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Volume 22,
Issue 2,
1960
Volume 22, Issue 2, 1960
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The Isolation of Anaerobic Cellulose-decomposing Bacteria from Soil
More LessSUMMARY: A strictly anaerobic mesophilic species of cellulose-decomposing bacteria was isolated from soil by a new technique. Cultures were made in screw-capped bottles with media containing finely divided cellulose. The method and apparatus used for filling these bottles with reduced media and nitrogen is described. Flocculation of cellulose particles in agar media was prevented by incorporating a low concentration of sodium carboxymethyl cellulose. Cellulolytic colonies in cellulose agar media were of two types, punctiform and spreading. The isolate derived from a punctiform colony digested cellulose with the formation of formic, acetic and malic acids, carbon dioxide and hydrogen. Essential growth factors were provided by yeast and soil extracts. Surface colonies on yeast peptone cellobiose agar were differentiated into convex entire central zones and thin transparent irregular margins. In deep culture with the same medium the isolate grew either as discrete lenticular colonies or spread rapidly throughout the agar. These growth forms were unstable, the type appearing in any one culture being unpredictable. In many respects the isolate resembles Clostridium cellobioparum Hungate, and is probably a strain of this species. It differs from C. cellobioparum, however, in producing little or no cellobiose but abundant glucose from cellulose in liquid culture.
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The Cultivation of Sheep Rumen Oligotrich Protozoa in vitro
More LessSUMMARY: Oligotrich protozoa from the sheep rumen, principally Entodinium caudatum, were maintained in culture in vitro and dividing every 2 days at a density of 15,000–30,000 protozoa/ml. for 18 months on a medium of rice starch, dried grass, 10% (v/v) rumen fluid (fresh or autoclaved) and 50 μg. chloramphenicol/ml. The effect on these organisms of varying each of these factors in turn and the use of different growth conditions is described. The protozoa have also been grown from an inoculum of 100’900/ml. to a density of over 50,000/ml. in 10 days.
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Studies on the Metabolism of Arthrobacter globiformis
More LessSUMMARY: A strain of Arthrobacter globiformis grew on a glucose + ammonium + salts medium (pH 7) when this was supplemented with biotin (10−8 m). Maximal and most rapid growth was obtained by aerobic incubation in shaken culture at 30°. A variety of sugars, sugar alcohols, dicarboxylic acids, some amino acids and miscellaneous compounds could replace the glucose in this medium, but various aromatic compounds, purines, pyrimidines and other amino acids did not support growth, though several of these substances were oxidized by washed suspensions. The organism was an obligate aerobe whose terminal electron transport was mediated by a cytochrome system. Enzymic analysis showed that glucose could be metabolized by the hexose monophosphate oxidation and Embden-Meyerhof pathways. No direct oxidation of glucose to gluconic and 2-oxogluconic acids, and no Entner-Dou- doroff pathway for the utilization of 6-phosphogluconate were demonstrable. Studies with differently [14C]-labelled samples of glucose confirmed these findings and showed that in suspensions of organisms depleted of endogenous metabolites, the Embden-Meyerhof pathway was fully functional, accounting for c. 65 % of glucose utilization, the remaining 35 % proceeding by way of the hexose monophosphate cycle. The pyruvate so formed was normally further oxidized by the tricarboxylic acid cycle. The growth yield of A. globiformis on limiting amounts of glucose was no greater than that of Escherichia coli under the same condition. These observations are considered in relation to the allocation of A. globiformis in the autochthonous group of soil micro-organisms.
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A Rapid Method for Obtaining Unordered Neurospora Tetrads
More LessSUMMARY: A method of collecting unordered asci of Neurospora crassa makes use of the natural ejection of the ascospores from perithecia in groups of eight. Genetic evidence from 2374 groups shows that they were derived from individual asci. The method is reliable and efficient.
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