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411.
The phosphorus of glucose-6-phosphate residue in starch (P(G6P)) was estimated specifically by means of glucose-6-phosphate dehydrogenase (E.C.1.1.1.49) after acid hydrolysis. Sixty to 70 % of total phosphorus in potato starch was found to be P(G6P)). It was shown that the rest of phosphorus (Px) was incorporated as glucose-2-phosphate and/or glucose-3-phosphate, since it was determined as glucose by periodate oxidation, borohydride reduction, acid hydrolysis and treatment with alkaline phosphatase. The Px was more labile to acid and heat than P(G6P) and decomposed yielding inorganic phosphate. The phospholigosacharide (D. P. 3.6), which was prepared by the limit hydrolysis of potato starch with glucoamylase of Rh. delemar (α-1,4-Glucan glucohydrolase E.C.3.2.1.3) was fractionated by gel-filtration through Sephadex G-25 into fractions with D.P. 2 to 7. Each fraction contained a mole of phosphorus per mole of the saccharide. The P(G6P) and the Px were enriched in the low and the high D.P. fractions, respectively. 相似文献
412.
Vladislav Stroganov Daniel Hüger Christof Neumann Tabata Noethel Michael Steinert Uwe Hübner Andrey Turchanin 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(29):2300282
Molecular thin carbon nanomembranes (CNMs) synthesized by electron irradiation induced cross-linking of aromatic self-assembled monolayers (SAMs) are promising 2D materials for the next generation of filtration technologies. Their unique properties including ultimately low thickness of ≈1 nm, sub-nanometer porosity, mechanical and chemical stability are attractive for the development of innovative filters with low energy consumption, improved selectivity, and robustness. However, the permeation mechanisms through CNMs resulting in, e.g., an ≈1000 times higher fluxes of water in comparison to helium have not been yet understood. Here, a study of the permeation of He, Ne, D2, CO2, Ar, O2 and D2O using mass spectrometry in the temperature range from room temperature to ≈120 °C is studied. As a model system, CNMs made from [1″,4′,1′,1]-terphenyl-4-thiol SAMs are investigated. It is found out that all studied gases experience an activation energy barrier upon the permeation which scales with their kinetic diameters. Moreover, their permeation rates are dependent on the adsorption on the nanomembrane surface. These findings enable to rationalize the permeation mechanisms and establish a model, which paves the way toward the rational design not only of CNMs but also of other organic and inorganic 2D materials for energy-efficient and highly selective filtration applications. 相似文献