RESUMO
New astronomical observations point to a nucleosynthesis picture that goes beyond what was accepted until recently. The intermediate "i" process was proposed as a plausible scenario to explain some of the unusual abundance patterns observed in metal-poor stars. The most important nuclear physics properties entering i-process calculations are the neutron-capture cross sections and they are almost exclusively not known experimentally. Here we provide the first experimental constraints on the ^{139}Ba(n,γ)^{140}Ba reaction rate, which is the dominant source of uncertainty for the production of lanthanum, a key indicator of i-process conditions. This is an important step towards identifying the exact astrophysical site of stars carrying the i-process signature.
RESUMO
The first complete measurement of the ß-decay strength distribution of _{17}^{45}Cl_{28} was performed at the Facility for Rare Isotope Beams (FRIB) with the FRIB Decay Station Initiator during the second FRIB experiment. The measurement involved the detection of neutrons and γ rays in two focal planes of the FRIB Decay Station Initiator in a single experiment for the first time. This enabled an analytical consistency in extracting the ß-decay strength distribution over the large range of excitation energies, including neutron unbound states. We observe a rapid increase in the ß-decay strength distribution above the neutron separation energy in _{18}^{45}Ar_{27}. This was interpreted to be caused by the transitioning of neutrons into protons excited across the Z=20 shell gap. The SDPF-MU interaction with reduced shell gap best reproduced the data. The measurement demonstrates a new approach that is sensitive to the proton shell gap in neutron rich nuclei according to SDPF-MU calculations.
RESUMO
The validity of the Brink-Axel hypothesis, which is especially important for numerous astrophysical calculations, is addressed for ^{116,120,124}Sn below the neutron separation energy by means of three independent experimental methods. The γ-ray strength functions (GSFs) extracted from primary γ-decay spectra following charged-particle reactions with the Oslo method and with the shape method demonstrate excellent agreement with those deduced from forward-angle inelastic proton scattering at relativistic beam energies. In addition, the GSFs are shown to be independent of excitation energies and spins of the initial and final states. The results provide a critical test of the generalized Brink-Axel hypothesis in heavy nuclei, demonstrating its applicability in the energy region of the pygmy dipole resonance.
RESUMO
At room temperature at stall, the flagellar motor of the bacterium Escherichia coli exerts a torque of ~1300 pN nm. At zero external load, it spins ~330 Hz. A robust method for studying the motor near zero load is reviewed here.
RESUMO
Paralyzed motors of motA and motB point and deletion mutants of Escherichia coli were repaired by synthesis of wild-type protein. As found earlier with a point mutant of motB, torque was restored in a series of equally spaced steps. The size of the steps was the same for both MotA and MotB. Motors with one torque generator spent more time spinning counterclockwise than did motors with two or more generators. In deletion mutants, stepwise decreases in torque, rare in point mutants, were common. Several cells stopped accelerating after eight steps, suggesting that the maximum complement of torque generators is eight. Each generator appears to contain both MotA and MotB.
Assuntos
Proteínas de Bactérias/fisiologia , Escherichia coli/fisiologia , Flagelos/fisiologia , Proteínas de Bactérias/genética , Eletroquímica , Escherichia coli/genética , Proteínas de Membrana/genética , Proteínas de Membrana/fisiologia , Movimento , Mutação , Plasmídeos , Prótons , Transformação BacterianaRESUMO
The MotA protein of Escherichia coli is an essential component of the torque-generating units that drive the flagellar rotary motor. A variety of evidence indicates that MotA is involved in transmembrane proton conduction. We have now mapped a number of MotA mutants, focusing primarily on those previously shown to be dominant. Fifty-six mutations (all dominant), each causing severe or complete impairment of function, were sequenced and found to correspond to 31 different alleles. All except two of these encoded amino acid substitutions clustered in four hydrophobic, presumably membrane-spanning segments, that together make up only one-third of the length of the polypeptide chain. In contrast, eight mutations (5 dominant), each causing only slight impairment of function (slow alleles), were sequenced and found to specify amino acid substitutions in three hydrophilic domains. The clustering of the mutations provides independent support for the suggestion that MotA is a transmembrane proton channel and places significant constraints on models for the molecular mechanism of ion conduction.
Assuntos
Proteínas de Bactérias/metabolismo , Escherichia coli/metabolismo , Canais Iônicos/metabolismo , Proteínas de Membrana/metabolismo , Alelos , Sequência de Aminoácidos , Proteínas de Bactérias/química , Proteínas de Bactérias/genética , Análise Mutacional de DNA , RNA Polimerases Dirigidas por DNA/metabolismo , Eletroforese em Gel de Poliacrilamida , Endopeptidase K , Escherichia coli/genética , Escherichia coli/crescimento & desenvolvimento , Genes Dominantes/genética , Canais Iônicos/química , Canais Iônicos/genética , Proteínas de Membrana/química , Proteínas de Membrana/genética , Dados de Sequência Molecular , Mutação/genética , Plasmídeos/genética , Prótons , Serina Endopeptidases/metabolismo , Esferoplastos/metabolismo , Proteínas ViraisRESUMO
Cells of a motile Streptococcus were starved, tethered to a quartz coverslip, energized with a potassium diffusion potential, and exposed to sudden decrements in external pH generated by flash photolysis of 2-hydroxyphenyl-1-(2-nitro)phenyl phosphate. The rotation rate of the cells increased following the flash but only after a brief time lag. Lags of the order of 0.1 second were observed in a dilute buffer (0.05 mM), confirming results obtained earlier. These lags were longer when the buffer was prepared in D2O. However, lags as short as 0.01 second were found in more concentrated buffers (1 and 3 mM). In this case, there was no deuterium solvent isotope effect. These differences arise from the extra time required for diffusion of protons from a dilute medium into the cell wall, which has a large buffering capacity. The short lags observed in concentrated media could be inherent to the flagellar motor, but the possibility that they are due to buffered diffusion through the cell wall or to elastic filtering by the tether has not been ruled out.
Assuntos
Flagelos/fisiologia , Rotação , Streptococcus/fisiologia , Movimento Celular , Concentração de Íons de Hidrogênio , PrótonsRESUMO
The motion of tethered cells of Streptococcus was analyzed at low values of protonmotive force (delta p). Cells repeatedly energized and de-energized stopped at discrete angular positions, indicating a rotational symmetry of barriers to rotation of order 5 or 6. At values of delta p smaller than -30 mV, constraints imposed by these barriers were evident when cells were starved and gradually energized, but not when they were energized first and then gradually de-energized. At values of delta p larger than about -30 mV, the cells behaved as if there were no barriers. Cells spinning in this regime also executed rotational Brownian movement. At energy levels above threshold, the motor determines torque; it does not fix the position of the rotor relative to the stator.
Assuntos
Flagelos/fisiologia , Rotação , Streptococcus/fisiologia , Difusão , Concentração de Íons de Hidrogênio , Matemática , Potássio , TermodinâmicaRESUMO
The ability of the flagellar motor of Escherichia coli to switch between clockwise and counterclockwise modes of operation is ultimately responsible for the swimming behavior of the cell. Three motor proteins, FliG, FliM, and FliN, have been implicated in this process. Using the two-hybrid system in Saccharomyces cerevisiae, we demonstrated strong interactions between FliG/FliM,FliM/FliM, and FliM/FliN. A screen for other components that might interact with FliG revealed interactions with FliF (the MS ring protein) and H-NS (a histone-like protein). Regions of proteins important for several of these interactions were identified by mutational analysis. The implications for motor assembly and function are discussed.
Assuntos
Proteínas de Bactérias/fisiologia , Escherichia coli/fisiologia , Flagelos/fisiologia , Proteínas de Saccharomyces cerevisiae , Fatores de Transcrição , Sequência de Bases , Análise Mutacional de DNA , Proteínas de Ligação a DNA , Escherichia coli/genética , Proteínas Fúngicas/genética , Dados de Sequência Molecular , Saccharomyces cerevisiae/genética , Ativação TranscricionalRESUMO
Two mutants with defects in hook-associated protein 3 (HAP3) were isolated that exhibit impaired swimming only when they interact with a solid surface or a semisolid matrix. Motility and chemotaxis were normal in liquid media, even in media containing viscous agents, but cells failed to swarm in 0.28% agar. Mutants appeared to carry a full complement of flagella of normal configuration and length. However, filaments rotating counterclockwise close to a glass surface transformed from normal to straight, while filaments rotating clockwise transformed from curly to straight. Both transformations propagated from base to tip, as expected if torsionally induced. The mutations mapped to the middle of flgL, to structural gene for HAP3, and sequence analysis revealed the same coding change in both mutants: a substitution of cysteine for arginine 168. Our results show that the ability of a filament composed of normal flagellin subunits to resist mechanical stress depends on the structure of the protein (HAP3) to which it is attached at its base. The N-terminal sequence of HAP3 was found to be similar to the N-terminal sequence of flagellin, and the possibility that it provides a nucleation site for the C-terminal region of flagellin is discussed.
Assuntos
Proteínas de Bactérias/fisiologia , Escherichia coli/fisiologia , Flagelos/fisiologia , Sequência de Aminoácidos , Proteínas de Bactérias/genética , Sequência de Bases , Fenômenos Biomecânicos , Movimento Celular/fisiologia , Mapeamento Cromossômico , Meios de Cultura , Escherichia coli/genética , Escherichia coli/ultraestrutura , Flagelos/ultraestrutura , Genes Bacterianos , Dados de Sequência Molecular , Mutação , RotaçãoAssuntos
Membrana Celular , Compostos de Diazônio , Eritrócitos , Ácidos Sulfônicos , Resinas Acrílicas , Antígenos de Grupos Sanguíneos , Proteínas Sanguíneas , Permeabilidade da Membrana Celular , Fenômenos Químicos , Química , Cromatografia , Detergentes , Eletroforese , Eritrócitos/citologia , Humanos , Lipídeos , Peso Molecular , Nitritos , Fosfolipases , Potássio , Sódio , Solubilidade , Coloração e Rotulagem , Isótopos de EnxofreAssuntos
Eritrócitos , Poli T , Polidesoxirribonucleotídeos , Separação Celular , Membrana Eritrocítica , Humanos , Células Híbridas , Poli AAssuntos
Amidinas , Membrana Celular/ultraestrutura , Eritrócitos/ultraestrutura , Imidas , Acetilcolinesterase/sangue , Sítios de Ligação , Transporte Biológico , Glicemia/metabolismo , Radioisótopos de Carbono , Membrana Celular/metabolismo , Eritrócitos/metabolismo , Humanos , Espectroscopia de Ressonância Magnética , Potássio/sangue , TrítioAssuntos
Membrana Celular/análise , Eritrócitos/análise , Peptídeo Hidrolases , Proteínas/análise , Transporte Biológico , Carboidratos/análise , Inibidores da Colinesterase , Detergentes , Compostos de Diazônio , Difusão , Eletroforese Descontínua , Eritrócitos/enzimologia , Glucose/metabolismo , Humanos , Hidrólise , Peso Molecular , Ácidos Neuramínicos/análise , Osmose , Potássio/metabolismo , Isótopos de Enxofre , TrometaminaRESUMO
Many bacteria swim by rotating thin helical filaments that extend into the external medium, as with common bacteria, or run beneath the outer membrane, as with spirochetes. Each filament is driven at its base by a motor that turns alternately clockwise and counterclockwise. The motor-filament complex is called a flagellum. Other kinds of bacteria glide, but their organelles of locomotion are not known. Since bacteria are microscopic and live in an aqueous environment, they swim at low Reynolds' number; cyclic motion works (e.g. rotation of a helix) but reciprocal motion does not (e.g. stroking of a singly hinged oar). By measuring concentrations of certain chemicals as they move through their environment, making temporal comparisons and modulating the direction of flagellar rotation, bacteria accumulate in regions that they find more favourable. Studies of bacterial chemotaxis are highly advanced, particularly for the peritrichously flagellated species Escherichia coli. A great deal is known about chemoreception, receptor-flagellar coupling and adaptation. Recently it has been found that E. coli can aggregate in response to signals generated by the cells themselves. Complex patterns form with remarkable symmetries.