增强UV-B辐射和He-Ne激光辐照对小麦离体叶绿体光化学活性的影响

利用低剂量的He-Ne激光和增强UV-B处理小麦叶绿体,研究了He-Ne激光对UV-B辐射损伤的修复效应.将提取的离体完整叶绿体分成CK(对照)、L(激光)、B(UV-B)和BL(UV-B和He-Ne激光复合处理)不同处理组.B、BL组经过不同剂量的紫外辐照处理(剂量依次为0.42 kJ·m－2·d－1,0.84 kJ·m－2·d－1 ,1.26 kJ·m－2·d－1),其中BL组被UV-B辐射处理后再用He-Ne激光(5 mW·mm－2)辐照.利用低温荧光法测定不同处理组小麦叶绿体荧光发射光谱的变化;用电导仪和Clark氧电极仪分别测量叶绿体膜透性和电子传递速率,膜透性的改变从一定程度上能反应膜的损伤程度;ATPase活性采用分光光度计测量.研究表明:He-Ne激光和增强UV-B辐射影响叶绿体激发能的分配,UV-B辐照达到1.26 kJ·m-2·d－1时,叶绿体几乎完全失去活性;He-Ne激光则从一定程度上能促进叶绿体的光化学活性.UV-B辐射后的叶绿体再经过He-Ne激光的辐照处理后,可以恢复部分光化学活性,但当叶绿体损伤严重,光化学活性完全丧失时,He-Ne激光对其没有激活作用.     

He-Ne激光和增强UV-B辐射对小麦TaRAN1蛋白的影响

采用He-Ne激光(5mW·mm-2)和增强UV-B(10.08kJ·m-2.d-1)辐照‘ML7113’小麦幼苗,6天后提取各处理组小麦幼苗的总蛋白和TaRAN1蛋白,用SDS-PAGE对其进行初步检测及Western Blot对目的蛋白进行鉴定,并采用考马斯亮蓝法测量不同处理组的TaRAN1蛋白的含量以做进一步的比较分析.结果表明:增强UV-B辐射使小麦TaRAN1蛋白电泳条带加宽颜色加深且含量显著增加;单独He-Ne激光处理,蛋白电泳条带较窄颜色较淡且所测的蛋白含量明显减少,表现出了抑制作用;经He-Ne激光辐照和UV-B辐射复合处理后,蛋白的含量明显低于B组而与对照组相差不明显.说明增强UV-B辐射后,小麦TaRAN1蛋白可能参与了植物的抗逆境反应.     

He-Ne激光和增强UV-B辐射对小麦TaRAN1蛋白的影响

采用He-Ne激光(5 mW· mm 2)和增强UV-B(10.08 kJ·m-2·d-1)辐照‘ML7113’小麦幼苗,6天后提取各处理组小麦幼苗的总蛋白和TaRAN1蛋白,用SDS-PAGE对其进行初步检测及Western Blot对目的蛋白进行鉴定,并采用考马斯亮蓝法测量不同处理组的TaRAN1蛋白的含量以做进一步的比较分析.结果表明:增强UV-B辐射使小麦TaRAN1蛋白电泳条带加宽颜色加深且含量显著增加;单独He-Ne激光处理,蛋白电泳条带较窄颜色较淡且所测的蛋白含量明显减少,表现出了抑制作用;经He-Ne激光辐照和UV-B辐射复合处理后,蛋白的含量明显低于B组而与对照组相差不明显.说明增强UV-B辐射后,小麦TaRAN1蛋白可能参与了植物的抗逆境反应.     

He-Ne激光对增强UV-B辐射拟南芥抗氧化系统的损伤修复

以培养6周左右的拟南芥为材料,采用UV-B辐射(剂量1 KJ/m2/d)和He-Ne激光器(波长632.8 nm,输出功率5 mW·mm2,辐照时间60 s)对材料进行处理,分成CK(没有经过UV-B或激光辐照)组、B(UV-B辐射)组、BL(UV-B和激光复合处理)组和L(激光辐照)组4个不同处理组.结果表明:增强的...     

脉冲软X光辐射三种材料的喷射冲量实验研究

 在强光一号脉冲加速器上进行了国内首次的实验室软X光辐射三种材料的喷射冲量研究。结果表明，在能量为(0.2～0.33)keV、平均脉宽为39ns左右的X光辐射下，对灰漆、白漆和硬铝，在能注量分别为(92～152)J/cm²、(115～136)J/cm²和(163～192)J/cm²时，它们的冲量耦合系数分别为(0.61～0.80)Pa·s/(J·cm^-2)、(0.58～0.97)Pa·s/(J·cm^-2)和(0.61～0.84)Pa·s/(J·cm^-2)。     

辅助光对NaCl(OH-)和KCl(Na+,OH-)晶体中的类F2+型色心激光输出的影响

文中报进了有关辅助光对NaCl(OH^-):(F₂⁺)_H及KCl(Na⁺,OH^-):(F₂⁺)_AH色心激光输出功率影响的主要研究结果。初步探讨了辅助光作用的物理机制。     

He-Ne激光对增强UV-B辐射拟南芥抗氧化系统的损伤修复

以培养6周左右的拟南芥为材料,采用UV-B辐射（剂量1 KJ/m2/d）和He-Ne激光器（波长632.8 nm,输出功率5 mW·mm2,辐照时间60 s）对材料进行处理,分成CK（没有经过UV-B或激光辐照）组、B(UV-B辐射)组、BL（UV-B和激光复合处理）组和L（激光辐照）组4个不同处理组.结果表明:增强的UV-B辐射拟南芥幼苗导致MDA(Malondialdehyde)、超氧阴离子含量升高,GSH(Glutathione)含量降低,PAL(phenylalanine ammomia-lyase)、CAT(catalase)和APX(ascorbate peroxidase)活性升高,SOD(supemxide dismutas)活性降低.单独He-Ne激光处理使MDA、超氧阴离子含量降低,GSH的含量升高,SOD、APX、CAT的活性升高,PAL的活性降低.UV-B辐射后再用He-Ne激光进行后处理,发现与单独UV-B辐照处理相比,MDA、超氧阴离子含量降低,GSH含量升高,SOD、APX、CAT的活性升高了,PAL的活性降低了.因此激光在一定程度上提高了拟南芥叶片抗氧化能力,在此基础上讨论了其可能的形成机理.     

X形色心激光谐振腔参数的确定及类F2+型色心激光运转

文中,针对X形谐振腔的特点及结合纵向泵浦理论,分析了X形谐振腔几何参数的确定条件和模式匹配条件;根据有关NaCl(OH^-):(F₂⁺)_H和KCl(Na⁺,OH^-):(F₂⁺)AH色心激光的主要研究结果,分析了提高色心激光输出效率的可能途径.     

激光诱变选育果胶酶高产菌株

采用Ar⁺、He-Ne、LD、YAP等激光辐照果胶酶产生菌,不同波长激光辐照均获高酶活菌株,其中从LD激光与He-Ne激光辐照组中选育出酶活达6×10⁴单位/g的高产菌株(比对照组提高122%),并稳定地应用于生产.文中从黑曲霉抱子与DNA的吸收光谱以及电镜观察黑曲霉抱子的结果出发,对激光诱变机制进行了初步探讨.     

COIL用变形反射镜介质反射膜

 报道COIL激光用变形反射镜的介质反射多层膜实验。在真空镀膜机内制备了膜系Sub/Ag(SiO₂/HfO₂)⁴/air和Sub/Ag(YbF₃/ZnS)³/air, 反射率分别为99.90%和99.87%。在经历109次循环后变形镜物理特性无变化。研究了COIL激光辐射下热畸变和损伤特性。分别在功率密度为1.52kW/cm²和1.18kW/cm²的COIL激光辐照下,这两种膜系的变形镜波前变化为0.37l 和0.54l 。因此对于变形镜1kW/cm²激光功率密度是安全可靠的。     

Development and evaluation of an optical fibre-based helium-neon laser irradiation system for tissue regeneration: A pilot study

Low level laser therapy is being extensively used to treat various medical ailments including wound healing. In the present study, an optical fibre-based helium-neon (He-Ne) laser irradiation system was designed, developed and evaluated for optimum tissue repair on mice excision wounds. Circular wounds of 15 mm diameter were created on the dorsum of animals and single exposure of uniformly distributed laser beam was administered at 1, 2 and 3 J/cm² to the respective test groups with suitable controls. Progression of healing was monitored by measuring wound contraction and mean healing time. Significant reduction in wound size and mean healing time (p <0.001) were observed in the test groups for the laser dose of 2 J/cm² compared to the unilluminated controls, suggesting the suitability of this dose.     

CO2激光预处理对UV-B辐射引起的小麦幼苗脂质过氧化伤害的防护作用

用20 mW·mm－2CO2激光对小麦萌发的种子分别照射1 min、3 min、5 min、7 min，待其长至幼苗期，在光背景（PAR）90 μmol·m－2·s－1条件下，用3.10 kJ·m－2 UV-B照射7 h·d－1,然后对其丙二醛（MDA）、还原型谷胱甘肽（GSH）、超氧化物岐化酶（SOD）、过氧化氢酶（CAT）、过氧化物酶（POD）以及抗坏血酸（AsA）等含量进行测定.结果发现，CO2激光预处理可提高小麦GSH和AsA含量以及SOD、CAT、POD酶活性，降低MDA含量，从而抑制了由UV-B辐射引起小麦的脂质过氧化作用，以处理5 min为最适时间.     

Mutagenic effect of accelerated heavy ions on bacterial cells

The heavy ion accelerators of the Joint Institute for Nuclear Research were used to study the regularities and mechanisms of formation of different types of mutations in prokaryote cells. The induction of direct (lac⁻, ton B⁻, col B) mutations for Esherichia coli cells and reverse his⁻ → His⁺ mutations of Salmonella typhimurium, Bacillus subtilis cells under the action of radiation in a wide range of linear energy transfer (LET) was studied. The regularities of formation of gene and structural (tonB trp-) mutations for Esherichia coli bacteria under the action of accelerated heavy ions were studied. It was demonstrated that the rate of gene mutations as a function of the dose under the action of Γ rays and accelerated heavy ions is described by linear-quadratic functions. For structural mutations, linear “dose-effect” dependences are typical. The quadratic character of mutagenesis dose curves is determined by the “interaction” of two independent “hitting” events in the course of SOS repair of genetic structures. The conclusion made was that gene mutations under the action of accelerated heavy ions are induced by δ electron regions of charged particle tracks. The methods of SOS chromotest, SOS lux test, and λ prophage induction were used to study the regularities of SOS response of cells under the action of radiations in a wide LET range. The following proposition was substantiated: the molecular basis for formation of gene mutations are cluster single-strand DNA breaks, and that for structural mutations, double-strand DNA breaks. It was found out that the LET dependence of the relative biological efficiency of accelerated ions is described by curves with a local maximum. It was demonstrated that the biological efficiency of ionizing radiations with different physical characteristics on cells with different genotype, estimated by the lethal action, induction of gene and deletion mutations, precision excision of transposons, is determined by the specific features of energy transfer of the radiations that affect the character of induced DNA damage, and the efficiency inducible and constitutive cell repair systems. The growth of relative biological efficiency of heavy charged particles is determined by the growth of the damage yield of the DNA participating in the formation of radiation-induced effects, and higher efficiency of inducible repair systems. It was established that the LET value (L _max) for which the maximum (according to the applied irradiation criteria) coefficients of relative biological efficiency are observed varies depending on the character of the registered radiation induced effect. It was demonstrated that for gene mutations and induction of precision excision of mobile elements the values of L _max are realized in a LET range of ≈20 keV/μm. For lethal effects of irradiation and induction of deletion mutations the value of L _max is ≈ 100 and 50 keV/μm, respectively. The differences in the L _max for the studied radiation gene effectis are determined by the different type of DNA damage participating in the mutation process. A molecular model of the formation of gene mutations in Escherichia coli cells under the action of ionizing radiation was proposed. Basic DNA radiation damage and main repair ways were considered in the framework of this model. The basis is the idea of the decisive role of mutagenic, error-prone, branch of SOS repair in fixing premutation DNA damage into point mutations. It was demonstrated that the central mechanism in this process is the formation of an inducible multi-enzymatic complex including the DNA polymerase V (Umu C), RecA-protease, SSB proteins, subunits of DNA polymerase III, performing erroneous DNA synthesis on the damaged matrix. A mathematical model of induction of gene mutations under ultraviolet cell irradiation was developed based on the molecular model.     

He-Ne激光、紫外线诱变氧化亚铁硫杆菌及耐砷菌株的选育

对适合氧化亚铁硫杆菌(Thiobacilus ferrooxidans)特点的诱变方法进行了研究:把菌体制成无铁细胞悬液进行小剂量、多次数的诱变.氧化亚铁硫杆菌菌株S₁经多次紫外线和激光照射,并结合逐级驯化处理,最终选育出了优良耐砷菌株S_x,它能在含11g/LA_s2O₃的环境中生长,比出发菌株的0.7g/L提高了近14.7倍.在用该菌株进行浸矿的实验结果表明:浸矿能力良好,在同样是10%接种量时,浸出时间比出发菌缩短了一天,并且砷元素的浸出率由原先的76%提高至85.7%.     

强激光辐照铝靶的辐射流体动力学模型及数值求解

本文改进了传统的辐射流体动力学模型,建立了完整的一维单流体双温度辐射流体力学方程组描述5×10⁸w/cm²高斯脉冲激光与一维半无界铝靶在真空中耦合所产生的靶外等离子体的发展过程,并建立了相应的数值模拟模型,计算结果与有关文献和实验比较,取得了定性与定量的一致.     

制备多孔硅的一种新方法

自从Canham观察到多孔硅(PS)的可见光致发光后,由于其可望成为可与Ⅲ—Ⅴ族半导体材料相媲美的新型光电子材料而引起了科学界极大的兴趣.目前,制备多孔硅一般都采用电化学腐蚀方法.     

DNA腺嘌呤阳离子自由基脱质子反应机理的研究

Among all the DNA components, extremely redox-active guanine (G) and adenine (A) bases are subject to facile loss of an electron and form cation radicals (G^+· and A^+·) when exposed to irradiation or radical oxidants. The subsequent deprotonation of G^+· and A^+· can invoke DNA damage or interrupt hole transfer in DNA. However, compared with intensive reports for G^+·, studies on the deprotonation of A^+· are still limited at present. Herein, we investigate the deprotonation behavior of A^+· by time-resolved laser flash photolysis. The deprotonation product of A(N₆-H)^· is observed and the deprotonation rate constant, (2.0±0.1)×10⁷ s^-1, is obtained at room temperature. Further, the deprotonation rate constants of A^+· are measured at temperatures varying from 280 K to 300 K, from which the activation energy for the N₆-H deprotonation is determined to be (17.1±1.0) kJ/mol by Arrhenius equation. In addition, by incorporating the aqueous solvent effect, we perform density functional theory calculations for A^+· deprotonation in free base and in duplex DNA. Together with experimental results, the deprotonation mechanisms of A^+· in free base and in duplex DNA are revealed, which are of fundamental importance for understanding the oxidative DNA damage and designing DNA-based electrochemical devices.