Skip to main content
Fig. 5 | Microbial Cell Factories

Fig. 5

From: Metabolic engineering of Acremonium chrysogenum for improving cephalosporin C production independent of methionine stimulation

Fig. 5

CPC production and intracellular SAM concentration in Acppm1DM. a CPC production of Acppm1DM in the MDFA medium supplemented with varying concentrations of methionine. One half (1.6 g/L), one-fifth (0.64 g/L), one-tenth (0.32 g/L), one-twentieth (0.16 g/L) and the normal concentration of methionine (3.2 g/L) were used in the MDFA medium for fermentation. b CPC production of WT, Acppm1DM, Acppm1CM and Acppm1OE in the MDFA medium supplemented with 0.32 g/L methionine. c Intracellular SAM concentration of WT and Acppm1DM. The concentrations of methionine supplemented in the MDFA medium were 3.2 g/L and 0.32 g/L, respectively. d CPC production of Acppm1DM with addition of exogenous SAM during fermentation. 4 μM and 1 mM of SAM were added after 3 or 4 days fermentation. Acppm1DM3d, SAM was added after 3 days fermentation; Acppm1DM4d, SAM was added after 4 days fermentation. WT, the wild-type strain; Acppm1DM, the Acppm1 disruption mutant; Acppm1CM, the complemented strain of Acppm1DM with a copy of Acppm1; Acppm1OE, the Acppm1 overexpressed strain. Met, methionine. CPC production was determined by bioassays against B. subtilis 1.1630 as described in the “Methods”. Error bars represent standard deviations from three independent experiments

Back to article page