Heme protein identified from scaly-foot gastropod can synthesize pyrite (FeS2) nanoparticles.

The scaly-foot gastropod (Chrysomallon squamiferum), which lives in the deep-sea zone of oceans around thermal vents, has a black shell and scales on the foot. Both the black shell and scales contain iron sulfide minerals such as greigite (Fe3S4) and pyrite (FeS2). Although pyrite nanoparticles can be used as materials for solar panels, it is difficult to synthesize stable and spherical nanoparticles in vitro. In this study, we extracted organic molecules that interact with nano-pyrite from the shell of the scaly-foot gastropod to develop a low-cost, eco-friendly method for pyrite nanoparticles synthesis. Myoglobin (csMG), a heme protein, was identified in the iron sulfide layer of the shell. We purified recombinant csMG (r-csMG) and demonstrated that r-csMG helped in the conversion of ferric ions, sulfide ions and sulfur into spherical shaped pyrite nanoparticles at 80°C. To reduce the effort and cost of production, we showed that commercially available myoglobin from Equus caballus (ecMG) also induced the in vitro synthesis of pyrite nanoparticles. Using structure-function experiments with digested peptides, we highlighted that the amino acid sequence of r-csMG peptides controlled the spherical shape of the nanoparticle while the hemin molecules, which the peptides interacted with, maintained the size of nanoparticles. Synthesized pyrite nanoparticles exhibited strong photoluminescence in the visible wavelength region, suggesting its potential application as a photovoltaic solar cell material. These results suggest that materials for solar cells can be produced at low cost and energy under eco-friendly conditions. STATEMENT OF SIGNIFICANCE: Pyrite is a highly promising material for photovoltaic devices because of its excellent optical, electrical, magnetic, and transport properties and high optical absorption coefficient. Almost all current pyrite synthesis methods use organic solvents at high temperature and pressure under reducing conditions. Synthesized pyrite nanoparticles are unstable and are difficult to use in devices. The scaly-foot gastropod can synthesize pyrite nanoparticles in vivo, meaning that pyrite nanoparticles can be generated in an aqueous environment at low temperature. In this study, we demonstrated the synthesis of pyrite nanoparticles using a heme protein identified in the iron sulfide layer of the scaly-foot gastropod shell. These results exemplify how natural products in organisms can inspire the innovation of new technology.

Non-degenerated photoluminescence excitation correlation spectroscopy using an optical sampling technique.

We have developed a highly time-resolved photoluminescence spectroscopy based on the excitation correlation method. Successive irradiation of a pair of ultrashort light pulses with different wavelength combinations taken from two sub-picosecond lasers has exposed both temporal and energetic correlation in photoluminescence intensity associated with a nonlinear response of a sample. An optical sampling technique has been introduced successfully in order to avoid consideration of the synchronization control of ultrashort light pulses. We have demonstrated the abilities of this technique by applying to the nonlinear photoluminescence dynamics of organic dye molecules in solution.

Production of Xylanase with a transformant of Aspergillus oryzae RIB40 in a Liquid-Surface Immobilization (LSI) System.

Xylanase production by a XynF1 (33 kDa)-transformant of Aspergillus oryzae RIB40 was compared between submerged cultivation (SmC) and liquid-surface immobilization (LSI) systems. While the accumulation of xylanase in the SmC decreased by prolonged incubation, LSI system enabled the continuation of xylanase production to afford 4.5-fold xylanase production compared with the SmC system.

Surface relaxation of polarized Xe atoms dissolved in deuterated ethanol.

We measured the spin relaxation of polarized xenon atoms dissolved in deuterated ethanol. Surface relaxation was suppressed by coating the cell walls with deuterated eicosane. From the dependence of the decay rate on temperature and static magnetic field, we obtained the correlation time of random fluctuations of the local field at the liquid-solid interface. By varying the cell volume, the wall coating, and the surface area of the eicosane, we measured the contribution of the spin-rotation interaction to the relaxation. The use of both deuterated molecules enables us to distinguish surface relaxation from the magnetic dipole-dipole and spin-rotation interactions in solution.

Highly time-resolved correlation measurement between laser and synchrotron radiation pulses without synchronization control.

A mode-locked laser has been introduced in combination with synchrotron radiation to establish a versatile technique for highly time-resolved correlation measurements utilizing the short-pulse and high-pulse frequency characteristics of both photon sources. Successive pulse timing delay detected by nonlinear optical mixing between the two sources yields a cross-correlation profile capable of accurate measurement of the picosecond pulse profile of the synchrotron radiation without any synchronization control. Although the experiment was performed in the visible spectral domain, the present technique opens up a methodology for time-resolved spectroscopy in femtosecond and higher-energy domains by introducing a suitable nonlinear process that informs of the pulse coincidence between the two radiation sources.

Magnetic resonance imaging of spin-polarization transfer of polarized Xe atoms dissolving into ethanol.

We detect the free-induction signals of xenon atoms polarized by spin-exchange optical pumping. The temperature dependence of dissolution and spin-polarization transfer of xenon atoms to ethanol is measured by simultaneous detection of both xenon and proton signals. The polarization of proton is efficiently enhanced in the xenon-saturated solution at low magnetic fields. The large polarization and chemical shift enable us to obtain clearly the distribution image of xenon atoms near the gas-liquid and liquid-liquid boundaries. Therefore the localization of polarized xenon atoms is observed near the surface. By time-resolved magnetic resonance imaging of polarized xenon and polarization-enhanced proton, the spin dynamics is qualitatively studied for the nuclear spins interacting with each other in a dense solution.