Monomolecular reassembly of a crystalline bacterial cell surface layer (S-layer) on untreated and modified silicon surfaces

Abstract Scanning force microscopy was used to investigate the recrystallization of isolated bacterial cell surface layer (S-layer) proteins of Bacillus stearothermophilus NRS 2004/3a variant V1 on untreated, cleaned, silanized and photoresist-coated silicon wafers. With the exception of the hydrophilic surface of cleaned wafers, all other surfaces showed hydrophobic surface characteristics. Recrystallization occurred only at the hydrophobic surfaces, and, with respect to the bacterial cell, the S-layer was always oriented with its more hydrophobic outer face against the interface. Monolayer formation was initiated by crystal growth from several distant randomly oriented nucleation points and terminated by neighbouring, also growing, crystalline areas. The size of the individual crystalline domains formed in this way was in the range of 5–10 μm in diameter. The entire silicon surface was covered by a coherent monolayer after a recrystallization time of approximately 1 h.