable homology as a result of a highly conserved protein domains.[1]

One such set of proteins is expressed from the propanediol utilisation (Pdu) operon in Salmonella enterica, which is involved in the coenzyme B(12)-dependent breakdown of the organic compound 1,2-propanediol. S. enterica synthesises its microcompartments during aerobic or anaerobic growth on 1,2-propanediol, but does not form them when grown on other carbon sources. Enzymes vital for the catabolic pathway are thought to be enclosed within the BMC.[2]

Figure 1: Gene organization in the Pdu Operon and Pdu metabolic pathway[1]

The Pdu operon is composed of 21 genes, which encode proteins involved in the Pdu microcompartment (Figure 1) either in formation of the shell or in the metabolic pathway contained inside. Of these 21 genes, seven have been identified as having a role in BMC shell assembly. These genes code for the proteins PduA, -B, -J, -K, -N, -T, and -U plus a truncated version of PduB termed PduB’.[3]