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1.
本文把数学和管理科学有机结合,为数学应用提出问题,得出新结果,推广了J.Michel
Harrison(1985)[1]第43页的命题27,并给出了在金融中的应用. 相似文献
2.
一类随机环境中的随机游动 总被引:5,自引:2,他引:3
在Solomn的模型的基础上对一类随机环境中随机游动进行了讨论,并得出了一个常返性准则和一些极限性质。 相似文献
3.
We investigate the links between Sobolev and Nash inequalities, capacity and hitting times estimates and ultracontractive semigroups, in a non-symmetric setting. 相似文献
4.
S. Yu. Troitskii A. L. Chuvilin D. I. Kochubei B. N. Novgorodov V. N. Kolomiichuk V. A. Likholobov 《Russian Chemical Bulletin》1995,44(10):1822-1826
The structure of polynuclear PdII hydroxocomplexes (PHC) formed as a result of alkaline hydrolysis of PdII chloride complexes was studied by EXAFS, SAXS, and TEM methods. It is established that in aqueous solutions a hydroxocomplex particle is a filament curled into a ball containing about 100 Pd atoms. The filament consists of planar coordination squares of PdO4 units linkedvia one or two oxygen bridges of different geometry. Aging of samples results in an increase in the number of single bridging ligands and a decrease in the diameter of particles. Interatomic distances around palladium atoms were determined.Translated fromIzvestiya Akademii Nauk. Seriya Khimlcheskaya, No. 10, pp. 1901–1905, October, 1995. 相似文献
5.
The addition of the macrocyclic polyether 18-Crown-6 (18C6) increases the selectivity of oxidation of ethylbenzene to -phenylethylhydroperoxide (PEH) in the presence of Ni(acac)2. The initial oxidation rate, selectivity and degree of conversion of ethylbenzene to PEH are greater than those catalyzed by Ni(acac)2 only. The efficiency of the macrocyclic ligand as an activator of Ni(acac)2 exceeds that of monodentate donor ligands. The high selectivity of the process is due to both the primary Ni(acac)2 · 18C6 complexes and the products of their transformation in the course of oxidation. The mechanism of ethylbenzene oxidation catalyzed by Ni(acac)2 · 18C6 complexes is discussed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1406–1411, August, 1994. 相似文献
6.
Shetty Kalidas Korus roger A. Crawford Dom L. 《Applied biochemistry and biotechnology》1989,(1):825-843
Glycine max was used as a model plant cell suspension culture to establish relationships among growth kinetics, phenolics production,
elicitor action, and peroxidase activity. Timing of elictor addition through monitoring of peroxidase provided an excellent
means of optimizing yields of phenolics and reduced the time span during which phenolics were formed, negating the need for
a secondary production medium. We have also determined that calcium and other cellular effectors like polyamines and organic
osmolytes, when used in conjunction with elicitors, enhance phenolics production. Calcium directly enhanced elicitation, whereas
polyamines and other osmolytes such as glycerol and proline extended cell viability. The study also demonstrated potential
for enhancing secondary metabolite production by a combination of elicitation, cell viability stabilizers, and by addition
of nutrients at the time of elicitation. 相似文献
7.
Shi Nian-Qing Prahl Kristine Hendrick Jim Cruz Jose Lu Ping Cho Jae-Yong Jones Sharon Jeffries Thomas 《Applied biochemistry and biotechnology》2000,84(1-9):201-216
Pichia stipitis CBS 6054 will grow on d-xylose, d-arabinose, and l-arabinose. d-Xylose and l-arabinose are abundant in seed hulls of maize, and their utilization is important in processing grain residues. To elucidate
the degradation pathway for l-arabinose, we obtained a mutant, FPL-MY30, that was unable to grow on d-xylose and l-arabinose but that could grow on d-arabinitol. Activity assays of oxidoreductase and pentulokinase enzymes involved in d-xylose, d-arabinose, and l-arabinose pathways indicated that FPL-MY30 is deficient in d-xylitol dehydrogenase (D-XDH), d- and l-arabinitol dehydrogenases, and d-ribitol dehydrogenase. Transforming FPL-MY30 with a gene for xylitol dehydrogenase (PsXYL2), which was cloned from CBS 6054 (Gen Bank AF127801), restored the D-XDH activity and the capacity for FPL-MY30 to grow on
l-arabinose. This suggested that FPL-MY30 is critically deficient in XYL2 and that the d-xylose and l-arabinose metabolic pathways have xylitolas a common intermediate. The capacity for FPL-MY30 to grow on d-arabinitol could proceed through d-ribulose. 相似文献
8.
A chiral liquid chromatographic method for determination of the enantiomeric purity of both l-carnitine and acetyl-l-carnitine is described. Separation of the enantiomers of dl-carnitine and acetyl-dl-carnitine was achieved on a commercial chiral column (Chiralcel OD-R) after derivatization with (alpha-bromo)methyl phenyl ketone. Introduction of this lipophilic UV chromophoric group to the carnitine and acetylcarnitine molecules improved their retention, resolution, and UV detection. The mobile phase was 74:26 (v/v) 0.5 mol L-1 sodium perchlorate–acetonitrile, pH 3.8, and the flow rate was 0.4 mL min-1. Detection was performed at 235 nm. The method is selective and reliable for determination of the enantiomeric purity of bulk drug substances l-carnitine and acetyl-l-carnitine. 相似文献
9.
Boris U. Stambuk Mary Ann Franden Arjun Singh Min Zhang 《Applied biochemistry and biotechnology》2003,106(1-3):255-263
The kinetics and regulation of d-xylose uptake were investigated in the efficient pentose fermentor Candida succiphila, and in Kluyveromyces marxianus, which assimilate but do not ferment pentose sugars. Active high-affinity (K
m
∼ 3.8 mM; V
max ∼ 15 nmol/[mg·min]) and putative facilitated diffusion low-affinity (K
m
∼ 140 mM; V
max ∼ 130 nmol/[mg·min]) transport activities were found in C. succiphila grown, respectively, on xylose or glucose. K. marxianus showed facilitated diffusion low-affinity (K
m
∼ 103 mM; V
max ∼ 190 nmol/[mg·min]) transport activity when grown on xylose under microaerobic conditions, and both a low-affinity and an
active high-affinity (K
m
∼ 0.2 mM; V
max ∼ 10 nmol/[mg·min]) transport activity when grown on xylose under fully aerobic conditions. 相似文献
10.
Z. A. Starikova A. I. Yanovsky Yu. T. Struchkov S. V. Zubkov I. I. Seifullina 《Russian Chemical Bulletin》1996,45(9):2157-2162
The crystal structure of the product of the condensation of (salicylideneamino)nitroguanidine with salicylaldehyde on a Ni2+ ion template, K[Ni(C15H10N5O4)] · DMF, has been studied. It was established that a planar Ni complex, consisting of isolated [NiL]– anions and solvated [K+ · DMF] cations, is formed. The negative charge of the anion is localized mainly on the O atoms of the nitro group. The nitroguanidine fragment of the ligand occurs in the tautomeric form, which was not reported previously.Deceased in 1995Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2273–2277, September, 1996. 相似文献