Complete genome structure of the unicellular cyanobacterium Synechocystis sp. PCC6803

Cyanobacteria are photoautotrophic organisms capable of oxygen-producing photosynthesis similar to that in eukaryotic algae and plants, and because of this, they have been used as model organisms for the study of the mechanism and regulation of oxygen-producing photosynthesis. To understand the entire genetic system in cyanobacteria, the nucleotide sequence of the entire genome of the unicellular cyanobacterium Synechocystis sp. PCC6803 has been determined. The total length of the circular genome is 3,573,470 bp, with a GC content of 47.7%. A total of 3,168 potential protein coding genes were assigned. Of these, 145 (4.6%) were identical to reported genes, and 1,259 (39.6%) and 342 (10.8%) showed similarity to reported and hypothetical genes, respectively. The remaining 1,422 (45.0%) showed no apparent similarity to any genes registered in the databases. Classification of the genes by their biological function and comparison of the gene complement with those of other organisms have revealed a variety of features of the genetic information characteristic of a photoautotrophic organism. The sequence data, as well as other information on the Synechocystis genome, is presented in CyanoBase on WWW [http:/(/)www.kazusa.or.jp/cyano/].     

Raman Spectroscopic Studies on the Formation Mechanism of Hydrous-Zirconia Fine Particles

The Raman spectra of hydrous-zirconia fine particles produced by the hydrolysis of various ZrOCl₂ solutions were investigated. The Raman spectra of hydrous zirconia synthesized at HCl concentrations below 1 mol/L were similar to those of monoclinic, crystalline ZrO₂; those of hydrous zirconia synthesized at HCl concentrations greater than 1 mol/L showed a crystal structure change. The line width of the Raman bands increased with increasing H⁺ ion concentration. Analyzing the relationship between Raman band width and particle size revealed that the primary particle size of hydrous zirconia was controlled by the H⁺ and Cl⁻ ions, because these ions interfered with the polymerization in a hydrolysis reaction. Based on the experimental results, the formation mechanism for primary particles of hydrous zirconia was determined.     

The vapour pressures and heats of sublimation of model disperse dyes

The vapour pressures and heats of sublimation of 23 model disperse dyes have been measured by the vapour saturation method (modified transpiration method). The data obtained were in good agreement with those produced by the other investigators using the effusion method. The heats of sublimation are discussed in terms of molecular structure.     

Electrostatic properties of antistatic cloth woven partly withelectrically conductive fibers

An electrically conductive fiber and an antistatic cloth woven partly with electrically conductive fibers have a high electrostatic elimination effect in wet as well as dry atmospheres. The electrostatic elimination effect of the antistatic cloth does not decay with repeated washing. Antistatic cloth has been widely used in industry to prevent the electrostatic risk caused by electrification of fiberware. Charge densities and discharge characteristics of various antistatic cloths, controlled primarily by weaving electrically conductive fibers into the cloth, have been investigated experimentally. The electrostatic elimination effect of these is evaluated     

Microprocessor-Based Adjustable-Speed DC Motor Drives Using Model Reference Adaptive Control

Model reference adaptive control (MRAC) is applied to microprocessor-based adjustable-speed dc motor drives. The algorithm of the MRAC is based on the linear model following control (LMFC) and is the combination of the adaptive controller with the LMFC. The MRAC-based speed controller allows the indistinctness and/or inaccuracy in the motor and load parameters in the system design stage. It also maintains the prescribed control performance in the presence of the motor parameter perturbations and the load disturbances. The experimental setup is constructed using a microprocessor. The experimental results confirm the useful effects of the MRAC-based speed controller.     

High-performance genetic analysis on microfabricated capillary array electrophoresis plastic chips fabricated by injection molding

We have developed a novel technique for mass production of microfabricated capillary array electrophoresis (mu-CAE) plastic chips for high-speed, high-throughput genetic analysis. The mu-CAE chips, containing 10 individual separation channels of 50-microm width, 50-microm depth, and a 100-microm lane-to-lane spacing at the detection region and a sacrificial channel network, were fabricated on a poly(methyl methacrylate) substrate by injection molding and then bonded manually using a pressure-sensitive sealing tape within several seconds at room temperature. The conditions for injection molding and bonding were carefully characterized to yield mu-CAE chips with well-defined channel and injection structures. A CCD camera equipped with an image intensifier was used to monitor simultaneously the separation in a 10-channel array with laser-induced fluorescence detection. High-performance electrophoretic separations of phiX174 HaeIII DNA restriction fragments and PCR products related to the human beta-globin gene and SP-B gene (the surfactant protein B) have been demonstrated on mu-CAE plastic chips using a methylcellulose sieving matrix in individual channels. The current work demonstrated greatly simplified the fabrication process as well as a detection scheme for mu-CAE chips and will bring the low-cost mass production and application of mu-CAE plastic chips for genetic analysis.     

Site-directed mutagenesis study of the antibody 2D7 which catalyzes a reaction for insertion of Cu2+ into mesoporphyrin

Monoclonal antibody 2D7 generated against a transition-state analog N-methyl mesoporphyrin catalyzes a reaction for insertion of a cupric ion into mesoporphyrin. To investigate amino acid residues responsible for the catalytic activity, site-directed mutagenesis of the amino acid residues in the third complementarity determining region of the heavy chain (CDRH3) was performed on the antigen-binding fragment (Fab) of the antibody. Recombinant Fab mutants, in which Arg95 is replaced with Ala (R95A), Asp96 with Asn (D96N) and Met97 with Gly (M97G), were examined in terms of the catalytic efficiency of the reaction (k/K(S)) and the dissociation constant for N-methyl mesoporphyrin binding (K(d)) and these values were compared with those of the wild type. The k/K(S) values of the R95A and D96N mutants were 0.96% and 1.0% of that of the wild type, respectively, whereas the M97G mutant had no detectable catalytic activity. The K(d) values of the R95A and D96N mutants were 165 and 69 times that of the wild type, respectively, while that of the M97G mutant was similar to that of the wild type. The relationship between the k/K(S) and 1/K(d) values in the wild type and the R95A and D96N mutants suggests that Arg95 and Asp96 are responsible for stabilizing the transition-state in the catalytic reaction. The results of the M97G mutant allow us to propose that Met97 plays an important role in the catalytic activity probably due to a subtle and specific conformation of the antibody.