RIG-I is a cytosolic receptor recognizing virus-specific RNA
structures and initiates an antiviral signaling that induces the
production of interferons and proinflammatory cytokines.
Because inappropriate RIG-I signaling affects either viral
clearance or immune toxicity, multiple regulations of RIG-I
have been investigated since its discovery as the viral RNA
detector. In this review, we describe the recent progress in
research on the regulation of RIG-I activity or abundance.
Specifically, we focus on the mechanism that modulates RIGI-
dependent antiviral response through post-translational
modifications of or protein-protein interactions with RIG-I.
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A novel halophilic bacterium, strain K7T, was isolated from
kimchi, a traditional Korean fermented food. The strain is
Gram-positive, motile, and produces terminal endospores.
The isolate is facultative aerobic and grows at salinities of
0.0–25.0% (w/v) NaCl (optimum 10–15% NaCl), pH 5.5–8.5
(optimum pH 7.0–7.5), and 15–42°C (optimum 37°C). The
predominant isoprenoid quinone in the strain is menaquinone-
7 and the peptidoglycan of the strain is meso-diaminopimelic
acid. The major fatty acids of the strain are anteisio-
C15:0, iso-C15:0, and, C16:0 (other components were < 10.0%),
while the major polar lipids are diphosphatidylglycerol, phosphatidylglycerol,
phosphatidylcholine, and three unidentified
lipids. A phylogenetic analysis of 16S rRNA gene sequence
similarity showed that the isolated strain was a cluster of the
genus Gracilibacillus. High levels of gene sequence similarity
were observed between strain K7T and Gracilibacillus orientalis
XH-63T (96.5%), and between the present strain and
Gracilibacillus xinjiangensis (96.5%). The DNA G+C content
of this strain is 37.7 mol%. Based on these findings, strain
K7T is proposed as a novel species: Gracilibacillus kimchii sp.
nov. The type strain is K7T (KACC 18669T; JCM 31344T).
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intestinal Lactobacillus species and diet of elderly subjects in
a longevity area in Southern China. Healthy elderly subjects
ranging from 80 to 99 years old were respectively selected
from the regions of Bama and Nanning, Guangxi, China.
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gel electrophoresis (PCR-DGGE) technology was used
to analyze the intestinal Lactobacillus community structure. Results showed that Weissella confusa, L. mucosae, L. crispatus,
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Lactobacillus of elderly subjects. Among them, L. crispatus
and L. delbrueckii were the dominant Lactobacillus of
all species. In comparison to Nanning elderly subjects, the
detection frequencies of W. confusa and L. salivarius were
significantly increased in Bama elderly subjects (P < 0.01),
whereas L. mucosae was significantly decreased (P < 0.01).
Interestingly, it was also found that there were 4 kinds of
representative Lactobacillus, which were significantly correlated
with dietary fiber. W. confusa (P < 0.01) and L. salivarius
(P < 0.05) were significantly positively correlated with
the intake of dietary fiber, while L. mucosae (P < 0.01) and
L. crispatus (P < 0.05) were significantly negatively correlated
with the intake of dietary fiber, respectively. Results confirmed
that different diets had obvious effects on the intestinal Lactobacillus
community structure of elderly subjects in Southern
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of soil bacterial communities in long-term converted
and fertilized red soils (a type of Ferralic Cambisol). We observed
that soil bacterial diversity was strongly affected by
different types of fertilization management. Oligotrophic bacterial
taxa demonstrated large relative abundances in chemically
fertilized soil, whereas copiotrophic bacterial taxa were
found in large relative abundances in organically fertilized
and fallow management soils. Only organic-inorganic fertilization
exhibited the same local taxonomic and phylogenetic
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independent use of organic or inorganic fertilizer reduced
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of the yeast species that cause food spoilage. A total 134 strains
belonging to 21 different yeast species were examined to evaluate
the discriminative power of HRM analysis. Two different
highly variable DNA regions on the 26 rRNA gene were
targeted to produce the HRM profiles of each strain. HRMbased
grouping was compared and confirmed by (GTG)5 rep-
PCR fingerprinting analysis. All of the yeast species belonging
to the genera Pichia, Candida, Kazachstania, Kluyveromyces,
Debaryomyces, Dekkera, Saccharomyces, Torulaspora,
Ustilago, and Yarrowia, which were produced as species-specific
HRM profiles, allowed discrimination at species and/or
strain level. The HRM analysis of both target regions provided
successful discrimination that correlated with rep-PCR fingerprinting
analysis. Consequently, the HRM analysis has the
potential for use in the rapid and accurate classification and
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The sco0765 gene was annotated as a glycosyl hydrolase family
5 endoglucanase from the genomic sequence of Streptomyces
coelicolor A3(2) and consisted of 2,241 bp encoding a
polypeptide of 747 amino acids (molecular weight of 80.5
kDa) with a 29-amino acid signal peptide for secretion. The
SCO0765 recombinant protein was heterogeneously overexpressed
in Streptomyces lividans TK24 under the control
of a strong ermE* promoter. The purified SCO0765 protein
showed the expected molecular weight of the mature form
(718 aa, 77.6 kDa) on sodium dodecyl sulfate-polyacryl amide
gel electrophoresis. SCO0765 showed high activity toward
β-glucan and carboxymethyl cellulose (CMC) and negligible
activity to Avicel, xylan, and xyloglucan. The SCO0765 cellulase
had a maximum activity at pH 6.0 and 40°C toward
CMC and at pH 9.0 and 50–60°C toward β-glucan. Thin
layer chromatography of the hydrolyzed products of CMC
and β-glucan by SCO0765 gave cellotriose as the major product
and cellotetraose, cellopentaose, and longer oligosaccharides
as the minor products. These results clearly demonstrate
that SCO0765 is an endo-β-1,4-cellulase, hydrolyzing
the β-1,4 glycosidic bond of cellulose into cellotriose.
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Autoinducer 2 (AI-2) is a quorum sensing molecule to which
bacteria respond to regulate various phenotypes, including
virulence and biofilm formation. AI-2 plays an important role
in the formation of a subgingival biofilm composed mostly of
Gram-negative anaerobes, by which periodontitis is initiated.
The aim of this study was to evaluate D-galactose as an inhibitor
of AI-2 activity and thus of the biofilm formation of
periodontopathogens. In a search for an AI-2 receptor of
Fusobacterium nucleatum, D-galactose binding protein (Gbp,
Gene ID FN1165) showed high sequence similarity with
the ribose binding protein (RbsB), a known AI-2 receptor of
Aggregatibacter actinomycetemcomitans. D-Galactose was
evaluated for its inhibitory effect on the AI-2 activity of Vibrio
harveyi BB152 and F. nucleatum, the major coaggregation
bridge organism, which connects early colonizing commensals
and late pathogenic colonizers in dental biofilms. The
inhibitory effect of D-galactose on the biofilm formation of
periodontopathogens was assessed by crystal violet staining
and confocal laser scanning microscopy in the absence or
presence of AI-2 and secreted molecules of F. nucleatum.
D-Galactose significantly inhibited the AI-2 activity of V.
harveyi and F. nucleatum. In addition, D-galactose markedly
inhibited the biofilm formation of F. nucleatum, Porphyromonas
gingivalis, and Tannerella forsythia induced by the
AI-2 of F. nucleatum without affecting bacterial growth. Our results demonstrate that the Gbp may function as an AI-2
receptor and that galactose may be used for prevention of the
biofilm formation of periodontopathogens by targeting AI-2
activity.
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