Alternatively, TraB might recruit other chromosomally

encoded proteins for the transfer process. 1. How to cross the PG barrier? A TraB–eGFP fusion was localized at the hyphal tip, suggesting that the selleck chemicals tips of the mycelium are involved in conjugation (Reuther et al., 2006a). Also, TraB was shown to bind isolated PG (Vogelmann et al., 2011a). Because TraB itself does not have a PG-lysing activity (Finger and Muth, unpublished), it is possible that TraB interacts with chromosomally encoded PG hydrolases at the tip to direct fusion of the PG layers of donor and recipient. 2. How to cross membranes of donor and recipient? In contrast to FtsK that is found in both compartments during cell division, TraB is present only in the donor mycelium. Therefore, the TraB pore has to traverse two membranes (one from the donor, one from the recipient) or the two membranes have to fuse. For SpoIIIE that mediates translocation of the chromosome into the forespore during Bacillus sporulation, a membrane fusing activity has been reported (Sharp & Pogliano, 2003). Therefore, it is tempting to speculate that also TraB might have a membrane

fusing activity allowing formation of a pore structure to the recipient. 3. How to translocate a circular covalently closed plasmid molecule? During cell division or sporulation, http://www.selleckchem.com/Caspase.html the septum closes, while chromosomal DNA is already present, allowing FtsK to assemble at both chromosomal arms to translocate the DNA. DNA translocation causes topological stress to the DNA, which has to be relieved by topoisomerases. The interaction of E. coli FtsK with topoisomerase

Glutathione peroxidase IV has been reported (Espeli et al., 2003). However, it is still unclear, how the remaining end of the circular chromosome becomes translocated through the membrane and fusion of the two FtsK hexamer structures has been postulated (Burton et al., 2007). During Streptomyces conjugation, the situation is even more complex. The translocase TraB is definitely present only on the donor site of the mating hyphae, and a mechanism translocating a circular double-stranded DNA molecule is not very plausible. Because the plasmid DNA is not processed during TraB binding at clt, one has to propose involvement of an additional enzymatic activity, for example, a topoisomerase, which might produce a linear molecule that can be transported through the TraB pore. 4. How to pass the septal cross-walls in the recipient mycelium? Crossing the septal cross-walls during intramycelial plasmid spreading seems to be an even more challenging task compared to the primary DNA transfer at the hyphal tip. It involves, in addition to TraB, several Spd proteins. The structure of the Streptomyces septal cross-walls has not been elucidated, and it is not clear whether preexisting channel structures in the cross-walls connect the compartments of the substrate mycelium (Jakimowicz & van Wezel, 2012).