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. 2006 Dec 8;189(5):1589–1596. doi: 10.1128/JB.01151-06

TABLE 2.

Phosphotransacylase activity in cell extracts from selected strains of S. entericaa

Strain (relevant genotype) PTAC activity (μmol min−1 mg−1)b
Propionyl-PO42− Acetyl-PO42− Propionyl-PO42− preferencec
Wild type (PduL+ Pta+) 8.9 3.5 2.5
BE188 (PduL Pta+) 2.6 3.2 0.8
BE527 (PduL+ Pta) 6.0 0.4 15.0
BE291 (PduL Pta) ND ND
a

Cells were grown on NCE succinate minimal medium supplemented with 1,2-PD to ensure induction of the pdu operon.

b

PTAC assay mixtures contained 0.2 mM HS-CoA and 1 mM propionyl-PO42− or acetyl-PO42− and assay buffer. Activity was determined by monitoring the absorbance of reaction mixtures at 232 nm. ND, not detected (the lower detection limit of the assay is estimated to be 0.03 μmol min−1 mg−1).

c

Propionyl-PO42− preference = (activity with propionyl-PO42−)/(activity with acetyl-PO42−).