Results 11 to 20 of about 78,380 (148)
The O2‐tolerant NAD+‐reducing hydrogenase (SH) from Ralstonia eutropha (Cupriavidus necator) has already been applied in vitro and in vivo for H2‐driven NADH recycling in coupled enzymatic reactions with various NADH‐dependent oxidoreductases.
Lars Lauterbach +17 more
core +1 more source
Membrane electrochemical reactors (MER) for NADH regeneration in HLADH-catalysed synthesis: comparison of effectiveness [PDF]
Two membrane electrochemical reactors(MER) were designed and applied to HLADH-catalysed reduction of cyclohexanone to cyclohexanol. The regeneration of the cofactor NADH was ensured electrochemically, using either methyl viologen or a rhodium complex as
Basséguy, Régine +2 more
core +1 more source
Unravelling the Chemolithoautotrophic Metabolism of the Carboxydotrophic Knallgas Bacterium Hydrogenophaga pseudoflava. [PDF]
Proteomics of the aerobic carboxydotroph Hydrogenophaga pseudoflava across trophic conditions revealed that an unphysiological CO concentration causes a redox imbalance and stress response. CO dehydrogenase I and the membrane‐bound hydrogenase were essential for CO and H2 oxidation, respectively, whereas the soluble hydrogenase likely supports redox ...
Grieshaber S +8 more
europepmc +2 more sources
A novel NADPH:(bound) NADP + reductase and NADH:(bound) NADP + transhydrogenase function in bovine liver catalase [PDF]
Many catalases have the shared property of containing bound NADPH and being susceptible to inactivation by their own substrate, H2O2. The presence of additional (unbound) NADPH effectively prevents bovine liver and human erythrocytic catalase from ...
KIRKMAN, Henry N. +3 more
core +3 more sources
Detection of NADH and NADPH levels in vivo identifies shift of glucose metabolism in cancer to energy production [PDF]
Profound changes in the metabolism of cancer cells have been known for almost 100 years, and many aspects of these changes have continued to be actively studied and discussed.
Shupletsov, Valery V. +15 more
core +4 more sources
Photobiocatalytic Linear Deracemization of β‐Hydroxynitriles [PDF]
Photosensitizers were screened for the oxidation of β‐hydroxynitriles under blue light irradiation, finding tetra‐n‐butyl decatungstate as the most suitable catalyst for accessing ketonitriles. Subsequently, bioreductions were carried out, leading to the identification of stereocomplementary alcohol dehydrogenases for the development of a linear ...
Filgueira S +2 more
europepmc +2 more sources
Normalised hybridisation signals of NADH dehydrogenase genes.
Solid lines: P. putida S12; dotted lines: P. putida S12ΔtrgI. ● NADH dehydrogenase (probe PS1205605_at), ♦ NADH dehydrogenase (probe PS1200059_at), ▲ NADH-quinine oxidoreductases chain A, × NADH-quinone oxidoreductases chain B, + NADH-quinone ...
Harald J. Ruijssenaars (771205) +3 more
core +1 more source
Pancreatic β-cells release insulin in response to elevation of glucose from basal (4–7 mM) to stimulatory (8–16 mM) levels. Metabolism of glucose by the β-cell results in the production of low levels of reactive oxygen intermediates (ROI), such as ...
Womack, Trayce +8 more
core +1 more source
Tools for controlled selenol delivery are crucial for exploring Se‐related biology and medicine, but compound platforms for triggerable release of CH3SeH remain lacking. Herein, we report the first general triggered platform (TD‐MSe) for efficient cyclization release of CH3SeH in live cells.
Wenfang Liang +7 more
wiley +1 more source
Objective: A poorly characterized phagocyte-type NADPH oxidase, which is reportedly NADH-rather than NADPH-dependent, is a major source of endothelial reactive oxygen species (ROS) production.
Li, J M, Shah, A M, J Li
core +1 more source

