1,809 research outputs found
Superfluidity versus localization in bulk 4He at zero temperature
We present a zero-temperature quantum Monte Carlo calculation of liquid
He immersed in an array of confining potentials. These external potentials
are centered in the lattice sites of a fcc solid geometry and, by modifying
their well depth and range, the system evolves from a liquid phase towards a
progressively localized system which mimics a solid phase. The superfluid
density decreases with increasing order, reaching a value when the Lindemann's ratio of the model equals the experimental
value for solid He.Comment: 5 pages,5 figure
Supersolidity in quantum films adsorbed on graphene and graphite
Using quantum Monte Carlo we have studied the superfluid density of the first
layer of He and H adsorbed on graphene and graphite. Our main focus has
been on the equilibrium ground state of the system, which corresponds to a
registered phase. The perfect solid phase of H shows
no superfluid signal whereas He has a finite but small superfluid fraction
(0.67%). The introduction of vacancies in the crystal makes the superfluidity
increase, showing values as large as 14% in He without destroying the
spatial solid order.Comment: 5 pages, accepted for publication in PR
Isolation, characterization and selection of bacterial isolates from a suppressive soil with beneficial traits to plants
Backgrounds
This study focused on the characterization and selection of bacterial strains obtained from a suppressive soil displaying antifungal activity against the soilborne phytopathogenic fungi Rosellinia necatrix. Bacterial profile from this suppressive soil were first obtained by 16S rRNA gene sequencing, revealing a significant increase in the bacterial class Gammaproteobacteria, especially in some antagonistic representatives of Pseudomonas spp.
Objectives
To obtain and characterize a collection of 246 bacterial isolates obtained from this suppressive soil, in order to identify new strains with antifungal activity against fungal phytopathogens.
Methods
To obtain the bacterial collection, we performed an isolation on a selective medium for Pseudomonas-like microorganisms. Further characterization tests were used in order to analyse the bacterial collection, including identification of the general metabolic profile of glucose, the profiling of antifungals produced, including both the putative production of antifungal compounds and lytic exoenzymes, and the evaluation of traits related with beneficial effects on plants.
Conclusions
A final selection of representative strains resulted in antifungal isolates belonging to the genus Pseudomonas, but also some representatives of the genera Serratia and Stenotrophomonas. These selected strains were tested for plant protection by an in vivo experiment using avocado and wheat plants challenged by the pathogen R. necatrix, showing all of them an antifungal ability and plant disease protection.
Pseudomonas-like strains isolated from suppressive soils constitute an excellent source for novel microbial biocontrol agents against soilborne fungal pathogens.
This work was supported by grant AGL2014-52518-C2-1-R. Carmen Vida and Sandra Tienda are supported by a PhD fellowship from the FPI program of the Spanish Government.This work was supported by grant AGL2014-52518-C2-1-R. Carmen Vida and Sandra Tienda are supported by a PhD fellowship from the FPI program of the Spanish Government; Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
Quantum Monte Carlo simulation of overpressurized liquid 4He
A diffusion Monte Carlo simulation of superfluid He at zero temperature
and pressures up to 275 bar is presented. Increasing the pressure beyond
freezing ( 25 bar), the liquid enters the overpressurized phase in a
metastable state. In this regime, we report results of the equation of state
and the pressure dependence of the static structure factor, the condensate
fraction, and the excited-state energy corresponding to the roton. Along this
large pressure range, both the condensate fraction and the roton energy
decrease but do not become zero. The roton energies obtained are compared with
recent experimental data in the overpressurized regime.Comment: 5 pages, accepted for publication in Phys. Rev. Let
Genomic analysis of eight native plasmids of the phytopathogen Pseudomonas syringae
Comunicación a conferenciaThe pPT23A family of plasmids (PFPs) appears to be indigenous to the plant pathogen Pseudomonas syringae and these plasmids are widely distributed and widely transferred among pathovars of P. syringae and related species. PFPs are sources of accessory genes for their hosts that can include genes important for virulence and epiphytic colonization of plant leaf surfaces. Further understanding of the evolution of the pPT23A plasmid family and the role of these plasmids in P. syringae biology and pathogenesis, requires the determination and analysis of additional complete, closed plasmid genome sequences. Therefore, our main objective was to obtain complete genome sequences from PFPs from three different P. syringae pathovars and perform a comparative genomic analysis. In this work plasmid DNA isolation, purification by CsCl-EtBr gradients, and sequencing using 454 platform, were used to obtain the complete sequence of P. syringae plasmids. Different bioinformatic tools were used to analyze the plasmid synteny, to identify virulence genes (i.e. type 3 effectors) and to unravel the evolutionary history of PFPs. Our sequence analysis revealed that PFPs from P. syringae encode suites of accessory genes that are selected at different levels (universal, interpathovar and intrapathovar). The conservation of type IVSS encoding conjugation functions also contributes to the distribution of these plasmids within P. syringae populations. Thus, this study contributes to unravel the genetic basis of the role of PFPs in different P. syringae lifestyles.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
Tracking advanced persistent threats in critical infrastructures through opinion dynamics
Advanced persistent threats pose a serious issue for modern industrial environments, due to their targeted and complex attack vectors that are difficult to detect. This is especially severe in critical infrastructures that are accelerating the integration of IT technologies. It is then essential to further develop effective monitoring and response systems that ensure the continuity of business to face the arising set of cyber-security threats. In this paper, we study the practical applicability of a novel technique based on opinion dynamics, that permits to trace the attack throughout all its stages along the network by correlating different anomalies measured over time, thereby taking the persistence of threats and the criticality of resources into consideration. The resulting information is of essential importance to monitor the overall health of the control system and cor- respondingly deploy accurate response procedures. Advanced Persistent Threat Detection Traceability Opinion Dynamics.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
Comparative genomic analysis of native pseudomonas syringae plasmids belonging to the ppt23 a family reveals their role in p. Syringae epiphytic and pathogenic lifestyles
Backgrounds
The pPT23A family of plasmids (PFPs) appears to be indigenous to the plant pathogen Pseudomonas syringae and these plasmids are widely distributed and widely transferred among pathovars of P. syringae and related species. PFPs are sources of accessory genes for their hosts that can include genes important for virulence and epiphytic colonization of plant leaf surfaces.
Objectives
Further understanding of the evolution of the pPT23A plasmid family and the role of these plasmids in P. syringae biology and pathogenesis, requires the determination and analysis of additional complete, closed plasmid genome sequences. Therefore, our main objective was to obtain complete genome sequences of PFPs from three different P. syringae pathovars and perform a comprehensive comparative genomic analysis.
Methods
In this work plasmid DNA isolation, purification by CsCl-EtBr gradients, and sequencing using 454 platform, were carried out to obtain the complete sequence of P. syringae plasmids. Different bioinformatic tools were used to analyze the plasmid synteny, to identify virulence genes (i.e. type 3 effectors) and to unravel the evolutionary history of PFPs.
Conclusions
Our sequence analysis revealed that PFPs from P. syringae encode suites of accessory genes that are selected at different levels (universal, interpathovar and intrapathovar). The conservation of type IVSS encoding conjugation functions also contributes to the distribution of these plasmids within P. syringae populations. Thus, this study contributes to unravel the genetic bases of the role of PFPs in different P. syringae lifestyles.
This work was supported by grants Proyecto de Excelencia, Junta de Andalucía (P07-AGR-02471; P12-AGR-1473) and by Michigan State University AgBioResearch.This work was supported by grants Proyecto de Excelencia, Junta de Andalucía (P07-AGR-02471; P12-AGR-1473) and by Michigan State University AgBioResearch; Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
Análisis comparativo de dos colecciones de pseudo monas syringae pv. syringae asociadas a mango
Pseudomonas syringae es una bacteria ubicua a nivel ambiental. Presenta una taxonomía compleja en la que se han descrito más de 60 patovares que causan enfermedad en muchas especies de plantas diferentes. Entre los patovares más importantes se encuentra el pv. syringae debido a su amplio rango de hospedador, y al arsenal de mecanismos de virulencia que posee. A principios de los años 90, se describió a Pseudomonas syringae pv. syringae (Pss) como el agente causal de la necrosis apical del mango (NAM). Pss aisladas de mango muestran características importantes para su biología, tanto en sus mecanismos de virulencia como para el fitness epifítico. En este trabajo, se plantea conocer en profundidad cómo han evolucionado las poblaciones de Pss a lo largo del tiempo sobre el mangoUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.
Este trabajo ha sido financiado por ayuda de la Consejería de Economía, Innovación y Ciencia, Junta de Andalucía (Pl2-AGR-1473), cofinanciados con fondos FEDER (UE
Analysis of Synaptic Proteins in the Cerebrospinal Fluid as a New Tool in the Study of Inborn Errors of Neurotransmission
Abstract In a few rare diseases, specialised studies in cerebrospinal fluid (CSF) are required to identify the underlying metabolic disorder. We aimed to explore the
possibility of detecting key synaptic proteins in the CSF, in particular dopaminergic and gabaergic, as new procedures
that could be useful for both pathophysiological and diagnostic purposes in investigation of inherited disorders
of neurotransmission. Dopamine receptor type 2 (D2R), dopamine transporter (DAT) and vesicular monoamine transporter type 2 (VMAT2) were analysed in CSF samplesfrom 30 healthy controls (11 days to 17 years) by western blot analysis. Because VMAT2 was the only protein with intracellular localisation, and in order to compare results, GABA vesicular transporter, which is another intracellular protein, was also studied. Spearman’s correlation and
Student’s t tests were applied to compare optical density signals between different proteins. All these synaptic proteins could be easily detected and quantified in the
CSF. DAT, D2R and GABA VT expression decrease with age, particularly in the first months of life, reflecting the expected intense synaptic activity and neuronal circuitry formation. A statistically significant relationship was found
between D2R and DAT expression, reinforcing the previous evidence of DAT regulation by D2R. To our knowledge, there are no previous studies on human CSF reporting a reliable
analysis of these proteins. These kinds of studies could help elucidate new causes of disturbed dopaminergic and gabaergic
transmission as well as understanding different responses to L-dopa in inherited disorders affecting dopamine metabolism.
Moreover, this approach to synaptic activity in vivo can be extended to different groups of proteins and diseases
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