Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
Add more filters










Language
Publication year range
1.
Rev Argent Microbiol ; 27(4): 175-83, 1995.
Article in Spanish | MEDLINE | ID: mdl-8850129

ABSTRACT

Ozone and chlorine are agents that disinfect by destroying, neutralizing or inhibiting the growth of pathogenic microorganisms. The treatment of drinking water with ozone has shown to be more efficient against spores of Bacillus subtilis. It was observed that the ozone already in dose of 0.35 mg/l produced the reduction of at least 5 log in populations of approximately 1 x 10(6) cells/ml of Escherichia coli, Vibrio cholerae, Salmonella typhi, Yersinia enterocolitica, Pseudomonas aeruginosa, Aeromonas hydrophila, Listeria monocytogenes and Staphylococcus aureus. With a dose of 0.50 mg/l of chlorine, the reduction was much smaller for the tested microorganisms (except Vibrio cholerae), while the effect of 2 mg/l of chlorine was similar to the ozone treatment. For spores of Bacillus subtilis, the reduction observed with ozone concentrations of 0.35 and 0.70 mg/l was of almost 3 log, while no considerable effect was obtained with chlorine in the tested conditions. Our results have shown that both disinfectans were consumed during the treatment period, probably because of the own water demand and the added bacterial mass.


Subject(s)
Bacteria/drug effects , Disinfectants/pharmacology , Ozone/pharmacology , Sodium Hypochlorite/pharmacology , Water Microbiology , Enterobacteriaceae/drug effects , Listeria monocytogenes/drug effects , Microbial Sensitivity Tests , Pseudomonas aeruginosa/drug effects , Staphylococcus aureus/drug effects , Thiosulfates/pharmacology , Vibrionaceae/drug effects
2.
Rev. argent. microbiol ; 27(4): 175-83, 1995 Oct-Dec.
Article in Spanish | LILACS-Express | LILACS, BINACIS | ID: biblio-1171657

ABSTRACT

Ozone and chlorine are agents that disinfect by destroying, neutralizing or inhibiting the growth of pathogenic microorganisms. The treatment of drinking water with ozone has shown to be more efficient against spores of Bacillus subtilis. It was observed that the ozone already in dose of 0.35 mg/l produced the reduction of at least 5 log in populations of approximately 1 x 10(6) cells/ml of Escherichia coli, Vibrio cholerae, Salmonella typhi, Yersinia enterocolitica, Pseudomonas aeruginosa, Aeromonas hydrophila, Listeria monocytogenes and Staphylococcus aureus. With a dose of 0.50 mg/l of chlorine, the reduction was much smaller for the tested microorganisms (except Vibrio cholerae), while the effect of 2 mg/l of chlorine was similar to the ozone treatment. For spores of Bacillus subtilis, the reduction observed with ozone concentrations of 0.35 and 0.70 mg/l was of almost 3 log, while no considerable effect was obtained with chlorine in the tested conditions. Our results have shown that both disinfectans were consumed during the treatment period, probably because of the own water demand and the added bacterial mass.

3.
Rev. argent. microbiol ; 27(4): 175-83, 1995 Oct-Dec.
Article in Spanish | BINACIS | ID: bin-37074

ABSTRACT

Ozone and chlorine are agents that disinfect by destroying, neutralizing or inhibiting the growth of pathogenic microorganisms. The treatment of drinking water with ozone has shown to be more efficient against spores of Bacillus subtilis. It was observed that the ozone already in dose of 0.35 mg/l produced the reduction of at least 5 log in populations of approximately 1 x 10(6) cells/ml of Escherichia coli, Vibrio cholerae, Salmonella typhi, Yersinia enterocolitica, Pseudomonas aeruginosa, Aeromonas hydrophila, Listeria monocytogenes and Staphylococcus aureus. With a dose of 0.50 mg/l of chlorine, the reduction was much smaller for the tested microorganisms (except Vibrio cholerae), while the effect of 2 mg/l of chlorine was similar to the ozone treatment. For spores of Bacillus subtilis, the reduction observed with ozone concentrations of 0.35 and 0.70 mg/l was of almost 3 log, while no considerable effect was obtained with chlorine in the tested conditions. Our results have shown that both disinfectans were consumed during the treatment period, probably because of the own water demand and the added bacterial mass.

4.
Rev Argent Microbiol ; 22(2): 86-9, 1990.
Article in Spanish | MEDLINE | ID: mdl-2287717

ABSTRACT

Fast lactose fermenting Leuconostoc species and subspecies were isolated from raw milk. Samples were obtained from dairy farms of the surroundings of Buenos Aires city. A lactose, non selective, isolation medium was employed (YCL). Differentiation of leuconostocs from Lactobacillus viridescens and L. confusus was avoided on account of the use of this medium. 801 typical colonies of lactic acid bacteria were selected from YCL agar; 710 of them were identified as lactic acid bacteria from which 114 strains belonged to the genus Leuconostoc. These last strains were then tested for species and subspecies differentiation by dextran production and sugar fermentation. Leuconostoc mesenteroides subsp. dextranicum and L. lactis were identified. Four strains identified as Leuconostoc spp do not belong to any known species.


Subject(s)
Leuconostoc/isolation & purification , Milk/microbiology , Animals , Cattle , Female , Lactobacillus/isolation & purification , Lactobacillus/metabolism , Lactose/metabolism , Leuconostoc/metabolism , Species Specificity
5.
Rev. argent. microbiol ; 22(2): 86-9, 1990 Apr-Jun.
Article in Spanish | BINACIS | ID: bin-51715

ABSTRACT

Fast lactose fermenting Leuconostoc species and subspecies were isolated from raw milk. Samples were obtained from dairy farms of the surroundings of Buenos Aires city. A lactose, non selective, isolation medium was employed (YCL). Differentiation of leuconostocs from Lactobacillus viridescens and L. confusus was avoided on account of the use of this medium. 801 typical colonies of lactic acid bacteria were selected from YCL agar; 710 of them were identified as lactic acid bacteria from which 114 strains belonged to the genus Leuconostoc. These last strains were then tested for species and subspecies differentiation by dextran production and sugar fermentation. Leuconostoc mesenteroides subsp. dextranicum and L. lactis were identified. Four strains identified as Leuconostoc spp do not belong to any known species.

6.
Rev Argent Microbiol ; 17(4): 225-8, 1985.
Article in Spanish | MEDLINE | ID: mdl-3870660

ABSTRACT

Prill and Hammer's method (4) for microdetermination of diacetyl was modified by several authors (1-3, 7), but retaining the same principle: diacetyl is converted into dimethylglyoxime by reaction with hydroxylamine; the oxime is subsequently converted into a pink ammonoferrous glyoximate and its colour is measured by absorbance at 530 nm. In the present communication a procedure based on the method of Pack et al. (3) is proposed with the following modifications: 1. Omission of carboy and suction flask; 2. Elongation of the connecting tubing between sample and trap tubes and relocation of the trap tubes to a higher level. 3. Replacement of rubber tubing by pvc connection and of rubber stoppers by neoprene ones. 4. A more accurate regulation of the nitrogen flow. 5. Protection of the Fe SO4 against oxidation. 6. Omission of the rinse of the trap tips with K2 HPO4 solution. 7. Use of diacetyl as a standard instead of dimethylglyoxime.


Subject(s)
Butanones/analysis , Diacetyl/analysis , Methods
7.
Rev. argent. microbiol ; 17(4): 225-8, 1985.
Article in Spanish | LILACS-Express | LILACS, BINACIS | ID: biblio-1171529

ABSTRACT

Prill and Hammer’s method (4) for microdetermination of diacetyl was modified by several authors (1-3, 7), but retaining the same principle: diacetyl is converted into dimethylglyoxime by reaction with hydroxylamine; the oxime is subsequently converted into a pink ammonoferrous glyoximate and its colour is measured by absorbance at 530 nm. In the present communication a procedure based on the method of Pack et al. (3) is proposed with the following modifications: 1. Omission of carboy and suction flask; 2. Elongation of the connecting tubing between sample and trap tubes and relocation of the trap tubes to a higher level. 3. Replacement of rubber tubing by pvc connection and of rubber stoppers by neoprene ones. 4. A more accurate regulation of the nitrogen flow. 5. Protection of the Fe SO4 against oxidation. 6. Omission of the rinse of the trap tips with K2 HPO4 solution. 7. Use of diacetyl as a standard instead of dimethylglyoxime.

8.
Rev. argent. microbiol ; 17(4): 225-8, 1985.
Article in Spanish | BINACIS | ID: bin-49149

ABSTRACT

Prill and Hammers method (4) for microdetermination of diacetyl was modified by several authors (1-3, 7), but retaining the same principle: diacetyl is converted into dimethylglyoxime by reaction with hydroxylamine; the oxime is subsequently converted into a pink ammonoferrous glyoximate and its colour is measured by absorbance at 530 nm. In the present communication a procedure based on the method of Pack et al. (3) is proposed with the following modifications: 1. Omission of carboy and suction flask; 2. Elongation of the connecting tubing between sample and trap tubes and relocation of the trap tubes to a higher level. 3. Replacement of rubber tubing by pvc connection and of rubber stoppers by neoprene ones. 4. A more accurate regulation of the nitrogen flow. 5. Protection of the Fe SO4 against oxidation. 6. Omission of the rinse of the trap tips with K2 HPO4 solution. 7. Use of diacetyl as a standard instead of dimethylglyoxime.

SELECTION OF CITATIONS
SEARCH DETAIL
...