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We realize the Belinschi–Nica semigroup of homomorphisms as a free multiplicative subordination. This realization allows to define more general semigroups of homomorphisms with respect to free multiplicative convolution. For these semigroups we show that a differential equation holds, generalizing the complex Burgers equation. We give examples of free multiplicative subordination and find a relation to the Markov–Krein transform, Boolean stable laws and monotone stable laws. A similar idea works for additive subordination, and in particular we study the free additive subordination associated to the Cauchy distribution and show that it is a homomorphism with respect to monotone, Boolean and free additive convolutions. 相似文献
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Risa Mutoh Hiroyuki Mino Reiko Murakami Tatsuya Uzumaki Masahiro Ishiura 《Applied magnetic resonance》2011,40(4):525-534
Site-directed spin labeling electron spin resonance (ESR) was applied to investigate the local environment of the cyanobacterial circadian clock protein KaiB. We prepared five cysteine residue-substituted mutants of KaiB labeled with maleimide spin label (MSL). By comparing the ESR spectra of KaiBs carrying MSL at different positions (Thr64, Lys67, Tyr94, Gly98, and Ala101), local conformational changes were identified. The ESR spectra of MSL-T64C and MSL-K67C showed the relatively slow motion of MSL characterized by τ?=?79 and 59?ns at 4°C, respectively. The spectra of MSL-Y94C, MSL-G98C and MSL-A101C showed relatively fast motion characterized by τ?=?8.0, 4.1 and 3.1?ns at 4°C, respectively. These differences were explained by the local environments of the position in KaiB. On incubation at 40°C for 24?h, all ESR spectra of the labeled KaiBs changed, which can be explained by the structural relaxation of KaiB. 相似文献
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This paper presents a low-capacity cation-exchange chromatography method for the analysis of UV-absorbing dipeptides and amino acids. A newly marketed low-capacity cation-exchange column packed with sulfo-functionalized highly cross-linked macroreticular poly(ethylstyrene-divinylbenzene) copolymer was used for the simultaneous determination of imidazole amino acids, aromatic amino acids, and creatinine in urine samples. A dual-mode binary gradient chromatography method was established using two solvents, A: 15 mM H3PO4/5 mM ethylenediamine and B: 15 mM H3PO4/5 mM ethylenediamine/40 (v/v) % CH3CN at 40 °C, with an optimized time program for changing the delivery ratio of A/B and the flow rate. Good chromatograms were obtained within an acceptable cycle time of 25 min. The quantification data were satisfactory for all analytes, showing the relative standard deviations (RSD) of retention times between 0.08 and 1.68 %; RSDs of area intensities between 0.23 and 2.60 %; and linear regression lines with r 2 more than 0.9994. The method could determine the creatinine ratios of the diagnostic markers on the single chromatographic run, which enabled to discriminate disease from health. For example, the creatinine ratios for phenylketonuria were significantly higher than those for controls. The method can provide highly cost-efficient information or useful knowledge for clinical and pharmaceutical studies. 相似文献
37.
Shinya Nakashima Dr. Hiromune Ando Risa Saito Hideki Tamai Dr. Hideharu Ishida Dr. Makoto Kiso 《化学:亚洲杂志》2012,7(5):1041-1051
The first total synthesis of the hybrid ganglioside X2, which consisted of a highly branched octasaccharide and ceramide moieties, was accomplished by using a glucosyl ceramide cassette approach. With a disaccharyl donor, the heptasaccharide could not be constructed by glycosylation of the C4 hydroxy group of galactose at the reducing end of the pentasaccharide. In contrast, through an alternative approach with two branched glycan units, a GM2-core trisaccharide, and a lacto-ganglio tetrasaccharide, the heptasaccharyl donor could be prepared and subsequently joined with a glucosyl ceramide cassette to afford the protected ganglioside, X2. Finally, global deprotection completed the synthesis, thus affording the pure ganglioside X2. 相似文献
38.
The principle of the signal amplification of a uric acid sensor based on dithiothreitol (DTT)-mediated intermediate regeneration of uricase was applied to a flow-injection system with an immobilized uricase reactor and a DTT-containing carrier. Highly sensitive detection for nM to microM order of uric acid was achieved when 10 mM TRIS-HCl buffer (pH 10.0) containing 20 mM DTT was used as a carrier at 0.6 ml min-1 and 37 degrees C. The sensitivity of the uric acid was much improved over a batch method using a uricase membrane-coupling electrode, and the detection limit (ca. peak current 8 nA) of uric acid was found to be down to 3 x 10(-10) M (amplification factor; more than 10,000). This chemically amplified flow-system is very useful for the direct assay of uric acid in highly diluted biological fluids (urine and serum) without complicated pretreatment of the samples, because this sensor has the potential to detect trace amounts (nM to microM) of uric acid in highly diluted body fluids in which the concentration of interfering constituents was decreased to negligible levels. Good correlation was observed between this system and conventional spectrophotometry. The immobilized uricase reactor could be re-used for at least 4 months of repeated analysis without loss of activity and was stable if stored at 4 degrees C in 10 mM TRIS-HCl buffer, pH 9.0. 相似文献
39.
Koichi Hasebe Akio Fujiwara Takashi Nozaki Koichi Miyamoto 《Macromolecular Symposia》2007,260(1):161-164
In this study, ultrahigh molecular weight polyethene homopolymer and copolymer were successfully produced with the metallocene and the Ziegler catalyst system. In case with the metallocene catalyst system, viscosity average molecular weight of the homopolymer was controlled from 2 million to 10 million. Also, the molecular weight of the copolymer was reached up to 6 million. In case with the Ziegler catalyst system, the molecular weight of the copolymer was reached up to 4 million. The transparency of the copolymer by the Ziegler catalyst, with which the copolymer with better uniformity was produced, could be comparable with that by the metallocene catalyst. 相似文献
40.
Satoshi Hikima Teiji Kakizaki Mitsuhiko Taga Kiyoshi Hasebe 《Fresenius' Journal of Analytical Chemistry》1993,345(8-9):607-609
Summary An amperometric enzyme sensor composed of a mercury film electrode and an enzyme-immobilized chitosan membrane is developed. This biosensor is based on both a mercury film electrode detecting the consumption of dissolved dioxygen following enzymatic reaction, and a chitosan membrane. The latter provides an excellent permselectivity and excludes electroactive interferents. The detection range of this biosensor was 1.0×10–5–3.0×10–4 mol/l and the relative standard deviation, R.S.D. at 5.0×10–5 mol/l was 1.4% (n=3). This biosensor was applied to the direct determination of L-lactate in human serum without pretreatment. 相似文献