Skip to main content
. Author manuscript; available in PMC: 2011 Feb 2.
Published in final edited form as: Biochemistry. 2010 Feb 2;49(4):718–726. doi: 10.1021/bi901890a

Fig. 6.

Fig. 6

Growth of strains JWC280 (ΔfabA ΔfadA::cml ΔfadIJ::kan) and GRT23 (ΔfabB Δcfa::kan) carrying the AasS encoding plasmid pYFJ85 in the presence or absence of cis-5-dodecenoic acid (0.5 mg/ml from Aldrich) and in the presence or absence of arabinose (0.2%). The LB plates were incubated for three days at 37oC. The plates are divided into halves by a wall. Both strains are derivatives of strain BW25111 (34) and were constructed by phage λ Red-mediated recombination and transduction (34). None of these media supported detectable growth of the same strains carrying the vector plasmid pBAD24 in place of pYFJ85 (data not shown