Taniguchi transfer

Imahori H, Hagiwara K, Akiyama T, Aoki M, Taniguchi S, Okada T, Shirakawa M and Sakata Y 1996 The small reorganization energy of Cgg in electron transfer Chem. Phys. Lett. 263 545-50... 

Katto, Y., S. Yokoya, S. Miake, and M. Taniguchi, 1987, CHF on a Uniformly Heated Cylinder in a Crossflow of Saturated Liquid over a Very Wide Range of Vapor-to-Liquid Density Ratio, Int. J. Heat Mass Transfer 30.1971-1977. (5)... 

I. Taniguchi, K. Watanabe, M. Tominaga, and F.M. Hawkridge, Direct electron transfer of horse heart myoglobin at an indium oxide electrode. J. Electroanal. Chem. 333, 331-338 (1992). 

M. Tominaga, T. Kumagai, S. Takita, and I. Taniguchi, Effect of surface hydrophilicity of an indium oxide electrode on direct electron transfer of myoglobins. Chem. Lett. 10, 1771-1774 (1993). 

Fujita S, Steenken S (1981) Pattern ofOFI radical addition to uracil and methyl-and carboxyl-substituted uracils. Electron transfer ofOFI adducts with N,N, Ar, Ar -tetramethyl-p-phenylenediamine and tetranitromethane. J Am Chem Soc 103 2540-2545 Fujita S, Nagata Y, Dohmaru T (1988) Radicals produced by the reactions of SO4 with uridine and its derivatives. Studies by pulse radiolysis and y-radiolysis. Int J Radiat Biol 54 417-427 Fujita S, Horii FI,Taniguchi R, Lakshmi S, Renganathan R (1996) Pulse radiolytic investigations on the reaction of the 6-yl radicals of the uracils with Cu(ll)-amino acid complexes. Radiat Phys Chem 48 643-649... 

The value of Eox for BH 4 is not known, but the borohydride radical, BH4 has been characterized by e.s.r and UV spectroscopy in oxidations of the anion by hydroxyl or azide radicals under pulse-radiolysis conditions (Symons et al., 1983 Horii and Taniguchi, 1986). Most borohydride reductions seem to be straightforward hydride transfers, but stepwise processes occur in the reductions of aryl bromides or iodides under photochemical or di-t-biftyl peroxide initiation. Radical intermediates are shown by the formation of 3-methyl-2,3-dihydrobenzofuran in the reduction of o-allyloxyiodobenzene (Abeywickrama and Beckwith, 1986). 

Mataga N, Chosrowjan H,Taniguchi S. Ultrafast charge transfer in excited electronic states and investigations into fundamental problems of exciplex chemistry Our early studies and recent developments. J Photochem Photobiol C Photochem Rev 2005 6 37-79. 

Hawkridge EM, Taniguchi I (1995) The direct electron transfer reactions of cytochrome c at electrode surfaces. Comments Inorg Chem 17 163-187... 

Taniguchi, S., Tatsuka, M., Nakamatsu, K., Inoue, M., Sadano, H., Okazaki, H., Iwamoto, H. and Baba, T. (1989). High invasiveness associated with augmentation of motility in a fos-transferred highly metastatic rat 3 Y1 cell line. Cancer Res. 49, 6738-6744. 

Taniguchi, S., Miyamoto, S., Sadano, H. and Kobayashi, H. (1991). Rat elongation factor 1 alpha sequence of cDNA from a highly metastatic fos-transferred cell line. Nucl. Acids Res. 19, 6949. 

This result may be explained by a combination of intraparticle diffusion and bulk mass transfer processes. As material is extracted from the exposed areas of the seed, the solvent must travel further through the pores to reach the solute. Also, as the entrance portion of the bed becomes depleted of soluble components, the effective bed length decreases until the residence time is insufficient to achieve equilibrium. Similar effects were observed in seed oil extraction by Fattori (1) and Taniguchi et al. (9). 

An alternative approach similar to the discrete transfer method was reported by Taniguchi et al. [115,116,117]. They showed that, for nonscattering media, the method yields very good results with significant computational time savings over standard Monte Carlo techniques. 

H. Taniguchi and M. Funazu, The Radiative Transfer of Gas in a Three-Dimensional System Calculated by Monte Carlo Method, Bulletin ofJSME, 13, p. 458,1970. 

W.-J. Yang, H. Taniguchi, and K. Kudo, Radiative Heat Transfer by the Monte Carlo Method, T. F. Irvine and J. P. Hartnett (eds.), Advances in Heat Transfer, Academic Press, New York, vol. 27, pp. 1-215,1995. 

Gou, P, Hanke, G.T., Kimata-Ariga, Y., Standley, D.M., Kubo, A., Taniguchi, I., Nakamura, H., and Hase, T. (2006). Higher order structure contributes to specific differences in redox potential and electron transfer efficiency of root and leaf ferredoxins. Biochemistry 45, 14389-14396. 

Osuka A, Shiratori H, Yoneshima R, Okada T, Taniguchi S, Malaga N (1995) Intiacomplex electron transfer in a hydrogen-bonded poiphyrin-diimide system. Chem Lett 24 913-194... 

Osuka, A. Yoneshima, R. Shiratori. H. Okada, T. Taniguchi, S. Malaga. N. Electron transfer in a hydrogen-bonded assembly consisting of porphyrin-diimide. Chem. Commun. 1998.15, 1567-1568. 

Uemura. S. Sakata, M. Taniguchi, I. Hirayama. C. Kunitake. M. In situ observation of coronene epitaxial adlayers on Au(lll) surfaces prepared by the transfer of Langmuir films. Thin Solid Films 2002. 409. 206-210. 

C.J., Ham, M.H., Sanchez-Yamagishi, J.D., Watanabe, K., Taniguchi, T. et al. (2012) Understanding and controlling the substrate effect on graphene electron-transfer chemistry via reactivity imprint lithography. Nat. Chem., 4, 724-732. 

K. Yase, E.-M. Han, K. Yamamoto, Y. Yoshida, N. Takada and N. Taniguchi, One-dimensional growth of phenylene oligomer single crystals of friction-transferred poly(p-phenylene) film, Jpn. J. Appl. Phys.. 36, 2843-2848 (1997). 

Fig. 1. Estimation of the size of mRNA for bovine poly(ADP-ribose) synthetase by in vitro translation of size fractionated poly (A) + RNA and Northern blot analysis. A. Size-fractionation of poly (A) + RNA and location of mRNA for the enzyme. Bovine thymus poly(A)+ RNA was size-fractionated by neutral sucrose density gradient centrifugation and RNA in each fraction was translated in vitro. The translated products were immunoprecipitated, and separated on a 7.5% SDS-polyacrylamide gel. B. Typical fluorogram of the gel. Lanes 1, 2, 3, 4, and 5, correspond to fractions 1, 3, 5, 7, and 9, respectively. Molecular weight markers a, p-galactosidase (116K), b, phosphorylase a(95K), c, bovine serum albumin (68K), d, ovalbumin (43K), e, lysozyme (14.3K). C. Northern blot analysis of bovine thymus poly(A)+ RNA. RNA (2 pg per lane) was separated on a 1.2% agarose/formaldehyde gel, transferred to a nitrocellulose filter, and hybridized with the p-iabelled 2.7 kb insert cDNA prepared from the clone ARS-1. Size markers used were 28 S(4.9 kb), 18 S(2.0 kb)rRNA, 3.8 kb, 2.7 kb, and 1.1 kb denatured DNA. Reprinted from Taniguchi etaL, Eur J Biochem 171 571-575,1988.

There now is no difficulty in achieving the electrochemistry of small redox proteins (see, for example, Armstrong et al., 1987, 1988, Frew and Hill, 1987, 1988) whether, e.g., cytochrome c, (Figure 1) ferredoxin, azurin, rubredoxin or flavodoxin (Figure 2), A variety of electrode surfaces exist at which the direct electrochemistry of proteins proceeds without the need for mediators. At some metal electrodes, what is required is the presence of some compound, called a promoter (Eddowes and Hill, 1977), which binds to the surface yet allows electron transfer to proceed (Figure 3). Over the years, many promoters have been reported (Taniguchi et al., 1982 Allen et al., 1984) and they are all bifunctional molecules, one part of which causes... 

Mataga, N., Chosrowjan, H., Taniguchi, S., Tanaka, F., Kido, N., et al. Femtosecond fluorescence dynamics of flavoproteins comparative studies on flavodoxin, its site-directed mutants, and riboflavin binding protein regarding ultrafast electron transfer in protein nanospaces. J. Phys. Chem. B 106, 8917-8920 (2002)... 

Taniguchi S, Kikuchi A, Hatsuzaki H, Bessho N (1988) Dispersion of bubbles and gas-liquid mass transfer in a gas-stirred system. Trans ISIJ 28 262-270... 

Since little is known about the interfacial behavior of enzymes other than glucose oxidase (GOD) at an electrode, Taniguchi et examined the electron-transfer reactions and adsorption behavior of several flavoen-zymes by fluorescence and SERRS measurements. They found that the intensities were useful in determining the location of flavin adenine dinucleotide (FAD) in the flavoenzymes, which suggested possible interfacial structures of these flavoenzymes. 

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