Direct observation of molecular preorganization for chirality transfer on a catalyst surface

The chemisorption of specific optically active compounds on metal surfaces can create catalytically active chirality transfer sites. However, the mechanism through which these sites bias the stereoselectivity of reactions (typically hydrogenations) is generally assumed to be so complex that continued progress in the area is uncertain. We show that the investigation of heterogeneous asymmetric induction with single-site resolution sufficient to distinguish stereochemical conformations at the submolecular level is finally accessible. A combination of scanning tunneling microscopy and density functional theory calculations reveals the stereodirecting forces governing preorganization into precise chiral modifier-substrate bimolecular surface complexes. The study shows that the chiral modifier induces prochiral switching on the surface and that different prochiral ratios prevail at different submolecular binding sites on the modifier at the reaction temperature.     

Galileo infrared imaging spectroscopy measurements at venus

During the 1990 Galileo Venus flyby, the Near Infaied Mapping Spectrometer investigated the night-side atmosphere of Venus in the spectral range 0.7 to 5.2 micrometers. Multispectral images at high spatial resolution indicate substanmial cloud opacity variations in the lower cloud levels, centered at 50 kilometers altitude. Zonal and meridional winds were derived for this level and are consistent with motion of the upper branch of a Hadley cell. Northern and southern hemisphere clouds appear to be markedly different. Spectral profiles were used to derive lower atmosphere abundances of water vapor and other species.     

Predominance of Dehalococcoides in the presence of different sulfate concentrations

Urban stormwater runoff is contaminated by nutrients that wash off of roadways, parking lots and lawns during storms. In-ground permeable filter systems that consist of carefully selected filter material have the potential to remove these nutrients from the run-off. In this paper, four filter materials, calcite, zeolite, sand and iron filings, were investigated using laboratory batch tests to evaluate their efficiency in the removal of nitrate and phosphate from the simulated stormwater at different initial concentrations under the same 24-h exposure time period. The range of removal for nitrate was from 39 % to 65 % for calcite, from 42 % to 77 % for zeolite, from 40 % to 70 % for sand, and from 74 % to 100 % for iron filings. The removal of phosphate ranged from 35 % to 41 % for calcite, 59 % to 100 % for zeolite, 49 % to 100 % for sand, and 73 % to 100 % for iron filings. The removal of nitrate is mainly attributed to electrostatic adsorption, except when iron filings were used as a filter material where additional processes such as electrochemical reduction, ligand complexation and precipitation may have contributed to the higher nitrate removal. Phosphate removal is also attributed to electrostatic adsorption in all filter materials; however, at higher phosphate concentrations, the precipitation process may be the dominant process for all of the filter materials except calcite. The Langmuir and Freundlich isotherms fitted the observed nonlinear adsorption results, but the mechanism of removal of phosphate changed from adsorption to precipitation at concentrations higher than 1 mg/l in zeolite, sand, and iron filings; therefore, the adsorption models are valid below this concentration limit. A typical application of these batch adsorption test results is presented in the design of a field in-ground permeable filter system.     

Correction to: Cacao,copoazu and macambo: Exploring Theobroma diversity in smallholder agroforestry systems of the Peruvian Amazon

Agroforestry Systems - In the original publication of the article, the article title was incorrectly published.     

Enzymes without borders: mobilizing substrates, delivering products

Many cellular reactions involve both hydrophobic and hydrophilic molecules that reside within the chemically distinct environments defined by the phospholipid-based membranes and the aqueous lumens of cytoplasm and organelles. Enzymes performing this type of reaction are required to access a lipophilic substrate located in the membranes and to catalyze its reaction with a polar, water-soluble compound. Here, we explore the different binding strategies and chemical tricks that enzymes have developed to overcome this problem. These reactions can be catalyzed by integral membrane proteins that channel a hydrophilic molecule into their active site, as well as by water-soluble enzymes that are able to capture a lipophilic substrate from the phospholipid bilayer. Many chemical and biological aspects of this type of enzymology remain to be investigated and will require the integration of protein chemistry with membrane biology.     

Wide Range Applications of Spirulina: From Earth to Space Missions

Spirulina is the most studied cyanobacterium species for both pharmacological applications and the food industry. The aim of the present review is to summarize the potential benefits of the use of Spirulina for improving healthcare both in space and on Earth. Regarding the first field of application, Spirulina could represent a new technology for the sustainment of long-duration manned missions to planets beyond the Lower Earth Orbit (e.g., Mars); furthermore, it could help astronauts stay healthy while exposed to a variety of stress factors that can have negative consequences even after years. As far as the second field of application, Spirulina could have an active role in various aspects of medicine, such as metabolism, oncology, ophthalmology, central and peripheral nervous systems, and nephrology. The recent findings of the capacity of Spirulina to improve stem cells mobility and to increase immune response have opened new intriguing scenarios in oncological and infectious diseases, respectively.