Strain 327 had a special requirement for methionine which was illustrated by the fact that in its absence, the bacteria Compound C datasheet started to die already after 24 h. This strain does not possess all the enzymes involved in synthesis of cellular methionine ( [29]). The modified CDB with 0.01 mM methionine was used in 2D gel analysis because no significant
difference in growth was observed between this concentration and the highest concentration (0.1 mM) investigated (P 305 = 0.07, P 11168 = 0.36, P 327 = 0.52) (Figure 1). The CDB with methionine supported good growth of all 13 strains tested. For nine of the strains the growth and generation times were comparable with BHI, while four of the strains showed either significantly faster or slower growth (unpublished observations). It has been shown that auxotyping markers, except cystine and cysteine, are stable after three cycles of freezing and thawing [30], and it is therefore possible to minimize the workload by preparing batches of double strength stocks and storing these at −20°C. [35 S]-methionine labelling during acid stress C. jejuni strains NCTC 11168, 327, and 305 were grown in CDB containing 0.01 mM methionine at 37°C in a microaerophilic atmosphere. Similar numbers of cells in late exponential Panobinostat in vivo phase were desirable
for comparability between the strains. To achieve cells in the late exponential phase with approximately 1 × 108 CFU/ml, strains of NCTC 11168 and 327 were grown for 26 hours, whereas strain 305 only
required 22 hours. The C. jejuni cells were exposed to relatively mild acid conditions (pH 5.2 with HCl and pH 5.7 with acetic acid) to prevent the cells from dying and closing down all metabolic activity. The gastric Coproporphyrinogen III oxidase pH during a meal has been measured to be 3.9-5.5 [36] and the experimental pH is therefore within the upper range. The effects of acid exposure on CFU for all strains are illustrated in Figure 2. Strain 305 was the most acid-tolerant strain while strain 327 was the most acid-sensitive at 37°C. This correlated well with earlier findings AMN-107 mouse showing that strain 305 was more tolerant than strain 327 towards tartaric acid at 4°C [23]. Growth of C. jejuni 305 was only slightly reduced during HCl and acetic acid stress (Figure 2C), whereas the number of cells for strain 327 decreased (Figure 2B). Proteomic analysis and identification of proteins Methionine labelled protein extracts from non-stressed, HCl or acetic acid-exposed cells were subjected to 2D-gel-electrophoresis analysis. The majority of proteins were repressed as expected. Relatively few (up to seven) induced proteins were identified with only five being significantly induced. The intensity (% volume) was calculated for induced proteins under the following conditions: control, HCl, and acetic acid (Table 3).
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