Measurement of Ankle Joint Movements Using IMUs during Running.

Gait analysis has historically been implemented in laboratory settings only with expensive instruments; yet, recently, efforts to develop and integrate wearable sensors into clinical applications have been made. A limited number of previous studies have been conducted to validate inertial measurement units (IMUs) for measuring ankle joint kinematics, especially with small movement ranges. Therefore, the purpose of this study was to validate the ability of available IMUs to accurately measure the ankle joint angles by comparing the ankle joint angles measured using a wearable device with those obtained using a motion capture system during running. Ten healthy subjects participated in the study. The intraclass correlation coefficient (ICC) and standard error of measurement were calculated for reliability, whereas the Pearson coefficient correlation was performed for validity. The results showed that the day-to-day reliability was excellent (0.974 and 0.900 for sagittal and frontal plane, respectively), and the validity was good in both sagittal (r = 0.821, p < 0.001) and frontal (r = 0.835, p < 0.001) planes for ankle joints. In conclusion, we suggest that the developed device could be used as an alternative tool for the 3D motion capture system for assessing ankle joint kinematics.

Cofactor-Free, Direct Photoactivation of Enoate Reductases for the Asymmetric Reduction of C=C Bonds.

Enoate reductases from the family of old yellow enzymes (OYEs) can catalyze stereoselective trans-hydrogenation of activated C=C bonds. Their application is limited by the necessity for a continuous supply of redox equivalents such as nicotinamide cofactors [NAD(P)H]. Visible light-driven activation of OYEs through NAD(P)H-free, direct transfer of photoexcited electrons from xanthene dyes to the prosthetic flavin moiety is reported. Spectroscopic and electrochemical analyses verified spontaneous association of rose bengal and its derivatives with OYEs. Illumination of a white light-emitting-diode triggered photoreduction of OYEs by xanthene dyes, which facilitated the enantioselective reduction of C=C bonds in the absence of NADH. The photoenzymatic conversion of 2-methylcyclohexenone resulted in enantiopure (ee>99 %) (R)-2-methylcyclohexanone with conversion yields as high as 80-90 %. The turnover frequency was significantly affected by the substitution of halogen atoms in xanthene dyes.

CO2 -Reductive, Copper Oxide-Based Photobiocathode for Z-Scheme Semi-Artificial Leaf Structure.

Green plants convert sunlight into high-energy chemicals by coupling solar-driven water oxidation in the Z-scheme and CO2 fixation in the Calvin cycle. In this study, formate dehydrogenase from Clostridium ljungdahlii (ClFDH) is interfaced with a TiO2 -coated CuFeO2 and CuO mixed (ClFDH-TiO2 |CFO) electrode. In this biohybrid photocathode, the TiO2 layer enhances the photoelectrochemical (PEC) stability of the labile CFO photocathode and facilitates the transfer of photoexcited electrons from the CFO to ClFDH. Furthermore, inspired by the natural photosynthetic scheme, the photobiocathode is combined with a water-oxidizing, FeOOH-coated BiVO4 (FeOOH|BiVO4 ) photoanode to assemble a wireless Z-scheme biocatalytic PEC device as a semi-artificial leaf. The leaf-like structure effects a bias-free biocatalytic CO2 -to-formate conversion under visible light. Its rate of formate production is 2.45 times faster than that without ClFDH. This work is the first example of a wireless solar-driven semi-biological PEC system for CO2 reduction that uses water as an electron feedstock.

Semiconducting Synthetic Melanin-Based Organic/Inorganic Hybrid Photoanodes for Solar Water Oxidation.

We report the development of semiconducting melanin-based organic/inorganic hybrid photoanodes for solar water oxidation. Synthetic melanin thin-film incorporating polyoxometalate (POM) water oxidation catalysts (WOCs) are readily deposited on the surface of various n-type inorganic semiconductors (e.g., Fe2 O3 , BiVO4 , and TiO2 ) by electropolymerization. The deposition of melanin and POM hybrid (MP) thin-film results in the remarkably improved performance of an underlying semiconductor photoanode for solar water oxidation with a significantly increased photocurrent density and decreased onset potential for water oxidation through the formation of a melanin-based p-n heterojunction structure. We believe that this study can provide insights into the design and fabrication of various melanin-based optoelectronic devices by utilizing its unique physicochemical properties.

Unbiased biocatalytic solar-to-chemical conversion by FeOOH/BiVO4/perovskite tandem structure.

Redox enzymes catalyze fascinating chemical reactions with excellent regio- and stereo-specificity. Nicotinamide adenine dinucleotide cofactor is essential in numerous redox biocatalytic reactions and needs to be regenerated because it is consumed as an equivalent during the enzymatic turnover. Here we report on unbiased photoelectrochemical tandem assembly of a photoanode (FeOOH/BiVO4) and a perovskite photovoltaic to provide sufficient potential for cofactor-dependent biocatalytic reactions. We obtain a high faradaic efficiency of 96.2% and an initial conversion rate of 2.4 mM h-1 without an external applied bias for the photoelectrochemical enzymatic conversion of α-ketoglutarate to L-glutamate via L-glutamate dehydrogenase. In addition, we achieve a total turnover number and a turnover frequency of the enzyme of 108,800 and 6200 h-1, respectively, demonstrating that the tandem configuration facilitates redox biocatalysis using light as the only energy source.