Preparation of Metal Immobilized Orange Waste Gel for Arsenic(V) Removal From Water

- The toxicity of arsenic is known to be a risk to aquatic flora and fauna and to human health even in relatively low concentration. In this research an adsorption gel was prepared from agricultural waste material (orange waste) through simple chemical modification in the view to remove arsenic (V) from water. Orange waste was crushed into small particles and saponified with Ca(OH)2 to prepare saponified orange waste, which was further modified by immobilizing gadolinium(III) to obtain desired adsorption material (Gd(III)-immobilized SOW gel). The effective pH range for arsenic adsorption was found to be 7.5 – 8.5. Adsorption capacity of the gel was evaluated to be 0.45 mol-arsenic (V)/kg. Dynamic adsorption of arsenic (V) in column-mode was conducted and a dynamic capacity was found to be 0.39 mol/kg. Elution of arsenate was tested after complete saturation of the column packed with gadolinium-immobilized orange waste adsorption gel. A complete elution of arsenate was achieved with the help of 1 M HCl and 28 times pre-concentration factor was attained. This study showed that a cheap and abundant agro-industrial waste material could be successfully employed for the remediation of arsenic pollution in aquatic environment

AGN feedback and gas mixing in the core of NGC 4636

Chandra observations of NGC 4636 show disturbances in the galaxy X-ray halo, including arm-like high surface brightness features (tentatively identified as AGN driven shocks) and a possible cavity on the west side of the galaxy core. We present Chandra and XMM spectral maps of NGC 4636 which confirm the presence of the cavity and show it to be bounded by the arm features. The maps also reveal a ~15 kpc wide plume of low temperature, high abundance gas extending 25-30 kpc to the southwest of the galaxy. The cavity appears to be embedded in this plume, and we interpret the structure as being entrained gas drawn out of the galaxy core during previous episodes of AGN activity. The end of the plume is marked by a well defined edge, with significant falls in surface brightness, temperature and abundance, indicating a boundary between galaxy and group/cluster gas. This may be evidence that as well as preventing gas cooling through direct heating, AGN outbursts can produce significant gas mixing, disturbing the temperature structure of the halo and transporting metals out from the galaxy into the surrounding intra-group medium.Comment: 4 Pages, 2 colour figures, accepted for publication in ApJ Letters. Version with high quality images at http://hea-www.harvard.edu/~ejos/files/N4636_hires.pd

Vibrational couplings and energy transfer pathways of water's bending mode

Yu, CC., Chiang, KY., Okuno, M. et al. Vibrational couplings and energy transfer pathways of water’s bending mode. Nat Commun 11, 5977 (2020). https://doi.org/10.1038/s41467-020-19759-

UTX mediates demethylation of H3K27me3 at muscle-specific genes during myogenesis

Polycomb (PcG) and Trithorax (TrxG) group proteins act antagonistically to establish tissue-specific patterns of gene expression. The PcG protein Ezh2 facilitates repression by catalysing histone H3-Lys27 trimethylation (H3K27me3). For expression, H3K27me3 marks are removed and replaced by TrxG protein catalysed histone H3-Lys4 trimethylation (H3K4me3). Although H3K27 demethylases have been identified, the mechanism by which these enzymes are targeted to specific genomic regions to remove H3K27me3 marks has not been established. Here, we demonstrate a two-step mechanism for UTX-mediated demethylation at muscle-specific genes during myogenesis. Although the transactivator Six4 initially recruits UTX to the regulatory region of muscle genes, the resulting loss of H3K27me3 marks is limited to the region upstream of the transcriptional start site. Removal of the repressive H3K27me3 mark within the coding region then requires RNA Polymerase II (Pol II) elongation. Interestingly, blocking Pol II elongation on transcribed genes leads to increased H3K27me3 within the coding region, and formation of bivalent (H3K27me3/H3K4me3) chromatin domains. Thus, removal of repressive H3K27me3 marks by UTX occurs through targeted recruitment followed by spreading across the gene

Morphine activates neuroinflammation in a manner parallel to endotoxin

Opioids create a neuroinflammatory response within the CNS, compromising opioid-induced analgesia and contributing to various unwanted actions. How this occurs is unknown but has been assumed to be via classic opioid receptors. Herein, we provide direct evidence that morphine creates neuroinflammation via the activation of an innate immune receptor and not via classic opioid receptors. We demonstrate that morphine binds to an accessory protein of Toll-like receptor 4 (TLR4), myeloid differentiation protein 2 (MD-2), thereby inducing TLR4 oligomerization and triggering proinflammation. Small-molecule inhibitors, RNA interference, and genetic knockout validate the TLR4/MD-2 complex as a feasible target for beneficially modifying morphine actions. Disrupting TLR4/MD-2 protein–protein association potentiated morphine analgesia in vivo and abolished morphine-induced proinflammation in vitro, the latter demonstrating that morphine-induced proinflammation only depends on TLR4, despite the presence of opioid receptors. These results provide an exciting, nonconventional avenue to improving the clinical efficacy of opioids.Xiaohui Wang, Lisa C. Loram, Khara Ramos, Armando J. de Jesus, Jacob Thomas, Kui Cheng, Anireddy Reddy, Andrew A. Somogyi, Mark R. Hutchinson, Linda R. Watkins and Hang Yi

Radio Bubbles in Clusters

We extend our earlier work on cluster cores with distinct radio bubbles, adding more active bubbles, i.e. those with Ghz radio emission, to our sample, and also investigating ``ghost bubbles,'' i.e. those without GHz radio emission. We have determined k, which is the ratio of the total particle energy to that of the electrons radiating between 10 MHz and 10 GHz. Constraints on the ages of the active bubbles confirm that the ratio of the energy factor, k, to the volume filling factor, f lies within the range 1 < k/f < 1000. In the assumption that there is pressure equilibrium between the radio-emitting plasma and the surrounding thermal X-ray gas, none of the radio lobes has equipartition between the relativistic particles and the magnetic field. A Monte-Carlo simulation of the data led to the conclusion that there are not enough bubbles present in the current sample to be able to determine the shape of the population. An analysis of the ghost bubbles in our sample showed that on the whole they have higher upper limits on k/f than the active bubbles, especially when compared to those in the same cluster. A study of the Brightest 55 cluster sample shows that 17, possibly 20, clusters required some form of heating as they have a short central cooling time, t_cool < 3 Gyr, and a large central temperature drop, T_centre/T_outer< 1/2. Of these between 12 (70 per cent) and 15 (75 per cent), contain bubbles. This indicates that the duty cycle of bubbles is large in such clusters and that they can play a major role in the heating process.Comment: 12 pages, Accepted for publication in MNRA

Effects of APETALA2 on embryo, endosperm, and seed coat development determine seed size in Arabidopsis

Arabidopsis APETALA2 (AP2) controls seed mass maternally, with ap2 mutants producing larger seeds than wild type. Here, we show that AP2 influences development of the three major seed compartments: embryo, endosperm, and seed coat. AP2 appears to have a significant effect on endosperm development. ap2 mutant seeds undergo an extended period of rapid endosperm growth early in development relative to wild type. This early expanded growth period in ap2 seeds is associated with delayed endosperm cellularization and overgrowth of the endosperm central vacuole. The subsequent period of moderate endosperm growth is also extended in ap2 seeds largely due to persistent cell divisions at the endosperm periphery. The effect of AP2 on endosperm development is mediated by different mechanisms than parent-of-origin effects on seed size observed in interploidy crosses. Seed coat development is affected; integument cells of ap2 mutants are more elongated than wild type. We conclude that endosperm overgrowth and/or integument cell elongation create a larger postfertilization embryo sac into which the ap2 embryo can grow. Morphological development of the embryo is initially delayed in ap2 compared with wild-type seeds, but ap2 embryos become larger than wild type after the bent-cotyledon stage of development. ap2 embryos are able to fill the enlarged postfertilization embryo sac, because they undergo extended periods of cell proliferation and seed filling. We discuss potential mechanisms by which maternally acting AP2 influences development of the zygotic embryo and endosperm to repress seed size

Adaptation of Arabidopsis to nitrogen limitation involves induction of anthocyanin synthesis which is controlled by the NLA gene

Plants can survive a limiting nitrogen (N) supply by developing a set of N limitation adaptive responses. However, the Arabidopsis nla (nitrogen limitation adaptation) mutant fails to produce such responses, and cannot adapt to N limitation. In this study, the nla mutant was utilized to understand further the effect of NLA on Arabidopsis adaptation to N limitation. Grown with limiting N, the nla mutant could not accumulate anthocyanins and instead produced an N limitation-induced early senescence phenotype. In contrast, when supplied with limiting N and limiting phosphorus (Pi), the nla mutants accumulated abundant anthocyanins and did not show the N limitation-induced early senescence phenotype. These results support the hypothesis that Arabidopsis has a specific pathway to control N limitation-induced anthocyanin synthesis, and the nla mutation disrupts this pathway. However, the nla mutation does not affect the Pi limitation-induced anthocyanin synthesis pathway. Therefore, Pi limitation induced the nla mutant to accumulate anthocyanins under N limitation and allowed this mutant to adapt to N limitation. Under N limitation, the nla mutant had a significantly down-regulated expression of many genes functioning in anthocyanin synthesis, and an enhanced expression of genes involved in lignin production. Correspondingly, the nla mutant grown with limiting N showed a significantly lower production of anthocyanins (particularly cyanidins) and an increase in lignin contents compared with wild-type plants. These data suggest that NLA controls Arabidopsis adaptability to N limitation by channelling the phenylpropanoid metabolic flux to the induced anthocyanin synthesis, which is important for Arabidopsis to adapt to N limitation

Desulfation of Heparan Sulfate by Sulf1 and Sulf2 Is Required for Corticospinal Tract Formation

Heparan sulfate (HS) has been implicated in a wide range of cell signaling. Here we report a novel mechanism in which extracellular removal of 6-O-sulfate groups from HS by the endosulfatases, Sulf1 and Sulf2, is essential for axon guidance during development. In Sulf1/2 double knockout (DKO) mice, the corticospinal tract (CST) was dorsally displaced on the midbrain surface. In utero electroporation of Sulf1/2 into radial glial cells along the third ventricle, where Sulf1/2 mRNAs are normally expressed, rescued the CST defects in the DKO mice. Proteomic analysis and functional testing identified Slit2 as the key molecule associated with the DKO phenotype. In the DKO brain, 6-O-sulfated HS was increased, leading to abnormal accumulation of Slit2 protein on the pial surface of the cerebral peduncle and hypothalamus, which caused dorsal repulsion of CST axons. Our findings indicate that postbiosynthetic desulfation of HS by Sulfs controls CST axon guidance through fine-tuning of Slit2 presentation