1954
DOI: 10.1021/ie50530a047
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Production of Clinical-Type Dextran - Partial Hydrolytic Depolymerization and Fractionation of the Dextran from Leuconostoc mesenteroides Strain NRRL B-512

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Cited by 31 publications
(14 citation statements)
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“…During fermentation, the pH drops from 7 to 5 due to the generation of lactic acid; therefore, non-ionic detergents are usually added to maintain the stability of the bacteria and its enzymes [8]. In the clinical area, dextran is usually obtained from the acid hydrolysis (e.g., sulfuric and hydrochloric acids) of the native dextran from Leuconostoc mesenteroides NRRL B512, which allows controlling the molecular weights of the resulting dextrans [26,27].…”
Section: Synthesis Of Dextranmentioning
confidence: 99%
“…During fermentation, the pH drops from 7 to 5 due to the generation of lactic acid; therefore, non-ionic detergents are usually added to maintain the stability of the bacteria and its enzymes [8]. In the clinical area, dextran is usually obtained from the acid hydrolysis (e.g., sulfuric and hydrochloric acids) of the native dextran from Leuconostoc mesenteroides NRRL B512, which allows controlling the molecular weights of the resulting dextrans [26,27].…”
Section: Synthesis Of Dextranmentioning
confidence: 99%
“…The relative similarity of the results of number and weight average methods indicates that while the individual fractions were not homogeneous they were considerably more so than the native dextrans, but similar to the clinical, ethyl alcoholfractionated dextrans (28).…”
Section: Ditionsmentioning
confidence: 89%
“…Dextran A, carefully hydrolyzed and converted to clinical dextrans with acid and then fractionated with ethyl alcohol, showed differences between number and weightaverage molecular weights, thus demonstrating heterogeneity (28). Furthermore, a light-scattering technique applied to various fractions of a native dextran gave a wide range of D P values (1) from 7.8 to 370 ( X lo4) , demonstrating heterogeneity.…”
Section: Experiments a N D Discussionmentioning
confidence: 99%
“…For clinical and technical dextran, the partial hydrolysis and further fractionation of native dextran gives products with the desired molecular sizes [79,80]. Variation of the concentration of the hydrochloric or sulfuric acid, the time and temperature of hydrolysis, and the nature and ratio of the precipitant (alcohol/water) for phase separation permits the control of the resultant average molecular weights.…”
Section: Industrial Productionmentioning
confidence: 99%