Baine T J, Sagstuen E
Department of Physics, University of Oslo, Norway.
Radiat Res. 1998 Aug;150(2):148-58.
Single crystals of disodium beta-glycerophosphate pentahemihydrate (betaGP), Na2x(HO)CH2CH(PO(4)2-)CH2(OH)x5 1/2H2O, were X-irradiated at 77 and 280 K. EPR, ENDOR and FSE techniques were used to study the formation of free radicals in these irradiated crystals to characterize possible reaction mechanisms leading to dephosphorylation. Irradiation at 77 K reveals the presence of four different radicals: two alkoxy radical conformations, AR1 and AR2, (HO)CH2CH(PO(4)2-)CH2O. and two carbon-centered hydroxyalkyl radicals, LTR1, (HO)CH2CH(PO(4)2-) C.HOH, and LTR2, with a tentative structure (HO)CH2C.H(PO(4)2-)CH2OH. AR1 and AR2 were determined to be formed on each of the two independent molecules A and B of the asymmetrical unit of betaGP, each on the 3-end of the molecule. Irradiation at 280 K reveals the presence of three hydroxyalkyl allyl radicals, R1, R2 and R3, with the common chemical structure (HO)C.H-H=CH(OH). Radicals R1 and R2 are determined to form on molecules B and A of the asymmetrical unit, respectively. The site of radical formation for R3 could not be ascertained absolutely from the available data, and there is also evidence that suggests the possibility that R3 has a hydroxyphospho-allyl radical structure. Possible reaction mechanisms for the formation of both the 77 K radicals and the 280 K radicals are suggested and discussed. The formation of an allyl-type radical in such a small-molecule single-crystal model system is an interesting and surprising result which may be relevant to the formation of the so-called 3alphaH radical species commonly observed in irradiated solid cytosine nucleosides and nucleotides. The result is also important because of the formation of the hydroxyalkyl allyl radical in solid beta-glycerophosphate is at variance with mechanisms and products shown to dominate for this and similar systems in solution radiolysis.
对五水合β -甘油磷酸二钠(βGP),即Na₂ₓ(HO)CH₂CH(PO₄²⁻)CH₂(OH)ₓ5 1/2H₂O的单晶在77K和280K下进行了X射线辐照。采用电子顺磁共振(EPR)、电子核双共振(ENDOR)和场扫电子自旋共振(FSE)技术研究了这些辐照晶体中自由基的形成,以表征可能导致去磷酸化的反应机制。在77K下辐照发现存在四种不同的自由基:两种烷氧基自由基构象,AR1和AR2,即(HO)CH₂CH(PO₄²⁻)CH₂O·;以及两种以碳为中心的羟烷基自由基,LTR1,(HO)CH₂CH(PO₄²⁻)C·HOH,和LTR2,其暂定结构为(HO)CH₂C·H(PO₄²⁻)CH₂OH。已确定AR1和AR2分别在βGP不对称单元的两个独立分子A和B上形成,均在分子的3'端。在280K下辐照发现存在三种羟烷基烯丙基自由基,R1、R2和R3,具有共同的化学结构(HO)C·H - H=CH(OH)。已确定自由基R1和R2分别在不对称单元的分子B和A上形成。根据现有数据无法绝对确定R3的自由基形成位点,并且也有证据表明R3可能具有羟磷烯丙基自由基结构。提出并讨论了形成77K自由基和280K自由基的可能反应机制。在这样一个小分子单晶模型系统中形成烯丙基型自由基是一个有趣且令人惊讶的结果,这可能与在辐照的固体胞嘧啶核苷和核苷酸中通常观察到的所谓3αH自由基物种的形成有关。该结果也很重要,因为在固体β -甘油磷酸中形成羟烷基烯丙基自由基与在溶液辐射分解中该体系及类似体系所显示的主导机制和产物不同。