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- Phylogenetic Assessment of Understudied Families in Hymenochaetales (Basidiomycota, Fungi)-Reporting Uncovered Species and Reflecting the Recent Taxonomic Updates in the Republic of Korea.
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Yoonhee Cho, Dohye Kim, Young Woon Lim
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J. Microbiol. 2024;62(6):429-447. Published online May 16, 2024
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DOI: https://doi.org/10.1007/s12275-024-00120-5
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Abstract
- Hymenochaetales Oberw. is an order classified in Basidiomycota of Fungi, and species in this order display notable diversity. They exhibit various fruiting body shapes, including clavarioid, effused-reflexed, and resupinate basidiomes.
Few mycorrhizal species have been reported in Hymenochaetales, but wood-decaying species dominate the order. Hymenochaetaceae Imazeki & Toki and Schizoporaceae Jülich are the most species-rich families within Hymenochaetales, and most species in the Republic of Korea belong to these two families. As such, current taxonomic classification and nomenclature are not reflected upon species in the remaining Hymenochaetales families. For this study, a multifaceted morphological and multigenetic marker-based phylogenetic investigation was conducted to, firstly, comprehensively identify understudied Hymenochaetales specimens in Korea and, secondly, reflect the updates on the species classification. Five genetic markers were assessed for the phylogenetic analysis: nuclear small subunit ribosomal DNA (nSSU), internal transcribed spacer (ITS), nuclear large subunit ribosomal DNA (nLSU), RNA polymerase II subunit 2 gene (RPB2), and translation elongation factor 1 gene (TEF1). The results from phylogenetic analysis supported 18 species classified under eight families (excluding Hymenochaetaceae and Schizoporaceae) in Korea. Species formerly placed in Rickenellaceae and Trichaptum sensu lato have been systematically revised based on recent taxonomic reconstructions. In addition, our findings revealed one new species, Rickenella umbelliformis, and identified five formerly nationally unreported species classified under five understudied families. Our findings contribute to a better understanding of Hymenochaetales diversity and highlight the need for continued research.
- Transcriptome‑based Mining of the Constitutive Promoters for Tuning Gene Expression in Aspergillus oryzae
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Kobkul Laoteng , Jutamas Anantayanon , Chanikul Chutrakul , Sarocha Panchanawaporn , Sukanya Jeennor
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J. Microbiol. 2023;61(2):199-210. Published online February 6, 2023
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DOI: https://doi.org/10.1007/s12275-023-00020-0
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Abstract
- Transcriptional regulation has been adopted for developing metabolic engineering tools. The regulatory promoter is a crucial
genetic element for strain optimization. In this study, a gene set of Aspergillus oryzae with highly constitutive expression
across different growth stages was identified through transcriptome data analysis. The candidate promoters were functionally
characterized in A. oryzae by transcriptional control of β-glucuronidase (GUS) as a reporter. The results showed that
the glyceraldehyde triphosphate dehydrogenase promoter (PgpdA1) of A. oryzae with a unique structure displayed the most
robust strength in constitutively controlling the expression compared to the PgpdA2 and other putative promoters tested. In
addition, the ubiquitin promoter (Pubi) of A. oryzae exhibited a moderate expression strength. The deletion analysis revealed
that the 5' untranslated regions of gpdA1 and ubi with the length of 1028 and 811 nucleotides, counted from the putative
translation start site (ATG), respectively, could efficiently drive the GUS expression. Interestingly, both promoters could
function on various carbon sources for cell growth. Glucose was the best fermentable carbon source for allocating high constitutive
expressions during cell growth, and the high concentrations (6–8% glucose, w/v) did not repress their functions. It
was also demonstrated that the secondary metabolite gene coding for indigoidine could express under the control of PgpdA1
or Pubi promoter. These strong and moderate promoters of A. oryzae provided beneficial options in tuning the transcriptional
expression for leveraging the metabolic control towards the targeted products.
- Salmonella Typhimurium ST313 isolated in Brazil revealed to be more invasive and inflammatory in murine colon compared to ST19 strains
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Amanda Aparecida Seribelli , Tamara R. Machado Ribeiro , Patrick da Silva† , Isabela Mancini Martins , Felipe Pinheiro Vilela , Marta I. Cazentini Medeiros , Kamila Chagas Peronni , Wilson Araújo da Silva Junior , Cristiano Gallina Moreira , Juliana Pfrimer Falcão
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J. Microbiol. 2021;59(9):861-870. Published online August 12, 2021
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DOI: https://doi.org/10.1007/s12275-021-1082-z
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Abstract
- Salmonella Typhimurium (ST313) has caused an epidemic of
invasive disease in sub-Saharan Africa and has been recently
identified in Brazil. As the virulence of this ST is poorly understood,
the present study aimed to (i) perform the RNAseq
in vitro of S. Typhimurium STm30 (ST313) grown in
Luria-Bertani medium at 37°C; (ii) compare it with the RNAseq
of the S. Typhimurium SL1344 (ST19) and S. Typhimurium
STm11 (ST19) strains under the same growing conditions;
and (iii) examine the colonization capacity and expression
of virulence genes and cytokines in murine colon. The
STm30 (ST313) strain exhibited stronger virulence and was
associated with a more inflammatory profile than the strains
SL1344 (ST19) and STm11 (ST19), as demonstrated by transcriptome
and in vivo assay. The expression levels of the hilA,
sopD2, pipB, and ssaS virulence genes, other Salmonella pathogenicity
islands SPI-1 and SPI-2 genes or effectors, and
genes of the cytokines IL-1β, IFN-γ, TNF-α, IL-6, IL-17, IL-22,
and IL-12 were increased during ST313 infection in C57BL/6J
mice. In conclusion, S. Typhimurium STm30 (ST313) isolated
from human feces in Brazil express higher levels of pathogenesis-
related genes at 37°C and has stronger colonization
and invasion capacity in murine colon due to its high expression
levels of virulence genes, when compared with the S.
Typhimurium SL1344 (ST19) and STm11 (ST19) strains.
STm30 (ST313) also induces stronger expression of pro-inflammatory
cytokines in this organ, suggesting that it causes
more extensive tissue damage.
- Effect of biostimulation and bioaugmentation on hydrocarbon degradation and detoxification of diesel-contaminated soil: a microcosm study
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Patricia Giovanella , Lídia de Azevedo Duarte , Daniela Mayumi Kita , Valéria Maia de Oliveira , Lara Durães Sette
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J. Microbiol. 2021;59(7):634-643. Published online May 15, 2021
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DOI: https://doi.org/10.1007/s12275-021-0395-2
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Abstract
- Soil contamination with diesel oil is quite common during
processes of transport and storage. Bioremediation is considered
a safe, economical, and environmentally friendly approach
for contaminated soil treatment. In this context, studies
using hydrocarbon bioremediation have focused on total
petroleum hydrocarbon (TPH) analysis to assess process effectiveness,
while ecotoxicity has been neglected. Thus, this
study aimed to select a microbial consortium capable of detoxifying
diesel oil and apply this consortium to the bioremediation
of soil contaminated with this environmental pollutant
through different bioremediation approaches. Gas chromatography
(GC-FID) was used to analyze diesel oil degradation,
while ecotoxicological bioassays with the bioindicators
Artemia sp., Aliivibrio fischeri (Microtox), and Cucumis
sativus were used to assess detoxification. After 90 days of
bioremediation, we found that the biostimulation and biostimulation/
bioaugmentation approaches showed higher rates
of diesel oil degradation in relation to natural attenuation
(41.9 and 26.7%, respectively). Phytotoxicity increased in the
biostimulation and biostimulation/bioaugmentation treatments
during the degradation process, whereas in the Microtox
test, the toxicity was the same in these treatments as that
in the natural attenuation treatment. In both the phytotoxicity
and Microtox tests, bioaugmentation treatment showed lower
toxicity. However, compared with natural attenuation, this
approach did not show satisfactory hydrocarbon degradation.
Based on the microcosm experiments results, we conclude
that a broader analysis of the success of bioremediation requires
the performance of toxicity bioassays.
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