Glycyrrhizic acid, glycyrrhetinic acid, and their oxo, ester, lactone, and other derivatives, are known for their anti-inflammatory,
anti-oxidant, and hypoglycemic pharmacological activities. In this study, chryseno[2,1-c]oxepin-12-carboxylic acid
(MG) was first biosynthesized from glycyrrhizic acid through sequential hydrolysis, oxidation, and esterification using
Aspergillus terreus TMZ05-2, providing a novel in vitro biosynthetic pathway for glycyrrhizic acid derivatives. Assessing
the influence of fermentation conditions and variation of strains during culture under stress-induction strategies enhanced
the final molar yield to 88.3% (5 g/L glycyrrhizic acid). CCK8 assays showed no cytotoxicity and good cell proliferation,
and anti-inflammatory experiments demonstrated strong inhibition of NO release (36.3%, low-dose MG vs. model), transcriptional
downregulation of classical effective cellular factors tumor necrosis factor-α (TNF-α; 72.2%, low-dose MG vs.
model), interleukin-6 (IL-6; 58.3%, low-dose MG vs. model) and interleukin-1β (IL-1β; 76.4%, low-dose MG vs. model),
and decreased abundance of P-IKK-α, P-IKB-α, and P-P65 proteins, thereby alleviating inflammatory responses through
the NF-κB pathway in LPS-induced RAW264.7 cells. The findings provide a reference for the biosynthesis of lactone compounds
from medicinal plants.
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Salmonella enterica serovar Typhimurium (S. Typhimurium) is a globally recognized foodborne pathogen that affects both
animals and humans. Endoribonucleases mediate RNA processing and degradation in the adaptation of bacteria to environmental
changes and have been linked to the pathogenicity of S. Typhimurium. Not much is known about the specific regulatory
mechanisms of these enzymes in S. Typhimurium, particularly in the context of environmental adaptation. Thus, this
study carried out a comparative transcriptomic analysis of wild-type S. Typhimurium SL1344 and its mutant (Δrnc), which
lacks the rnc gene encoding RNase III, thereby elucidating the detailed regulatory characteristics that can be attributed to the
rnc gene. Global gene expression analysis revealed that the Δrnc strain exhibited 410 upregulated and 301 downregulated
genes (fold-change > 1.5 and p < 0.05), as compared to the wild-type strain. Subsequent bioinformatics analysis indicated
that these differentially expressed genes are involved in various physiological functions, in both the wild-type and Δrnc
strains. This study provides evidence for the critical role of RNase III as a general positive regulator of flagellar-associated
genes and its involvement in the pathogenicity of S. Typhimurium.
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of evidence supporting heterogeneous distributions for bacteria, archaea and protists is accumulating, and more recently
a few efforts have targeted microscopic fungi. We propose an insight into this latter kingdom by looking at a group of soil
nematode-trapping fungi whose species are well-known and easily recognizable. We chose a pure culture approach because
of its reliable isolation procedures for this specific group. After morphologically and molecularly identifying all species
collected from 2250 samples distributed in 228 locations across Yunnan province of China, we analyzed occurrence frequencies
and mapped species, genera, and richness. Results showed an apparent cosmopolitan tendency for this group of
fungi, including species richness among sites. However, only four species were widespread across the region, while nonrandom
heterogeneous distributions were observed for the remaining 40 species, both in terms of statistical distribution of
species richness reflected by a significant variance-to-mean ratio, as well as in terms of visually discernible spatial clusters
of rare species and genera on the map. Moreover, several species were restricted to only one location, raising the question
of whether endemicity exists for this microbial group. Finally, environmental heterogeneity showed a marginal contribution
in explaining restricted distributions, suggesting that other factors such as geographical isolation and dispersal capabilities
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J. Microbiol. 2021;59(12):1104-1111. Published online October 26, 2021
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cell’s state is its fatty acid (FA) profile, reflecting membrane
lipid composition. Consideration of FA composition
enables assessment of bacterial responses to cultivation conditions
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factors impacting cellular metabolism. In this work,
soil SDS-degrading Pseudomonas helmanticensis was studied
at the fatty acid profile level, including analysis of rearrangement
between planktonic and aggregated forms. The set of
substrates included fat hydrolysates, SDS, and their mixtures
with glucose. Such media are useful in bioplastic production
since they can help incrementally lower overall costs. Conventional
gas chromatography-mass spectrometry was used
for FA analysis. Acridine orange-stained aggregates were observed
by epifluorescence microscopy. The bacterium was
shown to change fatty acid composition in the presence of
hydrolyzed fats or SDS. These changes seem to be driven by
the depletion of metabolizable substrates in the culture medium.
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unsaturated FA ratios) do not always sufficiently characterize
a cell's physiological state, and morphological examination
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Paenibacillus polymyxa is a promising plant-growth-promoting
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the exopolysaccharides (EPSs) of these strains increased the
mitotic index 1.9-fold (P. polymyxa CCM 1465) and 2.8-fold
(P. polymyxa 92). These increases indicate activation of cell
division in the root meristems. Analysis of the morphometric
variables of the seedlings showed that P. polymyxa CCM
1465, P. polymyxa 92, and their EPSs promoted wheat growth,
increasing root and shoot length up to 22% and root and
shoot dry weight up to 28%, as compared with the control.
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seedling root surface. Thus, P. polymyxa EPSs are active metabolites
that, along with whole cells, are responsible for the
contact interactions of the bacteria with wheat roots and are
implicated in the induction of plant responses to these interactions.
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mechanisms of plant–bacterial interactions and to develop
effective biofertilizers for agricultural purposes.
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with antibiotic treatment failure. However, we do not know
how widespread the colistin heteroresistance is in carbapenem-
resistant K. pneumoniae isolates. In this study, we performed
colistin disc diffusion assays, E-tests, and population
analysis profiling for KPC-2-producing K. pneumoniae isolates
to identify colistin heteroresistance. Although no colistin-
resistant colonies were detected by the disc diffusion
test and E-test, a colistin-resistant subpopulation was identified
in population analysis profiling in all colistin-susceptible,
KPC-2-producing K. pneumoniae isolates. Colistin-resistant
subpopulations were also identified even when isolates
had no colistin exposure. The ratio of colistin-resistant
subpopulations to the total population increased as the exposure
concentration of colistin increased. In in vitro time-kill
assays, regrowth was observed in all isolates after 2 h upon
exposure to colistin. We identified common amino acid alterations
in PhoQ, PhoP, and PmrB in colistin-resistant subpopulations
from some isolates, but no substitutions were
found in most resistant subpopulations from other isolates.
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PhoQ and PbgP was observed. In this study, we demonstrated
that colistin heteroresistance may be common in KPC-2-producing
K. pneumoniae isolates, which could not be detected
in the disc diffusion method and E-test. Colistin heteroresistance
may cause colistin treatment failure in part and may
evolve into resistance. Thus, development of more reliable
diagnostic methods is required to detect colistin heteroresistance.
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Aquatic microorganisms in the sediment and water column
are closely related; however, their distribution patterns between
these two habitats still remain largely unknown. In this
study, we compared sediment and water microeukaryotic and
bacterial microorganisms in aquaculture ponds from different
areas in China, and analyzed the influencing environmental
factors as well as the inter-taxa relationships. We found that
bacteria were significantly more abundant than fungi in both
sediment and water, and the bacterial richness and diversity
in sediment were higher than in water in all the sampling
areas, but no significant differences were found between the
two habitats for microeukaryotes. Bacterial taxa could be
clearly separated through cluster analysis between the sediment
and water, while eukaryotic taxa at all classification
levels could not. Spirochaetea, Deltaproteobacteria, Nitrospirae,
Ignavibacteriae, Firmicutes, Chloroflexi, and Lentimicrobiaceae
were more abundantly distributed in sediment,
while Betaproteobacteria, Alphaproteobacter, Cyanobacteria,
Roseiflexaceae, Dinghuibacter, Cryomorphaceae, and Actinobacteria
were more abundant in water samples. For eukaryotes,
only Cryptomonadales were found to be distributed
differently between the two habitats. Microorganisms in sediment
were mainly correlated with enzymes related to organic
matter decomposition, while water temperature, pH, dissolved
oxygen, and nutrient levels all showed significant correlation
with the microbial communities in pond water. Intensive interspecific
relationships were also found among eukaryotes
and bacteria. Together, our results indicated that eukaryotic
microorganisms are distributed less differently between sediment
and water in aquaculture ponds compared to bacteria.
This study provides valuable data for evaluating microbial
distributions in aquatic environments, which may also be of
practical use in aquaculture pond management.
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Human intestinal microbiota is affected by the exogenous
microenvironment. This study aimed to determine the effects
of cigarettes and alcohol on the gut microbiota of healthy
men. In total, 116 healthy male subjects were enrolled and
divided into four groups: non-smoking and non-drinking
(Group A), smoking only (Group B), drinking only (Group
C), and smoking and drinking combined (Group D). Fecal
samples were collected and sequenced using 16S rRNA to
analyze the microbial composition. Short-chain fatty acid
(SCFAs) levels in feces were determined by gas chromatography.
We found that cigarette and alcohol consumptions
can alter overall composition of gut microbiota in healthy
men. The relative abundances of phylum Bacteroidetes and
Firmicutes and more than 40 genera were changed with cigarette
and alcohol consumptions. SCFAs decreased with smoking
and alcohol consumption. Multivariate analysis indicated
that when compared with group A, group B/C/D had higher
Bacteroides, and lower Phascolarctobacterium, Ruminococcaceae_
UCG-002, Ruminococcaceae_UCG-003, and Ruminiclostridium_
9 regardless of BMI and age. Additionally, the
abundance of Bacteroides was positively correlated with the
smoking pack-year (r = 0.207, p < 0.05), the abundance of predicted
pathway of bacterial toxins (r = 0.3672, p < 0.001) and
the level of carcinoembryonic antigen in host (r = 0.318, p
< 0.01). Group D shared similar microbial construction with
group B, but exerted differences far from group C with lower
abundance of Haemophilus. These results demonstrated that
cigarette and alcohol consumption separately affected the
intestinal microbiota and function in healthy men; furthermore,
the co-occurrence of cigarette and alcohol didn’t exacerbate
the dysbiosis and cigarette played the predominated
role on the alteration.
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We measured the grazing and growth response of the mixotrophic
chrysomonad flagellate Poterioochromonas malhamensis
on four closely related picocyanobacterial strains isolated
from subalpine lakes in central Europe. The picocyanobacteria
represented different pigment types (phycoerythrin-
rich, PE, and phycocyanin-rich, PC) and phylogenetic
clusters. The grazing experiments were conducted with laboratory
cultures acclimated to 10 μmol photon/m2/sec (low
light, LL) and 100 μmol photon/m2/sec (moderate light, ML),
either in the dark or at four different irradiances ranging from
low (6 μmol photon/m2/sec) to high (1,500 μmol photon/m2/
sec) light intensity. Poterioochromonas malhamensis preferred
the larger, green PC-rich picocyanobacteria to the smaller,
red PE-rich picocyanobacterial, and heterotrophic bacteria.
The feeding and growth rates of P. malhamensis were sensitive
to the actual light conditions during the experiments;
the flagellate performed relatively better in the dark and at
LL conditions than at high light intensity. In summary, our results found strain-specific ingestion and growth rates of
the flagellate; an effect of the preculturing conditions, and,
unexpectedly, a direct adverse effect of high light levels. We
conclude that this flagellate may avoid exposure to high surface
light intensities commonly encountered in temperate
lakes during the summer.
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Intrauterine growth restriction (IUGR) predisposes newborns
to inflammatory and metabolic disturbance. Disequilibrium
of gut microbiota in early life has been implicated
in the incidence of inflammation and metabolic diseases in
adulthood. This study aimed to investigate the difference in
gut microbiota colonization, cytokines and plasma metabolome
between IUGR and normal birth weight (NBW) piglets
in early life. At birth, reduced (P < 0.05) body, jejunum, and
ileum weights, as well as decreased (P < 0.05) small intestinal
villi and increased (P < 0.05) ileal crypt depth were observed
in IUGR piglets compared with their NBW counterparts. Imbalanced
inflammatory and plasma metabolome profile was
observed in IUGR piglets. Furthermore, altered metabolites
were mainly involved in fatty acid metabolism and inflammatory
response. At 12 h after birth and after suckling colostrum,
reduced (P < 0.05) postnatal growth and the small intestinal
maturation retardation (P < 0.05) continued in IUGR
piglets in comparison with those in NBW littermates. Besides,
the gut microbiota structure was significantly altered
by IUGR. Importantly, the disruption of the inflammatory
profile and metabolic status mainly involved the pro-inflammatory
cytokines (IL-1β and IFN-γ) and amino acid metabolism.
Moreover, spearman correlation analysis showed
that the increased abundance of Escherichia-Shigella and decreased
abundance of Clostridium_sensu_stricto_1 in IUGR
piglets was closely associated with the alterations of slaughter
weight, intestinal morphology, inflammatory cytokines, and
plasma metabolites. Collectively, IUGR significantly impairs
small intestine structure, modifies gut microbiota colonization, and disturbs inflammatory and metabolic profiles during
the first 12 h after birth. The unbalanced gut microbiota
mediated by IUGR contributes to the development of inflammation
and metabolic diseases.
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analysis, strain SK68 has been identified as a Streptomyces
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Tricholoma matsutake is an ectomycorrhizal fungus usually
associated with Pinus densiflora in South Korea. Fruiting
bodies (mushrooms) of T. matsutake are economically important
due to their attractive aroma; yet, T. matsutake is
uncultivatable and its habitat is rapidly being eradicated due
to global climate change. Root-associated bacteria can influence
the growth of ectomycorrhizal fungi that co-exist in the
host rhizosphere and distinctive bacterial communities are
associated with T. matsutake. In this study, we investigated
how these bacterial communities affect T. matsutake growth
by isolating bacteria from the roots of P. densiflora colonized
by ectomycorrhizae of T. matsutake and co-culturing rootassociated
bacteria with T. matsutake isolates. Thirteen species
of bacteria (27 isolates) were found in pine roots, all
belonging to the orders Bacillales or Burkholderiales. Two
species in the genus Paenibacillus promoted the growth of
T. matsutake in glucose poor conditions, likely using soluble
metabolites. In contrast, other bacteria suppressed the growth
of T. matsutake using both soluble and volatile metabolites.
Antifungal activity was more frequent in glucose poor conditions.
In general, pine rhizospheres harbored many bacteria
that had a negative impact on T. matsutake growth and the
few Paenibacillus species that promoted T. matsutake growth.
Paenibacillus species, therefore, may represent a promising
resource toward successful cultivation of T. matsutake.
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Brassica rapa (Chinese cabbage) is an essential component
of traditional Korean food. However, the crop is often subject
to zinc (Zn+) toxicity from contaminated irrigation water,
which, as a result, compromises plant growth and production,
as well as the health of human consumers. The present study
investigated the bioaccumulation of Zn+ by Burkholderia cepacia
CS2-1 and its effect on the heavy metal tolerance of
Chinese cabbage. Strain CS2-1 was identified and characterized
on the basis of 16S rRNA sequences and phylogenetic
analysis. The strain actively produced indole-3-acetic acid
(3.08 ± 0.21 μg/ml) and was also able to produce siderophore,
solubilize minerals, and tolerate various concentrations of Zn+.
The heavy metal tolerance of B. rapa plants was enhanced
by CS2-1 inoculation, as indicated by growth attributes, Zn+
uptake, amino acid synthesis, antioxidant levels, and endogenous
hormone (ABA and SA) synthesis. Without inoculation,
the application of Zn+ negatively affected the growth and
physiology of B. rapa plants. However, CS2-1 inoculation
improved plant growth, lowered Zn+ uptake, altered both
amino acid regulation and levels of flavonoids and phenolics,
and significantly decreased levels of superoxide dismutase,
endogenous abscisic acid, and salicylic acid. These findings
indicate that B. cepacia CS2-1 is suitable for bioremediation
against Zn+-induced oxidative stress.
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Auricularia auricula-judae is a traditional edible fungus that
is cultivated widely in China. In this study, a genetic linkage
map for A. auricula-judae was constructed using a mapping
population consisting of 138 monokaryons derived from a
hybrid strain (A119-5). The monokaryotic parent strains
A14-5 and A18-119 were derived from two cultivated varieties,
A14 (Qihei No. 1) and A18 (Qihei No. 2), respectively.
In total, 130 simple sequence repeat markers were mapped.
These markers were developed using the whole genome sequence
of A. auricula-judae and amplified in A14-5, A18-
119, and the mapping population. The map consisted of 11
linkage groups (LGs) spanning 854 cM, with an average interval
length of 6.57 cM. A testcross population was derived
from crossing between the monokaryon A184-57 (from the
wild strain A184 as a tester strain) and the mapping population.
Important agronomic trait-related QTLs, including
mycelium growth rate on potato dextrose agar for the mapping
population, mycelium growth rate on potato dextrose
agar and sawdust for the testcross population, growth period
(days from inoculation to fruiting body harvesting), and yield
for the testcross population, were identified using the composite
interval mapping method. Six mycelium growth raterelated
QTLs were identified on LG1 and LG4, two growth
period-related QTLs were identified on LG2, and three yieldrelated
QTLs were identified on LG2 and LG6. The results
showed no linkage relationship between mycelium growth
rate and growth period. The present study provides a foundation
for locating genes for important agronomic characteristics
in A. auricula-judae in the future.
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Cell phones and electronic appliances and devices are inseparable
from most people in modern society and the electromagnetic
field (EMF) from the devices is a potential health
threat. Although the direct health effect of a cell phone and its
radiofrequency (RF) EMF to human is still elusive, the effect
to unicellular organisms is rather apparent. Human microbiota,
including skin microbiota, has been linked to a very
significant role in the health of a host human body. It is important
to understand the response of human skin microbiota
to the RF-EMF from cell phones and personal electronic
devices, since this may be one of the potential mechanisms
of a human health threat brought about by the disruption
of the intimate and balanced host-microbiota relationship.
Here, we investigated the response of both laboratory culture
strains and isolates of skin bacteria under static magnetic
field (SMF) and RF-EMF. The growth patterns of laboratory
cultures of Escherichia coli, Pseudomonas aeruginosa,
and Staphylococcus epidermidis under SMF were variable
per different species. The bacterial isolates of skin microbiota
from 4 subjects with different cell phone usage history also
showed inconsistent growth responses. These findings led us
to hypothesize that cell phone level RF-EMF disrupts human
skin microbiota. Thus, the results from the current study lay
ground for more comprehensive research on the effect of
RF-EMF on human health through the human-microbiota
relationship.
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