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1.
Akihiko Yukie 《Mathematische Annalen》1992,292(1):355-374
Partially supported by NSF Grant DMS-8803085, DMS-8610730 相似文献
2.
S Ozaki T Akiyama T Morita M Kumegawa T Nagase N Uehara A Hoshi 《Chemical & pharmaceutical bulletin》1990,38(11):3164-3166
Various kinds of 5'-O-unsaturated acyl 5-fluorouridines were synthesized to obtain 5-fluorouridine derivatives with low toxicity and high antitumor activity. Antitumor activity of the compounds against L-1210 leukemia in mice was examined, and the 5'-O-4-pentenoyl derivative showed the highest antitumor activity. 相似文献
3.
The antitumor activity of (1----3)-beta-D-glucans was tested in order to clarify its conformation-dependent response together with conformational elucidation by carbon-13 nuclear magnetic resonance (13C-NMR) spectroscopy. It was shown that the following three conformations, single chain, single helix and triple helix, are readily distinguished by the high-resolution solid-state 13C-NMR method. It turned out that preparations of linear (1----3)-beta-D-glucans of a triple helical conformation were ineffective in the inhibition of tumor growth. These linear (1----3)-beta-D-glucans were converted to an effective form in the inhibition of tumor growth when they were lyophilized from dimethyl sulfoxide (DMSO) solutions as a result of a conformational change from the triple helical to the single chain forms. They were not effective, however, when assayed in DMSO solution. In contrast, it was found that a branched (1----3)-beta-D-glucan is effective not only in either saline solutions of the triple helical sample or the lyophilized sample from DMSO, but also in DMSO solution. The aforementioned drastic change in antitumor activity was interpreted in terms of resulting conformational changes as analyzed by the 13C-NMR method. 相似文献
4.
5.
T. Takeuchi S. Uehara T. Hayashi 《Journal of Radioanalytical and Nuclear Chemistry》1980,56(1-2):25-35
Several dead time correction methods were compared experimentally with the exact correction method and their limits were discussed.
These correction methods were applied to neutron activation analysis of a biological sample. A special electronic circuit
and an additional counting equipment were used to obtain the fractional dead time with a suficiently high frequency. 相似文献
6.
R- and S-epimerization at the 3(1) position of bacteriochlorophyll (BChl) c and the formation of rod-like aggregates in chlorosomes of green sulfur bacteria were markedly affected in Chlorobium (Cb.) tepidum and Cb. limicola by cultivation under various light intensities (photon fluence rate). The stronger the light, the higher the ratio of the S-epimer to the R-epimer for each homolog of BChl c in the bacteria. S[P,E] BChl cF and S[I,E] BChl cF were found to be the major S-epimers in Cb. tepidum and Cb. limicola, respectively. R[P,E] BChl cF decreased markedly compared to R[E,E] BChl cF in Cb. tepidum, whereas no observable change in the ratio of R[P,E]/R[E,E] was detected for Cb. limicola. With increase in light intensity the Qy absorption maximum of the bacteria shifted to shorter wavelengths. In vitro spectroscopic studies of the aggregates showed a marked difference in the formation of aggregates from R- and S-epimers of BChl c; the S-epimers formed aggregates much more slowly than did the R-epimers. These results suggest that the ratio of the epimers of BChl c might significantly affect the aggregation of BChl in the chlorosome. We propose different roles for the R- and S-epimers in chlorosomes of Cb. limicola and Cb. tepidum. 相似文献
7.
The synchronized self-motion of two camphor boats on polygonal water chambers was investigated. The two boats synchronously moved depending on the number of corners in the polygon by changing the distance between the two boats through the corners. We regard the self-motion of a camphor boat as an oscillator; i.e., one cycle on the polygonal chamber corresponds to 2pi. Phase-locked synchronization at a phase difference of 2pi/3, which corresponds to the length of one side of the chamber, was observed with a triangular chamber. Two types of synchronized motion at phase differences of pi/2 and pi, which correspond to the length of one and two sides of the chamber, respectively, were observed with a square chamber. These characteristic features of synchronized self-motion were qualitatively reproduced by a numerical calculation that regarded the surface tension as the driving force and the number of corners in the chamber as a velocity-regulating mechanism. We believe that the present system may be a simple model of synchronization which depends on the geometry of the system. 相似文献
8.
Katsutoshi Kubota Makoto Minakata Shoichi Saito Shingo Uehara 《Optical and Quantum Electronics》1978,10(3):205-210
A low drive-voltage optical modulator using a Ti-diffused UNbO3 optical waveguide has been fabricated. Stabilization against ambient temperature change was realized by using a miniature halfwave plate. The halfwave voltage, 3 dB bandwidth, optical insertion loss and extinction ratio were 3·8 V (at 1·06m wavelength), 850 MHz, 10 dB and 13 dB, respectively. A reduction scheme for the optical absorption caused by metallic electrodes, and an analysis of the modulator high frequency response are also reported. 相似文献
9.
Abe I Oguro S Utsumi Y Sano Y Noguchi H 《Journal of the American Chemical Society》2005,127(36):12709-12716
The chalcone synthase (CHS) superfamily of type III polyketide synthases (PKSs) produces a variety of plant secondary metabolites with remarkable structural diversity and biological activities (e.g., chalcones, stilbenes, benzophenones, acrydones, phloroglucinols, resorcinols, pyrones, and chromones). Here we describe an octaketide-producing novel plant-specific type III PKS from aloe (Aloe arborescens) sharing 50-60% amino acid sequence identity with other plant CHS-superfamily enzymes. A recombinant enzyme expressed in Escherichia coli catalyzed seven successive decarboxylative condensations of malonyl-CoA to yield aromatic octaketides SEK4 and SEK4b, the longest polyketides known to be synthesized by the structurally simple type III PKS. Surprisingly, site-directed mutagenesis revealed that a single residue Gly207 (corresponding to the CHS's active site Thr197) determines the polyketide chain length and product specificity. Small-to-large substitutions (G207A, G207T, G207M, G207L, G207F, and G207W) resulted in loss of the octaketide-forming activity and concomitant formation of shorter chain length polyketides (from triketide to heptaketide) including a pentaketide chromone, 2,7-dihydroxy-5-methylchromone, and a hexaketide pyrone, 6-(2,4-dihydroxy-6-methylphenyl)-4-hydroxy-2-pyrone, depending on the size of the side chain. Notably, the functional diversity of the type III PKS was shown to evolve from simple steric modulation of the chemically inert single residue lining the active-site cavity accompanied by conservation of the Cys-His-Asn catalytic triad. This provided novel strategies for the engineered biosynthesis of pharmaceutically important plant polyketides. 相似文献
10.
Yoshitaka Ogiwara Yukie Ogiwara Hitoshi Kubota 《Journal of polymer science. Part A, Polymer chemistry》1967,5(11):2791-2805
Graft copolymerization of methyl methacrylate on cellulosic materials of various carbonyl and aldehyde contents with the use of a ceric salt as an initiator was studied. It was found that the concentration of the ceric salt which gives the maximum per cent grafting is in good agreement with the equivalent of total carbonyl content in the cellulosic material, and the number of grafted chains in copolymers is roughly proportional to it. However, the molar ratio of the number of grafted chains to total carbonyl content is quite small, being approximately 1:50, and the graft copolymerization can be explained kinetically on the assumption that the number of radicals produced on cellulose by the ceric salt leading to branching is very much smaller than the number of radicals destroyed by the ceric salt, and growing radicals can be stabilized by the termination reaction with the ceric salt or with a cellulose radical. Although both aldehyde and carbonyl groups contribute to the formation of grafted chains, the former are effective mainly at low concentrations of the ceric salt; both groups participate in the production of graft copolymers showing the maximum per cent grafting. 相似文献