Doak et al. (1959) demonstrated the beneficial effects of low concentrations of sodium and potassium ions and the detrimental effect of higher concentrations of sodium ion on the survival in vitro of Treponema pallidum. Since this microorganism has not been cultivated in vitro, it cannot be said that either ion is essential for growth. However, most bacteria require potassium for growth (Lester, 1958), and it is not surprising that this ion prolongs survival time. The beneficial effect of sodium ion was unexpected, although MacLeod demonstrated that certain marine bacteria require sodium (MacLeod et al., 1954; MacLeod and Onofrey, 1956). The red halophile, Pseudomonas salinaria, also requires this ion (Brown and Gibbons, 1955). Many investigators have demonstrated that rubidium ion can replace potassium ion as a growth factor for bacteria and as an activator for isolated enzyme systems (Lester, 1958; Brown and Gibbons, 1955; Kachmar and Boyer, 1953; Black, 1931). An exception lhas recently been found in certain marine bacteria in which rubidium does not replace potassium (MacLeod and Onofrey, 1957). Cesium, in isolated enzyme systems, can partially replace potassium (Pressman and Lardy, 1952), but ammonium ion is known to sometimes replace potassium (Kachmar and Boyer, 1953; Stadtman, 1952; Von Korff, 1953) and at other times to be inhibitory (Black, 1931). Again, in certain isolated enzyme systems inhibited by sodium ion, this same inhibition can be achieved with lithium ion (Kachmar and Boyer, 1953; Black, 1931). The present work