Bezuglyĭ S V, Skripal' I G, Babichev V V, Malinovskaia L P
Mikrobiol Zh (1978). 1992 Jul-Aug;54(4):21-7.
The biological and physico-chemical properties of DNA-dependent DNA-polymerases of Acholeplasma laidlawii PG-8 have been studied. The optimal parameters of maximal enzymatic activity are determined. It is stated that N-ethylmaleimide in concentration of 1 mM activated DNA-polymerase I by 52%, whereas DNA-polymerase II with reagent concentration of 0.5 mM demonstrated the peak of activity exceeding the control only by 10%. Spermidine in concentration of 1.5 mM for the first form of DNA-polymerase and 0.15 mM-for the second one increased the ability of both forms of polymerases to synthesize DNA by 10%. Aphidicolin added to the reaction medium up to concentration of 10 mg/ml decreased activity of forms I and II of enzymes by 83 and 68%, respectively. The presence of 0.6 mM of EDTA in the medium also negatively affected the activity of polymerases inhibiting it by 83% in form I and by 77%-in form II.
对莱氏无胆甾原体PG - 8的依赖DNA的DNA聚合酶的生物学和物理化学性质进行了研究。确定了最大酶活性的最佳参数。结果表明,浓度为1 mM的N - 乙基马来酰亚胺可使DNA聚合酶I的活性提高52%,而试剂浓度为0.5 mM时,DNA聚合酶II的活性峰值仅比对照高出10%。对于第一种形式的DNA聚合酶,浓度为1.5 mM的亚精胺,对于第二种形式的DNA聚合酶,浓度为0.15 mM的亚精胺,可使两种形式的聚合酶合成DNA的能力提高10%。添加到反应介质中的浓度高达10 mg/ml的阿非迪霉素分别使酶的I型和II型活性降低了83%和68%。培养基中存在0.6 mM的EDTA也对聚合酶的活性产生负面影响,使I型聚合酶的活性降低83%,II型聚合酶的活性降低77%。