oneidensis to form pellicles in the presence of EDTA completely. In contrast, Mg(II) shows mild effects on relieving EDTA inhibition whereas Fe(II) and Fe(III) Liproxstatin-1 cell line counteracted EDTA in a way different from other tested cations evidenced by the fragile pellicles. In combination, these

data suggest that the relative stability constants of metal cations (Cu(II) [5.77], Mg(II) [8.83], Ca(II) [10.61], Mn(II) [15.6], Zn(II) [17.5], Fe(II) [25.0], and Fe(III) [27.2]) and their affect on EDTA inhibition are not correlated. It is particularly worth discussing roles of Fe(II) and Fe(III) in pellicle formation of S. oneidensis. In recent years, many reports have demonstrated that the iron cations are important, if not essential, in bacterial biofilm formation [34, 45–47]. In P. aeruginosa, influence of Fe(II) and Fe(III) on the process was equivalent to that of Ca(II) [34]. In S. oneidensis, irons in forms of Fe(II) and Fe(III) were PF-573228 research buy not only unable to neutralize MK-0457 the inhibitory effect of EDTA on pellicle formation

completely but also resulted in structurally impaired pellicles although these agents indeed play a role in pellicle formation. This observation indicates that irons are not so crucial as Cu(II), Ca(II), Mn(II), and Zn(II) in pellicle formation of S. oneidensis. In fact, this may not be surprising. In Acinetobacter baumannii and Staphylococcus aureus, iron limitation improved biofilm formation

[48, 49]. Therefore, it is possible that different bacteria respond to irons in a different way with respect to biofilm formation. Like SSA biofilms, pellicles require EPS to form a matrix to support embedded cells. Although EPS are now widely recognized as the essential components for biofilm formation and development in all biofilm-forming microorganisms studied so far, diversity in their individual composition and relative abundance of certain elements is substantial [50]. For example, extracellular nucleic acids, which are not important in most biofilm-forming microorganisms, are required for SSA biofilm formation in a variety check details of bacteria [11, 36, 37, 51, 52]. In S. oneidensis, proteins not extracellular DNAs are required to pellicle formation. While essential extracellular proteins for S. oneidensis pellicle formation are largely unknown, results from this study demonstrated that the AggA TISS is crucial in the process, likely at the development of the monolayer. One of substrates of this transporter is predicted to be SO4317, a large ‘putative RTX toxin’ [35], implicating that the protein may be involved in pellicle formation. In the case of polysaccharides, mannose dominates not only in pellicles but also in supernatants, implicating that mannose-based polysaccharides may have a more general role in the bacterial physiology. Like in B. subtilis, mutations in S.