324 research outputs found
Long-term Benefits of GM crops: Potential for Diabrotica Suppression in Europe using Bt Maize
Transgenic crops producing insecticidal proteins from _Bacillus thuringiensis_ (Bt) have been widely adopted since 1996 in the United States of America to combat important pests of maize and cotton. There is growing evidence that several target pest populations have been dramatically reduced in areas where the Bt crops have been most intensively adopted over multiple years. The evidence is most dramatic for nonmigratory monophagous and oligophagous species that show high mortality on Bt crops, such as European corn borer (_Ostrinia nubilalis_), and tobacco budworm (_Heliothis virescens_). Bt cotton is currently being used in the southwestern USA as part of an area-wide eradication program for pink bollworm (_Pectinophora gossypiella_). Single, stacked, and pyramided Bt maize lines producing coleopteran-active insecticidal proteins have been shown in some cases to cause >99% mortality of western corn rootworm (_Diabrotica virgifera virgifera_) larvae every year. Simulation models suggest that long-term area-wide cultivation of these Bt corn lines can lead to dramatic population reduction, and even local extinction, of corn rootworms. An eradication program for this economically important pest, based around Bt maize and incorporating a combination of other tools, would benefit European agriculture and the environment. Post-commercial monitoring programs should be designed to investigate long-term benefits to agricultural production systems that can be reasonably expected from the widespread cultivation of Bt crops in Europe
Luminescence conversion of blue light emitting diodes,”
Abstract: Solid state lighting seeks to replace both, incandescent and fluorescent lighting by energy efficient light-emitting diodes (LEDs). Just like compact fluorescent tubes, current white LEDs employ costly rare earth-based phosphors, a drawback we propose to overcome with direct emitting LEDs of all colors. We show the benefits of homoepitaxial LEDs on bulk GaN substrate for wavelength-stable green spectrum LEDs. By use of non-polar growth orientation we avoid big color shifts with drive current and demonstrate polarized light emitters that prove ideal for pairing with liquid crystal display modulators in back light units of television monitors. We further offer a comparison of the prospects of non-polar a-and m-plane growth over conventional c-plane growth
Magnetic switching in granular FePt layers promoted by near-field laser enhancement
Light-matter interaction at the nanoscale in magnetic materials is a topic of
intense research in view of potential applications in next-generation
high-density magnetic recording. Laser-assisted switching provides a pathway
for overcoming the material constraints of high-anisotropy and high-packing
density media, though much about the dynamics of the switching process remains
unexplored. We use ultrafast small-angle x-ray scattering at an x-ray
free-electron laser to probe the magnetic switching dynamics of FePt
nanoparticles embedded in a carbon matrix following excitation by an optical
femtosecond laser pulse. We observe that the combination of laser excitation
and applied static magnetic field, one order of magnitude smaller than the
coercive field, can overcome the magnetic anisotropy barrier between "up" and
"down" magnetization, enabling magnetization switching. This magnetic switching
is found to be inhomogeneous throughout the material, with some individual FePt
nanoparticles neither switching nor demagnetizing. The origin of this behavior
is identified as the near-field modification of the incident laser radiation
around FePt nanoparticles. The fraction of not-switching nanoparticles is
influenced by the heat flow between FePt and a heat-sink layer
Irreversible transformation of ferromagnetic ordered stripe domains in single-shot IR pump - resonant X-ray scattering probe experiments
The evolution of a magnetic domain structure upon excitation by an intense,
femtosecond Infra-Red (IR) laser pulse has been investigated using single-shot
based time-resolved resonant X-ray scattering at the X-ray Free Electron laser
LCLS. A well-ordered stripe domain pattern as present in a thin CoPd alloy film
has been used as prototype magnetic domain structure for this study. The
fluence of the IR laser pump pulse was sufficient to lead to an almost complete
quenching of the magnetization within the ultrafast demagnetization process
taking place within the first few hundreds of femtoseconds following the IR
laser pump pulse excitation. On longer time scales this excitation gave rise to
subsequent irreversible transformations of the magnetic domain structure. Under
our specific experimental conditions, it took about 2 nanoseconds before the
magnetization started to recover. After about 5 nanoseconds the previously
ordered stripe domain structure had evolved into a disordered labyrinth domain
structure. Surprisingly, we observe after about 7 nanoseconds the occurrence of
a partially ordered stripe domain structure reoriented into a novel direction.
It is this domain structure in which the sample's magnetization stabilizes as
revealed by scattering patterns recorded long after the initial pump-probe
cycle. Using micro-magnetic simulations we can explain this observation based
on changes of the magnetic anisotropy going along with heat dissipation in the
film.Comment: 16 pages, 6 figure
Ultrafast Laser-Induced Melting of Long-Range Magnetic Order in Multiferroic TbMnO3
We performed ultrafast time-resolved near-infrared pump, resonant soft X-ray
diffraction probe measurements to investigate the coupling between the
photoexcited electronic system and the spin cycloid magnetic order in
multiferroic TbMnO3 at low temperatures. We observe melting of the long range
antiferromagnetic order at low excitation fluences with a decay time constant
of 22.3 +- 1.1 ps, which is much slower than the ~1 ps melting times previously
observed in other systems. To explain the data we propose a simple model of the
melting process where the pump laser pulse directly excites the electronic
system, which then leads to an increase in the effective temperature of the
spin system via a slower relaxation mechanism. Despite this apparent increase
in the effective spin temperature, we do not observe changes in the wavevector
q of the antiferromagnetic spin order that would typically correlate with an
increase in temperature under equilibrium conditions. We suggest that this
behavior results from the extremely low magnon group velocity that hinders a
change in the spin-spiral wavevector on these time scales.Comment: 9 pages, 4 figure
BCAT1 redox function maintains mitotic fidelity
The metabolic enzyme branched-chain amino acid transaminase 1 (BCAT1) drives cell proliferation in aggressive cancers such as glioblastoma. Here, we show that BCAT1 localizes to mitotic structures and has a non-metabolic function as a mitotic regulator. Furthermore, BCAT1 is required for chromosome segregation in cancer and induced pluripotent stem cells and tumor growth in human cerebral organoid and mouse syngraft models. Applying gene knockout and rescue strategies, we show that the BCAT1 CXXC redox motif is crucial for controlling cysteine sulfenylation specifically in mitotic cells, promoting Aurora kinase B localization to centromeres, and securing accurate chromosome segregation. These findings offer an explanation for the well-established role of BCAT1 in promoting cancer cell proliferation. In summary, our data establish BCAT1 as a component of the mitotic apparatus that safeguards mitotic fidelity through a moonlighting redox functionality
Two canine CD1a proteins are differentially expressed in skin
Lipid antigens are presented to T cells by the CD1 family of proteins. In this study, we characterize the complete dog (Canis familiaris) CD1 locus, which is located on chromosome 38. The canine locus contains eight CD1A genes (canCD1A), of which five are pseudogenes, one canCD1B, one canCD1C, one canCD1D, and one canCD1E gene. In vivo expression of canine CD1 proteins was shown for canCD1a6, canCD1a8, and canCD1b, using a panel of anti-CD1 monoclonal antibodies (mAbs). CanCD1a6 and canCD1a8 are recognized by two distinct mAbs. Furthermore, we show differential transcription of the three canCD1A genes in canine tissues. In canine skin, the transcription level of canCD1A8 was higher than that of canCD1A6, and no transcription of canCD1A2 was detected. Based on protein modeling and protein sequence alignment, we predict that both canine CD1a proteins can bind different glycolipids in their groove. Besides differences in ectodomain structure, we observed the unique presence of three types of cytoplasmic tails encoded by canCD1A genes. cDNA sequencing and expressed sequence tag sequences confirmed the existence of a short, human CD1a-like cytoplasmic tail of four amino acids, of an intermediate length form of 15 amino acids, and of a long form of 31 amino acids
Annexin A1-dependent tethering promotes extracellular vesicle aggregation revealed with single–extracellular vesicle analysis
Extracellular vesicles (EVs) including plasma membrane-derived microvesicles and endosomal-derived exosomes aggregate by unknown mechanisms, forming microcalcifications that promote cardiovascular disease, the leading cause of death worldwide. Here, we show a framework for assessing cell-independent EV mechanisms in disease by suggesting that annexin A1 (ANXA1)-dependent tethering induces EV aggregation and microcalcification. We present single-EV microarray, a method to distinguish microvesicles from exosomes and assess heterogeneity at a single-EV level. Single-EV microarray and proteomics revealed increased ANXA1 primarily on aggregating and calcifying microvesicles. ANXA1 vesicle aggregation was suppressed by calcium chelation, altering pH, or ANXA1 neutralizing antibody. ANXA1 knockdown attenuated EV aggregation and microcalcification formation in human cardiovascular cells and acellular three-dimensional collagen hydrogels. Our findings explain why microcalcifications are more prone to form in vulnerable regions of plaque, regulating critical cardiovascular pathology, and likely extend to other EV-associated diseases, including autoimmune and neurodegenerative diseases and cancer
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