Mengpei Guo , Xiaolong Ma , Yan Zhou , Yinbing Bian , Gaolei Liu , Yingli Cai , Tianji Huang , Hongxia Dong , Dingjun Cai , Xueji Wan , Zhihong Wang , Yang Xiao , Heng Kang
J. Microbiol. 2023;61(1):83-93. Published online February 1, 2023
The basidiomycetous edible mushroom Stropharia rugosoannulata has excellent nutrition, medicine, bioremediation, and
biocontrol properties. S. rugosoannulata has been widely and easily cultivated using agricultural by-products showing strong
lignocellulose degradation capacity. However, the unavailable high-quality genome information has hindered the research
on gene function and molecular breeding of S. rugosoannulata. This study provided a high-quality genome assembly and
annotation from S. rugosoannulata monokaryotic strain QGU27 based on combined Illumina-Nanopore data. The genome
size was about 47.97 Mb and consisted of 20 scaffolds, with an N50 of 3.73 Mb and a GC content of 47.9%. The repetitive
sequences accounted for 17.41% of the genome, mostly long terminal repeats (LTRs). A total of 15,726 coding gene
sequences were putatively identified with the BUSCO score of 98.7%. There are 142 genes encoding plant cell wall degrading
enzymes (PCWDEs) in the genome, and 52, 39, 30, 11, 8, and 2 genes related to lignin, cellulose, hemicellulose, pectin,
chitin, and cutin degradation, respectively. Comparative genomic analysis revealed that S. rugosoannulata is superior in
utilizing aldehyde-containing lignins and is possible to utilize algae during the cultivation.
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Bacillus velezensis strain GH1-13 contains a (2R,3R)-butanediol
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mutation of three cysteines in BdhA. The C37S mutant
had no enzyme activity and the C34S and C177S mutants
differed from each other and wild type (WT). After zinc affinity
chromatography, 1 mM ZnCl2 treatment resulted in a
3-fold enhancement of the WT activity, but reduced activity
of the C34S mutant by more than 2 folds compared to the untreated
ones. However, ZnCl2 treatment did not affect the activity
of the C177S mutant. Most of the double and triple mutant
proteins (C34S/C37S, C34S/C177S, C37S/C177S, and
C34S/C37S/C177S) were aggregated in zinc resins, likely due
to the decreased protein stability. All of the purified WT and
single mutant proteins increased multiple intermolecular disulfide
bonds in the presence of H2O2 as the buffer pH decreased
from 7.5 to 5.5, whereas an intramolecular disulfide
bond of cysteine 177 and another cysteine in the CGIC motif
region was likely formed at pH higher than pKa of 7.5. When
pH varied, WT and its C34S or C177S mutants reduced acetoin
to R-BD at the optimum pH 5.5 and oxidized R-BD to
acetoin at the optimum pH 10. This study demonstrated that
cysteine residues in BdhA play a regulatory role for the production
of acetoin and R-BD depending on pH as well as
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The genome is highly organized hierarchically by the function
of structural maintenance of chromosomes (SMC) complex
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remain unclear. Condensin and cohesin have distinct
binding sites and mediate long-range and short-range genomic
associations, respectively, to form cell cycle-specific
genome organization. Condensin can be recruited to highly
expressed genes as well as dispersed repeat genetic elements,
such as Pol III-transcribed genes, LTR retrotransposon, and
rDNA repeat. In particular, mitotic transcription factors Ace2
and Ams2 recruit condensin to their target genes, forming
centromeric clustering during mitosis. Condensin is potentially
involved in various chromosomal processes such as the
mobility of chromosomes, chromosome territories, DNA reannealing,
and transcription factories. The current knowledge
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help us understand how condensin mediates genome organization
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using MiSeq, and the amount of short chain fatty acids
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mechanisms underlying the elaborate crosstalk between those
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energy source. Unexpectedly, the culture with yeast extract
as a sole energy source showed enhanced growth by 2-fold
in the presence of O2. Genome-wide transcriptome analysis
revealed the upregulation of several antioxidant-related genes
encoding thioredoxin peroxidase (TON_0862), rubrerythrin
(TON_0864), rubrerythrin-related protein (TON_0873),
NAD(P)H rubredoxin oxidoreductase (TON_0865), or thioredoxin
reductase (TON_1603), which can couple the detoxification
of reactive oxygen species with the regeneration
of NAD(P)+ from NAD(P)H. We present a plausible mechanism
by which O2 serves to maintain the intracellular redox
balance. This study demonstrates an unusual strategy of an
obligate anaerobe underlying O2-mediated growth enhancement
despite not having heme-based or cytochrome-type
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Hypocrellin A (HA) is a perylenequinone (PQ) isolated from
Shiraia bambusicola that shows antiviral and antitumor activities,
but its application is limited by the low production
from wild fruiting body. A gene overexpressing method was
expected to augment the production rate of HA in S. bambusicola.
However, the application of this molecular biology
technology in S. bambusicola was impeded by a low genetic
transformation efficiency and little genomic information. To
enhance the plasmid transformant ratio, the Polyethylene
Glycol-mediated transformation system was established and
optimized. The following green fluorescent protein (GFP)
analysis showed that the gene fusion expression system we
constructed with a GAPDH promoter Pgpd1 and a rapid 2A
peptide was successfully expressed in the S. bambusicola S4201
strain. We successfully obtained the HA high-producing strains
by overexpressing O-methyltransferase/FAD-dependent monooxygenase
gene (mono) and the hydroxylase gene (hyd),
which were the essential genes involved in our putative HA
biosynthetic pathway. The overexpression of these two genes
increased the production of HA by about 200% and 100%,
respectively. In general, this study will provide a basis to identify
the genes involved in the hypocrellin A biosynthesis. This
improved transformation method can also be used in genetic
transformation studies of other fungi.
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The genome sequences of two pyrene-degrading bacterial
strains of Mycobacterium spp. PYR10 and PYR15, isolated
from the estuarine wetland of the Han river, South Korea,
were determined using the PacBio RS II sequencing platform.
The complete genome of strain PYR15 was 6,037,017 bp in
length with a GC content of 66.5%, and contained 5,933 protein-
coding genes. The genome of strain PYR10 was 5,999,427
bp in length with a GC content of 67.7%, and contained
5,767 protein-coding genes. Based on the average nucleotide
identity values, these strains were designated as M. gilvum
PYR10 and M. pallens PYR15. A genomic comparison
of these pyrene-degrading Mycobacterium strains with pyrene-
non-degrading strains revealed that the genomes of
pyrene-degrading strains possessed similar repertoires of ringhydroxylating
dioxygenases (RHDs), including the pyrenehydroxylating
dioxygenases encoded by nidA and nidA3,
which could be readily distinguished from those of pyrenenon-
degraders. Furthermore, genomic islands, containing
catabolic gene clusters, were shared only among the pyrenedegrading
Mycobacterium strains and these gene clusters
contained RHD genes, including nidAB and nidA3B3. Our
genome data should facilitate further studies on the evolution
of the polycyclic aromatic hydrocarbon-degradation
pathways in the genus Mycobacterium.
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Reactive oxygen species (ROS) produced by NADPH oxidases
can serve as signaling molecules to regulate a variety of
physiological processes in multi-cellular organisms. In the
nematophagous fungus Arthrobotrys oligospora, we found
that ROS were produced during conidial germination, hyphal
extension, and trap formation in the presence of nematodes.
Generation of an AoNoxA knockout strain demonstrated
the crucial role of NADPH oxidase in the production
of ROS in A. oligospora, with trap formation impaired in
the AoNoxA mutant, even in the presence of the nematode
host. In addition, the expression of virulence factor serine
protease P186 was up-regulated in the wild-type strain, but
not in the mutant strain, in the presence of Caenorhabditis
elegans. These results indicate that ROS derived from AoNoxA
are essential for full virulence of A. oligospora in nematodes.
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that was isolated from a freshwater lake using the floating
filter culture technique. Based on a phylogenetic analysis of
16S rRNA gene sequences, the isolate was found to be closely
related to the genus Methylomonas in the family Methylococcaceae
of the class Gammaproteobacteria with 94.2–97.4%
16S rRNA gene similarity to Methylomonas type strains. Comparison
of chemotaxonomic and physiological properties
further suggested that strain EMGL16-1 was taxonomically
distinct from other species in the genus Methylomonas. The
isolate was versatile in utilizing nitrogen sources such as molecular
nitrogen, nitrate, nitrite, urea, and ammonium. The
genes coding for subunit of the particulate form methane
monooxygenase (pmoA), soluble methane monooxygenase
(mmoX), and methanol dehydrogenase (mxaF) were detected
in strain EMGL16-1. Phylogenetic analysis of mmoX indicated
that mmoX of strain EMGL16-1 is distinct from those
of other strains in the genus Methylomonas. This isolate probably
represents a novel species in the genus. Our study provides
new insights into the diversity of species in the genus
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physiological features depending on their biological niches.
Interestingly, organisms exhibiting high radiation resistance
have been discovered in the three domains of life (Bacteria,
Archaea, and Eukarya), even though a naturally radiationintensive
environment has not been found. To counteract
the deleterious effects caused by radiation exposure, radiation-
resistant organisms employ a series of defensive systems,
such as changes in intracellular cation concentration, excellent
DNA repair systems, and efficient enzymatic and non-enzymatic
antioxidant systems. Here, we overview past and recent
findings about radiation-resistance mechanisms in the
three domains of life for potential usage of such radiationresistant
microbes in the biotechnology industry.
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Kaposi’s sarcoma-associated herpesvirus (KSHV) is the major
etiologic agent of Kaposi’s sarcoma, primary effusion lymphoma,
and multicentric Castleman’s disease. Recent studies
have indicated that KSHV can be detected at high frequency
in patient-derived bladder cancer tissue and might be associated
with the pathogenesis of bladder cancer. Bladder cancer
is the second most common cancer of the genitourinary
tract, and it has a high rate of recurrence. Because drug resistance
is closely related to chemotherapy failure and cancer
recurrence, we investigated whether KSHV infection is associated
with drug resistance of bladder cancer cells. Some
KSHV-infected bladder cancer cell lines showed resistance to
an anti-cancer drug, cisplatin, possibly as a result of downregulation
of reactive oxygen species. Additionally, drug resistance
acquired from KSHV infection could partly be overcome
by HDAC1 inhibitors. Taken together, the data suggest
the possible role of KSHV in chemo-resistant bladder
cancer, and indicate the therapeutic potential of HDAC1 inhibitors
in drug-resistant bladder cancers associated with
KSHV infection.
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elaborate mechanisms. MMOs express particulate methane
monooxygenase (pMMO) in most strains and soluble methane
monooxygenase (sMMO) under copper-limited conditions.
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sMMO belonging to the bacterial multicomponent monooxygenase
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sites where different types of hydrocarbons are oxidized through
orchestrated hydroxylase, regulatory and reductase components
for precise control of hydrocarbons, oxygen, protons,
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structural and enzymatic achievements for sMMO, have
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