Characterization of flower-inducing compound in Lemna paucicostata exposed to drought stress

A flower-inducing compound, LDS1, was isolated from a free-floating aquatic plant, Lemna paucicostata. The chemical structure and the absolute stereochemistry of LDS1 were determined as (9R,13R,11E,15Z)-9,13-dihydroxy-10-oxooctadeca-11,15-dienoic acid for its most abundant diastereomer. LDS1 was enzymatically produced when the plant was exposed to drought stress, and induced flowering at a concentration of 10 nM.     

Relaxation Behavior of Laser-Polarized Xe Gas: Size Dependency and Wall Effect of the T1 Relaxation Time in Glass and Gelatin Bulbs

Size dependency of the relaxation time T₁ was measured for laser-polarized ¹²⁹Xe gas encapsulated in different sized cavities made by glass bulbs or gelatin capsules. The use of laser-polarized gas enhances the sensitivity a great deal, making it possible to measure the longer ¹²⁹Xe relaxation time in quite a short time. The size dependency is analyzed on the basis of the kinetic theory of gases and a relationship is derived in which the relaxation rate is connected with the square inverse of the diameter of the cavity. Such an analysis provides a novel parameter which denotes the wall effect on the relaxation rate when a gas molecule collides with the surface once in a second. The relaxation time of ¹²⁹Xe gas is also dependent on the material which forms the cavity. This dependency is large and the relaxation study using polarized ¹²⁹Xe gas is expected to offer important information about the state of the matter of the cavity wall.     

Reinvestigation into the ring‐opening process of monochloroethylene oxide by quantum chemical calculations

Density functional theory (DFT) computation with B3LYP/6‐31++G** has been performed for the ring‐opening process of monochloroethylene oxide. In this study, the energy changes of an isolated monochloroethylene oxide, an O‐protonated one and a Cl‐protonated one, were investigated with respect to the stretching of the C? O bond length. The increased energy in an O‐protonated system is fairly slow compared with that in a neutral system. In an O‐protonated system, rupturing of the C? O bond, in which the carbon atom in the bond binds to the chlorine atom, occurs more easily than another C? O bond rupture. This fact is in agreement with ideas accepted in organic chemistry. Intrinsic reaction coordinate (IRC) calculations were performed for the O‐protonated system, which gave the activation energy of the ring rupture as 3.89 kcal/mol. This also revealed that the production of an aldehyde occurred by a two‐step reaction, that is, the first ring‐opening process and following transfer of the chlorine atom. LMO wave functions were used to analyze the reaction mechanism. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2006     

Ion conduction mechanisms and thermal properties of hydrated and anhydrous phosphoric acids studied with 1H, 2H, and 31P NMR

To understand the behaviors of phosphoric acids in fuel cells, the ion conduction mechanisms of phosphoric acids in condensed states without free water and in a monomer state with water were studied by measuring the ionic conductivity (sigma) using AC impedance, thermal properties, and self-diffusion coefficients (D) and spin-lattice relaxation times (T1) with multinuclear NMR. The self-diffusion coefficient of the protons (H+ or H3O+), H2O, and H located around the phosphate were always larger than the diffusion coefficients of the phosphates and the disparity increased with increasing phosphate concentration. The diffusion coefficients of the samples containing D2O paralleled those in the protonated samples. Since the 1H NMR T1 values exhibited a minimum with temperature, it was possible to determine the correlation times and they were found to be of nanosecond order for a distance of nanometer order for a flip. The agreement of the ionic conductivities measured directly and those calculated from the diffusion coefficients indicates that the ion conduction obeys the Nernst-Einstein equation in the condensed phosphoric acids. The proton diffusion plays a dominant role in the ion conduction, especially in the condensed phosphoric acids.     

An investigation of pipeline materials for continuous hyperpolarized 129Xe gas spectroscopy

In order to establish a continuous hyperpolarized xenon-129 (HP-129Xe) gas delivery system for MR imaging, the effect of the metallic materials in the gas pipeline on the signal intensity was investigated. In the gas pipeline, an appropriate surface is needed to minimize wall relaxation by the HP-129Xe gas caused by the interaction between the HP gas and the surface, which can lead to signal loss. Although Pyrex glass is a popular material for the HP gas chamber, it is fragile under heat or physical stress. In this study, five stainless steel tubes (STs) prepared with different surface film-forming processes were examined. The MR signal intensities of HP-129Xe gas that passed through each tube were then compared. The film passivated by iron fluoride maintained the highest level of hyperpolarization, whereas that passivated by chromium oxide maintained the lowest. A ST with an appropriate passive film may be a useful alternative to a Pyrex glass pipeline.     

Structure-activity relationship study of flowering-inducer FN against Lemna paucicostata

FN1 (1) and FN2 (2), cycloadducts of α-ketol octadecadienoic acid (3) with norepinephrine (NE), induce flowering in Lemna paucicostata. In order to broaden our understanding of structural requirements of FN for flower induction, nine analogs of 3 (4-12) were synthesized and reacted with NE under basic conditions. These analogs, except for 8, 10, and 12, exhibited significant activity regarding to floral induction in L. paucicostata. Similar experiments were carried out by using 3 and epinephrine, and it was demonstrated that these products also possessed biological activity.     

Enantio-selective reduction of the flowering related compound KODA and its analogues in Pharbitis nil cv. Violet

Plant oxylipins are an important class of signaling molecules in plants. The cyclic adducts of epinephrine or norepinephrine with the naturally occurring oxylipin (12Z,15Z)-9-hydroxy-10-oxo-octadeca-12,15-dienoic acid (KODA, 1) or its synthetic analogues (2–6) have been reported to possess flower-inducing activity toward Lemna paucicostata. By in vivo and in vitro experiments with seedlings of Pharbitis nil cv. Violet carbonyl groups of the α-ketols (1 and 3) and the ketones (7 and 9) were enantio-selectively reduced to give their corresponding vicinal diols (2 and 4) and alcohols (8 and 10). The stereo-chemistry at the oxymethine carbon was determined based on the long range C–H coupling constants and the modified Mosher's method. Orientation of the adjacent hydroxyl group in (1 and 3) did not affect the enantio-selectivity, whereas the conversion was slightly affected and higher yields were obtained with the R-enantiomers of the α-ketols.     

A Simple Model of a Two-Layered High-Temperature Liquid-Dominated Geothermal Reservoir as a Part of a Large-Scale Hydrothermal Convection System

The Kakkonda geothermal reservoir, Japan, is a typical high-temperature liquid-dominated geothermal reservoir, except for its distinctive two-layered temperature structure. It has a shallow permeable reservoir of 230–260°, and a deep less permeable reservoir of 350–360°. Geology and hydrology indicate that the shallow reservoir is one to two orders of magnitude more permeable than the deep reservoir, but that the two reservoirs communicate. It has been widely assumed in engineering and scientific circles that the connection between the two reservoirs is a zero or low permeability barrier to fluid flow. We show that this hypothesis is untenable, based on both physical evidence and numerical simulation. We numerically model the evolution of the geothermal system as it heats after emplacement of an intrusion. The two-layered temperature structure is found to be a consequence of the permeability difference, i.e. the two-layered permeability structure.     

Partial molar volumes and adiabatic compressibilities ofN-acetyl-DL-serinamide andN-acetyl-L-threonmamide in dilute aqueous solutions

Densities and sound velocities in dilute aqueous solutions ofN-acetyl-DL-serinamide andN-acetyl-L-threoninamide were measured at 5, 15, 25, 35, and 45°C. Partial molar volumes and partial molar adiabatic compressibilities of these amino acid derivatives at infinite dilution were determined. The partial molar quantities for the parent amino acids, serine and threonine, were also determined and compared with the acetyl amide derivatives. The contribution of the side chain of theN-acetyl amino acid amide or amino acid to the partial molar quantities were estimated from the difference between the partial molar quantities for the solute studied and those for the corresponding species,N-acetyl-glycinamide or glycine, without the side chain.