328 research outputs found
A Plasmodium falciparum S33 proline aminopeptidase is associated with changes in erythrocyte deformability
Infection with the apicomplexan parasite Plasmodium falciparum is a major cause of morbidity and mortality worldwide. One of the Striking features of this parasite is its ability to remodel and decrease the deformability of host red blood cells, a process that contributes to disease. To further understand the virulence of Pf we investigated the biochemistry and function of a putative Pf S33 proline aminopeptidase (PJPAP). Unlike other P. falciparum aminopeptidases, PJPAP contains a predicted protein export element that is non-syntenic with other human infecting Plasmodium species. Characterization of PJPAP demonstrated that it is exported into the host red blood cell and that it is a prolyl aminopeptidase with a preference for N-terminal proline substrates. In addition genetic deletion of this exopeptidase was shown to lead to an increase in the deformability of parasite-infected red cells and in reduced adherence to the endothelial cell receptor CD36 under flow conditions. Our studies suggest that PJPAP plays a role in the rigidification and adhesion of infected red blood cells to endothelial surface receptors, a role that may make this protein a novel target for anti-disease interventions strategies. (C) 2016 Elsevier Inc. All rights reserved
Effects of CO 2 and nutrient availability on mineral weathering in controlled tree growth experiments
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/94968/1/gbc911.pd
Detection of brown dwarf-like objects in the core of NGC3603
We use near-infrared data obtained with the Wide Field Camera 3 (WFC3) on the
Hubble Space Telescope to identify objects having the colors of brown dwarfs
(BDs) in the field of the massive galactic cluster NGC 3603. These are
identified through use of a combination of narrow and medium band filters
spanning the J and H bands, and which are particularly sensitive to the
presence of the 1.3-1.5{\mu}m H2O molecular band - unique to BDs. We provide a
calibration of the relationship between effective temperature and color for
both field stars and for BDs. This photometric method provides effective
temperatures for BDs to an accuracy of {\pm}350K relative to spectroscopic
techniques. This accuracy is shown to be not significantly affected by either
stellar surface gravity or uncertainties in the interstellar extinction. We
identify nine objects having effective temperature between 1700 and 2200 K,
typical of BDs, observed J-band magnitudes in the range 19.5-21.5, and that are
strongly clustered towards the luminous core of NGC 3603. However, if these are
located at the distance of the cluster, they are far too luminous to be normal
BDs. We argue that it is unlikely that these objects are either artifacts of
our dataset, normal field BDs/M-type giants or extra-galactic contaminants and,
therefore, might represent a new class of stars having the effective
temperatures of BDs but with luminosities of more massive stars. We explore the
interesting scenario in which these objects would be normal stars that have
recently tidally ingested a Hot Jupiter, the remnants of which are providing a
short-lived extended photosphere to the central star. In this case, we would
expect them to show the signature of fast rotation.Comment: 26 Pages, 8 Figures, Accepted for publication on Ap
The suppressive effect of a commercial extract from Durvillaea potatorum and Ascophyllum nodosum on infection of broccoli by Plasmodiophora brassicae
Symbiotic Legume Nodules Employ Both Rhizobial Exo- and Endo-Hydrogenases to Recycle Hydrogen Produced by Nitrogen Fixation
BACKGROUND: In symbiotic legume nodules, endosymbiotic rhizobia (bacteroids) fix atmospheric N(2), an ATP-dependent catalytic process yielding stoichiometric ammonium and hydrogen gas (H(2)). While in most legume nodules this H(2) is quantitatively evolved, which loss drains metabolic energy, certain bacteroid strains employ uptake hydrogenase activity and thus evolve little or no H(2). Rather, endogenous H(2) is efficiently respired at the expense of O(2), driving oxidative phosphorylation, recouping ATP used for H(2) production, and increasing the efficiency of symbiotic nodule N(2) fixation. In many ensuing investigations since its discovery as a physiological process, bacteroid uptake hydrogenase activity has been presumed a single entity. METHODOLOGY/PRINCIPAL FINDINGS: Azorhizobium caulinodans, the nodule endosymbiont of Sesbania rostrata stems and roots, possesses both orthodox respiratory (exo-)hydrogenase and novel (endo-)hydrogenase activities. These two respiratory hydrogenases are structurally quite distinct and encoded by disparate, unlinked gene-sets. As shown here, in S. rostrata symbiotic nodules, haploid A. caulinodans bacteroids carrying single knockout alleles in either exo- or-endo-hydrogenase structural genes, like the wild-type parent, evolve no detectable H(2) and thus are fully competent for endogenous H(2) recycling. Whereas, nodules formed with A. caulinodans exo-, endo-hydrogenase double-mutants evolve endogenous H(2) quantitatively and thus suffer complete loss of H(2) recycling capability. More generally, from bioinformatic analyses, diazotrophic microaerophiles, including rhizobia, which respire H(2) may carry both exo- and endo-hydrogenase gene-sets. CONCLUSIONS/SIGNIFICANCE: In symbiotic S. rostrata nodules, A. caulinodans bacteroids can use either respiratory hydrogenase to recycle endogenous H(2) produced by N(2) fixation. Thus, H(2) recycling by symbiotic legume nodules may involve multiple respiratory hydrogenases
Improved direct diabatization and coupled potential energy surfaces for the photodissociation of ammonia
Classification schemes for knowledge translation interventions: a practical resource for researchers
History, Commemoration, and Belief: Abraham Lincoln in American Memory, 1945-2001
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/91765/1/Schuman-History_Commemoration_Belief.pd
The Physics of the B Factories
This work is on the Physics of the B Factories. Part A of this book contains a brief description of the SLAC and KEK B Factories as well as their detectors, BaBar and Belle, and data taking related issues. Part B discusses tools and methods used by the experiments in order to obtain results. The results themselves can be found in Part C
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