Results 31 to 40 of about 1,700 (151)
Rational Redesign of the 4-Chlorobenzoate Binding Site of 4-Chlorobenzoate: Coenzyme A Ligase for Expanded Substrate Range,, [PDF]
Environmental aromatic acids are transformed to chemical energy in bacteria that possess the requisite secondary pathways. Some of these pathways rely on the activation of the aromatic acid by coenzyme A (CoA) thioesterification catalyzed by an aromatic acid: CoA ligase.
Rui, Wu +4 more
openaire +2 more sources
2,3-Diaminopyridinium 3-chlorobenzoate–3-chlorobenzoic acid (1/1)
The asymmetric unit of the title compound, C5H8N3+·C7H4ClO2−·C7H5ClO2, contains an ion pair and a 3-chlorobenzoic acid molecule. In the cation, the pyridine N atom is protonated. In the crystal, the components are connected via N—H...O, O—H...O and C—H...O hydrogen bonds, thereby forming sheets ...
Madhukar Hemamalini +2 more
openaire +1 more source
Reduction of 3-chlorobenzoate, 3-bromobenzoate, and benzoate to corresponding alcohols by Desulfomicrobium escambiense, isolated from a 3-chlorobenzoate-dechlorinating coculture [PDF]
An anaerobic bacterial coculture which dechlorinated 3-chlorobenzoate (3CB) to benzoate was obtained by single-colony isolation from an anaerobic bacterial consortium which completely degraded 3CB in defined medium. Of 29 additional halogenated aromatic compounds tested, the coculture removed the meta halogen from 2,3- and 2,5-dichlorobenzoate, 3 ...
B R, Genthner +2 more
openaire +2 more sources
Substrate‐Based Ligand Design for Phenazine Biosynthesis Enzyme PhzF
The isomerase PhzF, a critical enzyme in the biosynthesis of the Pseudomonas aeruginosa virulence factor pyocyanin, was investigated as a pathoblocker target. Structures of the two distinct enzyme conformations provide insights for PhzF‐inhibitor development.
Janosch Baumgarten +6 more
wiley +1 more source
Enhancement of co-metabolism of chlorobenzoates by the co-substrate enrichment technique.
Chlorinated benzoates were degraded by bacteria contained in an activated sludge inoculum by a co-metabolic mechanism. This decomposition began after an initial lag period of 4 days and accounted for 63 to 69% degradation in 28 days.
R. Horvath
semanticscholar +1 more source
Metal‐Free Ammonia Borane‐Catalyzed Hydroboration of Lactones and Esters to Alcohols
Ammonia borane (NH3BH3) serves as an easy‐to‐handle and efficient pre‐catalyst for the hydroborative cleavage of lactones and esters with HBPin (Pin=pinacol). The reactions proceed under mild conditions, do not require any additional external stimuli, can be performed under solvent‐free conditions in air.
Azamat Yessengazin +4 more
wiley +1 more source
S. Samsuar +5 more
semanticscholar +1 more source
Curcuma Longa: Nutraceutical Use and Association With Nanotechnology
Curcumin, a natural origin compound, is increasingly gaining prominence in the scientific community for its various benefits for human health, being considered a hope for many patients. Therefore, this review seeks to update and compile important points, from its cultivation to human application, including its association with nanotechnology, an ...
Gabriela Corrêa Carvalho +5 more
wiley +1 more source
Decarboxylative C(sp2)−C(sp3) bond formation using a metallaphotoredox approach is a key method for rapidly building molecular complexity. In this work, we demonstrate that graphitic carbon nitride, a heterogeneous semiconductor, can act as a suitable photocatalyst to induce decarboxylative bond formation.
Florian Lukas +8 more
wiley +1 more source
This review aims to provide an overview of the synthetic methodologies with reduced environmental impact developed over the last 25 years for phthalocyanine synthesis, relating them to the Environmental factor (E‐factor), a key metric in green chemistry that allows for a rapid, effective, and versatile evaluation of the quantity of waste produced ...
Gloria Zanotti +2 more
wiley +1 more source

