Chemiosmotic Energy Conservation in : Proton Translocation Driven by Aerobic Respiration, Denitrification, and Photosynthetic Light Reaction.

is an aerobic anoxygenic phototroph and able to utilize light energy to support its aerobic energy metabolism. Since the cells can also grow anaerobically with nitrate and nitrite as terminal electron acceptor, we were interested in how the cells profit from photosynthesis during denitrification and what the steps of chemiosmotic energy conservation are. Therefore, we conducted proton translocation experiments and compared O, NO, and NO respiration during different light regimes and in the dark.

Propidium ion enters viable cells with high membrane potential during live-dead staining.

Live-dead staining with propidium iodide can give erroneous results for bacteria showing high membrane potentials. We observed uptake of propidium ions across intact cell membranes for Dinoroseobacter shibae and Bacillus subtilis. Apparently, a high membrane potential facilitates breakthrough of the double-charged propidium ion and can mark viable cells as dead.

Boosted Membrane Potential as Bioenergetic Response to Anoxia in .

DFL 12 is a metabolically versatile member of the world-wide abundant Roseobacter clade. As an epibiont of dinoflagellates is subjected to rigorous changes in oxygen availability. It has been shown that it loses up to 90% of its intracellular ATP when exposed to anoxic conditions.

Isolation and characterization of the ejectisomes of the prasinophyte Pyramimonas grossii.

For the first time, ejectisome-enriched fractions were isolated from the marine prasinophyte Pyramimonas grossii. Transmission electron microscopy revealed that most of the ejectisomes were discharged and formed long, spirally twisted filaments. Some ejectisomes were still fully or partly furled.

Effects of common antitussive drugs on the hERG potassium channel current.

A common over-the-counter (OTC) non-opioid antitussive drug, clobutinol, was recently withdrawn from the market due to its potential to induce cardiac arrhythmias by a blockade of the potassium channel coded by the human ether-à-go-go-related gene (hERG). In this study, we investigated the effects of a number of antitussive compounds on the hERG ion channel current using patch-clamp electrophysiology, and compared the effects to that of clobutinol. The compounds clobutinol, pentoxyverine, dextromethorphan, and codeine inhibited the outward current in hERG transfected cells with half-maximal inhibition concentrations (IC50) of 1.

Investigation of 3 industry-wide applied storage conditions for compound libraries.

The appropriate storage conditions for a compound file are a crucial factor for the success of drug discovery projects. In this study, 778 highly diverse compounds dissolved in 100% DMSO were stored under 3 industry-wide accepted storage conditions, and the compound integrity was monitored for a period of 6 months. The storage conditions selected were (1) under argon at +15 degrees C, (2) under argon at -20 degrees C, and (3) under ambient atmosphere at -20 degrees C.

Identification of novel Kv1.3 blockers using a fluorescent cell-based ion channel assay.

A functional cell-based assay was developed using a generic proprietary assay protocol, based on a membrane-potential sensitive dye, for the identification of small-molecule antagonists against the Kv1.3 potassium ion channel. A high-throughput screen (HTS) was subsequently performed with 20,000 compounds from the Evotec library, preselected using known small molecule antagonists for both sodium and potassium ion channels.