Chemoenzymatic Syntheses of Fluorine-18-Labeled Disaccharides from [F] FDG Yield Potent Sensors of Living Bacteria .

Chemoenzymatic techniques have been applied extensively to pharmaceutical development, most effectively when routine synthetic methods fail. The regioselective and stereoselective construction of structurally complex glycans is an elegant application of this approach that is seldom applied to positron emission tomography (PET) tracers. We sought a method to dimerize 2-deoxy-[F]-fluoro-d-glucose ([F]FDG), the most common tracer used in clinical imaging, to form [F]-labeled disaccharides for detecting microorganisms based on their bacteria-specific glycan incorporation. When [F]FDG was reacted with β-d-glucose-1-phosphate in the presence of maltose phosphorylase, the α-1,4- and α-1,3-linked products 2-deoxy-[F]-fluoro-maltose ([F]FDM) and 2-deoxy-2-[F]-fluoro-sakebiose ([F]FSK) were obtained. This method was further extended with the use of trehalose (α,α-1,1), laminaribiose (β-1,3), and cellobiose (β-1,4) phosphorylases to synthesize 2-deoxy-2-[F]fluoro-trehalose ([F]FDT), 2-deoxy-2-[F]fluoro-laminaribiose ([F]FDL), and 2-deoxy-2-[F]fluoro-cellobiose ([F]FDC). We subsequently tested [F]FDM and [F]FSK , showing accumulation by several clinically relevant pathogens including and , and demonstrated their specific uptake Both [F]FDM and [F]FSK were stable in human serum with high accumulation in preclinical infection models. The synthetic ease and high sensitivity of [F]FDM and [F]FSK to including methicillin-resistant (MRSA) strains strongly justify clinical translation of these tracers to infected patients. Furthermore, this work suggests that chemoenzymatic radiosyntheses of complex [F]FDG-derived oligomers will afford a wide array of PET radiotracers for infectious and oncologic applications.