Osland A, Kleppe K
Biochim Biophys Acta. 1978 Sep 27;520(2):317-30. doi: 10.1016/0005-2787(78)90230-7.
The influence of polyamines on the various activities of DNA polymerase I from Escherichia coli (EC 2.7.7.7) has been investigated. For all high molecular weight DNAs spermine and spermidine caused up to 80% inhibition when present in high concentrations, i.e. above 1 mM for spermine and 2 mM for spermidine. In the presence of low concentrations of polyamines a small activation was seen for some DNAs. The diamines cadaverine and putrescine had little influence on the rate of synthesis with natural occurring DNAs. In the case of d(A--T)n the activation/inhibition was found to be markedly dependent on the molecular weight of the samples used. With a low molecular weight DNA, 5.6 S, addition of spermidine resulted in up to 3-fold stimulation of activity. The activation was dependent on the concentration of MgCl2 and ionic strength; increasing concentration of these gave a decrease in the degree of activation. Polyamines also had a dramatic effect on the rate of synthesis using the homopolymers (dA)n . (dT)10 and (rA)n . (dT)10 . (20:1) as primers. Putrescine, in particular, increased the activity up to 10-fold with (rA)n . (dT)10 and somewhat less for (dA)n . (dT)10. The apparent Km for the primer (rA)n . (dT)10 decreased approx. 35-fold in the presence of 6.6 mM putrescine. There was no influence on the apparent Km for dTTP. The influence of polyamines on both the 5' leads to 3' and 3' leads to 5' nuclease activity was also investigated. Inhibition of nuclease activity was observed in the presence of polyamines, particularly with spermine. Thus with d(A--T)n and T7 DNA as substrates addition of 0.7 mM spermine resulted in almost complete inhibition of the activity. The dramatic inhibition observed with high concentrations of spermine (spermidine) both in the case of polymerizing and nuclease activity is thought to be due to polyamine-induced aggregation of DNA molecules.
已对多胺对大肠杆菌DNA聚合酶I(EC 2.7.7.7)各种活性的影响进行了研究。对于所有高分子量DNA,当精胺和亚精胺以高浓度存在时,即精胺高于1 mM、亚精胺高于2 mM时,会导致高达80%的抑制。在低浓度多胺存在下,一些DNA会出现轻微激活。二胺尸胺和腐胺对天然DNA的合成速率影响很小。对于d(A--T)n,发现激活/抑制明显取决于所用样品的分子量。对于低分子量DNA(5.6 S),添加亚精胺可使活性提高多达3倍。这种激活取决于MgCl2的浓度和离子强度;这些浓度增加会使激活程度降低。多胺对使用均聚物(dA)n、(dT)10和(rA)n、(dT)10(20:1)作为引物的合成速率也有显著影响。特别是腐胺,使用(rA)n、(dT)10时可使活性提高多达10倍,使用(dA)n、(dT)10时提高幅度稍小。引物(rA)n、(dT)10的表观Km在6. mM腐胺存在下大约降低35倍。对dTTP的表观Km没有影响。还研究了多胺对5'至3'和3'至5'核酸酶活性的影响。在多胺存在下观察到核酸酶活性受到抑制,尤其是精胺。因此,以d(A--T)n和T7 DNA为底物,添加0.7 mM精胺几乎完全抑制了活性。在聚合和核酸酶活性方面,高浓度精胺(亚精胺)观察到的显著抑制被认为是由于多胺诱导的DNA分子聚集。