55 research outputs found

    De Novo Peroxisome Biogenesis in Penicillium Chrysogenum Is Not Dependent on the Pex11 Family Members or Pex16

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    We have analyzed the role of the three members of the Pex11 protein family in peroxisome formation in the filamentous fungus Penicillium chrysogenum. Two of these, Pex11 and Pex11C, are components of the peroxisomal membrane, while Pex11B is present at the endoplasmic reticulum. We show that Pex11 is a major factor involved in peroxisome proliferation. We also demonstrate that P. chrysogenum cells deleted for known peroxisome fission factors (all Pex11 family proteins and Vps1) still contain peroxisomes. Interestingly, we find that, unlike in mammals, Pex16 is not essential for peroxisome biogenesis in P. chrysogenum, as partially functional peroxisomes are present in a pex16 deletion strain. We also show that Pex16 is not involved in de novo biogenesis of peroxisomes, as peroxisomes were still present in quadruple Δpex11 Δpex11B Δpex11C Δpex16 mutant cells. By contrast, pex3 deletion in P. chrysogenum led to cells devoid of peroxisomes, suggesting that Pex3 may function independently of Pex16. Finally, we demonstrate that the presence of intact peroxisomes is important for the efficiency of ß-lactam antibiotics production by P. chrysogenum. Remarkably, distinct from earlier results with low penicillin producing laboratory strains, upregulation of peroxisome numbers in a high producing P. chrysogenum strain had no significant effect on penicillin production

    A Deep Insight into the Sialotranscriptome of the Gulf Coast Tick, Amblyomma maculatum

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    Background: Saliva of blood sucking arthropods contains compounds that antagonize their hosts ’ hemostasis, which include platelet aggregation, vasoconstriction and blood clotting; saliva of these organisms also has anti-inflammatory and immunomodullatory properties. Perhaps because hosts mount an active immune response against these compounds, the diversity of these compounds is large even among related blood sucking species. Because of these properties, saliva helps blood feeding as well as help the establishment of pathogens that can be transmitted during blood feeding. Methodology/Principal Findings: We have obtained 1,626,969 reads by pyrosequencing a salivary gland cDNA library from adult females Amblyomma maculatum ticks at different times of feeding. Assembly of this data produced 72,441 sequences larger than 149 nucleotides from which 15,914 coding sequences were extracted. Of these, 5,353 had.75 % coverage to their best match in the non-redundant database from the National Center for Biotechnology information, allowing for the deposition of 4,850 sequences to GenBank. The annotated data sets are available as hyperlinked spreadsheets. Putative secreted proteins were classified in 133 families, most of which have no known function. Conclusions/Significance: This data set of proteins constitutes a mining platform for novel pharmacologically activ

    Riemann-Hilbert problems for multiple orthogonal polynomials

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    In the early nineties, Fokas, Its and Kitaev observed that there is a natural Riemann-Hilbert problem (for 2 2 matrix functions) associated which a system of orthogonal polynomials. This Riemann-Hilbert problem was later used by Deift et al. and Bleher and Its to obtain interesting results on orthogonal polynomials, in particular strong asymptotics which hold uniformly in the complex plane. In this paper we will show that a similar Riemann-Hilbert problem (for (r + 1) (r + 1) matrix functions) is associated with multiple orthogonal polynomials. We show how this helps in understanding the relation between two types of multiple orthogonal polynomials and the higher order recurrence relations for these polynomials. Finally we indicate how an extremal problem for vector potentials is important for the normalization of the Riemann-Hilbert problem. This extremal problem also describes the zero behavior of the multiple orthogonal polynomials. 1 Introduction Recently it was observed that ..

    Electroweak parameters of the z0 resonance and the standard model

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    Contains fulltext : 124399.pdf (publisher's version ) (Open Access
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