Iron Isotope Fractionation during Fe(II) Oxidation Mediated by the Oxygen-Producing Marine Cyanobacterium Synechococcus PCC 7002

In this study, we couple iron isotope analysis to microscopic and mineralogical investigation of iron speciation during circumneutral Fe(II) oxidation and Fe(III) precipitation with photosynthetically produced oxygen. In the presence of the cyanobacterium Synechococcus PCC 7002, aqueous Fe(II) (Fe(II)aq) is oxidized and precipitated as amorphous Fe(III) oxyhydroxide minerals (iron precipitates, Feppt), with distinct isotopic fractionation (ε56Fe) values determined from fitting the δ56Fe(II)aq (1.79‰ and 2.15‰) and the δ56Feppt (2.44‰ and 2.98‰) data trends from two replicate experiments. Additional Fe(II) and Fe(III) phases were detected using microscopy and chemical extractions and likely represent Fe(II) and Fe(III) sorbed to minerals and cells. The iron desorbed with sodium acetate (FeNaAc) yielded heavier δ56Fe compositions than Fe(II)aq. Modeling of the fractionation during Fe(III) sorption to cells and Fe(II) sorption to Feppt, combined with equilibration of sorbed iron and with Fe(II)aq using published fractionation factors, is consistent with our resulting δ56FeNaAc. The δ56Feppt data trend is inconsistent with complete equilibrium exchange with Fe(II)aq. Because of this and our detection of microbially excreted organics (e.g., exopolysaccharides) coating Feppt in our microscopic analysis, we suggest that electron and atom exchange is partially suppressed in this system by biologically produced organics. These results indicate that cyanobacteria influence the fate and composition of iron in sunlit environments via their role in Fe(II) oxidation through O2 production, the capacity of their cell surfaces to sorb iron, and the interaction of secreted organics with Fe(III) minerals

Multi-channel Nonlinearity Compensation of 128-Gb/s PDM-QPSK Signals in Dispersion-Managed Transmission Using Dispersion-Folded Digital Backward Propagation

We demonstrate nonlinearity compensation of 37.5-GHz-spaced 128-Gb/s PDM-QPSK signals using dispersion-folded digital-backward-propagation and a spectrally-sliced receiver that simultaneously receives three WDM signals, showing mitigation of intra-channel and inter-channel nonlinear effects in a 2560-km dispersion-managed TWRS-fiber link. Intra-channel and adjacent inter-channel nonlinear compensation gains when WDM channels are fully populated in the C-band are estimated based on the GN-model

Differences in the high-temperature tolerance of Aphis craccivora (Hemiptera: Aphididae) on cotton and soybean: Implications for ecological niche switching among hosts

To forecast the effects of climate change and extreme temperature events on insect population dynamics, the high-temperature tolerance of insects must be taken into account. We compared the life-history characteristics of cowpea aphid (Aphis craccivora Koch) across different temperature regimes on two different host plants, soybean (a preferred host) and cotton (a non-preferred host). Most demographic parameters were superior for the aphid on soybean than on cotton. Temperatures affected aphid development more on cotton than on soybean. The intrinsic rate of increase, reproduction rate, number of progeny per adult, and longevity were significantly higher on soybean than on cotton for the same temperature regime. Temperatures that fluctuated to extreme levels caused a rapid decline in each of these parameters for aphids fed on cotton, but not for those fed on soybean. To our knowledge, this is the first report to note that the high-temperature tolerance of A. craccivora is host-specific (cotton vs. soybean). Our findings may partly explain the observed niche switching of the cowpea aphid (Aphis craccivora) from cotton to soybean at the beginning of summer when the temperature goes up in the Xinjiang cotton-growing zone (Northwest China). This host mediation of high-temperature tolerance in aphids should be taken into account when modeling population dynamics under the influence of global warming, host adaptation, and the risk analysis of alien pest invasions

Broadly neutralizing anti-HIV-1 antibodies disrupt a hinge-related function of gp41 at the membrane interface

A vaccine capable of stimulating protective antiviral antibody responses is needed to curtail the global AIDS epidemic caused by HIV-1. Although rarely elicited during the course of natural infection or upon conventional vaccination, the membrane-proximal ectodomain region (MPER) of the HIV-1 glycoprotein of Mr 41,000 (gp41) envelope protein subunit is the target of 3 such human broadly neutralizing antibodies (BNAbs): 4E10, 2F5, and Z13e1. How these BNAbs bind to their lipid-embedded epitopes and mediate antiviral activity is unclear, but such information might offer important insight into a worldwide health imperative. Here, EPR and NMR techniques were used to define the manner in which these BNAbs differentially recognize viral membrane-encrypted residues configured within the L-shaped helix–hinge–helix MPER segment. Two distinct modes of antibody-mediated interference of viral infection were identified. 2F5, like 4E10, induces large conformational changes in the MPER relative to the membrane. However, although 4E10 straddles the hinge and extracts residues W672 and F673, 2F5 lifts up residues N-terminal to the hinge region, exposing L669 and W670. In contrast, Z13e1 effects little change in membrane orientation or conformation, but rather immobilizes the MPER hinge through extensive rigidifying surface contacts. Thus, BNAbs disrupt HIV-1 MPER fusogenic functions critical for virus entry into human CD4 T cells and macrophages either by preventing hinge motion or by perturbing MPER orientation. HIV-1 MPER features important for targeted vaccine design have been revealed, the implications of which extend to BNAb targets on other viral fusion proteins