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Zöllner, R.

Publications and source records attributed to Zöllner, R..

2 recordsLinked to original sources

Motor properties of PilT-independent type 4 pilus retraction in gonococci

Bacterial type 4 pili (T4P) belong to the strongest molecular machines. The gonococcal T4P retraction ATPase PilT supports forces exceeding 100 pN during T4P retraction. Here, we address the question whether gonococcal T4P retract in the absence of PilT. We show that pilT deletion strains indeed retract their T4P but the maximum force is reduced to 5 pN. Similarly, the speed of T4P retraction is lower by orders of magnitude compared to T4P retraction driven by PilT. Deleting the pilT paralogues pilU and pilT2 in the{Delta} pilT background did not inhibit T4P retraction, indicating that the PilT-like proteins do not compensate for PilT. Furthermore, we show that depletion of proton motive force did not inhibit pilT-independent T4P retraction. We conclude that the retraction ATPase is not essential for gonococcal T4P retraction. However, the force generated in the absence of PilT is too low to support important functions of T4P including twitching motility, fluidization of colonies, or induction of host cell response.\n\nIMPORTANCEBacterial type 4 pili (T4P) have been termed the swiss army knive of bacteria because they perform numerous functions including host cell interaction, twitching motility, colony formation, DNA uptake, protein secretion, and surface sensing. The pilus fibre continuously elongates or retracts and these dynamics are functionally important. Curiously, only a subset of T4P systems employs T4P retraction ATPases to power T4P retraction. Here we show that one of the strongest T4P machines, the gonococcal T4P, retracts without a retraction ATPase. Biophysical characterization reveal strongly reduced force and speed compared to retraction with ATPase. We propose that bacteria encode for retraction ATPases when T4P have to generate high force supporting functions like twitching motility, triggering host cell response, or fluidizing colonies.

biophysics↗

Type IV pilin post-translational modifications modulate materials properties of bacterial colonies

Bacterial type 4 pili (T4P) are extracellular polymers that initiate the formation of microcolonies and biofilms. T4P continuously elongate and retract. These pilus dynamics crucially affects the local order, shape, and fluidity of microcolonies. The major pilin subunit of the T4P bears multiple post-translational modifications. By interfering with different steps of the pilin glycosylation and phosphoform modification pathways, we investigated the effect of pilin post-translational modification on the shape and dynamics of microcolonies formed by Neisseria gonorrhoeae. Deleting the phosphotransferase responsible for phosphoethanolamine modification at residue serine 68 (S68) inhibits shape relaxations of microcolonies after pertubation and causes bacteria carrying the phosphoform modification to segregate to the surface of mixed colonies. We relate these mesoscopic phenotypes to increased attractive forces generated by T4P between cells. Moreover, by deleting genes responsible for the pilin glycan structure, we show that the number of saccharides attached at residue serine 63 (S63) affect the ratio between surface tension and viscosity and cause sorting between bacteria carrying different pilin glycoforms. We conclude that different pilin post-translational modifications moderately affect the attractive forces between bacteria but have severe effects on the materials properties of microcolonies.

biophysics↗