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1.
Commun Biol ; 1: 52, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30271935

RESUMO

Biofilms are intricate communities of microorganisms embedded in a self-produced matrix of extracellular polymer, which provides microbes survival advantages in stressful environments and can cause chronic infections in humans. Curli are functional amyloids that assemble on the extracellular surface of enteric bacteria such as Escherichia coli during biofilm development and colonization. The molecular chaperone DnaK, a bacterial Hsp70 homologue, promotes curli biogenesis via unknown mechanism(s). Here we show that DnaK increases the expression of CsgA and CsgB-the major and minor structural components of curli, respectively-via a quantity and quality control of RpoS, a stationary phase-specific alternative sigma factor regulating bacterial transcription, and CsgD, the master transcriptional regulator of curli formation. DnaK also keeps CsgA and CsgB in a translocation-competent state by binding to their signal peptides prone to aggregation. Our findings suggest that DnaK controls the homoeostasis of curli biogenesis at multiple stages to organize the biofilm matrix.

2.
Sci Rep ; 6: 31208, 2016 08 10.
Artigo em Inglês | MEDLINE | ID: mdl-27506289

RESUMO

Several studies have suggested that flavan-3-ols/procyanidins are associated with a reduced risk of developing obesity and metabolic syndrome. However, the role of highly polymeric procyanidins (PP), which are major non-absorbable flavonoids, in the biological effects, is not completely understood. Here, we show that 0.5% PP administration for 20 weeks alleviated obesity and regulate expression of genes related to lipid metabolism in C57BL/6J mice fed a high-fat/high-sucrose diet. PP-treatment attenuated weight gain and inflammatory effects including lipopolysaccharide and gut permeability. Additionally, metabolic urine profiling using high-performance liquid chromatography-quadrupole time-of-flight/mass spectrometry demonstrated that PP-treatment decreased the levels of endogenous metabolites associated with insulin resistance. Furthermore, microbial 16S rRNA gene sequencing of the cecum demonstrated that PP administration markedly decreased the Firmicutes/Bacteroidetes ratio and increased eight times the proportion of Akkermansia. These data suggest that PPs influence the gut microbiota and the intestinal metabolome to produce beneficial effects on metabolic homeostasis.


Assuntos
Microbioma Gastrointestinal , Malus/química , Obesidade/prevenção & controle , Proantocianidinas/química , Animais , Bacteroidetes , Ceco/metabolismo , Ceco/microbiologia , Dieta Hiperlipídica , Açúcares da Dieta , Firmicutes , Homeostase , Inflamação/tratamento farmacológico , Resistência à Insulina , Lipopolissacarídeos/metabolismo , Masculino , Metaboloma , Metabolômica , Camundongos Endogâmicos C57BL , Permeabilidade , Proantocianidinas/análise , RNA Ribossômico 16S/metabolismo , Aumento de Peso/efeitos dos fármacos
3.
Biosci Biotechnol Biochem ; 79(2): 271-9, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25351253

RESUMO

We previously described potential probiotic Lactobacillus rhamnosus strains, isolated from fermented mare milk produced in Sumbawa Island, Indonesia, which showed high adhesion to porcine colonic mucin (PCM) and extracellular matrix (ECM) proteins. Recently, mucus-binding factor (MBF) was found in the GG strain of L. rhamnosus as a mucin-binding protein. In this study, we assessed the ability of recombinant MBF protein from the FSMM22 strain, one of the isolates of L. rhamnosus from fermented Sumbawa mare milk, to adhere to PCM and ECM proteins by overlay dot blot and Biacore assays. MBF bound to PCM, laminin, collagen IV, and fibronectin with submicromolar dissociation constants. Adhesion of the FSMM22 mbf mutant strain to PCM and ECM proteins was significantly less than that of the wild-type strain. Collectively, these results suggested that MBF contribute to L. rhamnosus host colonization via mucin and ECM protein binding.


Assuntos
Aderência Bacteriana , Proteínas de Bactérias/metabolismo , Proteínas da Matriz Extracelular/metabolismo , Lacticaseibacillus rhamnosus/metabolismo , Mucinas/metabolismo , Proteínas de Bactérias/genética , Parede Celular/metabolismo , Clonagem Molecular , Lacticaseibacillus rhamnosus/citologia , Lacticaseibacillus rhamnosus/genética , Lacticaseibacillus rhamnosus/fisiologia , Mutação , Análise de Sequência
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