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1.
J Food Prot ; 63(11): 1591-3, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11079706

RESUMO

To evaluate the presence of Yersinia enterocolitica in raw chicken, 70 samples of chicken carcasses were obtained from a Buenos Aires, Argentina, processing plant. The detection of this psychotropic microorganism was carried out using the whole carcass rinse method and enrichment in phosphate-buffered saline, 0.067 M, pH 7.6, at 4 degrees C, followed by alkaline treatment and isolation on cefsulodin-irgasan-novobiocin nutrient agar. Y. enterocolitica or related species were detected in 7 of 70 samples. From them, 4.3% were identified as Y. enterocolitica, 1.4% as Yersinia intermedia, and 4.3% as Yersinia frederiksenii. The serotype and phagotype of Y. intermedia isolates were O:5(2), 5(3), and Xz and those of Y. frederiksenii were O:4.16 and Xo. All Y. enterocolitica isolates belong to the biogroup 1A, serotype O:5, phagotype Xz, which presents uncertain pathogenic potential. These findings reinforce the worldwide concern on the microbiological quality of food products. Quality assurance programs on the whole poultry process are increasingly being adopted in Argentina.


Assuntos
Galinhas/microbiologia , Microbiologia de Alimentos , Yersinia enterocolitica/isolamento & purificação , Animais , Argentina , Sorotipagem , Virulência , Yersinia enterocolitica/classificação , Yersinia enterocolitica/patogenicidade
2.
Rev Argent Microbiol ; 30(1): 42-51, 1998.
Artigo em Espanhol | MEDLINE | ID: mdl-9629607

RESUMO

A wide variety of techniques are available for the preservation of bacteria and it may be difficult to choose a method for a particular strain, which not only assures survival, but which also makes certain that the genotype and hence the unique characteristics do not change. This paper provides a summary of the main features of various available methods with references to recent research and applications.


Assuntos
Técnicas Bacteriológicas , Preservação Biológica/métodos , Criopreservação , Meios de Cultura , Dessecação , Liofilização , Gelatina , Papel , Sílica Gel , Dióxido de Silício , Esporos Bacterianos , Suspensões
3.
Rev. argent. microbiol ; Rev. argent. microbiol;30(1): 42-51, ene.-mar. 1998.
Artigo em Espanhol | LILACS | ID: lil-223474

RESUMO

Se dispone de una amplia variedad de técnicas para la preservación de cultivos bacteriano. Sin embargo puede resultar dificultoso elegir el método apropiado para la preservación de una determinada cepa, que no sólo asegure la viabilidad sino que también preserve el genotipo y en consecuencia, las características particulares de la misma. Este trabajo provee un compendio de los aspectos más importantes de los métodos disponibles, con referencias a investigaciones y aplicaciones recientes


Assuntos
Criopreservação/métodos , Meios de Cultura/normas , Liofilização/métodos , Preservação Biológica/métodos , Argentina
4.
Rev. argent. microbiol ; 30(1): 42-51, ene.-mar. 1998.
Artigo em Espanhol | BINACIS | ID: bin-17394

RESUMO

Se dispone de una amplia variedad de técnicas para la preservación de cultivos bacteriano. Sin embargo puede resultar dificultoso elegir el método apropiado para la preservación de una determinada cepa, que no sólo asegure la viabilidad sino que también preserve el genotipo y en consecuencia, las características particulares de la misma. Este trabajo provee un compendio de los aspectos más importantes de los métodos disponibles, con referencias a investigaciones y aplicaciones recientes (AU)


Assuntos
Meios de Cultura/normas , Criopreservação/métodos , Liofilização/métodos , Preservação Biológica/métodos , Argentina
5.
World J Microbiol Biotechnol ; 10(6): 673-6, 1994 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24421193

RESUMO

The conjugative enterococcal transposons Tn916 and Tn919 were introduced into Bacillus megaterium by a filtermating technique. The transfer frequencies obtained ranged from 1.3×10(-6) to 6.6×10(-7). The transposons integrated stably into the B. megaterium chromosome. Tn916 could generate auxotrophs and was transferred from B. megaterium Tn916 transconjugants to other species.

6.
Rev Argent Microbiol ; 23(1): 26-9, 1991.
Artigo em Espanhol | MEDLINE | ID: mdl-1815264

RESUMO

Centrifugation through sucrose gradients was adapted to separate spore-forming cells of B. megaterium deficient in poly-beta-hydroxybutyrate synthesis from wild type cells. The conditions described allowed the detection of mutant clones screening a low percentage of the mutagenized population.


Assuntos
Bacillus megaterium/genética , Hidroxibutiratos/metabolismo , Poliésteres/metabolismo , Bacillus megaterium/isolamento & purificação , Bacillus megaterium/metabolismo , Centrifugação com Gradiente de Concentração , Esporos Bacterianos
7.
Rev. argent. microbiol ; Rev. argent. microbiol;23(1): 26-9, 1991 Jan-Feb.
Artigo em Espanhol | BINACIS | ID: bin-51361

RESUMO

Centrifugation through sucrose gradients was adapted to separate spore-forming cells of B. megaterium deficient in poly-beta-hydroxybutyrate synthesis from wild type cells. The conditions described allowed the detection of mutant clones screening a low percentage of the mutagenized population.

8.
Rev Argent Microbiol ; 18(1): 49-51, 1986.
Artigo em Espanhol | MEDLINE | ID: mdl-3685381

RESUMO

A procedure was optimized for the formation and regeneration of protoplasts in a Clostridium acetobutylicum strain isolated from cassava roots in Misiones, Argentina. The regeneration frequency was calculated as the ratio of regenerants (colony forming units on regeneration plates minus colony forming units from osmotically resistant cells) per initial cell number (colony forming units before protoplast formation). The percentage regeneration varied from 10 to 15%.


Assuntos
Clostridium/genética , Protoplastos , Transformação Genética , Clostridium/crescimento & desenvolvimento
9.
Rev. argent. microbiol ; Rev. argent. microbiol;18(1): 49-51, 1986.
Artigo em Espanhol | BINACIS | ID: bin-52822

RESUMO

A procedure was optimized for the formation and regeneration of protoplasts in a Clostridium acetobutylicum strain isolated from cassava roots in Misiones, Argentina. The regeneration frequency was calculated as the ratio of regenerants (colony forming units on regeneration plates minus colony forming units from osmotically resistant cells) per initial cell number (colony forming units before protoplast formation). The percentage regeneration varied from 10 to 15


.

10.
Rev Argent Microbiol ; 16(2): 57-66, 1984.
Artigo em Espanhol | MEDLINE | ID: mdl-6400723

RESUMO

Schiemann's medium was used for the isolation of Yersinia enterocolitica and Yersinia enterocolitica-like organisms. These bacteria were isolated in 90% of the samples of sewage of the city of Buenos Aires, both from direct and cold enriched samples. From a total of 19 strains, 8 were classified as Y. enterocolitica (lactose positive), 7 as Y. frederiksenii and 2 as Y. intermedia. Two strains could be included in the latter species (biotypes 4 and 5 from Brenner et al. (14] but a confirmation by DNA hybridization would be useful. All the Y. enterocolitica and Y. frederiksenii were sero and lysotyped according to the Center for Yersinia (Paris, France).


Assuntos
Esgotos/análise , Yersinia/isolamento & purificação , Argentina , Técnicas Bacteriológicas , Meios de Cultura , Yersinia/classificação , Yersinia enterocolitica/classificação , Yersinia enterocolitica/isolamento & purificação
11.
Rev. argent. microbiol ; Rev. argent. microbiol;16(2): 57-66, 1984.
Artigo em Espanhol | BINACIS | ID: bin-49434

RESUMO

Schiemanns medium was used for the isolation of Yersinia enterocolitica and Yersinia enterocolitica-like organisms. These bacteria were isolated in 90


of the samples of sewage of the city of Buenos Aires, both from direct and cold enriched samples. From a total of 19 strains, 8 were classified as Y. enterocolitica (lactose positive), 7 as Y. frederiksenii and 2 as Y. intermedia. Two strains could be included in the latter species (biotypes 4 and 5 from Brenner et al. (14] but a confirmation by DNA hybridization would be useful. All the Y. enterocolitica and Y. frederiksenii were sero and lysotyped according to the Center for Yersinia (Paris, France).

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