Propagating slow magnetoacoustic waves in coronal loops observed by Hinode/EIS

We present the first Hinode/EIS observations of 5 min quasi-periodic oscillations detected in a transition-region line (He II) and five coronal lines (Fe X, Fe XII, Fe XIII, Fe XIV, and Fe XV) at the footpoint of a coronal loop. The oscillations exist throughout the whole observation, characterized by a series of wave packets with nearly constant period, typically persisting for 4-6 cycles with a lifetime of 20-30 min. There is an approximate in-phase relation between Doppler shift and intensity oscillations. This provides evidence for slow magnetoacoustic waves propagating upwards from the transition region into the corona. We find that the oscillations detected in the five coronal lines are highly correlated, and the amplitude decreases with increasing temperature. The amplitude of Doppler shift oscillations decrease by a factor of about 3, while that of relative intensity decreases by a factor of about 4 from Fe X to Fe XV. These oscillations may be caused by the leakage of the photospheric p-modes through the chromosphere and transition region into the corona, which has been suggested as the source for intensity oscillations previously observed by TRACE. The temperature dependence of the oscillation amplitudes can be explained by damping of the waves traveling along the loop with multithread structure near the footpoint. Thus, this property may have potential value for coronal seismology in diagnostic of temperature structure in a coronal loop.Comment: 13 pages, 11 color figures, 4 tables, Astrophys.J, May 2009 - v696 issue, (in press

Inferring yeast cell cycle regulators and interactions using transcription factor activities

BACKGROUND: Since transcription factors are often regulated at the post-transcriptional level, their activities, rather than expression levels may provide valuable information for investigating functions and their interactions. The recently developed Network Component Analysis (NCA) and its generalized form (gNCA) provide a robust framework for deducing the transcription factor activities (TFAs) from various types of DNA microarray data and transcription factor-gene connectivity. The goal of this work is to demonstrate the utility of TFAs in inferring transcription factor functions and interactions in Saccharomyces cerevisiae cell cycle regulation. RESULTS: Using gNCA, we determined 74 TFAs from both wild type and fkh1 fkh2 deletion mutant microarray data encompassing 1529 ORFs. We hypothesized that transcription factors participating in the cell cycle regulation exhibit cyclic activity profiles. This hypothesis was supported by the TFA profiles of known cell cycle factors and was used as a basis to uncover other potential cell cycle factors. By combining the results from both cluster analysis and periodicity analysis, we recovered nearly 90% of the known cell cycle regulators, and identified 5 putative cell cycle-related transcription factors (Dal81, Hap2, Hir2, Mss11, and Rlm1). In addition, by analyzing expression data from transcription factor knockout strains, we determined 3 verified (Ace2, Ndd1, and Swi5) and 4 putative interaction partners (Cha4, Hap2, Fhl1, and Rts2) of the forkhead transcription factors. Sensitivity of TFAs to connectivity errors was determined to provide confidence level of these predictions. CONCLUSION: By subjecting TFA profiles to analyses based upon physiological signatures we were able to identify cell cycle related transcription factors consistent with current literature, transcription factors with potential cell cycle dependent roles, and interactions between transcription factors

Wave propagation and shock formation in different magnetic structures

Velocity oscillations "measured" simultaneously at the photosphere and the chromosphere -from time series of spectropolarimetric data in the 10830 A region- of different solar magnetic features allow us to study the properties of wave propagation as a function of the magnetic flux of the structure (i.e. two different-sized sunspots, a tiny pore and a facular region). While photospheric oscillations have similar characteristics everywhere, oscillations measured at chromospheric heights show different amplitudes, frequencies and stages of shock development depending on the observed magnetic feature. The analysis of the power and the phase spectra, together with simple theoretical modeling, lead to a series of results concerning wave propagation within the range of heights of this study. We find that, while the atmospheric cut-off frequency and the propagation properties of the different oscillating modes depend on the magnetic feature, in all the cases the power that reaches the high chromosphere above the atmospheric cut-off comes directly from the photosphere by means of linear vertical wave propagation rather than from non-linear interaction of modes.Comment: Accepted for publication in The Astrophysical Journal. 29 pages, 9 figures, 12pt, preprin

Chromospheric jets around the edges of sunspots

Aims. Evidence is beginning to be put forward that demonstrates the role of the chromosphere in supplying energy and mass to the corona. We aim to asses the role of chromospheric jets in active region dynamics. Methods. Using a combination of the Hinode/SOT Ca II H and TRACE 1550 Å and 1600 Å filters we examine chromospheric jets situated at the edge of a sunspot. Results. Analysis reveals a near continuous series of jets, that raise chromospheric material into the low corona above a sunspot. The jets have average rise speeds of 30 km/s and a range of 10−100 km/s. Enhanced emission observed at the jets leading edge suggests the formation of a shock front. Increased emission in TRACE bandpasses above the sunspot and the disappearance of the jets from the Ca II filter suggests that some of the chromospheric jet material is at least heated to ∼ 0.1 MK. The evidence suggests that the jets could be a mechanism which provides a steady, low-level heating for active region features

Thermodynamic analysis of regulation in metabolic networks using constraint-based modeling

<p>Abstract</p> <p>Background</p> <p><it>Geobacter sulfurreducens </it>is a member of the <it>Geobacter </it>species, which are capable of oxidation of organic waste coupled to the reduction of heavy metals and electrode with applications in bioremediation and bioenergy generation. While the metabolism of this organism has been studied through the development of a stoichiometry based genome-scale metabolic model, the associated regulatory network has not yet been well studied. In this manuscript, we report on the implementation of a thermodynamics based metabolic flux model for <it>Geobacter sulfurreducens</it>. We use this updated model to identify reactions that are subject to regulatory control in the metabolic network of <it>G. sulfurreducens </it>using thermodynamic variability analysis.</p> <p>Findings</p> <p>As a first step, we have validated the regulatory sites and bottleneck reactions predicted by the thermodynamic flux analysis in <it>E. coli </it>by evaluating the expression ranges of the corresponding genes. We then identified ten reactions in the metabolic network of <it>G. sulfurreducens </it>that are predicted to be candidates for regulation. We then compared the free energy ranges for these reactions with the corresponding gene expression fold changes under conditions of different environmental and genetic perturbations and show that the model predictions of regulation are consistent with data. In addition, we also identify reactions that operate close to equilibrium and show that the experimentally determined exchange coefficient (a measure of reversibility) is significant for these reactions.</p> <p>Conclusions</p> <p>Application of the thermodynamic constraints resulted in identification of potential bottleneck reactions not only from the central metabolism but also from the nucleotide and amino acid subsystems, thereby showing the highly coupled nature of the thermodynamic constraints. In addition, thermodynamic variability analysis serves as a valuable tool in estimating the ranges of Δ_rG' of every reaction in the model leading to the prediction of regulatory sites in the metabolic network, thereby characterizing the regulatory network in both a model organism such as <it>E. coli </it>as well as a non model organism such as <it>G. sulfurreducens</it>.</p

Substrate protein folds while it is bound to the ATP-independent chaperone Spy

Chaperones assist the folding of many proteins in the cell. While the most well studied chaperones use cycles of ATP binding and hydrolysis to assist protein folding, a number of chaperones have been identified that promote protein folding in the absence of highenergy cofactors. Precisely how ATP-independent chaperones accomplish this feat is unclear. Here we have characterized the kinetic mechanism of substrate folding by the small, ATP-independent chaperone, Spy. Spy rapidly associates with its substrate, Immunity protein 7 (Im7), eliminating its potential for aggregation. Remarkably, Spy then allows Im7 to fully fold into its native state while remaining bound to the surface of the chaperone. These results establish a potentially widespread mechanism whereby ATP-independent chaperones can assist in protein refolding. They also provide compelling evidence that substrate proteins can fold while continuously bound to a chaperone

Potentiating antibacterial activity by predictably enhancing endogenous microbial ROS production

The ever-increasing incidence of antibiotic-resistant infections combined with a weak pipeline of new antibiotics has created a global public health crisis1. Accordingly, novel strategies for enhancing our antibiotic arsenal are needed. As antibiotics kill bacteria in part by inducing reactive oxygen species (ROS)2–4, we reasoned that targeting microbial ROS production might potentiate antibiotic activity. Here we show that ROS production can be predictably enhanced in Escherichia coli, increasing the bacteria’s susceptibility to oxidative attack. We developed an ensemble, genome-scale metabolic modeling approach capable of predicting ROS production in E. coli. The metabolic network was systematically perturbed and its flux distribution analyzed to identify targets predicted to increase ROS production. In silico–predicted targets were experimentally validated and shown to confer increased susceptibility to oxidants. Validated targets also increased susceptibility to killing by antibiotics. This work establishes a systems-based method to tune ROS production in bacteria and demonstrates that increased microbial ROS production can potentiate killing by oxidants and antibiotics

RegNetB: Predicting Relevant Regulator-Gene Relationships in Localized Prostate Tumor Samples

<p>Abstract</p> <p>Background</p> <p>A central question in cancer biology is what changes cause a healthy cell to form a tumor. Gene expression data could provide insight into this question, but it is difficult to distinguish between a gene that causes a change in gene expression from a gene that is affected by this change. Furthermore, the proteins that regulate gene expression are often themselves not regulated at the transcriptional level. Here we propose a Bayesian modeling framework we term RegNetB that uses mechanistic information about the gene regulatory network to distinguish between factors that cause a change in expression and genes that are affected by the change. We test this framework using human gene expression data describing localized prostate cancer progression.</p> <p>Results</p> <p>The top regulatory relationships identified by RegNetB include the regulation of RLN1, RLN2, by PAX4, the regulation of ACPP (PAP) by JUN, BACH1 and BACH2, and the co-regulation of PGC and GDF15 by MAZ and TAF8. These target genes are known to participate in tumor progression, but the suggested regulatory roles of PAX4, BACH1, BACH2, MAZ and TAF8 in the process is new.</p> <p>Conclusion</p> <p>Integrating gene expression data and regulatory topologies can aid in identifying potentially causal mechanisms for observed changes in gene expression.</p

Engineering Corynebacterium glutamicum for isobutanol production

The production of isobutanol in microorganisms has recently been achieved by harnessing the highly active 2-keto acid pathways. Since these 2-keto acids are precursors of amino acids, we aimed to construct an isobutanol production platform in Corynebacterium glutamicum, a well-known amino-acid-producing microorganism. Analysis of this host’s sensitivity to isobutanol toxicity revealed that C. glutamicum shows an increased tolerance to isobutanol relative to Escherichia coli. Overexpression of alsS of Bacillus subtilis, ilvC and ilvD of C. glutamicum, kivd of Lactococcus lactis, and a native alcohol dehydrogenase, adhA, led to the production of 2.6 g/L isobutanol and 0.4 g/L 3-methyl-1-butanol in 48 h. In addition, other higher chain alcohols such as 1-propanol, 2-methyl-1-butanol, 1-butanol, and 2-phenylethanol were also detected as byproducts. Using longer-term batch cultures, isobutanol titers reached 4.0 g/L after 96 h with wild-type C. glutamicum as a host. Upon the inactivation of several genes to direct more carbon through the isobutanol pathway, we increased production by ∼25% to 4.9 g/L isobutanol in a ∆pyc∆ldh background. These results show promise in engineering C. glutamicum for higher chain alcohol production using the 2-keto acid pathways