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Fig. 4 | Biotechnology for Biofuels

Fig. 4

From: Production of the biocommodities butanol and acetone from methanol with fluorescent FAST-tagged proteins using metabolically engineered strains of Eubacterium limosum

Fig. 4

Fluorescence intensity of recombinant E. limosum strains grown on methanol (100 mM) in presence of the fluorogen TFLime. a OD600 and fluorescence intensity of E. limosum [pMTL83251], b E. limosum [pMTL83251_PthlA_FAST], c E. limosum [pMTL83251_PbgaL_FAST], and d E. limosum [pMTL83251_PbgaL_tdFAST2] were monitored. Gene expression of E. limosum [pMTL83251_PbgaL_FAST] and E. limosum [pMTL83251_PbgaL_tdFAST2] was either induced by lactose or non-induced. Time of induction with lactose is indicated with the vertical dotted line. n=3, error bars show standard deviation. e Genetic maps of plasmids representing pMTL83251_PthlA_FAST (top), pMTL83251_PbgaL_FAST (middle), and pMTL83251_PbgaL_tdFAST2 (bottom). Fluorescence during growth of cells harboring respective plasmids are shown in panel b, c, and d, respectively. f Maximal fluorescence intensity of recombinant E. limosum strains in the presence of the fluorogen TFLime or TFCoral. Mean fluorescence was determined during stationary growth phase at an OD600 of ~ 1.5, n = 3, error bars show standard deviation. n = 3

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