Fluorinated carbohydrates : Part XIII. 2-deoxy-2-fluoro-D-galactose

Reaction of trifluoro(fluoroxy)methane at ca. −80° with 3,4,6-tri-O-acetyl-D-galactal affords trifluoromethyl 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-galactopyranoside (2, 39%), 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-galactopyranosyl fluoride (3, 37%), trifluoromethyl 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-talopyranoside (4, 3%), and 3,4,6-tri-O-acetyl-2-deoxy-2-fluor-α-D-talopyranosyl fluoride (5, 2%). The structures of compounds 2–5 have been established by n.m.r. spectroscopy. Acid hydrolysis of 2 or 3 allords 2-deoxy-2-fluoro-D-galactose.     

The oxidation of D-glucose and D-fructose with oxygen in aqueous,alkaline solutions : Part II. The overall kinetics

Based on a previously reported, integral reaction-scheme, a very simple, kinetic model for the homogeneous oxidation of D-glucose and D-fructose in aqueous, alkaline solutions has been developed. It involves the influence of the type and concentration of the hexose, the hydroxyl-ion concentration, the oxygen concentration in the liquid phase, and the temperature on the rate of formation of the acidic reaction products. No attention is paid to the product distribution.     

Metabolism of 2-deoxy-d-glucose by baker's yeast : IV. Incorporation of 2-deoxy-d-glucose into cell wall mannan

1.

1. Saccharomyces cerevisiae grown in the presence of 2-deoxy-d-glucose incorporate this glucose and mannose analogue into cell wall polysaccharides. Fractionation of cell walls to mannan- and glucan-containing fractions followed by analysis for glucose, mannose and deoxyglucose showed that deoxyglucose was incorported mainly, if not exclusively, into cell wall mannan.     

Sub-lethal autolysis : Modification of cell periphery by lysosomal enzymes

Lysosomal activation was induced in dog kidney and HEp-2 cells by treatment with anticellular serum and high concentrations (20 μg/ml) of vitamin A alcohol. The morphological changes accompanying the release of enzymes from activated lysosomes were described. Measurements of cell coat thickness by ellipsometry revealed that lysosomal enzymes released extracellularly were able to digest the coat. The scale of enzyme release was an important factor in determining the amount of coat digested. Complement-sufficient anticellular sera and high concentrations of vitamin A induced marked lysosomal activation and extensive digestion of the coat. Complement-deficient anticellular serum produced significantly less lysosomal labilization and only limited digestion of the coat. The digestion of the cell coat induced by these agents was prevented by pretreatment of the cells with either hydrocortisone or chloroquine.     

Intracellular pH electrode : Experiments on the giant squid axon

A new, easy method to produce and calibrate a 1-μm tip intracellular pH electrode is described. This antimony electrode and a micro-calomel electrode were inserted into the giant axon of Loligo pealii. The potential obtained when the axon was bathed in seawater corresponded to a pH of 7.0 ± 0.2. It was found that acidification of the external perfusate induced a drop in axoplasmatic pH leading to changes in the membrane electrical properties. Changes of resting or action potentials did not influence intracellular pH.     

Heterocycles from saccharide hydrazones : Part I. Saccharide 1,3,4-oxadiazoles

Oxidation, with iodine-mercuric oxide, of acetylated saccharide aroylhydrazones and of aromatic aldehyde hydrazones yields 5-aryl-2-(polyacetoxyalkyl)-1,3,4-oxadiazoles and 2,5-diaryl-1,3,4-oxadiazoles, respectively. On de-O-acetylation, saccharide oxadiazole acetates rearrange to the tautomeric, cyclic iminolactones which, on reacetylation, regenerate the starting oxadiazoles. Attempted dehydration of saccharide acetyl- and benzoyl-hydrazones by treatment with boiling acetic anhydride under reflux resulted in the formation of peracetylated N,N-diacetylhydrazones and-N-acetyl-N-benzoylhydrazones, respectively.     

Quinacrine fluorescence of metaphase chromosomes : Identical patterns in different tissues

The quinacrine mustard fluorescence patterns of the metaphase chromosomes of different tissues of the same plant species were found to be identical. Similar studies of the chromosome regions on human material gave the same result.     

Light scattering by cellulose : IV. Fibers with helical morphology

Solid-state light scattering has been used to study the scattering by the helically wound microfibrils in wood fibers. Scattering envelopes have been recorded from a section of Eastern spruce wood as well as a single fiber of Black spruce. Theoretical expressions for the intensity of light scattered by a continuous helix have been derived and found to be in fair agreement with the experimental results. A method of estimating the “pitch” and “tilt” of the helical segments is outlined.