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1.
J Sci Food Agric ; 100(9): 3598-3607, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32100298

ABSTRACT

BACKGROUND: Pingwu Fuzhuan brick tea is a type of post-fermented tea manufactured from leaves of the tea plant, Camellia sinensis var. sinensis, the quality of which is influenced by numerous factors, especially microorganisms. Currently, there is little research on the effect of microorganisms on the fermentation and quality characteristics of Pingwu Fuzhuan brick tea. Investigation of the main fungus in this tea and its effect on the fermentation process and tea quality can provide insights into the manufacturing of 'western road' border-selling tea and could lay the foundation for the popularization of Pingwu Fuzhuan brick tea. RESULTS: The main 'golden flower fungus' in Pingwu Fuzhuan brick tea was isolated and identified as Eurotium cristatum (GenBank accession number: MF800948.1; strain PW-1). Compared with natural fermentation, PW-1 inoculated fermentation accelerated biotransformation of phenolic compounds, which provided tea samples with better taste and tea infusion color. The proportions of velvety and sweet-tasting amino acids increased after 16-day fermentation with PW-1. Alcohols were the most abundant volatiles, with 40.13% and 39.43% content in NF16d and IF16d tea samples, respectively. Orthogonal partial least-squares discriminant analysis (OPLS-DA) and hierarchical clustering analysis (HCA) further revealed that naturally fermented and PW-1 fermented teas were significantly different. CONCLUSION: Strain PW-1 plays an important role in the fermentation process of Fuzhuan brick tea. Considering fermentation efficiency and tea quality, fermentation inoculated with E. cristatum PW-1 can be applied in the manufacturing of 'western road' border-selling tea. © 2020 Society of Chemical Industry.


Subject(s)
Camellia sinensis/chemistry , Eurotium/metabolism , Plant Leaves/microbiology , Camellia sinensis/microbiology , Eurotium/classification , Eurotium/genetics , Eurotium/isolation & purification , Fermentation , Plant Leaves/chemistry , Tea/chemistry
2.
J Appl Microbiol ; 128(6): 1658-1668, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31975478

ABSTRACT

OBJECTIVE: Eurotium sp. are the sexual states of the genus Aspergillus, and their ascospore is a spherical closed capsule with a golden colour. The growth of Eurotium sp. during tea production is a key step in achieving the unique quality of dark tea. This study aimed to evaluate the relationship between Eurotium sp. amount and Liupao tea quality. METHODS AND RESULTS: The amounts of Eurotium sp. in 26 differently aged Liupao tea samples from several factories were studied. Indicators related to the quality of Liupao tea were investigated. The amounts of Eurotium sp. were divided into 0, 105 and 106 levels, and quantitative real-time polymerase chain reaction (qPCR) was performed. Using ultrahigh-performance liquid chromatography and high-performance liquid chromatography, the amounts of emodin and physcion were determined to be closely related to the amount of Eurotium sp. Emodin was not found or occurred in minimal amounts in all raw Liupao tea samples. By contrast, physcion was found in Liupao tea at the 106 level of Eurotium sp. Liupao tea samples with varying levels of Eurotium sp. also exhibited evident differences in aroma and chromaticity. Result of the Pearson correlation test showed that the amount of Eurotium sp. plays a key role in creating the unique quality of Liupao tea. CONCLUSION: The amount of Eurotium sp. in dark tea detected via qPCR can be used as a quantitative quality indicator for evaluating dark tea. SIGNIFICANCE AND IMPACT OF THE STUDY: The present study provides an efficient method for identifying the different qualities of dark tea and addressing quality control issues in fermenting dark tea.


Subject(s)
Camellia sinensis/microbiology , Eurotium/isolation & purification , Food Quality , Tea/microbiology , Camellia sinensis/chemistry , Emodin/analogs & derivatives , Emodin/analysis , Eurotium/genetics , Fermentation , Real-Time Polymerase Chain Reaction , Tea/chemistry
3.
Mar Drugs ; 17(4)2019 Apr 11.
Article in English | MEDLINE | ID: mdl-30978942

ABSTRACT

The emergence of antibiotic resistance and viruses with high epidemic potential made unexplored marine environments an appealing target source for new metabolites. Marine fungi represent one of the most suitable sources for the discovery of new compounds. Thus, the aim of this work was (i) to isolate and identify fungi associated with the Atlantic sponge Grantia compressa; (ii) to study the fungal metabolites by applying the OSMAC approach (one strain; many compounds); (iii) to test fungal compounds for their antimicrobial activities. Twenty-one fungal strains (17 taxa) were isolated from G. compressa. The OSMAC approach revealed an astonishing metabolic diversity in the marine fungus Eurotium chevalieri MUT 2316, from which 10 compounds were extracted, isolated, and characterized. All metabolites were tested against viruses and bacteria (reference and multidrug-resistant strains). Dihydroauroglaucin completely inhibited the replication of influenza A virus; as for herpes simplex virus 1, total inhibition of replication was observed for both physcion and neoechinulin D. Six out of 10 compounds were active against Gram-positive bacteria with isodihydroauroglaucin being the most promising compound (minimal inhibitory concentration (MIC) 4-64 µg/mL) with bactericidal activity. Overall, G. compressa proved to be an outstanding source of fungal diversity. Marine fungi were capable of producing different metabolites; in particular, the compounds isolated from E. chevalieri showed promising bioactivity against well-known and emerging pathogens.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antiviral Agents/pharmacology , Biotechnology/methods , Eurotium/metabolism , Porifera/microbiology , Animals , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/isolation & purification , Antiviral Agents/chemistry , Antiviral Agents/isolation & purification , Aquatic Organisms/genetics , Aquatic Organisms/isolation & purification , Aquatic Organisms/metabolism , Biodiversity , Chlorocebus aethiops , Dogs , Eurotium/genetics , Eurotium/isolation & purification , Gram-Positive Bacteria/drug effects , Herpesvirus 1, Human/drug effects , Influenza A virus/drug effects , Madin Darby Canine Kidney Cells , Microbial Sensitivity Tests , Vero Cells , Virus Replication/drug effects
4.
Fungal Genet Biol ; 104: 1-5, 2017 07.
Article in English | MEDLINE | ID: mdl-28427933

ABSTRACT

Purification of high quality genomic DNA (gDNA) from filamentous fungi suitable for whole genome sequencing has previously involved many steps. Here, we report a simple and easy-to-follow mini-preparation protocol for high molecular weight (∼20kb) gDNA from filamentous fungi including Aspergillus and Eurotium. This comprehensive protocol includes graphic step-by-step instructions for inoculation, homogenization, and purification of gDNA. The most critical step is a thorough 3-5min homogenization of the freeze-dried mycelium using a motorized hand-held homogenizer with a mini spatula inserted. Approximately 20mg of the fine mycelial powder is then subjected to a modified procedure for the DNeasy Plant Mini Kit (Qiagen). This Qiagen spin column protocol avoids precipitation, dryness, and resuspension of gDNA, which can cause shearing and loss of gDNA. Final gDNA yields from ∼20mg of fine mycelial powder are 8 to 20µg with a consistent 260/280nm absorbance ratio of ∼1.9. All 30 gDNA samples we purified using our method were of high molecular weight (∼20kb). Whole genome sequencing of these DNA samples resulted in 160-260 X coverage with 2×150 reads using NextSeq 500. These gDNAs are also of a suitable quality for Southern blotting and PCR-based amplification of various genes in filamentous fungi.


Subject(s)
DNA, Fungal/isolation & purification , Fungi/genetics , Aspergillus/genetics , Blotting, Southern , DNA, Fungal/chemistry , Eurotium/genetics , Genetic Techniques , Molecular Weight
5.
Biocontrol Sci ; 19(3): 139-45, 2014.
Article in English | MEDLINE | ID: mdl-25252646

ABSTRACT

We offer the first description of the development of a multiple detection technique for fungi by DNA microarray with the simultaneous use of internal transcribed spacer region (ITS) of ribosomal RNA gene and ß-tubulin gene probes. The assay uses 12 oligonucleotide probes and multiplex amplification to detect fungal species belonging to various sections of Aspergillus, the Eurotium genus, and the Penicillium genus. The specificity of each probe was tested using 231 reference fungal strains, including 79 target and 152 non-target strains in 102 species of 24 genera. We determined the optimum concentration of the primer pairs for multiplex PCR to be 0.5 µM for the ß-tubulin gene and 0.125 µM for the ITS region. In the field trial using 76 specimens containing 323 fungi (up to five fungal strains were included in one specimen), the concordance rate between the DNA microarray and the DNA sequencing results was 97.4% at the species or genus levels.


Subject(s)
Aspergillus/isolation & purification , DNA, Ribosomal Spacer/genetics , Eurotium/isolation & purification , Microbiological Techniques/methods , Oligonucleotide Array Sequence Analysis/methods , Penicillium/isolation & purification , Tubulin/genetics , Aspergillus/genetics , DNA, Fungal/genetics , Eurotium/genetics , Molecular Diagnostic Techniques/methods , Oligonucleotide Probes/genetics , Penicillium/genetics , Sensitivity and Specificity
6.
Nat Commun ; 5: 3745, 2014 May 09.
Article in English | MEDLINE | ID: mdl-24811710

ABSTRACT

The Dead Sea is one of the most hypersaline habitats on Earth. The fungus Eurotium rubrum (Eurotiomycetes) is among the few species able to survive there. Here we highlight its adaptive strategies, based on genome analysis and transcriptome profiling. The 26.2 Mb genome of E. rubrum shows, for example, gains in gene families related to stress response and losses with regard to transport processes. Transcriptome analyses under different salt growth conditions revealed, among other things differentially expressed genes encoding ion and metabolite transporters. Our findings suggest that long-term adaptation to salinity requires cellular and metabolic responses that differ from short-term osmotic stress signalling. The transcriptional response indicates that halophilic E. rubrum actively counteracts the salinity stress. Many of its genes encode for proteins with a significantly higher proportion of acidic amino acid residues. This trait is characteristic of the halophilic prokaryotes as well, supporting the theory of convergent evolution under extreme hypersaline stress.


Subject(s)
Acclimatization/genetics , Adaptation, Biological/genetics , Adaptation, Physiological/genetics , Eurotium/genetics , Osmotic Pressure/physiology , Amino Acid Sequence , Fungi/genetics , Gene Expression Profiling , Gene Expression Regulation, Fungal , Israel , Oceans and Seas , Phylogeny , RNA, Untranslated/genetics , Salinity , Transcriptome/genetics
7.
J Microbiol Biotechnol ; 23(9): 1206-11, 2013 Sep 28.
Article in English | MEDLINE | ID: mdl-23770564

ABSTRACT

The selective inhibition of PTP1B has been widely recognized as a potential drug target for the treatment of type 2 diabetes and obesity. In the course of screening for PTP1B inhibitory fungal metabolites, the organic extracts of several fungal species isolated from marine environments were found to exhibit significant inhibitory effects, and the bioassay-guided investigation of these extracts resulted in the isolation of fructigenine A (1), cyclopenol (2), echinulin (3), flavoglaucin (4), and viridicatol (5). The structures of these compounds were determined mainly by analysis of NMR and MS data. These compounds inhibited PTP1B activity with 50% inhibitory concentration values of 10.7, 30.0, 29.4, 13.4, and 64.0 micrometer, respectively. Furthermore, the kinetic analysis of PTP1B inhibition by compounds 1 and 5 suggested that compound 1 inhibited PTP1B activity in a noncompetitive manner, whereas compound 5 inhibited PTP1B activity in a competitive manner.


Subject(s)
Enzyme Inhibitors/metabolism , Eurotium/metabolism , Penicillium/metabolism , Protein Tyrosine Phosphatase, Non-Receptor Type 1/antagonists & inhibitors , Seawater/microbiology , Alkaloids/chemistry , Alkaloids/metabolism , Benzodiazepinones/chemistry , Benzodiazepinones/metabolism , Enzyme Inhibitors/chemistry , Eurotium/chemistry , Eurotium/genetics , Eurotium/isolation & purification , Gentisates/chemistry , Gentisates/metabolism , Heterocyclic Compounds, 4 or More Rings/chemistry , Heterocyclic Compounds, 4 or More Rings/metabolism , Humans , Kinetics , Molecular Structure , Penicillium/chemistry , Penicillium/genetics , Penicillium/isolation & purification , Protein Tyrosine Phosphatase, Non-Receptor Type 1/chemistry , Secondary Metabolism
8.
Mycologia ; 105(4): 912-37, 2013.
Article in English | MEDLINE | ID: mdl-23396159

ABSTRACT

Aspergillus section Aspergillus contains economically important, xerophilic fungi that are widely distributed in nature and the human environment and are known for their ability to grow on substrates with low water activity. The taxa were revised based on sequence data from four loci, PCR fingerprinting, micro- and macromorphology, and physiology. The number of taxa was reduced to 17 species, all of which can be distinguished with sequence data from either the caM or RPB2 locus. The original description of A. proliferans was supplemented by a description of its teleomorph. This species seems to be relatively common and often has been confused with A. glaucus. In addition, green sporulating isolates of A. niveoglaucus isolated from food and several other substrates are indistinguishable in phenotype from A. glaucus. A dichotomous key based on ascospore size and ornamentation and the ability to grow at specific combinations of temperature and water activity is provided for identification of species. In response to recent changes in the botanical code, we transferred the Eurotium species to Aspergillus and selected one name for each species.


Subject(s)
Aspergillus/classification , Eurotium/classification , Ecosystem , Eurotium/genetics , Eurotium/growth & development , Sequence Analysis, DNA , Terminology as Topic
9.
Mikrobiologiia ; 80(5): 707-13, 2011.
Article in English | MEDLINE | ID: mdl-22168015

ABSTRACT

Thirty milled rice samples were collected from retailers in 4 provinces of Malaysia. These samples were evaluated for Aspergillus spp. infection by direct plating on malt extract salt agar (MESA). All Aspergillus holomorphs were isolated and identified using nucleotide sequences of ITS 1 and ITS 2 of rDNA. Five anamorphs (Aspergillus flavus, A. oryzae, A. tamarii, A. fumigatus and A. niger) and 5 teleomorphs (Eurotium rubrum, E. amstelodami, E. chevalieri, E. cristatum and E. tonophilum) were identified. The PCR-sequencing based technique for sequences of ITS 1 and ITS 2 is a fast technique for identification of Aspergillus and Eurotium species, although it doesn't work flawlessly for differentiation of Eurotium species. All Aspergillus and Eurotium isolates were screened for their ability to produce aflatoxin and ochratoxin A (OTA) by HPLC and TLC techniques. Only A. flavus isolate UPM 89 was able to produce aflatoxins B1 and B2.


Subject(s)
Aflatoxins/metabolism , Aspergillus/isolation & purification , Eurotium/isolation & purification , Ochratoxins/metabolism , Oryza/microbiology , Aflatoxins/chemistry , Aflatoxins/isolation & purification , Aspergillus/classification , Aspergillus/genetics , Aspergillus/metabolism , Base Sequence , Eurotium/classification , Eurotium/genetics , Eurotium/metabolism , Malaysia , Molecular Sequence Data , Ochratoxins/chemistry , Ochratoxins/isolation & purification , Phylogeny , RNA, Ribosomal, 18S/genetics
10.
J Microbiol ; 49(4): 669-74, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21887653

ABSTRACT

Eurotium strains were isolated from 77 loaves of meju (dried fermented soybeans), in various regions of Korea from 2008 to 2010. Morphological characteristics and DNA sequences of ß-tubulin were examined. They were identified as Eurotium amstelodami, E. chevalieri, E. herbariorum, E. repens, E. rubrum, and E. tonophilum. Of these species, E. chevalieri and E. tonophilum had not been previously reported in association with meju. E. chevalieri and E. repens were the species isolated most frequently. This paper summarizes the morphological characteristics of six Eurotium species and provides key to identify the species from meju.


Subject(s)
Eurotium/classification , Food Microbiology , Bacterial Typing Techniques , Eurotium/genetics , Eurotium/isolation & purification , Korea , Phenotype , Phylogeny , Tubulin/genetics
11.
FEMS Microbiol Ecol ; 77(1): 186-99, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21477006

ABSTRACT

Previous studies of hypersaline environments have revealed the dominant presence of melanized yeast-like fungi and related Cladosporium spp. In this study, we focused on the genera Aspergillus and Penicillium and their teleomorphic forms. From oligotrophic and eutrophic hypersaline waters around the world, 60 different species were identified, according to their morphological characteristics and extrolite profiles. For the confirmation of five new species, additionally, sequence analysis of the internal transcribed spacer region, the partial large subunit-rDNA and the partial ß-tubulin gene was performed. The species Aspergillus niger, Eurotium amstelodami and Penicillium chrysogenum were detected with the highest frequencies at all of the sampled sites; thus, they represent the pan-global stable mycobiota in hypersaline environments. Possible candidates were also Aspergillus sydowii and Eurotium herbariorum, as they were quite evenly distributed among the sampled sites, and Aspergillus candidus, which was abundant, but more locally distributed. These species and their byproducts can accumulate downstream following evaporation of brine, and they can become entrapped in the salt crystals. Consequently, marine salt used for consumption can be a potential source of food-borne fungi and their byproducts. For example, ochratoxin-A-producing species Penicillium nordicum was recovered from brine, salt and salted meat products.


Subject(s)
Aspergillus/isolation & purification , Penicillium/isolation & purification , Salinity , Water Microbiology , Aspergillus/genetics , Biodiversity , DNA, Fungal/genetics , DNA, Ribosomal Spacer/genetics , Environment , Eurotium/genetics , Eurotium/isolation & purification , Food Contamination , Meat Products/microbiology , Multivariate Analysis , Penicillium/genetics , Salts/chemistry , Sequence Analysis, DNA , Sodium Chloride/chemistry , Tubulin/genetics , Water/chemistry
12.
Int J Food Microbiol ; 144(3): 331-6, 2011 Jan 05.
Article in English | MEDLINE | ID: mdl-21093088

ABSTRACT

Xerophilic moulds cause contamination and spoilage of low moisture foods. This study examined the effect of ozone fumigation on growth of a Eurotium species isolated from naan bread. Two ozone treatments were used - a low-level long-term exposure (0.4 µmol/mol for 21 days) and high-level short-term exposure (300 µmol/mol for 5 to 120 min). For the low level exposure the combination of different media sucrose concentrations (0, 5, 10 and 20% w/v) with ozone treatment was also assessed. The growth of the isolate was found to be sensitive to low-level ozone fumigation depending on the media sucrose concentration and duration of the exposure. Low-level ozone exposure significantly (p<0.05) reduced the number of asexual spores formed in media with no added sucrose, an effect not observed in media with higher sucrose levels. Electron microscope observations of colonies indicated that ozone exposed cultures produced lower numbers of cleistothecia. High-level ozone exposure for short durations reduced spore viability although 100% reduction in viability was achieved only after 120 min exposure. This work demonstrates that ozone may be used to reduce spore production in Eurotium but that the ozone effect can be mediated by sucrose levels in the growth medium.


Subject(s)
Bread/microbiology , Eurotium/drug effects , Oxidants, Photochemical/pharmacology , Ozone/pharmacology , Culture Media , Eurotium/genetics , Fumigation , Molecular Sequence Data , RNA, Ribosomal, 28S/genetics , Spores/drug effects , Sucrose/metabolism
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