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D B JOHNSTONE

Publications and source records attributed to D B JOHNSTONE.

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EXTRACELLULAR POLYSACCHARIDES OF AZOTOBACTER VINELANDII.

Cohen, Gary H. (University of Vermont, Burlington), and Donald B. Johnstone. Extracellular polysaccharides of Azotobacter vinelandii. J. Bacteriol. 88:329-338. 1964.-Extracellular polysaccharides synthetized by Azotobacter vinelandii strains 155, 102, and 3A were shown to be carboxylic acid heteropolysaccharides of apparent high molecular weight. Cells were grown in a nitrogen-free, mineral broth medium with 2% sucrose. Extracellular slime was recovered by centrifugation and purified by repeated alcohol precipitation and Sevag deproteinization. Capsular polysaccharide was recovered from washed cells by mild alkaline digestion. Methods of isolation and purification appeared to provide polysaccharide showing no evidence of heterogeneity when examined by chemical and physical methods. Infrared analysis of purified slime from the three strains suggested fundamental structural similarities. Colorimetric, paper chromatographic, and enzymatic analyses on both intact and acid-hydrolyzed slime polysaccharide indicated that the polymers contained in common galacturonic acid, [alpha] d-glucose, and rhamnose at a ratio of approximately 43:2:1, as well as a hexuronic acid lactone, probably mannurono-lactone. However, as shown by chemical and infrared analysis, minor differences did exist; namely, slime from strain 155 and 102 contained o-acetyl groups, whereas slime from strain 3A contained none. A sialic acid-like component (1.5% of dry weight of the polysaccharide, calculated as N-acetyl neuraminic acid), was found only in the slime of strain 155. Capsular polysaccharide composition closely resembled that for slime. It is of interest that the major slime components were identical whether the energy source provided for the cells was sucrose, glucose, fructose, or ethanol.

Azotobacter↗

CAPSULAR POLYSACCHARIDE OF AZOTOBACTER AGILIS.

Cohen, Gary H. (University of Vermont, Burlington), and Donald B. Johnstone. Capsular polysaccharide of Azotobacter agilis. J. Bacteriol. 88:1695-1699. 1964.-Capsular polysaccharide from Azotobacter agilis strain 132 was recovered from washed cells by alkaline digestion. The polysaccharide was purified by centrifugation, repeated alcohol precipitation, Sevag deproteinization, and treatment with ribonuclease and charcoal-cellulose. Methods of isolation and purification appeared to provide a polymer showing no evidence of heterogeneity when examined by chemical and physical methods. Colorimetric, paper chromatographic, and enzymatic analyses on both intact and acid-hydrolyzed polysaccharide indicated that the polymer contained galactose and rhamnose at a molar ratio of approximately 1.0:0.7. A sialic acid-like component was also present in the polysaccharide. The study shows significant differences in the chemical composition of the extra-cellular polysaccharide of A. agilis and that of A. vinelandii. This adds further biochemical evidence for the right of these species to independent status.

Azotobacter↗

Growth of Azotobacter in deuterium oxide.

Johnstone, D. B. (University of Vermont, Burlington). Growth of Azotobacter in deuterium oxide. J. Bacteriol. 83:867-870. 1962.-To the small list of bacteria that are reported to have been cultured in fully deuterated media can be added Azotobacter agilis and A. vinelandii. Moreover, these bacteria, although growing in a deuterium oxide medium with deuterated carbon sources, will fix atmospheric nitrogen. Lag periods occur prior to growth, and wide morphological variation is apparent during adaptation to a deuterated environment. A convenient method is presented for measuring, by infrared spectroscopy, the amount of water that accumulates in a D(2)O medium; during incubation this amounts to about 1% per day. Prevention of this accumulation of water indicates that growth, after a lag period, probably is not supported by accumulated hydrogen.

Adaptation, Physiological↗