Assessing the effect of oxygen and microbial inhibitors to optimize ferricyanide-mediated BOD assay

Methods for short-term BOD analysis (BOD_st) based on ferricyanide mediator reduction have succeeded in overcoming some problems associated with the standard BOD test analysis (BOD₅) such as long-term incubations (5 days), the need to dilute samples and low reproducibility. Here we present a bioassay where a Klebsiella pneumoniae environmental strain successfully reduces ferricyanide without de-aeration of the samples with linear BOD₅ ranges between 30 and 500 mg L⁻¹ or 30 and 200 mg L⁻¹, using glucose-glutamic acid solution (GGA) or OECD standards respectively. We further propose a new assay termination solution that allows higher reproducibility and standardization of the cell-based assay, employing formaldehyde (22.7 g L⁻¹) or other compounds in order to stop ferricyanide reduction without affecting the amperometric detection and therefore replace the centrifugation step normally used to stop microbial-driven reactions in ferricyanide-mediated bioassays. These improvements led to an accurate determination of real municipal wastewater samples.     

Imaging of the structure of the argon and neon dimer, trimer, and tetramer

We Coulomb explode argon and neon dimers, trimers, and tetramers by multiple ionization in an ultrashort 800 nm laser pulse. By measuring all momentum vectors of the singly charged ions in coincidence, we determine the ground state nuclear wave function of the dimer, trimer, and tetramer. Furthermore we retrieve the bond angles of the trimer in position space by applying a classical numerical simulation. For the argon and neon trimer, we find a structure close to the equilateral triangle. The width of the distribution around the equilateral triangle is considerably wider for neon than for argon.     

Isolation and Structural Elucidation of Armeniaspirols A–C: Potent Antibiotics against Gram‐Positive Pathogens

In an antibiotic lead discovery program, the known strain Streptomyces armeniacus DSM19369 has been found to produce three new natural products when cultivated on a malt‐containing medium. The challenging structural elucidation of the isolated compounds was achieved by using three independent methods, that is, chemical degradation followed by NMR spectroscopy, a computer‐assisted structure prediction algorithm, and X‐ray crystallography. The compounds, named armeniaspirol A–C ( 2 – 4 ), exhibit a compact, hitherto unprecedented chlorinated spiro[4.4]non‐8‐ene scaffold. Labeling experiments with [1‐¹³C] acetate, [1,2‐¹³C2] acetate, and [U‐¹³C] proline suggest a biosynthesis through a rare two‐chain mechanism. Armeniaspirols displayed moderate to high in vitro activities against Gram‐positive pathogens such as methicillin‐resistant S. aureus (MRSA) or vancomycin resistant E. faecium (VRE). As analogue 2 was active in vivo in an MRSA sepsis model, and showed no development of resistance in a serial passaging experiment, it represents a new antibiotic lead structure.     

Tellurophenes with delocalized π-systems and their extended valence adducts

The π-conjugated 2,5-substituted tellurophene compounds 2,5-bis(2-(9,9-dihexylfluorene))tellurophene (1) and 2,5-diphenyltellurophene (3) were synthesized through ring closing reactions of 1,4-substituted butadiyne. The oxidative addition of Br(2) to tellurophene compounds 1 and 3 was studied through absorption spectroscopy, NMR, electrochemistry, X-ray crystallography, and density functional theory (DFT) calculations. When Br(2) adds to the tellurium center the absorption spectrum shifts to a lower energy. From electrochemistry and DFT calculations we show that this is caused by lowering the lowest unoccupied orbital. The highest occupied orbital is also lowered, but to a lesser extent. This shift in absorption spectrum and lowering of the oxidation potential can provide a method to modify tellurophene containing materials. The two-electron oxidative addition is promising for catalyzing energy storage reactions.     

Coulomb asymmetry in strong field multielectron ionization of diatomic molecules

We measure the angular distribution of an electron emitted by a strong elliptically polarized two-color laser field from exploding doubly charged molecular nitrogen. This angular distribution is vastly different for emission of the electron from the up-field core of the molecule as compared to that from the down-field core. The emission from the down-field core leads to a slight rotation with respect to the internuclear axis in the direction expected by the Coulomb effect of the remaining ion, while, for the emission from the up-field core, this direction is inversed. Our semiclassical simulations suggest that this unexpected angular distribution is caused by an initial longitudinal momentum of the electron freed by over-the-barrier ionization above the inner barrier in the molecule. The initial kinetic energy is in the range of the potential energy of the Stark-shifted orbital above the barrier.     

Spatial imaging of the H2(+) vibrational wave function at the quantum limit

We experimentally obtained a direct image of the nuclear wave functions of H(2)(+) by dissociating the molecule via electron attachment and determining the vibrational state using the cold target recoil ion momentum spectroscopy technique. Our experiment visualizes the nodal structure of different vibrational states. We compare our results to the widely used reflection approximation and to quantum simulations and discuss the limits of position measurements in molecules imposed by the uncertainty principle.     

Normal-state hourglass dispersion of the spin excitations in FeSexTe(1-x)

We use cold neutron spectroscopy to study the low-energy spin excitations of superconducting (SC) FeSe0.4Te0.6 and essentially nonsuperconducting (NSC) FeSe0.45Te0.55. In contrast with BaFe2-x(Co,Ni)xAs2, where the low-energy spin excitations are commensurate both in the SC and normal state, the normal-state spin excitations in SC FeSe0.4Te0.6 are incommensurate and show an hourglass dispersion near the resonance energy. Since similar hourglass dispersion is also found in the NSC FeSe0.45Te0.55, we argue that the observed incommensurate spin excitations in FeSe(1-x)Tex are not directly associated with superconductivity. Instead, the results can be understood within a picture of Fermi surface nesting assuming extremely low Fermi velocities and spin-orbital coupling.     

A new ¹⁵N tracer method to determine N turnover and denitrification of Pseudomonas stutzeri

Although denitrification is one of the key processes of ecosystem N turnover, the understanding of the regulation of the denitrification pathway is still limited due to the lack of feasible methods for the quantification of N? formation. Based on the previously developed isotope pairing method, we present a new in vitro 1?N tracer method for the quantification of N? released from denitrification by bacterial cultures. The application of the new method was enabled by replacing the background air in the sample flasks with a gas mixture of He and O? with an approximately 50-fold reduced N? background (1.7% v/v), allowing for a direct and sensitive quantification of N? formation with isotope-ratio mass spectrometry after 1?N-labelling on the one hand, but leaving the method relatively insensitive to intrusion of ambient N? on the other hand. The method was tested on bacterial cultures of Pseudomonas stutzeri grown at different oxygen levels. Additionally, NO and N?O formation were determined with a chemoluminescence analyser and a gas chromatograph, respectively. Following labelling with 1?N-ammonium and 1?N-nitrate, it could be shown that P. stutzeri used ammonium preferably for biomass build-up, and nitrate preferably as electron acceptor. Between 84-107% of the total available N could be recovered. Due to the high sensitivity of the new method only low levels of 1?N tracer were necessary, minimising substrate-induced effects and making this method also an appropriate tool for the use on soil cores. By that it offers a new method for studying denitrification in terrestrial ecosystems.