Naturally Derived Iron Oxide Nanowires from Bacteria for Magnetically Triggered Drug Release and Cancer Hyperthermia in 2D and 3D Culture Environments: Bacteria Biofilm to Potent Cancer Therapeutic.

Iron oxide nanowires produced by bacteria (Mariprofundus ferrooxydans) are demonstrated as new multifunctional drug carriers for triggered therapeutics release and cancer hyperthmia applications. Iron oxide nanowires are obtained from biofilm waste in the bore system used to pump saline groundwater into the River Murray, South Australia (Australia) and processed into individual nanowires with extensive magnetic properties. The drug carrier capabilities of these iron oxide nanowires (Bac-FeOxNWs) are assessed by loading anticancer drug (doxorubicin, Dox) followed by measuring its elution under sustained and triggered release conditions using alternating magnetic field (AMF). The cytotoxicity of Bac-FeOxNWs assessed in 2D (96 well plate) and 3D (Matrigel) cell cultures using MDA-MB231-TXSA human breast cancer cells and mouse RAW 264.7 macrophage cells shows that these Bac-FeOxNWs are biocompatible even at concentrations as high as 250 µg/mL after 24 h of incubation. Finally, we demonstrate the capabilities of Bac-FeOxNWs as potential hyperthermia agent in 3D culture setup. Application of AMF increased the local temperature by 14 °C resulting in approximately 34% decrease in cell viability. Our results demonstrate that these naturally produced nanowires in the form of biofilm can efficiently act as drug carriers with triggered payload release and magnetothermal heating features for potential anticancer therapeutics applications.

The application of activated carbon for the treatment and reuse of the aqueous phase derived from the hydrothermal liquefaction of a halophytic Tetraselmis sp.

The aim of this study was to determine how the treatment of the HTL AP with activated carbon would affect both growth and chemical composition of the microalgae. Tetraselmis MUR233 was grown in HTL AP (filtered and unfiltered) at 500 ×, 1000 ×, and 2000 × dilutions in hyper saline conditions. The organic nitrogen and carbon component of the HTL AP was greatly reduced with the activated carbon treatment (TKN 52,000 ± 520 mg/L to 5900 ± 59 mg/L; TOC 19,000 ± 190 mg/L to 13,000 ± 130 mg/L). Growth of Tetraselmis MUR233 was achieved on all dilutions of HTL AP, with a maximum growth observed in the AP filtered 1000 × dilution treatment (0.41 ± 0.09 g/L), this compares to a yield of 0.49 ± 0.10 g/L when grown in traditional culture media.

The influence of protozoa with a filtered and non-filtered seawater culture of Tetraselmis sp., and effects to the bacterial and algal communities over 10 days.

In this study a filter was used to remove protozoa and its effects on a Tetraselmis sp. culture were evaluated in terms of final total lipid, final total dry weight, cell counts, and both the bacterial and algal communities. The protozoa species observed within this study was identified as Cohnilembus reniformis. It was observed that on the final day no C. reniformis were present in filtered cultures compared to the non-filtered culture which contained 40±3 C. reniformis/mL. The presence of C. reniformis within the culture did not affect the total lipid or the total dry weight recovered, suggesting that Tetraselmis sp. was capable of surviving and growing in the presence of C. reniformis. Overall it is suggested that an 11 µm filter was effective at removing protozoa, though growing a microalgae culture without filtration did not show any significant effect.

Microalgae digestate effluent as a growth medium for Tetraselmis sp. in the production of biofuels.

This study investigated an alternative nutrient source arising from anaerobically digested Tetraselmis sp. effluent (MDE) as a nutrient feed stock to form a closed loop nutrient system. To determine MDE suitability the following factors were observed: growth, lipid content, and the bacterial diversity. MDE was diluted according to the concentration of NH4(+) content (20, 40, 60, 80 mg/L) and compared against F/2 medium a standard medium for Tetraselmis sp. The growth rate on the MDE medium was not as rapid as the F/2 medium and the less diluted MDE correlated (R(2)) with lower total lipid contents (R(2), 0.927), additionally acyl carrier proteins (ACP) gene expression rates displayed lower gene expression within MDE treatments. Lastly, higher concentrations of MDE were correlated with a higher bacterial diversity throughout the investigation. The suitability of MDE as a nutrient supplement for the production of Tetraselmis sp. biomass and lipid is feasible.

The influences of the recycle process on the bacterial community in a pilot scale microalgae raceway pond.

The use of recycled media has been shown to be a necessary step within the lifecycle of microalgal biofuels for economic sustainability and reducing the water footprint. However the impact of the harvesting of microalgae on the bacterial load of the recycled water has yet to be investigated. Within this study PCR-DGGE and real-time PCR was used to evaluate the bacterial community dynamics within the recycled water following harvest and concentration steps for a pilot scale open pond system (120,000L), which was developed for the production of green crude oil from Tetraselmis sp. in hyper saline water. Two stages were used in the harvesting; Stage 1 electroflocculation, and Stage 2 centrifugation. Electroflocculation was shown to have little effect on the bacterial cell concentration. In contrast bacterial diversity and cell concentration within the centrifugation step was greatly reduced.

Sustainable remediation--the application of bioremediated soil for use in the degradation of TNT chips.

Environmental contamination by TNT (2,4,6 trinitrotoluene), historically used in civilian industries and the military as an explosive is of great concern due to its toxicity. Scientific studies have however shown that TNT is susceptible to microbial transformation. The aim of this study was to assess the potential of a previously bioremediated hydrocarbon contaminated soil (PBR) to increase TNT degradation rates. This was investigated by adding TNT chips to PBR and uncontaminated soils (PNC) in laboratory based studies (up to 16 weeks). Residual TNT chip analysis showed greater TNT degradation in PBR soils (70%) and significantly higher metabolic rates (4.5 fold increase in cumulative CO(2) levels) than in PNC soils (30%). Molecular analysis (PCR-DGGE-cluster analysis) showed substantial shifts in soil microbial communities associated with TNT contamination between day 0 and week 4 especially in PBR soils. Bacterial communities appeared to be more sensitive to TNT contamination than fungal communities in both soils. Quantitative PCR analysis showed ~3 fold increase in the abundance of nitroreductase genes (pnrA) in PBR soils with a gradual reduction in community evenness (Pareto-Lorenz curves) in contrast to PNC soils. These results suggest that microbial response to TNT contamination was dependent on the history of soil use. The results also confirm that the microbial potential of waste soils such as PBR soil (usually disposed of via landfill) can be successfully used for accelerated TNT chip degradation. This promotes sustainable re-use of waste soils extending the life span of landfill sites.