Publications by authors named "A S C Navazo"

The upcoming UCNProBe experiment at Los Alamos National Laboratory will measure the beta decay rate of free neutrons with different systematic uncertainties than previous beam-based neutron lifetime experiments. We have tested a new 10B-coated Yttrium Aluminum Perovskite (YAP:Ce) scintillator and present its properties. The advantages of the YAP:Ce scintillator include its high Fermi potential, which reduces the probability for upscattering of ultracold neutrons (UCN), and its short decay time, which increases sensitivity at high counting rates.

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A study of the dead layer thickness and quenching factor of a plastic scintillator for use in ultracold neutron (UCN) experiments is described. Alpha spectroscopy was used to determine the thickness of a thin surface dead layer to be 630 ± 110 nm. The relative light outputs from the decay of 241Am and Compton scattering of electrons were used to extract Birks' law coefficient, yielding a kB value of 0.

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The genomic sequence of F113 has shown the presence of a 41 kb cluster of genes that encode the production of a second flagellar apparatus. Among 2,535 pseudomonads strains with sequenced genomes, these genes are only present in the genomes of F113 and other six strains, all but one belonging to the cluster of species, in the form of a genetic island. The genes are homologous to the flagellar genes of the soil bacterium .

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Diguanylate cyclase and phosphodiesterase enzymatic activities control c-di-GMP levels modulating planktonic versus sessile lifestyle behavior in bacteria. The PilZ domain is described as a sensor of c-di-GMP intracellular levels and the proteins containing a PilZ domain represent the best studied class of c-di-GMP receptors forming part of the c-di-GMP signaling cascade. In P.

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Background: Pseudomonas fluorescens F113 is a plant growth-promoting rhizobacterium (PGPR) isolated from the sugar-beet rhizosphere. This bacterium has been extensively studied as a model strain for genetic regulation of secondary metabolite production in P. fluorescens, as a candidate biocontrol agent against phytopathogens, and as a heterologous host for expression of genes with biotechnological application.

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