Mononuclear molybdenum enzymes catalyze a variety of reactions that are essential in the cycling of nitrogen, carbon, arsenic, and sulfur. For decades, the structure and function of these crucial enzymes have been investigated to develop a fundamental knowledge for this vast family of enzymes and the chemistries they carry out. Therefore, obtaining abundant quantities of active enzyme is necessary for exploring this family's biochemical capability. This mini-review summarizes the methods for overexpressing mononuclear molybdenum enzymes in the context of the challenges encountered in the process. Effective methods for molybdenum cofactor synthesis and incorporation, optimization of expression conditions, improving isolation of active vs. inactive enzyme, incorporation of additional prosthetic groups, and inclusion of redox enzyme maturation protein chaperones are discussed in relation to the current molybdenum enzyme literature. This article summarizes the heterologous and homologous expression studies providing underlying patterns and potential future directions.
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http://dx.doi.org/10.1007/s00775-020-01787-y | DOI Listing |
Acc Chem Res
July 2024
State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, Dalian University of Technology, Dalian 116024, P. R. China.
Int J Mol Sci
April 2024
Division of Materials Chemistry, Ruđer Bošković Institute, Bijenička 54, 10000 Zagreb, Croatia.
This study aimed to synthesize molybdenum complexes coordinated with an aroyl hydrazone-type ligand (HL), which was generated through the condensation of 2-hydroxy-5-nitrobenzaldehyde with benzhydrazide. The synthesis yielded two types of mononuclear complexes, specifically [MoO(L)(MeOH)] and [MoO(L)(HO)], as well as a bipyridine-bridged dinuclear complex, [(MoO(L))(4,4'-bpy)]. Those entities were thoroughly characterized using a suite of analytical techniques, including attenuated total reflectance infrared spectroscopy (IR-ATR), elemental analysis (EA), thermogravimetric analysis (TGA), and single-crystal X-ray diffraction (SCXRD).
View Article and Find Full Text PDFMolecules
February 2024
Department of Chemistry, Graduate School of Science, Osaka Metropolitan University, Sumiyoshi-ku, Osaka 558-8585, Japan.
The reaction of molybdenum complexes with a tris(pyrazolyl)borate ligand (EtN[TpMo(CO)] and EtN[Tp*Mo(CO)] (Tp = hydridotris(pyrazolyl)borate, Tp* = hydridotris(3,5-dimethylpyrazolyl)borate)) and InBr at a 1:1 molar ratio afforded molybdenum-indane complexes (EtN[TpMo(CO)(InBr)] and EtN[Tp*Mo(CO)(InBr)] ). In addition, tungsten-indane complexes, EtN[TpW(CO)(InBr)] and EtN[Tp*W(CO)(InBr)] , were obtained by the reaction of corresponding tungsten complexes. Complex reacted with HO to form the hydrido complex Tp*W(CO)H, in which the W-In bond was cleaved.
View Article and Find Full Text PDFChemistry
April 2024
Bioinorganic Chemistry, Institute of Biochemistry, University of Greifswald, 17489, Greifswald, Germany.
Based on their general spacial flexibility, their Lewis and Brønsted basicity, and ability to mimic second sphere effects the 1,5-diaza-3,7-diphosphacyclooctane ligand family and their complexes have regained substantial scientific interest. It was now possible to structurally analyze a recently reported member of this family with p-tolyl and t-butyl substituents on P and N, respectively, (P N ). Notably, the ligand crystallizes with a 'twisted' backbone.
View Article and Find Full Text PDFInt J Mol Sci
January 2024
Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, 10000 Zagreb, Croatia.
A series of polynuclear, dinuclear, and mononuclear Mo(VI) complexes were synthesized with the hydrazonato ligands derived from 5-methoxysalicylaldehyde and the corresponding hydrazides (isonicotinic hydrazide (HL), nicotinic hydrazide (HL), 2-aminobenzhydrazide (HL), or 4-aminobenzhydrazide (HL)). The metallosupramolecular compounds obtained from non-coordinating solvents, [MoO(L)] ( and ) and [MoO(L)] ( and ), formed infinite structures and metallacycles, respectively. By blocking two coordination sites with cis-dioxo ligands, the molybdenum centers have three coordination sites occupied by the donor atoms from the rigid hydrazone ligands and one by the N atom of pyridyl or amine-functionalized ligand subcomponents from the neighboring Mo building units.
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