The Pseudomonas dacunhael-aspartate-beta-decarboxylase (ABDC, aspartate 4-decarboxylase, aspartate 4-carboxylyase, E.C. 4.1.1.12) is a pyridoxal-5'-phosphate (PLP)-dependent enzyme that catalyzes the beta-decarboxylation of l-aspartate to produce l-alanine and CO(2). This catalytically versatile enzyme is known to form functional dodecamers at its optimal pH and is thought to work in conjunction with an l-Asp/l-Ala antiporter to establish a proton gradient across the membrane that can be used for ATP biosynthesis. We have solved the atomic structure of ABDC to 2.35 A resolution using single-wavelength anomalous dispersion phasing. The structure reveals that ABDC oligomerizes as a homododecamer in an unknown mode among PLP-dependent enzymes and has highest structural homology with members of the PLP-dependent aspartate aminotransferase subfamily. The structure shows that the ABDC active site is very similar to that of aspartate aminotransferase. However, an additional arginine side chain (Arg37) was observed flanking the re-side of the PLP ring in the ABDC active site. The mutagenesis results show that although Arg37 is not required for activity, it appears to be involved in the ABDC catalytic cycle.
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http://dx.doi.org/10.1016/j.jmb.2009.02.055 | DOI Listing |
Int J Biol Macromol
May 2022
Department of Chemistry, College of Science, Kind Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
In this present investigation, aluminium (Al) fabricated 2-aminobenzene-1,4-dicarboxylic acid (ABDC) namely Al@ABDC metal organic frameworks (MOFs) was developed for defluoridation studies. The unique advantages of developed MOFs possess high selectivity, high porosity and enhanced surface area but the developed powder form of Al@ABDC MOFs has several limitations in field applications like slow filtration and column blockage. To prevail over these troubles, biopolymer namely chitosan (CS) supported Al@ABDC MOFs namely Al@ABDC-CS beads were developed for effective fluoride adsorption from water.
View Article and Find Full Text PDFChemistry
October 2021
WestCHEM, School of Chemistry, University of Glasgow, University Avenue, Glasgow, G12 8QQ, UK.
Photophysical studies of chromophoric linkers in metal-organic frameworks (MOFs) are undertaken commonly in the context of sensing applications, in search of readily observable changes of optical properties in response to external stimuli. The advantages of the MOF construct as a platform for investigating fundamental photophysical behaviour have been somewhat overlooked. The linker framework offers a unique environment in which the chromophore is geometrically constrained and its structure can be determined crystallographically, but it exists in spatial isolation, unperturbed by inter-chromophore interactions.
View Article and Find Full Text PDFBioorg Med Chem Lett
March 2021
College of Pharmacy, Kinjo Gakuin University, 2-1723 Omori, Moriyamaku, Nagoya, Aichi 463-8521, Japan. Electronic address:
RSC Adv
March 2020
Institute for Inorganic Chemistry, ZFM - Center for Solid State Chemistry and New Materials, Leibniz Universität Callinstr. 9 30167 Hannover Germany
A MIL-140D- framework has been used as a highly stable backbone for the introduction of 4,4'-azobenzene dicarboxylic acid (H ) solvent-assisted ligand exchange (SALE). The implemented azo groups can serve as coordination sites for copper ions. These can exchange ligands with different gases, but show a high selectivity against HS, which makes this material promising for potential sensor applications.
View Article and Find Full Text PDFNat Chem
September 2017
Department of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, UK.
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