Ishige K, Noguchi T
Biochemicals Division, YAMASA Corporation, Choshi, Chiba, 288-0056, Japan.
Biochem Biophys Res Commun. 2001 Mar 2;281(3):821-6. doi: 10.1006/bbrc.2001.4415.
In Pseudomonas aeruginosa PAO1, we have found massive polyphosphate:AMP phosphotransferase activity and polyphosphate:ADP phosphotransferase activity known as the reverse catalytic activity of polyphosphate kinase which participates in polyphosphate synthesis in the bacterium. Biochemical analysis using the partially purified polyphosphate:ADP phosphotransferase has revealed that it is independent of polyphosphate kinase and can function as polyphosphate-dependent nucleoside diphosphate kinase which most prefers GDP to the other three nucleoside diphosphates as a phospho-acceptor. It has been also demonstrated that polyphosphate:AMP phosphotransferase activity marked in the bacterium mainly originates from the combined action of the polyphosphate:ADP phosphotransferase described above and adenylate kinase. Both of the polyphosphate-utilizing activities require short polyP as a phospho-donor whose chain length is <75.
在铜绿假单胞菌PAO1中,我们发现了大量的多聚磷酸盐:AMP磷酸转移酶活性和多聚磷酸盐:ADP磷酸转移酶活性,这是参与该细菌多聚磷酸盐合成的多聚磷酸盐激酶的反向催化活性。使用部分纯化的多聚磷酸盐:ADP磷酸转移酶进行的生化分析表明,它独立于多聚磷酸盐激酶,并且可以作为多聚磷酸盐依赖性核苷二磷酸激酶发挥作用,与其他三种核苷二磷酸相比,它最倾向于将GDP作为磷酸受体。还证明了该细菌中显著的多聚磷酸盐:AMP磷酸转移酶活性主要源于上述多聚磷酸盐:ADP磷酸转移酶和腺苷酸激酶的共同作用。两种多聚磷酸盐利用活性都需要链长<75的短链多聚磷酸作为磷供体。