4.4 Review

Functional mononuclear molybdenum enzymes: challenges and triumphs in molecular cloning, expression, and isolation

Journal

JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
Volume 25, Issue 4, Pages 547-569

Publisher

SPRINGER
DOI: 10.1007/s00775-020-01787-y

Keywords

Molybdenum; Pterin; Xanthine oxidase family; Sulfite oxidase family; Dimethyl sulfoxide reductase family

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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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