Nature-inspired trapped air cushion surfaces for environmentally sustainable antibiofouling

Feathers of seabirds and waterfowl (for example the mallard duck (Anas platyrhynchos)) consist of hierarchical fibrillar structures encapsulated with hydrophobic preen oil. These characteristics afford waterproofing through the entrapment of air pockets, enabling swimming and diving for such bird species. This liquid repellency mechanism for bird feathers is mimicked by surface hydrophobisation of fibrous nonwoven polypropylene textiles to create large volumes of trapped air at the solid–liquid interface (plastron). Higher static water contact angle values correlate to a greater resistance towards water ingress (akin to the behaviour of mallard feathers). In order to extend the trapped gas layer lifetimes, the transportation of air from the water surface to a submerged air bubble by the diving bell spider (Argyroneta aquatica) for respiration is mimicked via short duration (< 1 s) solar-powered air bubble bursts once every 2 h. This combination of ornithological and arachnological inspired approaches yields stable trapped gas layers at the solid–liquid interface which are shown to inhibit biofouling in real-world outdoor wet environments

An Ovarian Bioreactor for In Vitro Culture of the Whole Bovine Ovary: a Preliminary Report

Background: Improved cancer therapeutics and enhanced cancer survivorship have emphasized the severe long-term side effects of chemotherapy. Specifically, studies have linked many chemotherapy agents with primary ovarian insufficiency, although an exact insult model has not yet been determined. To investigate and ultimately solve this problem, a novel device for extended study of mammalian ovaries in vitro was developed. Methods: A bioreactor was fabricated for bovine ovarian culture that provides intravascular delivery of media to the ovary through isolation and cannulation of a main ovarian artery branch. Whole ovaries were cultured in vitro using three methods: (1) continuously supplied fresh culture media, (2) recirculated culture media, or (3) continuously supplied fresh culture media supplemented with 500 nM doxorubicin for 24 or 48 h. TUNEL assay was used to assess apoptotic cell percentages in the three groups as compared to uncultured baseline ovaries. Results: The ovary culture method was shown to maintain cell viability by effectively delivering nutrient-enriched pH-balanced media at a constant flow rate. Lower apoptosis observed in ovaries cultured in continuously supplied fresh culture media illustrates that this culture device and method are the first to sustain whole bovine ovary viability for 48 h. Meanwhile, the increase in the percentage of cell apoptosis with doxorubicin treatment indicates that the device can provide an alternative model for testing chemotherapy and chemoprotection treatments to prevent primary ovarian insufficiency in cancer patients. Conclusions: An ovarian bioreactor with consistent culture media flow through an ovarian vasculature-assisted approach maintains short-term whole bovine ovary viability

An Ovarian Bioreactor for In Vitro Culture of the Whole Bovine Ovary: a Preliminary Report

Background: Improved cancer therapeutics and enhanced cancer survivorship have emphasized the severe long-term side effects of chemotherapy. Specifically, studies have linked many chemotherapy agents with primary ovarian insufficiency, although an exact insult model has not yet been determined. To investigate and ultimately solve this problem, a novel device for extended study of mammalian ovaries in vitro was developed. Methods: A bioreactor was fabricated for bovine ovarian culture that provides intravascular delivery of media to the ovary through isolation and cannulation of a main ovarian artery branch. Whole ovaries were cultured in vitro using three methods: (1) continuously supplied fresh culture media, (2) recirculated culture media, or (3) continuously supplied fresh culture media supplemented with 500 nM doxorubicin for 24 or 48 h. TUNEL assay was used to assess apoptotic cell percentages in the three groups as compared to uncultured baseline ovaries. Results: The ovary culture method was shown to maintain cell viability by effectively delivering nutrient-enriched pH-balanced media at a constant flow rate. Lower apoptosis observed in ovaries cultured in continuously supplied fresh culture media illustrates that this culture device and method are the first to sustain whole bovine ovary viability for 48 h. Meanwhile, the increase in the percentage of cell apoptosis with doxorubicin treatment indicates that the device can provide an alternative model for testing chemotherapy and chemoprotection treatments to prevent primary ovarian insufficiency in cancer patients. Conclusions: An ovarian bioreactor with consistent culture media flow through an ovarian vasculature-assisted approach maintains short-term whole bovine ovary viability

Homologous Expression of a Subcomplex of Pyrococcus furiosus Hydrogenase that Interacts with Pyruvate Ferredoxin Oxidoreductase

Hydrogen gas is an attractive alternative fuel as it is carbon neutral and has higher energy content per unit mass than fossil fuels. The biological enzyme responsible for utilizing molecular hydrogen is hydrogenase, a heteromeric metalloenzyme requiring a complex maturation process to assemble its O2-sensitive dinuclear-catalytic site containing nickel and iron atoms. To facilitate their utility in applied processes, it is essential that tools are available to engineer hydrogenases to tailor catalytic activity and electron carrier specificity, and decrease oxygen sensitivity using standard molecular biology techniques. As a model system we are using hydrogen-producing Pyrococcus furiosus, which grows optimally at 100°C. We have taken advantage of a recently developed genetic system that allows markerless chromosomal integrations via homologous recombination. We have combined a new gene marker system with a highly-expressed constitutive promoter to enable high-level homologous expression of an engineered form of the cytoplasmic NADP-dependent hydrogenase (SHI) of P. furiosus. In a step towards obtaining ‘minimal’ hydrogenases, we have successfully produced the heterodimeric form of SHI that contains only two of the four subunits found in the native heterotetrameric enzyme. The heterodimeric form is highly active (150 units mg−1 in H2 production using the artificial electron donor methyl viologen) and thermostable (t1/2 ∼0.5 hour at 90°C). Moreover, the heterodimer does not use NADPH and instead can directly utilize reductant supplied by pyruvate ferredoxin oxidoreductase from P. furiosus. The SHI heterodimer and POR therefore represent a two-enzyme system that oxidizes pyruvate and produces H2 in vitro without the need for an intermediate electron carrier

Characterizing novel transducers for high temperature thermal measurements using time domain thermoreflectance

Time domain thermoreflectance (TDTR) is an optical pump-probe technique used to measure thermal properties of material systems. Samples are typically coated with a thin metal transducer layer, such as aluminum or gold. At temperatures approaching 2,000°C, most transducers become limited by melting temperature, chemical reactions, or other phase transitions. Hafnium Nitride (HfN) is a conductive ceramic with a melting point exceeding 3300°C. It is estimated to have a constant reflectance of 17% and 64% at 400nm and 800nm, respectively. Iridium (Ir) has a melting temperature of 2,447°C. Our work characterizes the thermal properties of HfN and Ir, respectively, and investigates their viability as transducers for TDTR measurements at high temperatures to the point of thermodynamically-driven failure. Thermal conductivity is measured as a function of temperature for HfN and Ir, respectively, and thermoreflectance coefficients are measured and compared to that of typical transducers. Thermal conductivities for MgO, Al2O3, SiO2, and diamond substrates are measured using the aforementioned thin films as transducers to test material reliability. Results and implications for future high temperature TDTR measurements are discussed. This work is supported by the U.S. Office of Naval Research MURI program (grant No. N00014-15- 1-2863)