Angewandte Chemie International Edition, EarlyView.The synergistic interplay of electricity, light and earth‐abundant, nontoxic iron catalysis allowed for the efficient recycling of post‐consumer polymers into value‐added products. This robust depolymerization strategy was viable on multigram‐scale, where the cathodic hydrogen evolution reaction presents an attractive opportunity for a green hydrogen ...
Maxime Hourtoule +5 more
wiley +1 more source
Trapping the substrate radical of heme synthase AhbD
Frontiers in ChemistryThe heme synthase AhbD catalyzes the last step of the siroheme-dependent heme biosynthesis pathway, which is operative in archaea and sulfate-reducing bacteria.
Lorenz Heidinger +3 more
doaj +1 more source
The PEP—pyruvate—oxaloacetate node as the switch point for carbon flux distribution in bacteria: We dedicate this paper to Rudolf K. Thauer, Director of the Max-Planck-Institute for Terrestrial Microbiology in Marburg, Germany, on the occasion of his 65th birthday [PDF]
, 2017 In many organisms, metabolite interconversion at the phosphoenolpyruvate (PEP)-pyruvate-oxaloacetate node involves a structurally entangled set of reactions that interconnects the major pathways of carbon metabolism and thus, is responsible for the ...
Eikmanns, Bernhard J., Sauer, Uwe
core
Structure and functional characterization of pyruvate decarboxylase from Gluconacetobacter diazotrophicus [PDF]
, 2014 BACKGROUND: Bacterial pyruvate decarboxylases (PDC) are rare. Their role in ethanol production and in bacterially mediated ethanologenic processes has, however, ensured a continued and growing interest.
A Bjork +83 more
core +2 more sources
Kinetic evaluation of human cloned coproporphyrinogen oxidase using a ring isomer of the natural substrate [PDF]
, 2005 Background: The enzyme coproporphyrinogen oxidase (copro\u27gen oxidase) converts coproporphyrinogen-Ill (GIII) to protoporphyrinogen-IX via an intermediary monovinyl porphyrinogen. The A ring isomer coproporphyrinogen-IV (C-IV) has previously been shown
Cooper, Christopher L +2 more
core +1 more source
Asparagine Decarboxylation by Lipid Oxidation Products in Model Systems
Journal of Agricultural and Food Chemistry, 2010 The decarboxylation of asparagine in the presence of alkanals, alkenals, and alkadienals, among other lipid derivatives, was studied in an attempt to understand the reaction pathways by which some lipid oxidation products are able to convert asparagine into acrylamide.
Hidalgo, Francisco J. +3 more
openaire +3 more sources
The role of remote flavin adenine dinucleotide pieces in the oxidative decarboxylation catalyzed by salicylate hydroxylase. [PDF]
Bioorg Chem, 2022 Pereira MS +4 more
europepmc +1 more source
Asia-Pacific Journal of Chemical Engineering, EarlyView.ABSTRACT Carbon materials synthesized from biomass are promising candidates for supercapacitor electrodes. Various activation processes for developing carbon materials with high surface areas have been investigated. Here, a manganese monoxide (MnO)–porous‐activated carbon (AC) composite was fabricated via the chemical activation of coconut shell by the
Seung‐Heon Ryu +3 more
wiley +1 more source
A mild oxidative decarboxylation of carbohydrate acids
Tetrahedron Letters, 1997 4 pages, 1 table, 1 scheme. The oxidative decarboxylation of carbohydrate uronic or ulosonic acids with simultaneous replacement by an acetoxy group has been accomplished using the (diacetoxyiodo)benzene and iodine system under mild conditions. A general synthesis of derivatives of tetrodialdoses, and pentodialdoses in furanose or pyranose form is ...
Francisco, Cosme G. +2 more
openaire +2 more sources