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Rasiella rasia gen. nov. sp. nov. within the family Flavobacteriaceae isolated from seawater recirculating aquaculture system
Seong-Jin Kim , Young-Sam Kim , Sang-Eon Kim , Hyun-Kyoung Jung , Jeeeun Park , Min-Ju Yu , Kyoung-Ho Kim
J. Microbiol. 2022;60(11):1070-1076.   Published online October 17, 2022
DOI: https://doi.org/10.1007/s12275-022-2099-7
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  • 2 Crossref
AbstractAbstract
A novel bacterium designated RR4-40T was isolated from a biofilter of seawater recirculating aquaculture system in Busan, South Korea. Cells are strictly aerobic, Gram-negative, irregular short rod, non-motile, and oxidase- and catalase-negative. Growth was observed at 15–30°C, 0.5–6% NaCl (w/v), and pH 5.0–9.5. The strain grew optimally at 28°C, 3% salinity (w/v), and pH 8.5. The phylogenetic analysis based on 16S rRNA gene sequences showed that strain RR4-40T was most closely related to Marinirhabdus gelatinilytica NH83T (94.16% of 16S rRNA gene similarity) and formed a cluster with genera within the family Flavobacteriaceae. The values of the average nucleotide identity (ANI), digital DNA-DNA hybridization (dDDH), and average amino acid identity (AAI) between genomes of strain RR4-40T and M. gelatinilytica NH83T were 72.91, 18.2, and 76.84%, respectively, and the values against the strains in the other genera were lower than those. The major fatty acids were iso-C15:0 (31.34%), iso-C17:0 3-OH (13.65%), iso-C16:0 3-OH (10.61%), and iso-C15:1 G (10.38%). The polar lipids comprised phosphatidylglycerol, diphosphatidylglycerol, aminophospholipid, aminolipid, glycolipid, and sphingolipid. The major respiratory quinone was menaquinone-6 (MK-6) and the DNA G + C content of strain RR4-40T was 37.4 mol%. According to the polyphasic analysis, strain RR4-40T is considered to represent a novel genus within the family Flavobacteriaceae, for which the name Rasiella rasia gen. nov, sp. nov. is proposed. The type strain is RR4-40T (= KCTC 52650T = MCCC 1K04210T).

Citations

Citations to this article as recorded by  
  • Rhodobacteraceae are Prevalent and Ecologically Crucial Bacterial Members in Marine Biofloc Aquaculture
    Meora Rajeev, Jang-Cheon Cho
    Journal of Microbiology.2024; 62(11): 985.     CrossRef
  • Validation List no. 215. Valid publication of new names and new combinations effectively published outside the IJSEM
    Aharon Oren, Markus Göker
    International Journal of Systematic and Evolutionary Microbiology .2024;[Epub]     CrossRef
Review
MINIREVIEW] The Potential Hazards of Aspergillus sp. in Foods and Feeds, and the Role of Biological Treatment: A Review
Sheikh Imranudin Sheikh-Ali , Akil Ahmad , Siti-Hamidah Mohd-Setapar , Zainul Akmal Zakaria , Norfahana Abdul-Talib , Aidee Kamal Khamis , Md Enamul Hoque
J. Microbiol. 2014;52(10):807-818.   Published online October 1, 2014
DOI: https://doi.org/10.1007/s12275-014-4294-7
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  • 16 Crossref
AbstractAbstract
The contamination of food and feed by Aspergillus has become a global issue with a significant worldwide economic impact. The growth of Aspergillus is unfavourable to the development of food and feed industries, where the problems happen mostly due to the presence of mycotoxins, which is a toxic metabolite secreted by most Aspergillus groups. Moreover, fungi can produce spores that cause diseases, such as allergies and asthma, especially to human beings. High temperature, high moisture, retarded crops, and poor food storage conditions encourage the growth of mold, as well as the development of mycotoxins. A variety of chemical, biological, and physical strategies have been developed to control the production of mycotoxins. A biological approach, using a mixed culture comprised of Saccharomyces cerevisiae and Lactobacillus rhamnosus resulted in the inhibition of the growth of fungi when inoculated into fermented food. The
results
reveal that the mixed culture has a higher potential (37.08%) to inhibit the growth of Aspergillus flavus (producer of Aflatoxin) compared to either single culture, L. rhamnosus NRRL B-442 and S. cerevisiae, which inhibit the growth by 63.07% and 64.24%, respectively.

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    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.2025; 324: 124965.     CrossRef
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    Rana R. El Sadda, Mai S. Eissa, Rokaya K. Elafndi, Elhossein A. Moawed, Mohamed M. El-Zahed, Hoda R. Saad
    BMC Chemistry.2024;[Epub]     CrossRef
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    Lawrence A. Isiofia, Emmanuel Nna, Francis O. Uzuegbunam, Eziyi O. Ibem
    International Journal of Building Pathology and Adaptation.2024; 42(6): 1147.     CrossRef
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    Zhengmei Ji, Wenjun Ma, Pengfei Liang, Xiaoyu Wang, Shuai Zhang, Yanhui Han, Yurong Guo
    International Journal of Biological Macromolecules.2024; 281: 136638.     CrossRef
  • In-situ synthesis of sepiolite-supported ceria nanocrystal composites for efficient removal of aflatoxin B1: Enhanced degradation of mycotoxins in the environment by sepiolite nanofibers
    Na Zhang, Ningxi Li, Xiaoyu Han, Hong Zhang, Junping Meng, Pengfei Zhou, Jinsheng Liang
    Journal of Alloys and Compounds.2023; 960: 170800.     CrossRef
  • High-throughput and point-of-care detection of wheat fungal diseases: Potentialities of molecular and phenomics techniques toward in-field applicability
    Sara Francesconi
    Frontiers in Agronomy.2022;[Epub]     CrossRef
  • Construction of a dual-functional CuO/BiOCl heterojunction for high-efficiently photoelectrochemical biosensing and photoelectrocatalytic degradation of aflatoxin B1
    Lebao Mao, Hao Liu, Linli Yao, Wei Wen, Miao-Miao Chen, Xiuhua Zhang, Shengfu Wang
    Chemical Engineering Journal.2022; 429: 132297.     CrossRef
  • Healthy Zerumbone: From Natural Sources to Strategies to Improve Its Bioavailability and Oral Administration
    María Dolores Ibáñez, Noelia M. Sánchez-Ballester, María Amparo Blázquez
    Plants.2022; 12(1): 5.     CrossRef
  • Coumarin derivative, 5′-hydroxy-auraptene, extracted from Lotus lalambensis, displays antifungal and anti-aflatoxigenic activities against Aspergillus flavus
    Enas M. Ali, Mayyadah A. Alkuwayti, Munirah F. Aldayel, Basem M. Abdallah
    Journal of King Saud University - Science.2021; 33(1): 101216.     CrossRef
  • Aspergillus Metabolome Database for Mass Spectrometry Metabolomics
    Alberto Gil-de-la-Fuente, Maricruz Mamani-Huanca, María C. Stroe, Sergio Saugar, Alejandra Garcia-Alvarez, Axel A. Brakhage, Coral Barbas, Abraham Otero
    Journal of Fungi.2021; 7(5): 387.     CrossRef
  • Behaviour of Aspergillus parasiticus in aflatoxin production as influenced by storage parameters using response surface methodology approach
    Stephen Abiola Akinola, Collins Njie Ateba, Mulunda Mwanza
    International Journal of Food Microbiology.2021; 357: 109369.     CrossRef
  • Updates on the Functions and Molecular Mechanisms of the Genes Involved in Aspergillus flavus Development and Biosynthesis of Aflatoxins
    Elisabeth Tumukunde, Rui Xie, Shihua Wang
    Journal of Fungi.2021; 7(8): 666.     CrossRef
  • Essential oils from the genus Thymus as antimicrobial food preservatives: Progress in their use as nanoemulsions-a new paradigm
    Abhay K. Pandey, Mónica L. Chávez-González, Ana Sanches Silva, Pooja Singh
    Trends in Food Science & Technology.2021; 111: 426.     CrossRef
  • Photocatalytic degradation of aflatoxin B1 by activated carbon supported TiO2 catalyst
    Shumin Sun, Ran Zhao, Yanli Xie, Yong Liu
    Food Control.2019; 100: 183.     CrossRef
  • Selected essential oil vapours inhibit growth of Aspergillus spp. in oats with improved consumer acceptability
    Matěj Božik, Miroslava Císarová, Dana Tančinová, Lenka Kouřimská, Lukáš Hleba, Pavel Klouček
    Industrial Crops and Products.2017; 98: 146.     CrossRef
  • Reduction of aflatoxin B1 in peanut meal by extrusion cooking
    Haiyan Zheng, Shuai Wei, Ying Xu, Mingtao Fan
    LWT - Food Science and Technology.2015; 64(2): 515.     CrossRef
Research Support, Non-U.S. Gov't
Heat- and Cold-Shock Responses in Fusarium graminearum 3 Acetyl- and 15 Acetyl-Deoxynivalenol Chemotypes
Vladimir Vujanovic , Yit Kheng Goh , Prasad Daida
J. Microbiol. 2012;50(1):97-102.   Published online February 27, 2012
DOI: https://doi.org/10.1007/s12275-012-1381-5
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  • 23 Scopus
AbstractAbstract
Fusarium graminearum Schwabe is the primary cause of Fusarium head blight (FHB) in North America. Chemically distinct F. graminearum sub-populations can be identified based on the type or composition of deoxynivalenol (DON) mycotoxin derivatives, including 3-acetyl (3-ADON) and 15-acetyl (15-ADON). The evaluation of randomly selected 3-ADON and 15-ADON isolates, collected from spring wheat throughout Canada, was performed using thin layer chromatography (TLC), high-performance liquid chromatography (HPLC), ice-nucleation activity (INA), and heat and cold tolerance tests conducted within a temperature range of -70°C to 65°C. The results indicated that the 3-ADON sub-population, which is responsible for the highest disease severity and has rapidly displaced the 15-ADON sub-population, produces more DON and zearalenone (ZEA) than the 15-ADON sub-population when exposed to heat and cold. Following exposures (1 and 2 h) to extremely high or low temperatures, 3-ADON isolates exhibited faster mycelial growth than 15-ADON isolates. In addition, the warmest temperature at which INA activity occurred was in 3-ADON (-3.6°C) vs. 15-ADON (-5.1°C). Taken together, these features suggest that the newly emerging 3-ADON sub-population is more resilient than the resident 15-ADON sub-population. Overall, the differences between the two sub-populations could provide new insights into FHB epidemiology and if validated under field conditions, may provide important information for predicting future FHB epidemics.
Review
Heterotrimeric G protein signaling and RGSs in Aspergillus nidulans
Jae-Hyuk Yu
J. Microbiol. 2006;44(2):145-154.
DOI: https://doi.org/2371 [pii]
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AbstractAbstract
Heterotrimeric G proteins (G proteins) are conserved in all eukaryotes and are crucial components sensing and relaying external cues into the cells to elicit appropriate physiological and biochemical responses. Basic units of the heterotrimeric G protein signaling system include a G protein-coupled receptor (GPCR), a G protein composed of α, β, and γ subunits, and variety of effectors. Sequential sensitization and activation of these G protein elements translates external signals into gene expression changes, resulting in appropriate cellular behaviors. Regulators of G protein signaling (RGSs) constitute a crucial element of appropriate control of the intensity and duration of G protein signaling. For the past decade, G protein signaling and its regulation have been intensively studied in a number of model and/or pathogenic fungi and outcomes of the studies provided better understanding on the upstream regulation of vegetative growth, mating, development, virulence/pathogenicity establishment, and biosynthesis of secondary metabolites in fungi. This review focuses on the characteristics of the basic upstream G protein components and RGS proteins, and their roles controlling various aspects of biological processes in the model filamentous ascomycete fungus Aspergillus nidulans. In particular, their functions in controlling hyphal proliferation, asexual spore formation, sexual fruiting, and the mycotoxin sterigmatocystin production are discussed.

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