Page 175 - The Biochemistry of Inorganic Polyphosphates
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               WU095-08
                        WU095/Kulaev
                                                                                  Yeast      159
                            400
                          PolyP ( µmol P (g dry biomass) −1 )  300




                            200



                            100



                              0
                                 12345    12345    12345    12345    12345     12345    12345
                                   A         B       C         D         E        F        G


                        Figure 8.24 The effect of inhibitors on the content of certain PolyP fractions in Saccharomyces
                        cerevisiae cells under phosphate overplus (Trilisenko et al., 2003). (A) PolyP in P i -starved cells;
                        (B–G) PolyP in cells grown at 2 h after re-inoculation on the complete medium (phosphate overplus):
                        (B) control conditions; (C) 10 mg ml −1  of cycloheximide; (D) 10 µM FCCP; (E) 20 µM FCCP; (F)
                        250 µM iodacetamide; (G) 50 nM bafilomycin A. PolyP fractions: (1) PolyP(I); (2) PolyP(II); (3)
                        PolyP(III); (4) PolyP(IV); (5) PolyP(V).





                        1980). It is possible that the ammonia-initiated PolyP hydrolysis provided the mechanisms
                        for maintenance of pH homeostasis in vacuoles.
                          The degradation of ‘NMR-visible’, probably vacuolar, PolyPs to short-chain polymers
                        in S. cerevisiae was observed under conditions where it was necessary to neutralize the
                        alkalization of cytoplasm (Castro et al., 1995, 1999).
                          Decrease in the PolyP level was observed under anaerobic conditions, probably because
                        PolyP biosynthesis requires a great deal of energy (Den Hollander et al., 1981; Beauvoit
                        et al., 1991; Castro et al., 1995). In energy-limited S. cerevisiae cells, a competition between
                        ion transport and PolyP biosynthesis was revealed: ion transport was only observed in
                        anaerobic cells without exogenous glucose with low ATP synthesis, whereas the addition
                        of glucose supported PolyP synthesis (Hofeler et al., 1987).
                          In a continuous culture of Candida utilis (glucose-containing medium), a direct and
                        almost linear relationship between the specific growth rate and the PolyP content in the
                        cells and vacuoles was observed. The relationship of the growth rate and chain length
                        of vacuolar PolyPs was an inverse one. At a low growth rate, two peaks with ∼ 35 and
                        ∼ 5P i residues were observed, while at an intermediate growth rate, a peak of 15–25 units
                        appeared with shorter chains of 5 units. When the growth rate was maximal, the short-chain
                        PolyPs (∼ 5 residues) prevailed (Nunez and Callieri, 1989).
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