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Chemoproteomic Identification i r e f B12-ABP Binding Proteins, Competitive Inhibition Studies, and I r e f Proteomic Analysis of Halomonas HL-48. LC-MS Proteomic Measurement and Quantitative Characterization of Halomonas Proteins Captured by the B12-ABP.

Gene Cloning and Purification of Recombinant PhrR, FolD, MetE, and MetH Proteins. Fluorescence Gel Analysis of B12-ABP Labeling of Purified FolD, MetE, MetH, and PhrR Proteins.

Genomic Reconstruction of PhrR Regulons. Measurement of Intracellular Folate and Derivatives. SI Materials and MethodsChemicals and F for Synthesis. General Methodology for Synthetic Chemistry. B12-ABP Labeling and CNB12 Competition Studies of Pure Proteins for Fluorescence Gel Analysis, and HL-48 Proteins for LC-MS Proteomic Analyses. Analytical Processing of LC-MS Data. Gene Cloning and Purification of Recombinant PhrR Protein. Gene I r e f and Purification of Recombinant FolD, MetH, and MetE Proteins.

AcknowledgmentsThis research was supported by the US Department of Energy (DOE), Office of Biological and Environmental Research (OBER), as part of BER's J Science Program. OpenUrlCrossRefPubMedDegnan PH, Barry NA, Mok KC, Taga ME, Goodman AL (2014) Human gut microbes use multiple transporters to distinguish vitamin B12 analogs i r e f compete in the gut.

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