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Inactivation of E. <strong>coli</strong> <strong>in</strong> UCFM 36.5.2 pHFigures 6 showed that the rate of pH decl<strong>in</strong>e dur<strong>in</strong>g fermentation and the ultimate pHachieved has an affect on the amount of <strong><strong>in</strong>activation</strong>. Grau (1996) considered the effect ofpH also, for all comb<strong>in</strong>ations of treatments and found the relationship shown <strong>in</strong> Figure 12.As with water activity, our earlier discussion queried whether faster <strong><strong>in</strong>activation</strong> rates arenecessarily due to lower pH. Rather, we suggested that that observation might be due lowerpH be<strong>in</strong>g associated with more rapid progression <strong>in</strong> the batter to conditions that prohibitE. <strong>coli</strong> growth. However, the results of Brown <strong>in</strong> Figure 9 <strong>in</strong>dicate that decreased pH does<strong>in</strong>crease the <strong><strong>in</strong>activation</strong> rate. Those data <strong>in</strong>dicate that a one pH unit difference <strong>in</strong> conditionsis associated with a difference <strong>in</strong> <strong><strong>in</strong>activation</strong> rate of ~3-fold.Figure 12.Correlation between f<strong>in</strong>al pH of matured fermented sausage and total <strong><strong>in</strong>activation</strong> for twostra<strong>in</strong>s of E. <strong>coli</strong> (Reproduced from Figure 4.3a of Grau, 1996).It is also noted from Figure 9a that the <strong><strong>in</strong>activation</strong> observed by Grau (1996) <strong>in</strong> broth at pH 4with 84 mM lactic acid (34 mM undissociated) is more rapid than that observed by Brown (<strong>in</strong>preparation) at pH 2.5 us<strong>in</strong>g HCl as acidulant. This may <strong>in</strong>dicate that organic acids are more‘lethal’ than m<strong>in</strong>eral acids at equivalent pH (a situation analogous to <strong>in</strong>hibition of E. <strong>coli</strong>growth rate) but there is <strong>in</strong>sufficient additional data by which to assess this possibilityrigorously.5.3 Water activityDespite the earlier discussion, Grau (1996) reported a correlation between water activity andthe amount of <strong><strong>in</strong>activation</strong> of E. <strong>coli</strong> <strong>in</strong> UCFM. His data are presented <strong>in</strong> Figure 13 below.It must be emphasised, however, that a correlation does not necessarily <strong>in</strong>dicate a causalrelationship. We <strong>in</strong>terpret the pattern seen <strong>in</strong> Figure 13 as not result<strong>in</strong>g from water activitydifferences directly, but to result from the longer dry<strong>in</strong>g times required to achieve lower wateractivities, i.e. that both the lower water activity and greater <strong><strong>in</strong>activation</strong> result from the samecause, but are not themselves causally related.Vanderl<strong>in</strong>de (1999) also presented results which suggest that, <strong>in</strong> the range of relevance toUCFM products, f<strong>in</strong>al water activity has little effect on <strong><strong>in</strong>activation</strong> rate dur<strong>in</strong>g maturation. Inthose data, there were no correlations between f<strong>in</strong>al water activity and either rate of<strong><strong>in</strong>activation</strong> (R 2 = 0.008) or total <strong><strong>in</strong>activation</strong> (R 2 = 0.292) but maturation time is significantlycorrelated with total <strong><strong>in</strong>activation</strong> (R 2 = 0.697). The results of Shadbolt et al. (1999) <strong>in</strong> Figures9 also <strong>in</strong>dicate, however, that water activity does affect <strong><strong>in</strong>activation</strong> rate and may cause up toa 2 – 3 fold difference <strong>in</strong> <strong><strong>in</strong>activation</strong> rates at the extremes of the range 0.7 – 0.9. The rangeof water activities of Australian UCFMs is likely to be lower than this (see Fig. 1).Page 36 of 59

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