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Six strains of Bacteroides fragilis were examined and all found to produce endo-beta-galactosidase, an enzyme that hydrolyses internal beta-galactosidic linkages of oligosaccharides belonging to the poly-N-acetyl-lactosamine series, with the common structure GlcNAc beta 1 leads to 3Gal beta 1 leads to 4GlcNAc/Glc. The enzyme was produced without the addition of an inducer such as keratan sulphate. It was purified 7000-fold from the culture supernatant and obtained with a yield 4-10-fold greater than from sources described previously. The specificity of the enzyme towards bovine corneal keratan sulphate, milk oligosaccharides and the glycolipids lacto-N-neotetraosylceramide and lacto-N-tetraosylceramide closely resembled that of the endo-beta-galactosidase isolated from Escherichia freundii. A novel observation was that both enzymes hydrolysed the type 2 sequence, Gal beta 1 leads to 4GlcNAc beta 1 leads to 3Gal beta 1 leads to 4Glc, at about twice the rate of the type 1 isomer, Gal beta 1 leads to 3GlcNAc beta 1 leads to 3Gal beta 1 leads to 4Glc. Because of the ease of purification of the enzyme and high yield in the absence of contaminating glycosidases and proteinases, Bacteroides fragilis is a valuable source of endo-beta-galactosidase for the structural analysis of carbohydrate chains.

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This paper describes a simple and reliable method of improving the surface insulation strength of a spacer used in vacuum. The method is to roughen the spacer surface to an average roughness R higher than 1 or 2 m. The material of the spacer a examined is SiO , PMMA, PTFE or Al O and their shape is a right cylinder with 2 2 3 10 mm in height and 54 mm in diameter. The spacer is subjected to a ramped dc voltage and its surface charging is observed by using an electrostatic probe embedded in the cathode. It has been found that R decisively affects the charging, which a decreases as R increases. Increasing R larger than about 2 m suppresses the a a charging until a higher applied voltage is reached, thus improving the insulation property.

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Multilayered manganese oxide films were prepared on a platinum electrode by potentiostatic oxidation of aqueous Mn2+ ions in the presence of n-tetra-alkylammonium compounds. Alkylammonium cations were intercalated between manganese oxide layers to balance the negative layer charge. Effects of several preparative parameters such as the size of alkylammonium molecules, counteranions, and bath composition on the structure of products were investigated. The interlayer distance of the products increased with increasing alkyl chain length up to C4, and the change became obviously small among C4–C6 compounds. The multilayer formation was achieved only when the manganese concentration was lower than 10 mM, and the highest crystallinity was obtained from a bath composed of 2 mM manganese sulfate and 50 mM alkylammonium chloride. At low concentrations of alkylammonium (<10 mM), a product intercalated with hydrated protons was formed, in which the protons were generated by anodic oxidation of Mn2+ with H2O.