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para-Aminobenzoic Acid (pABA) HPLC Assay Protocol

Purpose

To test for para-aminobenzoic acid levels in E. coli overexpressing the pABA synthesis genes pabA and pabB.

Materials

• Buffer A: 0.1% formic acid in H2O
• Buffer B: 0.1% formic acid in MeOH
• A high performance liquid chromatography machine.
• Column size ?

Procedure

Sample Prep

1. Centrifuge the cell culture max speed, 10 minutes.
2. Separate pellet from supernatant.
3. Resuspend the pellet in 1mL 0.1M Tris-HCl buffer
4. Sonicate the resuspended pellet for 1 minute, alternating between 0 and 12Hz.
5. Filter sterilize the cell lysate and the supernatant.
6. Load 500uL of each into the HPLC.

HPLC Method

1. Injection volume was 20uL, column temperature was kept at 40°C.
2. Flush the lines individually with Buffer A and B for two minutes each, flush the column with 92% A, 8% B for 10 minutes.
3. From the source: "The starting eluent was 92% A mixed with 8% B; the proportion of B was increased linearly to 50% in 7 min, then to 100% in 3 min. The mobile phase was then immediately adjusted to its initial composition and held for 4 min in order to re-equilibrate the column."
4. We found the retention time of pABA to be 4.9-5.0 minutes, however the literature states the retention time as 6.0 minutes.

pABA eluting at 4.9-5.0 minutes for the standard curve.

Standard Curve

1. Run 1:3 dilutions starting from 10ug/ml pABA in wild type bacterial lysate using the same protocol to generate a linear standard (see below).

pABA HPLC standard curve with 1:3 dilutions starting from 10ug/ml pABA. The integral of the peak is plotted against the known pABA amount.

Sources