40 research outputs found

    Induced gene expression in wheat seedlings treated with a crude extract of Agapanthus africanus L. prior to leaf rust infection

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    It was previously shown that a crude extract of Agapanthus africanus L. (Hoffman), applied as a foliar spray to wheat (Triticum aestivum L.) seedlings, significantly increased the in vitro activities of three pathogenesis related (PR) proteins (β-1,3-glucanase, chitinase and peroxidase). This was the case in both susceptible and resistant wheat lines whether the plants were uninfected or infected with leaf rust (Puccinia triticina). The aim of this study was to determine the influence of the A. africanus extract on both the intercellular PR-protein profile and PR gene expression in leaf rust infected wheat lines. Pretreatment of infected resistant and susceptible wheat with the extract led to increased β-1,3-glucanase levels that were higher as compared to the untreated controls. Similarly, treatment with the extract led to greater expression of both the PR3 and PR9 genes in infected resistant and susceptible seedlings as compared to the controls. This is also applied to a retrotransposon protein encoding gene whose expression was strongly induced following extract treatment. The induced expression of all these defence-related genes suggests that the crude A. africanus extract has the ability to prime the resistance response of wheat prior to leaf rust infection.Keywords: Wheat leaf rust, induced resistance, priming, gene expression, immunoblotting, crude Agapanthus africanus extractAfrican Journal of Biotechnology Vol. 12(20), pp. 2876-288

    Bioorthogonal, Bifunctional Linker for Engineering Synthetic Glycoproteins

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    Post-translational glycosylation of proteins results in complex mixtures of heterogeneous protein glycoforms. Glycoproteins have many potential applications from fundamental studies of glycobiology to potential therapeutics, but generating homogeneous recombinant glycoproteins using chemical or chemoenzymatic reactions to mimic natural glycoproteins or creating homogeneous synthetic neoglycoproteins is a challenging synthetic task. In this work, we use a site-specific bioorthogonal approach to produce synthetic homogeneous glycoproteins. We develop a bifunctional, bioorthogonal linker that combines oxime ligation and strain-promoted azide–alkyne cycloaddition chemistry to functionalize reducing sugars and glycan derivatives for attachment to proteins. We demonstrate the utility of this minimal length linker by producing neoglycoprotein inhibitors of cholera toxin in which derivatives of the disaccharide lactose and GM1os pentasaccharide are attached to a nonbinding variant of the cholera toxin B-subunit that acts as a size- and valency-matched multivalent scaffold. The resulting neoglycoproteins decorated with GM1 ligands inhibit cholera toxin B-subunit adhesion with a picomolar IC50

    Cryptic Disc Structures Resembling Ediacaran Discoidal Fossils from the Lower Silurian Hellefjord Schist, Arctic Norway

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    The Hellefjord Schist, a volcaniclastic psammite-pelite formation in the Caledonides of Arctic Norway contains discoidal impressions and apparent tube casts that share morphological and taphonomic similarities to Neoproterozoic stem-holdfast forms. U-Pb zircon geochronology on the host metasediment indicates it was deposited between 437 ± 2 and 439 ± 3 Ma, but also indicates that an inferred basal conglomerate to this formation must be part of an older stratigraphic element, as it is cross-cut by a 546 ± 4 Ma pegmatite. These results confirm that the Hellefjord Schist is separated from underlying older Proterozoic rocks by a thrust. It has previously been argued that the Cambrian Substrate Revolution destroyed the ecological niches that the Neoproterozoic frond-holdfasts organisms occupied. However, the discovery of these fossils in Silurian rocks demonstrates that the environment and substrate must have been similar enough to Neoproterozoic settings that frond-holdfast bodyplans were still ecologically viable some hundred million years later

    Nucleolus: the fascinating nuclear body

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    Nucleoli are the prominent contrasted structures of the cell nucleus. In the nucleolus, ribosomal RNAs are synthesized, processed and assembled with ribosomal proteins. RNA polymerase I synthesizes the ribosomal RNAs and this activity is cell cycle regulated. The nucleolus reveals the functional organization of the nucleus in which the compartmentation of the different steps of ribosome biogenesis is observed whereas the nucleolar machineries are in permanent exchange with the nucleoplasm and other nuclear bodies. After mitosis, nucleolar assembly is a time and space regulated process controlled by the cell cycle. In addition, by generating a large volume in the nucleus with apparently no RNA polymerase II activity, the nucleolus creates a domain of retention/sequestration of molecules normally active outside the nucleolus. Viruses interact with the nucleolus and recruit nucleolar proteins to facilitate virus replication. The nucleolus is also a sensor of stress due to the redistribution of the ribosomal proteins in the nucleoplasm by nucleolus disruption. The nucleolus plays several crucial functions in the nucleus: in addition to its function as ribosome factory of the cells it is a multifunctional nuclear domain, and nucleolar activity is linked with several pathologies. Perspectives on the evolution of this research area are proposed

    Earth: Atmospheric Evolution of a Habitable Planet

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    Our present-day atmosphere is often used as an analog for potentially habitable exoplanets, but Earth's atmosphere has changed dramatically throughout its 4.5 billion year history. For example, molecular oxygen is abundant in the atmosphere today but was absent on the early Earth. Meanwhile, the physical and chemical evolution of Earth's atmosphere has also resulted in major swings in surface temperature, at times resulting in extreme glaciation or warm greenhouse climates. Despite this dynamic and occasionally dramatic history, the Earth has been persistently habitable--and, in fact, inhabited--for roughly 4 billion years. Understanding Earth's momentous changes and its enduring habitability is essential as a guide to the diversity of habitable planetary environments that may exist beyond our solar system and for ultimately recognizing spectroscopic fingerprints of life elsewhere in the Universe. Here, we review long-term trends in the composition of Earth's atmosphere as it relates to both planetary habitability and inhabitation. We focus on gases that may serve as habitability markers (CO2, N2) or biosignatures (CH4, O2), especially as related to the redox evolution of the atmosphere and the coupled evolution of Earth's climate system. We emphasize that in the search for Earth-like planets we must be mindful that the example provided by the modern atmosphere merely represents a single snapshot of Earth's long-term evolution. In exploring the many former states of our own planet, we emphasize Earth's atmospheric evolution during the Archean, Proterozoic, and Phanerozoic eons, but we conclude with a brief discussion of potential atmospheric trajectories into the distant future, many millions to billions of years from now. All of these 'Alternative Earth' scenarios provide insight to the potential diversity of Earth-like, habitable, and inhabited worlds.Comment: 34 pages, 4 figures, 4 tables. Review chapter to appear in Handbook of Exoplanet

    Phytotoxicity of fumonisins and TA-toxin to corn and tomato

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    The phytotoxic effects of 5 fumonisin mycotoxins produced by Fusarium moniliforme [Gibberella fujikuroi], i.e., fumonisin A1 (FA1), A2 (FA2), B1 (FB1), B2 (FB2) and B3 (FB3), together with the aminopolyol hydrolysis products of FB1 and FB2 (AP1 and AP2, respectively) and tricarballylic acid (TCA) were compared with the host-specific phytotoxin TA-toxin (TA) produced by Alternaria alternata f.sp. lycopersici. A leaf assay was performed on detached leaves of the tomato genotypes Asc/Asc (tolerant of TA) and asc/asc (sensitive to TA) at 4 concn (0.1, 1, 10 and 100 µsmallcap˜M) of each toxin. Seedlings of maize cultivars A1849W and PNR 473 and the 2 tomato genotypes were also used to assay TA, FB1, FB2 and FB3. The fumonisins caused leaf necrosis identical to that caused by TA and FB1, FB2, FB3, and TA caused significantly (P=0.01) more necrosis than the other metabolites tested. Sterile distilled water (control) and TCA caused no necrosis. Significantly (P=0.01) more necrosis was observed on the asc/asc genotype compared with the Asc/Asc genotype. There was no significant (P>0.05) difference between necrosis caused by autoclaved metabolites and that caused by nonautoclaved metabolites. The fumonisins caused dose-dependent reductions in shoot and root length and dry mass of maize and tomato seedlings identical to those caused by TA. The results indicated that TA and FB1 are more toxic to seedlings than are FB2 and FB3. The effects of all 4 toxins were more pronounced on seedlings of the sensitive tomato genotype asc/asc than on the tolerant genotype Asc/Asc. No significant differences were recorded in the reaction of the 2 maize cultivars. The structural similarity of the fumonisin B mycotoxins and TA is therefore reflected by their phytotoxicity to detached tomato leaves as well as to maize and tomato seedlings
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