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. Author manuscript; available in PMC: 2017 Jul 1.
Published in final edited form as: Plasmid. 2016 May 24;86:1–6. doi: 10.1016/j.plasmid.2016.05.001

Fig. 3.

Fig. 3

Growth analysis and complementation of S. enterica acs phenotype. S.e. acs+ was cloned into pCV1-pCV3 and transformed into a acs strain to assess the effectiveness of the vectors. Cells were grown in NCE medium with acetate (10 mM) and transcription of acs+ in each vector was induced with L(+)-arabinose (250 μM). Growth curves were obtained using a microplate reader (BioTek Instruments).