David R. Salem

Cyanobacteria biomass sources have the potential to contribute to the replacement of fossil fuels and to the reduction in global warming by sustainable conversion of atmospheric CO₂ into biofuels and high-value chemicals. Cyanobacteria cultivation in photobioreactors (PBRs) results in biofouling on their transparent inner walls, which reduces photosynthetic efficiency and productivity. While cyanobacteria biofouling in PBRs is recognized as a significant operating challenge, this review draws attention to the lack of studies on antifouling strategies for PBRs involving cyanobacteria and discusses several areas related to cyanobacteria fouling mechanisms on PBR materials, which require further investigation. These include an in-depth analysis of conditioning films, the role of pili and EPS in gliding and adhesion, potential revisions to existing theoretical models for predicting adhesion, and material properties that affect cyanobacteria adhesion. We use knowledge from marine, medical, and industrial biofouling management to help identify strategies to combat cyanobacteria fouling in PBRs, and we review the applicability of various bioinspired physical and chemical strategies, as well as genetic engineering approaches to prevent cyanobacteria biofilm formation in PBRs.

Particulate methane monooxygenase (pMMO), a membrane-bound enzyme having three subunits (α, β, and γ) and copper-containing centers, is found in most of the methanotrophs that selectively catalyze the oxidation of methane into methanol. Active sites in the pMMO of Methylosinus trichosporium OB3b were determined by docking the modeled structure with ethylbenzene, toluene, 1,3-dibutadiene, and trichloroethylene. The docking energy between the modeled pMMO structure and ethylbenzene, toluene, 1,3-dibutadiene, and trichloroethylene was −5.2, −5.7, −4.2, and −3.8 kcal/mol, respectively, suggesting the existence of more than one active site within the monomeric subunits due to the presence of multiple binding sites within the pMMO monomer. The evaluation of tunnels and cavities of the active sites and the docking results showed that each active site is specific to the radius of the substrate. To increase the catalysis rates of methane in the pMMO of M. trichosporium OB3b, selected amino acid residues interacting at the binding site of ethylbenzene, toluene, 1,3-dibutadiene, and trichloroethylene were mutated. Based on screening the strain energy, docking energy, and physiochemical properties, five mutants were downselected, B:Leu31Ser, B:Phe96Gly, B:Phe92Thr, B:Trp106Ala, and B:Tyr110Phe, which showed the docking energy of −6.3, −6.7, −6.3, −6.5, and −6.5 kcal/mol, respectively, as compared to the wild type (−5.2 kcal/mol) with ethylbenzene. These results suggest that these five mutants would likely increase methane oxidation rates compared to wild-type pMMO.

The U.S. Department of Energy's Office of Scientific and Technical Information

Graphene nanomaterials have demonstrated simultaneous enhancement of both the thermal and mechanical properties of many base polymer systems, but for application as a reinforcement in multifunctional thermally insulating polymer foam the graphene additive must not significantly increase the macroscopic thermal conductivity. In an effort to study and decouple these mechanical and thermal properties, low loadings of reduced graphene oxide nanoplatelets have been added into epoxy formulations to comprise the matrix structure of hollow microchannel nanocomposite foams. Substantial improvements of 226% were achieved in the microchannel foam specific flexural modulus at only 0.15% graphene nanoplatelet loading without compromising the foam flexural strength and while also maintaining the low thermal conductivity of the baseline epoxy foam material. These results support the use of these nanocomposite foams as mechanically reinforced thermal insulation, with the addition of the graphene nanoplatelets potentially providing additional multifunctional improvements to the foam such as reduced UV‐radiation transmittance, improved electrical surface conductivity for diminished static charge buildup, and/or lowering of the coefficient of thermal expansion for enhanced structural stability in extreme environments. This particular combination of multifunctional properties makes these materials well suited as high‐performance structural thermal insulation materials in support of next generation space system applications.

Adsorption of conditioning films on a solid surface is the first step in the development of biofilms. With the goal of understanding the preliminary adhesion mechanisms of cyanobacteria on photobioreactor (PBR) materials to prevent biofouling, the physical changes occurring on PBR materials were investigated during the initial adhesion and biofilm formation by Anabaena sp. PCC 7120, a cyanobacterium that is genetically modified to produce linalool. Atomic force microscopy (AFM) revealed that the conditioning film deposition was in the form of spike-like structures on all the materials except PVC. The average heights (in the range 9 − 16 nm) of the conditioning films deposited on glass, PMMA, PC and HDPE were 11 to 20 times higher than on PVC at 96 h. The time dependent change in thickness of conditioning films correlated well with Anabaena cell attachment to the PBR materials. The rapid and significant colonization of Anabaena on glass within 48 h was consistent with the increase in thickness of the conditioning film within this time period. Lack of the conditioning film spike structures and no change in thickness of the conditioning films with time on the PVC together with comparatively delayed cell attachment and conditioning-film protein deposition on this material, indicated that the nanoscale spike structures on the other PBR materials may be accelerating the cell attachment process but are not a prerequisite for cell attachment. These results suggest that PVC should be explored further as an antifouling material for photobioreactors. The thickness of the conditioning films on glass measured by a scratch and scan method was in good agreement with the thickness values measured by an adhesive tape method, indicating that both these methods can be used for fast and reliable AFM thickness determination of bacterial conditioning films.

Firmicutes is almost a ubiquitous phylum. Several genera of this group, for instance, Geobacillus, are recognized for decomposing plant organic matter and for producing thermostable ligninolytic enzymes. Amplicon sequencing was used in this study to determine the prevalence and genetic diversity of the Firmicutes in two distinctly related environmental samples—South Dakota Landfill Compost (SDLC, 60 °C), and Sanford Underground Research Facility sediments (SURF, 45 °C). Although distinct microbial community compositions were observed, there was a dominance of Firmicutes in both the SDLC and SURF samples, followed by Proteobacteria. The abundant classes of bacteria in the SDLC site, within the phylum Firmicutes, were Bacilli (83.2%), and Clostridia (2.9%). In comparison, the sample from the SURF mine was dominated by the Clostridia (45.8%) and then Bacilli (20.1%). Within the class Bacilli, the SDLC sample had more diversity (a total of 11 genera with more than 1% operational taxonomic unit, OTU). On the other hand, SURF samples had just three genera, about 1% of the total population: Bacilli, Paenibacillus, and Solibacillus. With specific regard to Geobacillus, it was found to be present at a level of 0.07% and 2.5% in SURF and SDLC, respectively. Subsequently, culture isolations of endospore-forming Firmicutes members from these samples led to the isolation of a total of 117 isolates. According to colony morphologies, and identification based upon 16S rRNA and gyrB gene sequence analysis, we obtained 58 taxonomically distinct strains. Depending on the similarity indexes, a gyrB sequence comparison appeared more useful than 16S rRNA sequence analysis for inferring intra- and some intergeneric relationships between the isolates.