We adopted a steady-state labeling strategy (2). The 13C-labeling experiment was performed with 20 mM 13C-bicarbonate or 13C-formate, respectively, supplemented into the CTFUD defined medium in addition to 14.6 mM cellobiose. For cell growth, C. thermocellum strains were inoculated into these media with a starting OD600 of 0.05. When late log-phase was reached (OD600 ∼ 0.8), 3 mL of cultures was sampled.
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