In order to define appropriate experimental conditions for the pH shift, growth tests in Vincent minimal medium were carried out by varying the pH from 5.5 to 7.0 in 0.25 increments. It turned out that S. meliloti 1021 is not able

to grow at pH 5.5 while above pH 6.0 only minor deviations from the growth curve at pH 7.0 occurred (data not shown). At pH 5.75 S. meliloti 1021 showed a reduced growth rate, but the cell titer counts documented that this pH was not yet lethal (data not shown). The aim of this study was to identify genes of S. meliloti that directly respond to changes of the environmental P505-15 chemical structure pH, the transcriptional short term response within the first hour after a pH change was therefore the focus of our interest. In a time course experiment the global gene expression of S. meliloti cells exposed Selleck Silmitasertib to a pH change from 7.0 to 5.75 was compared

to the gene expression of untreated cells. To ensure identical conditions and treatment S. meliloti 1021 cells were grown in VMM at pH 7.0 until an o.D.580 of 0.8 was reached (Fig. 1), subsequently the culture was split in two and centrifuged. After centrifugation of the split cultures, the used growth medium was decanted and exchanged by fresh VMM adjusted to pH 5.75 (as testing condition) and to pH 7.0 (as reference), respectively. All manipulation steps were carried out very gently by using pre-warmed equipment and material to avoid any unwanted influences on the cells. The growth curves show the effect of the lowered pH on the growth of the S. meliloti 1021 culture (Fig. 1). The culture that was shifted to pH 5.75 grew slower than the pH 7.0 culture. For the duration of the time course experiment, the pH value of both cultures did not change.

At later time points an alkalisation of the growth medium could be observed for the low pH culture (data not shown). Figure 1 Growth of S. meliloti 1021 before and after a shift to low pH. An S. meliloti 1021 selleckchem preculture has been grown in VMM buffered at pH 7.0 until it reached an o.D.580 of 0.8 (dotted line with triangles). Afterwards the pre-culture has been separated into even parts, centrifuged and re-suspended in VMM at pH 5.75 and VMM Verteporfin clinical trial at pH 7.0, respectively. The growth of the pH 5.75 culture is given by lines with crosses and the growth of the pH 7.0 culture is given by lines with plus-symbols. The arrows in the diagram indicate the time points where cell culture probes were taken for transcriptional profiling. Remarks indicate the time in minutes passed after the splitting of the S. meliloti preculture. Cluster analysis of expression profiles of S. meliloti genes following a shift to acidic pH Cells were harvested from both cultures grown at pH 7.0 and pH 5.75 after 3, 8, 13, 18, 33 and 63 minutes (Fig. 1). Because both the sample (pH 5.75) and control (pH 7.