Zipper P, Wilfing R, Kriechbaum M, Durchschlag H
Z Naturforsch C Biosci. 1985 May-Jun;40(5-6):364-72. doi: 10.1515/znc-1985-5-614.
The sulfhydryl enzyme malate synthase from baker's yeast was X-irradiated with 6 kGy in air-saturated aqueous solution (enzyme concentration: congruent to 10 mg/ml; volume: 120 microliters), in the absence or presence of the specific scavengers formate, superoxide dismutase, and catalase. After X-irradiation, a small aliquot of the irradiated solutions was tested for enzymic activity while the main portion was investigated by means of small-angle X-ray scattering. Additionally, an unirradiated sample without additives was investigated as a reference. Experiments yielded the following results: X-irradiation in the absence of the mentioned scavengers caused considerable aggregation, fragmentation, and inactivation of the enzyme. The dose Dt37 for total (= repairable + non-repairable) inactivation resulted as 4.4 kGy. The mean radius of gyration was found to be about 13 nm. The mean degree of aggregation was obtained as 5.7, without correction for fragmentation. An estimation based on the thickness factor revealed that about 19% of material might be strongly fragmented. When this amount of fragments was accordingly taken into account, a value of 7.1 was obtained as an upper limit for the mean degree of aggregation. The observed retention of the thickness factor and the finding of two different cross-section factors are in full accord with the two-dimensional aggregation model established previously (Zipper and Durchschlag, Radiat. Environ. Biophys. 18, 99-121 (1980)). The presence of catalytic amounts of superoxide dismutase and/or catalase, in the absence of formate, during X-irradiation reduced both aggregation and inactivation significantly. The presence of formate (10 or 100 mM) during X-irradiation led to a strong decrease of aggregation and inactivation.(ABSTRACT TRUNCATED AT 250 WORDS)
在空气饱和的水溶液中(酶浓度:约10mg/ml;体积:120微升),对来自面包酵母的巯基酶苹果酸合酶进行6kGy的X射线辐照,辐照时不存在或存在特定清除剂甲酸盐、超氧化物歧化酶和过氧化氢酶。X射线辐照后,取一小份辐照溶液检测酶活性,而主要部分则通过小角X射线散射进行研究。此外,还研究了一份未添加添加剂的未辐照样品作为对照。实验得出以下结果:在不存在上述清除剂的情况下进行X射线辐照会导致酶大量聚集、断裂并失活。总(即可修复 + 不可修复)失活的剂量Dt37为4.4kGy。发现回转半径约为13nm。在未校正断裂的情况下,平均聚集度为5.7。基于厚度因子的估计表明,约19%的物质可能严重断裂。当相应考虑这部分断裂物质时,得到平均聚集度的上限值为7.1。观察到的厚度因子保留情况以及两个不同截面因子的发现与先前建立的二维聚集模型完全一致(Zipper和Durchschlag,《辐射与环境生物物理学》18,99 - 121(1980))。在X射线辐照期间,在不存在甲酸盐的情况下,催化量的超氧化物歧化酶和/或过氧化氢酶的存在显著降低了聚集和失活。在X射线辐照期间甲酸盐(10或100mM)的存在导致聚集和失活大幅降低。(摘要截断于250字)