“…Remarkably, human mitochondrial NAD kinase has been recently identified to have the ability to utilize both ATP and polyP as the phosphoryl donor (Ohashi et al, 2012). Neglected and long regarded a molecular fossil, polyP has a variety of significant functions in bacteria such as a (i) source of energy (Kulaev, 1979; Wood and Clark, 1988; Kulaev et al, 1999b), (ii) phosphate reservoir (Kulaev et al, 1999b), (iii) donor for sugar and adenylate kinases (Bonting et al, 1991; Hsieh et al, 1993; Phillips et al, 1993), (iv) chelator for divalent cations (Van Veen et al, 1993), (v) buffer against alkaline stress (Pick et al, 1990), (vi) regulator of development (Gezelius et al, 1973), and (vii) structural element in competence for DNA entry and transformation (Reusch and Sadoff, 1988). Even though most of polyP research has been performed in microorganisms, the presence of polyP has been demonstrated in many mammalian tissues (Figure 4) such as rodent liver, kidney, lungs, brain, and heart (Kumble and Kornberg, 1995), rabbit heart (Seidlmayer et al, 2012a,b), as well as in human granulocytes (Cowling and Birnboim, 1994), platelets (Smith et al, 2006; Smith and Morrissey, 2008a; Morrissey et al, 2012), and fibroblasts (Pisoni and Lindley, 1992).…”