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. 2013 Feb 20;8(2):e56529. doi: 10.1371/journal.pone.0056529

Table 3. FepABC role in heme acquisition.

Growth halo diameter (mm)
Strain name Relevant mutation 50 µM 10 µM 5 µM 1 µM
SET 535 none 28±2 20±2 14±2 12±2
SET 536 ΔyfeX::Apra 19±2 15±2 ndg ndg
SET 537 ΔefeUOB::Cm 19±2 13±2 ndg ndg
SET 538 ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 538 (pMD1) ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 538 (pMD1-fepB) ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 538 (pMD1-fepA) ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 538 (pMD1-fepAB) ΔyfeX::ApraΔefeUOB::Cm 25±2 22±2 17±2 11±2
SET 538 (pMD1-fepABC) ΔyfeX::ApraΔefeUOB::Cm 23±2 22±2 17±2 11±2
SET 538 (pSU19-fepB-6His), ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 538 (pSU19-fepB-6His)(pBAD24-fepA) ΔyfeX::ApraΔefeUOB::Cm 25±2 22±2 17±2 11±2
SET 538 (pMD1-fepAAkiA-B) ΔyfeX::ApraΔefeUOB::Cm 25±2 22±2 17±2 11±2
SET 538 (pBAD24-efeB) ΔyfeX::ApraΔefeUOB::Cm 17±2 15±2 ndg ndg
SET 538 (pBAD24-efeB)(pDIA561-efeO) ΔyfeX::ApraΔefeUOB::Cm 20±2 19±2 17±2 14±2
SET 538 (pMD1-fepB)(pDIA561-efeO) ΔyfeX::ApraΔefeUOB::Cm ndg ndg ndg ndg
SET 539 (pMD1-fepAB) ΔefeUOB::CmΔdppF::Km ndg ndg ndg ndg
SET 539(pMD1- fepABC) ΔefeUOB::CmΔdppF::Km ndg ndg ndg ndg

(a) ndg: no detectable growth around wells.

Names of strains and plasmid-borne complementing genes carried on pDIA561, pBAD24 and pMD1 are indicated in the first column. Aliquots of 50 µl of bovine hemoglobin at various concentrations calculated on the basis of the heme monomer were provided in wells punched into solidified agar. Plates were incubated for 48 h at 37°C and the growth halo diameter in mm around the wells was measured. All experiments were repeated three times.