Page 152 - The Biochemistry of Inorganic Polyphosphates
P. 152

WU095/Kulaev
               WU095-08
                                     Peculiarities of polyphosphate metabolism
                            136    March 9, 2004  20:32  Char Count= 0























                            Figure 8.9 Accumulation of PolyPs in Aerobacter aerogenes (Harold, 1966): (a) sulfur deprivation,
                            cells placed at 0 h in a P i - free medium; (b) phosphate overplus, cells placed at0hinaP i -free medium,
                            with P i was added after 4 h: (1) PolyP; (2) polyphosphate kinase activity; (3) exopolyphosphatase
                            activity.



                            of the latter the growth was restored and PolyP was utilized for biosynthetic processes. It
                            is probable that such mechanisms are realized by the same way as in other bacteria by the
                            ppGpp and rpoS controlling genes (see earlier in Chapter 7).
                               In contrast to E. coli, K. aerogenes exhibits rapid and extensive PolyP accumulation
                            (known as ‘PolyP overplus’) when P i is added to cells previously subjected to P i starvation
                            (Harold, 1966). The changes in PolyP content, polyphosphate kinase and exopolyphos-
                            phatase activities under phosphate overplus are presented in Figure 8.9(b). It was shown
                            that the absence of P i in the medium de-repressed the polyphosphate kinase (Harold, 1964;
                            Harold and Harold, 1963, 1965).
                               The mutant, which was devoid of polyphosphate kinase, had no PolyP accumulation in-
                            dependent of the growth conditions (Harold, 1964). Later, using specific gene constructions
                            with a cloned ppk gene, it was confirmed that in K. aerogenes,asin E. coli, polyphosphate
                            kinase is responsible for the synthesis of the most part of PolyP and for PolyP overplus
                            (Kato et al., 1993b; Ohtake et al., 1999; Kuroda and Ohtake, 2000). A ppk mutant of
                            K. aerogenes showed no PolyP overplus. Like the E. coli ppk-ppx operon, the ppx gene is
                            located immediately ‘downstream’ of the ppk gene (Kato et al., 1993b). As expected, the
                            polyphosphate kinase activity increased in response to P i starvation and decreased upon
                            addition of P i . However, unlike polyphosphate kinase, the exopolyphosphatase activity did
                            not increase but rather slightly decreased under conditions of P i starvation, although the
                            ppx mRNA was induced (Kuroda and Ohtake, 2000). Earlier, it had been shown that PolyP
                            degradation was completely inhibited in the mutant without exopolyphosphatase (Harold,
                            1966).
   147   148   149   150   151   152   153   154   155   156   157