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Immobilized FhuD2 Siderophore-Binding Protein Enables Purification of Salmycin Sideromycins from Streptomyces violaceus DSM 8286.

ACS Infect Dis. 2018; 
RiveraGerry Sann M,BeamishCatherine R,WencewiczTimot
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Codon Optimization Codon-optimized fhuD2∆24 was purchased from GenScript in a pET28a vector for heterologous expression in E. coli BL21(DE3) with an N-terminal hexahistidine tag (Supplementary Tables 2,3). Get A Quote

摘要

Siderophores are a structurally diverse class of natural products common to most bacteria and fungi as iron(III)-chelating ligands. Siderophores, including trihydroxamate ferrioxamines, are used clinically to treat iron overload diseases and show promising activity against many other iron-related human diseases. Here, we present a new method for the isolation of ferrioxamine siderophores from complex mixtures using affinity chromatography based on resin-immobilized FhuD2, a siderophore-binding protein (SBP) from Staphylococcus aureus. The SBP-resin enabled purification of charge positive, charge negative, and neutral ferrioxamine siderophores. Treatment of culture supernatants from Streptomyces viol... More

关键词

affinity chromatography,desferrioxamine B,drug delivery,iron transport,metal chelation therapy,siderophore−antibiotic conju