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. Author manuscript; available in PMC: 2023 Oct 23.
Published in final edited form as: J Am Chem Soc. 2023 Sep 21;145(39):21361–21369. doi: 10.1021/jacs.3c06354

Figure 3.

Figure 3.

Screening of potential C2 donor substrates for the AprG-catalyzed transaldolation reaction. (A) Structures of possible C2 donors. (B) Extracted ion chromatograms (EICs) at m/z 903.2035 corresponding to [M – H] for the tridinitrophenyl (DNP)-derivatives of 7, which was obtained after workup of the BtrQ/AprG reactions and then treated with 1-fluoro-2,4-dinitrobenzene (DNFB). Each EIC trace (a–f) is labeled with the compound number of the C2 donor candidate used in the assay.