We report the biological synthesis of titania that is integrated into the silica-based cell walls of a titaniumresistant diatom, Fistulifera solaris. Titania is deposited across the diatom cell walls by simply incubating F. solaris in a culture medium containing a high concentration (2 mM) of a water-soluble organo-titanium compound, titanium(IV) bis(ammonium lactato) dihydroxide (TiBALDH) that would otherwise inhibit the growth of other diatom species. Furthermore, we genetically engineered the interfaces of the diatom cell walls with a titanium-associated peptide, which subsequently increased the Ti/Si atomic ratio by more than 50% (i.e., from 6.2 ± 0.2% to 9.7 ± 0.5%, as identified by inductively coupled plasma−atomic emission spectrometry). The titanium content on the F. solaris silica cell walls is one of the highest reported to date, and comparable to that of chemically synthesized TiO 2 −silica composites. Subsequent thermal annealing at 500 °C in air converted the cell wall-bound titania to nanocrystalline anatase TiO 2 , a highly photocatalytically active phase. We propose that incubation of the titanium-resistant F. solaris with TiBALDH as demonstrated in this study could be a promising bioprocess toward the scalable synthesis of TiO 2 . In addition, the genetic engineering we used to modulate the surface properties of diatom silica cell walls could be extended to synthesize controlled nanomaterials for multiple applications including bioremediation, water purification, and energy conversion/storage.
Chitosan membranes were prepared by the casting method combined with alkali treatment. The molecular weight of chitosan and the alkali treatment influenced the water content and water permeability of the chitosan membranes. The water content increased as the NaOH concentration was increased from 1 to 5 mol/L. The water permeation flux of chitosan membranes with three different molecular weights increased linearly with the operating pressure and was highest for the membrane formed from chitosan with the lowest molecular weight. Membranes with a lower water content had a higher water flux. The membranes blocked 100% of compounds with molecular weights above methyl orange (MW = 327 Da). At 60 ≤ MW ≤ 600, the blocking rate strongly depended on the substance. The results confirmed that the membranes are suitable for compound separation, such as in purification and wastewater treatment.
BackgroundProduction of biofuels from microalgae has been recognized to be a promising route for a sustainable energy supply. However, the microalgae harvesting process is a bottleneck for industrialization because it is energy intensive. Thus, by displaying interactive protein factors on the cell wall, oleaginous microalgae can acquire the auto- and controllable-flocculation function, yielding smarter and energy-efficient harvesting.ResultsTowards this goal, we established a cell-surface display system using the oleaginous diatom Fistulifera solaris JPCC DA0580. Putative cell wall proteins, termed frustulins, were identified from the genome information using a homology search. A selected frustulin was subsequently fused with green fluorescent protein (GFP) and a diatom cell-surface display was successfully demonstrated. The antibody-binding assay further confirmed that the displayed GFP could interact with the antibody at the outermost surface of the cells. Moreover, a cell harvesting experiment was carried out using silica-affinity peptide-displaying diatom cells and silica particles where engineered cells attached to the silica particles resulting in immediate sedimentation.ConclusionThis is the first report to demonstrate the engineered peptide-mediated harvesting of oleaginous microalgae using a cell-surface display system. Flocculation efficiency based on the silica-affinity peptide-mediated cell harvesting method demonstrated a comparable performance to other flocculation strategies which use either harsh pH conditions or expensive chemical/biological flocculation agents. We propose that our peptide-mediated cell harvest method will be useful for the efficient biofuel production in the future.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-015-0406-9) contains supplementary material, which is available to authorized users.
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