Magnetic field measurements and wind-line variability of OB-type stars

Context. The first magnetic fields in O- and B-type stars that do not belong to the Bp-star class, have been discovered. The cyclic UV wind-line variability, which has been observed in a significant fraction of early-type stars, is likely to be related to such magnetic fields. Aims. We attempt to improve our understanding of massive-star magnetic fields, and observe twenty-five carefully-selected, OB-type stars. Methods. Of these stars we obtain 136 magnetic field strength measurements. We present the UV wind-line variability of all selected targets and summarise spectropolarimetric observations acquired using the MUSICOS spectropolarimeter, mounted at the TBL, Pic du Midi, between December 1998 and November 2004. From the average Stokes I and V line profiles, derived using the LSD method, we measure the magnetic field strengths, radial velocities, and first moment of the line profiles. Results. No significant magnetic field is detected in any OB-type star that we observed. Typical 1{\sigma} errors are between 15 and 200 G. A possible magnetic-field detection for the O9V star 10 Lac remains uncertain, because the field measurements depend critically on the fringe- effect correction in the Stokes V spectra. We find excess emission in UV-wind lines, centred about the rest wavelength, to be a new indirect indicator of the presence of a magnetic field in early B-type stars. The most promising candidates to host magnetic fields are the B-type stars {\delta} Cet and 6 Cep, and a number of O stars. Conclusions. Although some O and B stars have strong dipolar field, which cause periodic variability in the UV wind-lines, such strong fields are not widespread. If the variability observed in the UV wind-lines of OB stars is generally caused by surface magnetic fields, these fields are either weak (<~few hundred G) or localised.Comment: A&A publishe

Discovery of the magnetic field in the pulsating B star beta Cephei

Although the star itself is not He enriched, the periodicity and the variability in the UV wind lines of the pulsating B1 IV star beta Cep are similar to what is observed in magnetic He-peculiar B stars, suggesting that beta Cep is magnetic. We searched for a magnetic field using spectropolarimetry. From UV spectroscopy, we analysed the wind variability and investigated the correlation with the magnetic data. Using 130 time-resolved circular polarisation spectra, obtained with the MuSiCoS spectropolarimeter at the 2m TBL from 1998 until 2005, we applied the least-squares deconvolution method on the Stokes V spectra and derived the longitudinal component of the integrated magnetic field over the visible hemisphere of the star. We performed a period analysis on the magnetic data and on EW measurements of UV wind lines obtained over 17 years. We also analysed the short- and long-term radial velocity variations, which are due to the pulsations and the 90-year binary motion. beta Cep hosts a sinusoidally varying magnetic field with an amplitude 97(4) G and an average value -6(3) G. From the UV wind line variability, we derive a period of 12.00075(11) days, which is the rotation period of the star, and is compatible with the observed magnetic modulation. Phases of maximum and minimum field match those of maximum emission in the UV wind lines, strongly supporting an oblique magnetic-rotator model. We discuss the magnetic behaviour as a function of pulsation behaviour and UV line variability. This paper presents the analysis of the first confirmed detection of a dipolar magnetic field in an upper main-sequence pulsating star. Maximum wind absorption originates in the magnetic equatorial plane. Maximum emission occurs when the magnetic north pole points to the Earth. Radial velocities agree with the ~90-y orbit around its Be-star binary companion.Comment: 14 pages, 10 figures, 5 table

Genomic Species Are Ecological Species as Revealed by Comparative Genomics in Agrobacterium tumefaciens

The definition of bacterial species is based on genomic similarities, giving rise to the operational concept of genomic species, but the reasons of the occurrence of differentiated genomic species remain largely unknown. We used the Agrobacterium tumefaciens species complex and particularly the genomic species presently called genomovar G8, which includes the sequenced strain C58, to test the hypothesis of genomic species having specific ecological adaptations possibly involved in the speciation process. We analyzed the gene repertoire specific to G8 to identify potential adaptive genes. By hybridizing 25 strains of A. tumefaciens on DNA microarrays spanning the C58 genome, we highlighted the presence and absence of genes homologous to C58 in the taxon. We found 196 genes specific to genomovar G8 that were mostly clustered into seven genomic islands on the C58 genome—one on the circular chromosome and six on the linear chromosome—suggesting higher plasticity and a major adaptive role of the latter. Clusters encoded putative functional units, four of which had been verified experimentally. The combination of G8-specific functions defines a hypothetical species primary niche for G8 related to commensal interaction with a host plant. This supports that the G8 ancestor was able to exploit a new ecological niche, maybe initiating ecological isolation and thus speciation. Searching genomic data for synapomorphic traits is a powerful way to describe bacterial species. This procedure allowed us to find such phenotypic traits specific to genomovar G8 and thus propose a Latin binomial, Agrobacterium fabrum, for this bona fide genomic species

Production of selenium nanoparticles in Pseudomonas putida KT2440

Selenium (Se) is an essential element for the cell that has multiple applications in medicine and technology; microorganisms play an important role in Se transformations in the environment. Here we report the previously unidentified ability of the soil bacterium Pseudomonas putida KT2440 to synthesize nanoparticles of elemental selenium (nano-Se) from selenite. Our results show that P. putida is able to reduce selenite aerobically, but not selenate, to nano-Se. Kinetic analysis indicates that, in LB medium supplemented with selenite (1 mM), reduction to nano-Se occurs at a rate of 0.444 mmol L−1 h−1 beginning in the middle-exponential phase and with a final conversion yield of 89%. Measurements with a transmission electron microscope (TEM) show that nano-Se particles synthesized by P. putida have a size range of 100 to 500 nm and that they are located in the surrounding medium or bound to the cell membrane. Experiments involving dynamic light scattering (DLS) show that, in aqueous solution, recovered nano-Se particles have a size range of 70 to 360 nm. The rapid kinetics of conversion, easy retrieval of nano-Se and the metabolic versatility of P. putida offer the opportunity to use this model organism as a microbial factory for production of selenium nanoparticles.Universidad de Costa Rica/[809-B5-A68]/UCR/Costa RicaCentro Nacional de Innovaciones Biotecnológicas/[]/CENIBiot/Costa RicaBio-SEA/[]//FranciaUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Estructuras Microscópicas (CIEMIC)UCR::Vicerrectoría de Docencia::Ciencias Básicas::Facultad de Ciencias::Escuela de QuímicaUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Electroquímica y Energía Química (CELEQ)UCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigaciones en Productos Naturales (CIPRONA

Electroanalysis may be used in the Vanillin Biotechnological Production

This study shows that electroanalysis may be used in vanillin biotechnological production. As a matter of fact, vanillin and some molecules implicated in the process like eugenol, ferulic acid, and vanillic acid may be oxidized on electrodes made of different materials (gold, platinum, glassy carbon). By a judicious choice of the electrochemical method and the experimental conditions the current intensity is directly proportional to the molecule concentrations in a range suitable for the biotechnological process. So, it is possible to imagine some analytical strategies to control some steps in the vanillin biotechnological production: by sampling in the batch reactor during the process, it is possible to determine out of line the concentration of vanillin, eugenol, ferulic acid, and vanillic acid with a gold rotating disk electrode, and low concentration of vanillin with addition of hydrazine at an amalgamated electrode. Two other possibilities consist in the introduction of electrodes directly in the batch during the process; the first one with a gold rotating disk electrode using linear sweep voltammetry and the second one requires three gold rotating disk electrodes held at different potentials for chronoamperometry. The last proposal is the use of ultramicroelectrodes in the case when stirring is not possible

The CouPSTU and TarPQM transporters in Rhodopseudomonas palustris: Redundant, promiscuous uptake systems for lignin-derived aromatic substrates

The biodegradation of lignin, one of the most abundant carbon compounds on Earth, has important biotechnological applications in the derivation of useful products from lignocellulosic wastes. The purple photosynthetic bacterium Rhodopseudomonas palustris is able to grow photoheterotrophically under anaerobic conditions on a range of phenylpropeneoid lignin monomers, including coumarate, ferulate, caffeate, and cinnamate. RPA1789 (CouP) is the periplasmic binding-protein component of an ABC system (CouPSTU; RPA1789, RPA1791–1793), which has previously been implicated in the active transport of this class of aromatic substrate. Here, we show using both intrinsic tryptophan fluorescence and isothermal titration calorimetry that CouP binds a range of phenylpropeneoid ligands with Kd values in the nanomolar range. The crystal structure of CouP with ferulate as the bound ligand shows H-bond interactions between the 4-OH group of the aromatic ring with His309 and Gln305. H-bonds are also made between the carboxyl group on the ferulate side chain and Arg197, Ser222, and Thr102. An additional transport system (TarPQM; RPA1782–1784), a member of the tripartite ATP-independent periplasmic (TRAP) transporter family, is encoded at the same locus as rpa1789 and several other genes involved in coumarate metabolism. We show that the periplasmic binding-protein of this system (TarP; RPA1782) also binds coumarate, ferulate, caffeate, and cinnamate with nanomolar Kd values. Thus, we conclude that R. palustris uses two redundant but energetically distinct primary and secondary transporters that both employ high-affinity periplasmic binding-proteins to maximise the uptake of lignin-derived aromatic substrates from the environment. Our data provide a detailed thermodynamic and structural basis for understanding the interaction of lignin-derived aromatic substrates with proteins and will be of use in the further exploitation of the flexible metabolism of R. palustris for anaerobic aromatic biotransformations