Skip to main content
. 2015 May 4;16(9):987–999. doi: 10.1111/mpp.12254

Figure 2.

figure

Defects of the ΔareA mutant in response to different nitrogen sources. (A) Cultures of the wild‐type strain PH‐1 and ΔareA mutant grown on complete medium (CM) with 50 mm sodium nitrate (NO3 –), glutamate (GLU) or glutamine (GLN) and 5 or 50 mm ammonium phosphate (NH4 +) as the nitrogen source. (B) Quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR) assays of the nitrate (FGSG_01947) and nitrite (FGSG_08402) reductase genes in PH‐1 and ΔareA mutant grown under nitrogen starvation (NS) and ammonium suppression (AS; arbitrarily set to 1) conditions.