Intact cells are the most stable form of nature's photosynthetic machinery. Coating-immobilized microbes have the potential to revolutionize the design of photoabsorbers for conversion of sunlight into fuels. Multi-layer adhesive polymer coatings could spatially combine photoreactive bacteria and algae (complementary biological irradiance spectra) creating high surface area, thin, flexible structures optimized for light trapping, and production of hydrogen (H(2)) from water, lignin, pollutants, or waste organics. We report a model coating system which produced 2.08 +/- 0.01 mmol H(2) m(-2) h(-1) for 4,000 h with nongrowing Rhodopseudomonas palustris, a purple nonsulfur photosynthetic bacterium. This adhesive, flexible, nanoporous Rps. palustris latex coating produced 8.24 +/- 0.03 mol H(2) m(-2) in an argon atmosphere when supplied with acetate and light. A simple low-pressure hydrogen production and trapping system was tested using a 100 cm(2) coating. Rps. palustris CGA009 was combined in a bilayer coating with a carotenoid-less mutant of Rps. palustris (CrtI(-)) deficient in peripheral light harvesting (LH2) function. Cryogenic field emission gun scanning electron microscopy (cryo-FEG-SEM) and high-pressure freezing were used to visualize the microstructure of hydrated coatings. A light interaction and reactivity model was evaluated to predict optimal coating thickness for light absorption using the Kubelka-Munk theory (KMT) of reflectance and absorptance. A two-flux model predicted light saturation thickness with good agreement to observed H(2) evolution rate. A combined materials and modeling approach could be used for guiding cellular engineering of light trapping and reactivity to enhance overall photosynthetic efficiency per meter square of sunlight incident on photocatalysts.

Two genes (mcrA and mcrB) from Streptomyces lavendulae that together confer resistance to mitomycin C were identified. This DNA appears to comprise a polycistronic operon with a drug-inducible leaderless mRNA. The deduced amino acid sequence of mcrA shows similarity to sequences of a special class of bacterial, plant, and animal oxygen oxidoreductases.

We describe a latex wet coalescence extrusive coating method that produces up to 10-fold specific photosynthetic rate enhancements by nitrate-limited non-growing cyanobacteria deposited onto paper, hydrated and placed in the gas-phase of small tube photobioreactors. These plant leaf-like biocomposites were used to study the tolerance of cyanobacteria strains to illumination and temperature using a solar simulator. We report sustained CO2 absorption and O2 production for 500 h by hydrated gas-phase paper coatings of non-growing Synechococcus PCC7002, Synechocystis PCC6803, Synechocystis PCC6308, and Anabaena PCC7120. Nitrate-starved cyanobacteria immobilized on the paper surface by the latex binder did not grow out of the coatings into the bulk liquid. The average CO2 consumption rate in Synechococcus coatings is 5.67 mmol m(-2)  h(-1) which is remarkably close to the rate reported in the literature for Arabidopsis thaliana leaves under similar experimental conditions (18 mmol m(-2)  h(-1) ). We observed average ratios of oxygen production to carbon dioxide consumption (photosynthetic quotient, PQ) between 1.3 and 1.4, which may indicate a strong dependence on nitrate assimilation during growth and was used to develop a non-growth media formulation for intrinsic kinetics studies. Photosynthetic intensification factors (PIF) (O2 production by nitrate-limited cyanobacteria in latex coatings/O2 produced by nitrate-limited cell suspensions) in cyanobacteria biocomposites prepared from wet cell pellets concentrated 100- to 300-fold show 7-10 times higher specific reactivity compared to cells in suspension under identical nitrate-limited non-growth conditions. This is the first report of changes of cyanobacteria tolerance to temperature and light intensities after deposition as a thin coating on a porous matrix, which has important implications for gas-phase photobioreactor design using porous composite materials. Cryo-fracture SEM and confocal microscopy images of cell coating distribution on the paper biocomposite suggest that the spatial arrangement of the cells in the coating can affect photoreactivity. This technique could be used to fabricate very stable, multi-organism composite coatings on flexible microfluidic devices in the gas-phase capable of harvesting light in a broader range of wavelengths, to optimize thermotolerant, desiccation tolerant, or halotolerant cyanobacteria that produce O2 with secretion of liquid-fuel precursors synthesized from CO2 .

Adhesive biocatalytic coatings (biocoatings) have a nanoporous microstructure generated by partially coalesced waterborne polymer particles that entrap highly concentrated living cells in a dry state stabilized by carbohydrate osmo-protectants. Biocoatings can be deposited by high speed coating technologies, aerosol delivery or ink-jet printed in multilayered, patterned coatings on flexible nonporous or nonwoven substrates, preserving 10 10-10 12 non-growing viable microorganisms per m 2 in 2-50 m thick layers. Cells are rehydrated to restore their metabolism. The layers reactive half-life following rehydration can be 1000 s of hours. The planar structure of biocoatings enable uniform illumination of a high concentration of photo-reactive microorganisms or algae and contact these microbe with thin liquid films for efficient mass transfer. This review highlights recent advances in biocoating technology for pollutants degradation, photo-reactive coatings, stabilization of hyperthermophiles for biocatalysis, environmental biosensors, and biocomposite fuel cells. Engineering cells for desiccation tolerance, unveiling the metabolism of nongrowing cells, and engineering the interaction between the cell surface and adhesive polymer binders are fundamental challenges to open the door to vast future applications of biocoatings for environmental sensing and remediation.