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1.
J Microbiol ; 47(1): 101-9, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19229497

RESUMO

A lactic acid bacterial strain was isolated from human fecal specimen and identified as Enterococcus faecalis SL-5. The isolated strain showed antimicrobial activity against Gram-positive pathogens assayed, especially the highest activity against Propionibacterium acnes. The antimicrobial substance was purified and verified as a bacteriocin (named ESL5) of E. faecalis SL-5 by activity-staining using P. acnes as an indicator. N-terminal sequence of ESL5 was determined (MGAIAKLVAK) and sequence analysis revealed that it is almost identical to the some of enterocins including L50A/B of E. faecium L50 and MR10A/B of E. faecalis MRR 10-3. From the sequencing data of L50A/B structural genes, the nucleotide sequence showed 100% identity with that of the MR10A/B structural genes, implying that ESL5 is an equivalent of enterocin MR10. Meanwhile, we also tested the therapeutic effect of anti-P. acnes activity in patients with mild to moderate acne because of its pathogenic role to acne vulgaris. For this purpose, a concentrated powder of CBT SL-5 was prepared using cell-free culture supernatant (CFCS) of E. faecalis SL-5 and included in a lotion for application in the patients. The study showed that CBT SL-5 lotion significantly reduced the inflammatory lesions like pustules compared to the placebo lotion. Therefore our results indicate that the anti-P. acnes activity produced by E. faecalis SL-5 has potential role to the treatment of acne as an alternative to topical antibiotics.


Assuntos
Acne Vulgar/tratamento farmacológico , Antibacterianos/administração & dosagem , Antibacterianos/biossíntese , Bacteriocinas/administração & dosagem , Bacteriocinas/biossíntese , Enterococcus faecalis/metabolismo , Propionibacterium acnes/efeitos dos fármacos , Administração Cutânea , Adolescente , Adulto , Antibacterianos/isolamento & purificação , Bacteriocinas/isolamento & purificação , Sequência de Bases , Criança , DNA Bacteriano/análise , Método Duplo-Cego , Enterococcus faecalis/genética , Enterococcus faecalis/isolamento & purificação , Fezes/microbiologia , Humanos , Testes de Sensibilidade Microbiana , Dados de Sequência Molecular , Filogenia , Análise de Sequência de DNA
2.
Neurobiol Aging ; 26(7): 1083-91, 2005 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15748788

RESUMO

Previous gene expression profiling studies in Drosophila have provided clues for understanding the aging process at the gene expression level. For a detailed understanding, studies of specific regions of the body are necessary. We therefore employed microarray analysis to examine gene expression changes in the Drosophila head during aging. Six hundred and eighty-four of the 5405 genes present in the microarray showed significant age-dependent changes as determined by significance analysis of microarray (SAM) (q < 0.05). The biological significance of the changes was analyzed using the gene annotations provided by the Gene Ontology Consortium. Major changes involved genes affecting energy metabolism (proton transport, energy pathways, oxidative phosphorylation) and neuronal function, especially responses to light. Genes involved in protein catabolism and several other metabolic processes also showed age-dependent changes. Most of the changes were reductions in gene expression and occurred before day 13 of adult life. After day 13, the age-dependent gene expression changes were relatively smaller than earlier life. Interestingly, the two biological processes of major gene expression changes are related to the two known environmental changes that increase life span in Drosophila: caloric restriction and light reduction. Our findings suggest that light signaling and energy metabolism may be important biological processes affected by aging and be interesting targets for the further investigation related to the longevity in Drosophila.


Assuntos
Envelhecimento/fisiologia , Regulação da Expressão Gênica/fisiologia , Expressão Gênica/fisiologia , Cabeça/fisiologia , Fatores Etários , Animais , Drosophila , Perfilação da Expressão Gênica/métodos , Hibridização In Situ/métodos , Análise em Microsséries/métodos
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