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2.
Braz. j. microbiol ; 44(4): 1181-1188, Oct.-Dec. 2013. ilus, tab
Artigo em Inglês | LILACS | ID: lil-705259

RESUMO

This study was developed in order to evaluate two alternatives for the control of Listeria monocytogenes in raw bovine meat pieces, both based on the use of Thymus vulgaris and Rosmarinus officinalis essential oils (EOs). The antilisterial activity of different concentrations of the EOs was tested in vitro using agar dilution and disk volatilization techniques. In addition, L. monocytogenes was inoculated in meat pieces, which were submerged in edible gelatin coatings containing 2% (v/v) EOs or submitted to the vapor of EOs (0.74 μL.cm-3). L. monocytogenes was quantified after one, 48 and 96 hours of storage (7 °C). In the in vitro tests, the EO of T. vulgaris presented higher activity. The two options used (edible gelatin coating and vapor activity), in spite of exercising effects with differentiated behaviors, presented antibacterial activity against L. monocytogenes inoculated in raw bovine meat (p < 0.05). Greatest antibacterial activity were obtained in the experiment that used edible coatings containing EOs, at 48 hours of storage reductions in bacterial counts between 1.09 and 1.25 Log CFU.g-1 were obtained. In the vapor effect experiment, the EO of T. vulgaris caused the highest reduction in the population of bacteria inoculated in raw bovine meat (p < 0.05), 0.40 Log CFU.g-1 at 96 hours of storage. This study supplied important information regarding new and promising natural alternatives, based on the concept of active packaging, for the control of L. monocytogenes in the meat industry.


Assuntos
Animais , Bovinos , Antibacterianos/farmacologia , Conservantes de Alimentos/farmacologia , Listeria monocytogenes/efeitos dos fármacos , Carne/microbiologia , Óleos Voláteis/farmacologia , Thymus (Planta)/química , Antibacterianos/isolamento & purificação , Carga Bacteriana , Conservantes de Alimentos/isolamento & purificação , Listeria monocytogenes/crescimento & desenvolvimento , Testes de Sensibilidade Microbiana , Óleos Voláteis/isolamento & purificação , Rosmarinus/química , Temperatura
3.
Rev. Inst. Adolfo Lutz ; 69(3): 277-284, jul.-set. 2010.
Artigo em Português | LILACS, SES-SP, SESSP-CTDPROD, SES-SP, SESSP-ACVSES, SESSP-IALPROD, SES-SP, SESSP-IALACERVO | ID: lil-583060

RESUMO

Biofilmes podem ser definidos como comunidades microbianas envoltas por uma matriz de polímeros extracelulares e aderidas a superfícies. Na indústria de alimentos, os microrganismos podem se aderir a resíduos orgânicos e inorgânicos presentes na superfície de equipamentos e utensílios, caso o processo de higienização seja aplicado incorretamente. Células sésseis, presentes no biofilme, além de reduzir a eficiência e vida útil de equipamentos, em função do fenômeno denominado corrosão microbiologicamente induzida, são mais resistentes ao processo de desinfecção. As células podem se desprender e contaminar os alimentos que passam pelo local, que causam prejuízos econômicos e risco de ocorrência de toxinfecções alimentares. A compreensão do conceito de biofilmes microbianos e de aspectos inerentes a sua estrutura e composição, bem como de seu processo de formação, são fundamentais para efetuar o desenvolvimento de estratégias de controle efetivas e entendimento do risco que estes representam para as indústrias de alimentos. Na presente revisão bibliográfica, estão descritos os principais aspectos de biofilmes microbianos de importância na indústria de alimentos: i) definição, estrutura e composição; ii) etapas envolvidas na formação; iii) mecanismos de resistência a antimicrobianos; iv) riscos; v) microrganismos envolvidos; vi)importância da higienização como ferramenta de controle.


Bacterial biofilms are defined as microbial communities surrounded by an extracellular matrix of polymers and adhered to surfaces. In food industry, the microorganisms can adhere to organic and inorganic waste occurring on the equipment and utensils surfaces, if the cleaning and sanitization procedures are done incorrectly. The presence of sessile cells in the biofilm reduces the efficiency and durability of equipments through the phenomenon called microbiologically induced corrosion. Additionally, they show muchgreater resistance to the sanitization process; the cells can be loosen and contaminate foods that pass through the place, causing economic losses and risk of occurrence of food borne diseases. Understanding the concept, the structure and composition inherent aspects, and also the producing process of microbial biofilms, are fundamental for establishing effective control strategies and being assured on the risks that they represent to the food industry. This article reviews the crucial aspects concerned with microbialbiofilms in the food industry i) definition, structure and composition; ii) steps involved in the formation; iii) mechanisms of resistance to antimicrobials; iv) risks; v) involved microorganisms; and vi) importance of hygienization as a control strategy.


Assuntos
Aderência Bacteriana , Biofilmes , Contaminação de Alimentos , Higiene
4.
Braz. j. microbiol ; 41(1): 97-106, Jan.-Mar. 2010. ilus, tab
Artigo em Inglês | LILACS | ID: lil-531740

RESUMO

An experimental model was proposed to study biofilm formation by Listeria monocytogenes ATCC 19117 on AISI 304 (#4) stainless steel surface and biotransfer potential during this process. In this model, biofilm formation was conducted on the surface of stainless steel coupons, set on a stainless steel base with 4 divisions, each one supporting 21 coupons. Trypic Soy Broth was used as bacterial growth substrate, with incubation at 37 ºC and stirring of 50 rpm. The number of adhered cells was determined after 3, 48, 96, 144, 192 and 240 hours of biofilm formation and biotransfer potential from 96 hours. Stainless steel coupons were submitted to Scanning Electron Microscopy (SEM) after 3, 144 and 240 hours. Based on the number of adhered cells and SEM, it was observed that L. monocytogenes adhered rapidly to the stainless steel surface, with mature biofilm being formed after 240 hours. The biotransfer potential of bacterium to substrate occurred at all the stages analyzed. The rapid capacity of adhesion to surface, combined with biotransfer potential throughout the biofilm formation stages, make L. monocytogenes a potential risk to the food industry. Both the experimental model developed and the methodology used were efficient in the study of biofilm formation by L. monocytogenes on stainless steel surface and biotransfer potential.


Assuntos
Biofilmes/crescimento & desenvolvimento , Crescimento Bacteriano/métodos , Listeria monocytogenes/isolamento & purificação , Substratos para Tratamento Biológico/métodos , Métodos , Microscopia Eletrônica de Varredura , Métodos
5.
Ciênc. agrotec., (Impr.) ; 32(6): 1893-1898, nov.-dez. 2008. tab
Artigo em Português | LILACS | ID: lil-508591

RESUMO

Foram avaliadas condições higiênico-sanitárias de máquinas de moer carne e mãos de manipuladores e observou-se a interferência na qualidade microbiológica da carne moída. Nas máquinas de moer carne e mãos de manipuladores, realizaram-se análises de microrganismos aeróbios mesófilos, fungos filamentosos e leveduras, coliformes totais e termotolerantes, Escherichia coli e estafilococos coagulase positiva. Nenhuma das máquinas enquadrou-se nos padrões da APHA. Para manipuladores, as contagens de aeróbios mesófilos, estafilococos coagulase positiva, fungos filamentosos e leveduras, coliformes totais e termotolerantes apresentaram-se elevadas. Nas amostras de carne inteira e moída, realizaram-se, além das citadas acima, análises de Salmonella sp. aeróbios psicrotróficos e clostrídios sulfito-redutores. Comparando-se os resultados das análises microbiológicas das carnes antes e após a moagem e manipulação, constatou-se aumento da contagem microbiana na maioria das amostras analisadas, indicando higienização inadequada das máquinas de moer e mão dos manipuladores.


Hygienic-sanitary conditions of meat grinding-machines and handlers' hands were evaluated and the interference on the microbiologic quality of the ground meat was observed. In the meat-ground machines and handlers' hands analyses of mesophyllic aerobic microorganisms, filamentous fungi and yeasts, total and heat-tolerant coliforms, Escherichia coli and positive coagulase staphylococcus were accomplished. None of the machines fitted in the APHA standards. For the handlers, the counts of mesophyllic aerobes, positive coagulase staphylococcus, filamentous fungi and yeasts, total and heat-tolerant coliforms proved elevated. In the samples of whole and ground meat, in addition to those above-cited, analyses of Salmonella sp. psychotrophic aerobes and sulfite-reducing clostridia were performed. By comparing the results of the microbiological analyses of the meats before and after grinding and handling, an increase of the microbial count in most of the samples analyzed was found, denoting inadequate cleaning of the grinding-machines and handlers' hands.

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