Furusawa Y, Maezawa H, Suzuki K, Yamamoto Y, Kobayashi K, Hieda K
Department of Molecular Biology, Tokai University School of Medicine, Kanagawa, Japan.
Int J Radiat Biol. 1993 Aug;64(2):157-64. doi: 10.1080/09553009314551241.
T1 phages with and without 5-bromo-2'-deoxyuridine (BrdU) labelling were irradiated in solids with monochromatic X-rays at 12.40 and 13.51 keV, below and just above the K-absorption edge of bromine (13.47 keV) in vacuum and wet states. Irradiated phages were assayed on uracil-DNA glycosylase (Udg) deficient (ung-1) and sufficient (ung+) host strains of Escherichia coli, in order to investigate the nature of the lethal damage induced by Auger cascade following X-ray absorption at the K-shell of bromine as a key atom. The results were: (1) An Auger-specific enhancement (1.15) was observed only when BrdU-labelled phages were irradiated in the wet state and assayed on ung+ host cells. (2) A Udg-specific enhancement was observed only for BrdU-labelled phages, not for unlabelled phages. (3) The sensitivities of BrdU-unlabelled phages were almost the same, despite the irradiation states and strains of the host cell, indicating that this sensitivity was a common fraction of the sensitivity under all conditions. (4) The lethal damage for the T1 phage was categorized into four fractions according to the sensitivities under different conditions: the general fraction was defined as being the sensitivity of unlabelled phages (G-fraction); BrdU-specific, but unrecognizable by Udg (B-fraction); Udg specific, but not Auger-specific (U-fraction); and Auger-specific (A-fraction). (5) Although the so-called indirect action of water radicals increased only the G-fraction by about three-fold, the B- and U-fractions were not affected by any change in the irradiation states, thus indicating that these two fractions were caused by the so-called direct action.
携带和未携带5-溴-2'-脱氧尿苷(BrdU)标记的T1噬菌体,在真空和湿态下,分别用能量为12.40和13.51 keV的单色X射线在固体中进行辐照,这两个能量分别低于和略高于溴的K吸收边(13.47 keV)。为了研究以溴作为关键原子在K壳层吸收X射线后俄歇级联诱导的致死损伤的性质,将辐照后的噬菌体在尿嘧啶-DNA糖基化酶(Udg)缺陷型(ung-1)和野生型(ung+)的大肠杆菌宿主菌株上进行检测。结果如下:(1)仅当用BrdU标记的噬菌体在湿态下辐照并在ung+宿主细胞上检测时,观察到俄歇效应特异性增强(1.15)。(2)仅在BrdU标记的噬菌体中观察到Udg特异性增强,未标记的噬菌体未出现该现象。(3)未标记BrdU的噬菌体的敏感性几乎相同,与宿主细胞的辐照状态和菌株无关,这表明该敏感性是所有条件下敏感性的共同部分。(4)根据不同条件下的敏感性,T1噬菌体的致死损伤分为四类:一般部分定义为未标记噬菌体的敏感性(G部分);BrdU特异性但无法被Udg识别的部分(B部分);Udg特异性但非俄歇效应特异性的部分(U部分);以及俄歇效应特异性部分(A部分)。(5)虽然水自由基的所谓间接作用仅使G部分增加了约三倍,但B部分和U部分不受辐照状态变化的影响,因此表明这两个部分是由所谓的直接作用引起的。