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. 1997 May 27;94(11):5882–5887. doi: 10.1073/pnas.94.11.5882

Table 3.

Siderophore production by urbs1 gene disruption mutant UMC015 transformed with plasmid containing epitope-tagged wild-type urbs1 (pAN15) and in vitro mutated urbs1 alleles (pAKR350L and pAKR494L) under low and high iron conditions

Strain Low iron High iron LI/HI
UMC015/pAN15 0.12  ±  0.04* 0.02  ±  0.00 6
UMC015/pAKR350L 0.12  ±  0.01 0.02  ±  0.00 6
UMC015/pAKR494L 0.17  ±  0.02 0.13  ±  0.02 1.3

Cells were grown for 48 h at 28°C in low iron medium with or without 10 μM FeSO4. Siderophore production was determined by the ferric perchlorate assay as described. Values were normalized to a cell growth of OD600 = 1.0. LI, low iron; HI, high iron. 

*

Means of three replications ± SE.