Page 112 - The Biochemistry of Inorganic Polyphosphates
P. 112

WU095/Kulaev
               WU095-07
                                     Functions of polyphosphate and polyphosphate-dependent enzymes
                            96     March 9, 2004  15:39  Char Count= 0



                                         µmol per g of  wet biomass              c







                                                                                  d

                                                                                  b

                                                                                  a




                                                            Time (min)

                            Figure 7.2 The content of (a) K , (b) high-molecular-weight PolyP, (c) Zn , and (d) low-molecular-
                                                   +
                                                                                 2+
                            weight PolyP during Zn 2+  uptake by the yeast Saccharomyces carlbergensis. The incubation medium
                            contained 100 mM glucose and 3 mM ZnSO 4 (Okorokov et al., 1983b).

                            cells.BoththetotalcontentanddistributionofPolyPbyfractionsintheyeastSaccharomyces
                            cerevisiae depend on the growth phase (Vagabov et al., 1998) (for details, see Chapter 8).
                            Before glucose was consumed from the medium, the biomass and total cellular PolyP
                            content had increased in parallel. After glucose depletion, the content of PolyP in the cells
                            fell sharply and then increased again. A significant decline of the content of intracellular
                            PolyP while P i was present in the growth medium at high concentrations may imply that
                            in this growth phase PolyP is an energy rather than a phosphate source (Vagabov et al.,
                            1998, 2000). The active synthesis of PolyPs, accompanied by a dramatic decrease in their
                            chain lengths in the logarithmic phase of S. cerevisiae growth in a carbon- and phosphorus-
                            sufficient medium, also suggests that the energy derived from PolyP hydrolysis is necessary
                            to maintain the high rate of yeast growth (Vagabov et al., 1998, 2000). It was reported that
                            PolyP participates in the repair of yeast cells after radiation damage as an alternative energy
                            supply and phosphate source (Holahan et al., 1988).
                               Furthermore, in an adenine-deficient mutant of N. crassa, where the concentrations
                            of ATP and other adenyl nucleotides are sharply reduced, PolyP is alternatively synthe-
                            sized during glycolytic phosphorylation by 1,3-diphosphoglicerate:PolyP phosphotrans-
                            ferase (Kulaev and Bobyk, 1971). Thus, under certain conditions PolyP can replace ATP as
                            an energy reserve in eukaryotes.
                               PolyPs of 12–25 P i residues were found in the mitochondria of S. cerevisiae (Beauvoit
                            et al., 1989). The amounts increase sharply under phosphate overplus (Pestov et al., 2003).
                            The function of PolyPs in mitochondria needs further investigation. PolyPs also occur
   107   108   109   110   111   112   113   114   115   116   117