Eupenicillium Shearii Research Articles

Synthetic Biology-Based Discovery of Diterpenoid Pyrones from the Genome of Eupenicillium shearii.

Diterpenoid pyrones are a type of mainly fungal meroterpenoid metabolite consisting of a diterpene connected to a pyrone, some of which show potent bioactivity. Through genome mining and heterologous expression, nine new diterpenoid pyrones, shearones A-I (1-9), were discovered from the fungus Eupenicillium shearii IFM 42152, and their biosynthetic enzyme activities were revealed. Some of these heterologously biosynthesized diterpenoid pyrones exhibited moderate antiaggregative ability against amyloid β42 in vitro.

Structure–activity relationship study at C9 position of kaitocephalin

Kaitocephalin (KCP) isolated from Eupenicillium shearii PF1191 is an unusual amino acid natural product in which serine, proline, and alanine moieties are liked with carbon–carbon bonds. KCP exhibits potent and selective binding affinity for one of the ionotropic glutamate receptor subtypes, NMDA receptors (Ki=7.8nM). In this study, new structure–activity relationship studies at C9 of KCP were implemented. Eleven new KCP analogs with different substituents at C9 were prepared and employed for binding affinity tests using native ionotropic glutamate receptors. Replacement of the 3,5-dichloro-4-hydroxybenzoyl group of KCP with a 3-phenylpropionyl group resulted in significant loss of binding affinity for NMDARs (Ki=1300nM), indicating an indispensable role of the aromatic ring of KCP in the potent and selective binding to NMDARs. Other analogs showed potent binding affinity in a range of 11–270nM. These findings would directly link to develop useful chemical tools toward imaging and labeling of NMDARs.

Electrochemical biosensor for carbofuran pesticide based on esterases from Eupenicillium shearii FREI-39 endophytic fungus

In this work, a biosensor was constructed by physical adsorption of the isolated endophytic fungus Eupenicillium shearii FREI-39 esterase on halloysite, using graphite powder, multi-walled carbon nanotubes and mineral oil for the determination of carbofuran pesticide by inhibition of the esterase using square-wave voltammetry (SWV). Specific esterase activities were determined each 2 days over a period of 15 days of growth in four different inoculation media. The highest specific activity was found on 6th day, with 33.08U on PDA broth. The best performance of the proposed biosensor was obtained using 0.5U esterase activity. The carbofuran concentration response was linear in the range from 5.0 to 100.0µgL−1 (r=0.9986) with detection and quantification limits of 1.69µgL−1 and 5.13µgL−1, respectively. A recovery study of carbofuran in spiked water samples showed values ranging from 103.8±6.7% to 106.7±9.7%. The biosensor showed good repeatability and reproducibility and remained stable for a period of 20 weeks. The determination of carbofuran in spiked water samples using the proposed biosensor was satisfactory when compared to the chromatographic reference method. The results showed no significant difference at the 95% confidence level with t-test statistics. The application of enzymes from endophytic fungi in constructing biosensors broadens the biotechnological importance of these microorganisms.

The Structure of (−)-Kaitocephalin Bound to the Ligand Binding Domain of the (S)-α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA)/Glutamate Receptor, GluA2

Glutamate receptors mediate the majority of excitatory synaptic transmission in the central nervous system, and excessive stimulation of these receptors is involved in a variety of neurological disorders and neuronal damage from stroke. The development of new subtype-specific antagonists would be of considerable therapeutic interest. Natural products can provide important new lead compounds for drug discovery. The only natural product known to inhibit glutamate receptors competitively is (-)-kaitocephalin, which was isolated from the fungus Eupenicillium shearii and found to protect CNS neurons from excitotoxicity. Previous work has shown that it is a potent antagonist of some subtypes of glutamate receptors (AMPA and NMDA, but not kainate). The structure of kaitocephalin bound to the ligand binding domain of the AMPA receptor subtype, GluA2, is reported here. The structure suggests how kaitocephalin can be used as a scaffold to develop more selective and high affinity antagonists for glutamate receptors.

Genome screening for reducing type I polyketide synthase genes in tropical fungi associated with medicinal plants

The aim of this work was to employ primers, which encode ketosynthase (KS) domains designed to detect Lovastatin-type PKSs (highly reduced molecules), to identify fungal species that have the potential for polyketide production. Using this strategy we have identified twenty-three KS sequences from twenty different fungal strains associated with medicinal plants found in Thailand. Phylogenetic analysis based on these sequences suggested that rapid screening provided the potential to explore significant PKS structural diversity. With this primer set a unique subclade of reducing type I PKS was identified. This encodes uncharacterized functional enzyme systems, which may suggest a novel function for these pks. Two fungi, Eupenicillium shearii and Myrothecium pandanicola within this novel clade, were investigated for polyketide synthesis. Three compounds, p-hydroxyphenopyrrozin (1) phenopyrrozin (2), and 2,3-dihydro-5-methoxy-2-methylchromen-4-one (3), were identified.

A New Antifungal Macrolide, Eushearilide (I), Isolated from Eupenicillium shearii.

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A New Antifungal Macrolide, Eushearilide, Isolated from Eupenicillium shearii

In screening for antifungal substances, a new macrolide, eushearilide (1), was isolated from Eupenicillium shearii IFM54447. The structure of 1 was established to be 24-membered macrolide having a non-conjugated diene and a choline phosphate ester moetiy on the basis of detailed investigation of NMR, UV, IR and MS spectral data. Compound 1 showed antifungal activity against various fungi and yeasts, including human pathogens Aspergillus fumigatus, Trichophyton spp. and Candida spp.

Prevention of UV Radiation‐Induced Premature Skin Aging in Hairless Mice by the Novel Compound Melanocin A

Repetitive exposure of the skin to UV radiation induces various harmful changes, such as thickening, wrinkle formation, inflammation and carcinogenesis. A variety of natural compounds and synthetic compounds have been studied to determine whether they can prevent UV-induced harmful effects. In this study, we investigated the effect of a novel compound, Melanocin A, which was isolated from Eupenicillium shearii F80695, on UV-induced premature skin aging. First, we studied the effect of Melanocin A on UV-induced matrix metalloproteinase (MMP)-9 expression in an immortalized human keratinocyte cell line, HaCaT, in vitro. Acute UV irradiation induced MMP-9 expression at both the mRNA and protein levels and Melanocin A suppressed this expression in a dose-dependent manner. We then investigated the effect of Melanocin A on UV-induced skin changes in hairless mice in vivo. Chronic exposure of hairless mouse dorsal skin to UV increased skin thickness and induced wrinkle formation and the gelatinase activities of MMP-2 and MMP-9. Moreover, Melanocin A significantly suppressed UV-induced morphologic skin changes and MMP-2 and MMP-9 expression. Taken together, these results show that Melanocin A can prevent the harmful effects of UV that lead to skin aging. Therefore, we suggest that Melanocin A should be viewed as a potential therapeutic agent for preventing and/or treating premature skin aging.

Melanocins A, B and C, New Melanin Synthesis Inhibitors Produced by Eupenicillium shearii. Part 1. Taxonomy, Fermentation, Isolation and Biological Properties.

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Melanocins A, B and C, New Melanin Synthesis Inhibitors Produced by Eupenicillium shearii. Part 2. Physico‐chemical Properties and Structure Elucidation.

Melanocins A, B and C, New Melanin Synthesis Inhibitors Produced by Eupenicillium shearii. Part 2. Physico‐chemical Properties and Structure Elucidation.

Genetic variation and recombination in Penicillium miczynskii and Eupenicillium species

Reproduction in the genus Penicillium is thought to be completely asexual. Sexual reproduction, as occurs in the related genus Eupenicillium, is thought to provide evolutionary benefits because it allows for new combinations of alleles and therefore increases the amount of variation within the species. This hypothesis was tested using inter-simple sequence repeats (ISSRs) to assess the amount of intraspecific and intra-population variation within Penicillium miczynskii and the closely related Eupenicillium shearii. The data for both genera were also used to test for clonal reproduction against the null hypothesis of panmixis, using measures of genotypic diversity, linkage disequilibrium and phylogenetic tree length. The ISSR fingerprints indicated that the 70 Eupenicillium strains actually included two distinct species, Eupenicillium shearii and Eupenicillium tropicum sp. nov., each represented by populations in both Costa Rica and India. While none of the species or populations were found to be randomly recombining, the relative strength of the clonal component differed among the species. Penicillium miczynskii had the smallest clonal component, with the highest genotypic diversity, lowest Index of Association, 40 % of alleles non-randomly associated, and phylogenetic tree length closer to that of recombined data sets than to the minimum possible. Eupenicillium tropicum showed nearly complete clonal reproduction with the lowest genotypic diversity and 100 % of alleles non-randomly associated in both populations. On the other hand, it also had the greatest amount of intraspecific variation, with as little as 38 % similarity among strains. The results indicate that Penicilliumspecies may, on rare occasion, genetically recombine; the regular occurrence of meiosis in the life cycle of Eupenicilliumspecies does not facilitate recombination; and the greatest amount of genetic variation was not associated with recombination, but with clonal propagation.

A new species from tropical soils, Eupenicillium tropicum

Forty-three strains of Eupenicillium tropicum sp. nov. were isolated from soils collected in India, Costa Rica and Galapagos, Ecuador. The species is characterized by biverticillate penicilli, slightly rough, subglobose to ovate conidia, brownish cleistothecia that become brown-gray with age, and ascospores with two equatorial flanges and slightly roughened valves. All strains produced a large number of indole alkaloids, and many types of unknown secondary metabolites with characteristic chromophores were produced by a majority of strains. Eupenicillium tropicum is morphologically most similar to E. shearii, but based on ITS-LSU sequences, is most closely related to Penicillium citrinum, P. sartoryi and P. westlingii. Eupenicillium shearii strains consistently produce paxillin, paspalinine and shearinins, while the latter three penicillia all produce citrinin consistently.

Shearamide A: A new cyclic peptide from the ascostromata of Eupenicillium shearii

A new antiinsectan cyclic peptide ( 3) was isolated from the ascostromata of Eupenicillium shearii (NRRL 3324). The structure was determined by analysis of NMR and FABMS data.

Structure of kaitocephalin, a novel glutamate receptor antagonist produced by Eupenicillium shearii

Kaitocephalin was isolated from Eupenicillium shearii as a glutamate receptor antagonist, which protected chick telencephalic neurons as well as rat hippocampal neurons from kainate toxicity. It consists of a pyrrolidine moiety with tricarboxylic acids and a dichlorohydroxybenzoate substructure as shown in Figure 1.

Antiinsectan alkaloids: Shearinines A-C and a new paxilline derivative from the ascostromata of Eupenicillium shearii

Four new antiinsectan indole alkaloids ( 1–4) have been isolated from organic extracts of the sclerotioid ascostromata of Eupenicillium shearii (NRRL 3324). These extracts also afforded five known, related metabolites ( 5–9). The structures of the new compounds were determined through analysis of 1H NMR, 13C NMR, HMQC, and HMBC experiments. Compounds 1–9 were isolated from fractions displaying activity in dietary assays against the corn earworm Helicoverpa zea and the dried-fruit beetle Carpophilus hemipterus, and most of the compounds show potent activity in these assays. Shearinine A ( 1) also exhibited activity in a topical assay against H. zea, and shearinine B ( 2) caused significant mortality in a leaf disk assay against the fall armyworm Spodoptera frugiperda.