UV-B辐射和NaCl胁迫对绿豆幼苗叶片DNA损伤的复合效应

研究了0·4W/m2UV-B辐射和0·4%NaCl胁迫对两绿豆品种中绿_1和秦豆-20(PhaseolusraditusL.cv.Zhongl櫣-1andQindou-20)幼苗叶片DNA损伤的复合效应。结果表明:(1)中绿-1抗UV-B辐射和NaCl胁迫的能力均强于秦豆-20;NaCl胁迫能降低中绿-1UV-B敏感性,但对秦豆-20UV-B敏感性无明显影响。(2)两逆境因子单独胁迫或复合胁迫下DNA增色效应均明显降低,但中绿-1降低程度小于秦豆-20,复合胁迫下降低程度小于单独NaCl胁迫下。(3)UV-B辐射诱导的中绿-1DNA链内环丁烷嘧啶二聚体(CPD)累积量明显低于秦豆-20;NaCl胁迫能降低UV-B诱导的中绿-1CPD累积,而对UV-B诱导的秦豆-20CPD累积无影响。(4)各种胁迫处理均导致两品种幼苗DNA含量降低,但两品种间相比中绿-1降低程度较大。结果说明UV-B辐射不仅能诱导DNA链内交联形成CPD,而且能诱导DNA链间交联和DNA含量降低,且不同绿豆品种或同一品种在有无NaCl胁迫时UV-B敏感性的差异主要与CPD累积量和DNA链间交联程度有关。     

环丁烷嘧啶二聚体累积与水稻UV—B敏感性的关系

利用单克隆抗体ELISA ,研究了UV_B对水稻DNA中环丁烷嘧啶二聚体 (CPD)的诱导形成及其光、暗修复 ,并对CPD累积与水稻UV_B敏感性的关系进行了分析。结果表明 ,我国南方的 5个水稻 (OryzasativaL .)品种经13.6kJ·m-2 ·d-1UV_B处理 15d后 ,在株高、生物量、光合作用等方面表现出明显的品种间差异。不同品种水稻的DNA中CPD累积比对照明显增加 ,且敏感品种CPD的累积比抗性品种显著提高。统计分析证实 ,CPD的累积与生物量的抑制呈显著正相关 (r2 =0 .6 2 2 )。UV_B诱导的水稻DNA中CPD的清除以光修复为主 ,不同品种CPD暗修复能力相似 ,而光修复能力存在明显差异。根据以上结果推测 ,不同水稻品种UV_B敏感性与CPD光修复能力的差异有关。     

UV-B辐射引起的绿豆幼苗叶片Rubisco量降低与H2O2含量升高有关

为了探讨UV-B辐射引起的Rubisco含量降低的可能机制,研究了两个绿豆品种(秦豆-20和中绿-1)幼苗在UV-B辐射下叶片Rubisco含量、蛋白水解酶活性和H2O2含量的变化.结果表明:UV-B辐射显著加速了两个绿豆品种幼苗叶片H2O2含量和蛋白水解酶活性上升,使Rubiscco含量下降.秦豆-20品种在UV-B辐射下H2O2含量和蛋白水解酶活性的上升程度明显大于中绿-1,相应其Rubisco含量的下降程度也大于中绿-1.抗坏血酸处理能明显降低UV-B辐射下两品种幼苗叶片H2O2含量,同时明显抑制蛋白水解酶活性的上升及Rubisco含量的下降.结果说明UV-B辐射诱导Rubisco含量的降低可能通过提高H2O2水平从而加强蛋白水解酶系统的活化而加速了Rubisco的降解.     

NaCl胁迫对菜用大豆种子膨大过程中抗氧化系统及渗透调节物质的影响

采用蛭石栽培试验,在100mmol.L-1 NaCl胁迫下,对耐盐性不同的两个菜用大豆品种种子膨大、抗氧化系统及渗透调节物质进行了研究。结果显示:(1)耐盐品种‘绿领特早’种子干质量及大小的增加在NaCl胁迫15d时未受显著影响,而盐敏感品种‘理想高产95-1’种子的膨大受到了显著抑制。(2)NaCl胁迫导致菜用大豆种子超氧阴离子(O2.-)、过氧化氢(H2O2)及丙二醛(MDA)的过量积累,但‘绿领特早’种子的相对积累量均低于‘理想高产95-1’。(3)与‘理想高产95-1’相比,‘绿领特早’在NaCl胁迫期间维持了相对较高的超氧化物歧化酶(SOD)、抗坏血酸过氧化物酶(APX)及谷胱甘肽还原酶(GR)活性,以及较高的抗坏血酸(AsA)、可溶性蛋白和可溶性糖含量;胁迫中期维持了相对较高的过氧化物酶(POD)活性,胁迫后期维持了相对较高的过氧化氢酶(CAT)活性;胁迫前中期维持了相对较高的谷胱甘肽(GSH)含量。研究发现,‘绿领特早’种子在NaCl胁迫期间能够保持较高且协调平衡的保护酶SOD、POD、CAT活性和较高的AsA-GSH循环效率,同时维持了较强的渗透调节能力,有效抑制了O2.-和H2O2的过量积累,进而有效降低了细胞膜质过氧化程度,这可能是其耐盐性较强的重要原因之一。     

DNA超甲基化在小麦耐盐胁迫中的作用

运用高效液相色谱技术测定小麦(Triticum aestivumL.)耐盐品种‘德抗961’和盐敏感品种‘豫麦34’盐胁迫后叶片和根DNA中5-甲基胞嘧啶百分含量的变化,结果表明,经150 mmol/L NaCl处理6 d后,‘德抗961’叶片和根DNA中的5-甲基胞嘧啶的百分含量显著下降,但经150 mmol/L NaCl处理10 d后,耐盐品种‘德抗961’叶片和根DNA中的5-甲基胞嘧啶的百分含量都比盐敏感品种‘豫麦34’的高。由此推测DNA超甲基化可能是植物耐盐机制的一部分。     

温度对UV-B诱导的烟草叶圆片DNA损伤的影响

环丁烷嘧啶二聚体(CPD)和6-4光产物(6-4PP)是两种主要的UV-B诱导的DNA光损伤产物。利用单克隆抗体酶联免疫吸附分析法(ELISA),研究了温度对UV-B诱导的烟草叶圆片DNA损伤的影响。室温(24℃)条件下,UV-B处理引起了烟草叶圆片DNA中CPD和6-4PP的积累。0℃条件下,UV-B处理的烟草叶圆片DNA中CPD和6-4PP的积累比室温下分别降低了9.8%和12%。UV-B诱导的DNA损伤曾被认为是纯粹的光化学过程而与不受温度影响,而本实验结果表明,UV-B诱导的烟草叶圆片DNA形成CPD和6-4PP的过程具有温度依赖性。这一特性有利于植物对全球变化的适应,因而具有重要的生态学意义。     

不同耐盐性花生品种对NaCl胁迫的光合和抗逆生理响应特征

以较耐盐花生品种‘花育25’、‘鲁花12’和盐敏感品种‘海花1’、‘花育20’为材料,采用盆栽试验,设置0、1.0、2.0、3.0 g/kg土壤NaCl胁迫浓度梯度,测定其净光合速率、表观量子效率、气孔导度等光合特性,以及抗氧化酶活性和渗透调节物质含量等指标,明确NaCl胁迫条件下不同耐盐性花生品种光合和生理生化特性的适应特征。结果表明：(1)NaCl胁迫明显抑制各品种花生叶片光合作用,净光合速率随盐胁迫浓度的升高呈明显降低的趋势。(2)各品种花生叶片净光合速率均先随光照强度的增强而升高,当光强达到一定数值时趋于平稳;光补偿点和光饱点因品种和盐胁迫浓度差异较大,较高的盐胁迫浓度使叶片光补偿点升高,盐敏感品种的光饱和点降低。(3)盐胁迫条件下,各品种叶片表观量子效率和最大净光合速率均随盐胁迫强度的增加呈显著降低趋势,盐敏感品种利用弱光的能力在低盐胁迫下强于耐盐品种,其最大净光合速率在较高盐胁迫浓度(3.0 g/kg)下明显低于耐盐品种,但两类品种的叶片表观量子效率降幅相近(78.65%~88.00%)。(4)在NaCl胁迫下,耐盐品种叶片自由水含量显著高于盐敏感品种;在2.0～3.0 g/kg NaCl胁迫下,耐盐品种叶片SOD、CAT、POD活性和MDA含量的升降幅度均低于盐敏感品种;耐盐品种在NaCl浓度低于2.0 g/kg时的抗氧化能力明显高于盐敏感品种。研究发现,盐胁迫下花生品种抗盐耐逆的主要生理响应特征是提高光补偿点和最大净光合速率,增强叶片持水能力和物质代谢能力,以及提升抗氧化和渗透调节能力。     

外源Spd对低温胁迫下甜瓜幼苗光合与抗氧化特性及其相关基因表达的影响

为探讨外源亚精胺(Spd)诱导甜瓜耐低温胁迫的生理与分子机制,该研究以甜瓜耐低温品种‘世纪蜜’和低温敏感品种‘GL-1’为试验材料,在人工气候箱内采用基质栽培法,对其叶面喷施外源Spd,对低温胁迫及恢复后甜瓜幼苗生长、光合作用、抗氧化酶活性等生理指标进行测定,并利用定量PCR技术分析4种抗氧化酶基因在低温胁迫条件下的表达特性,分析外源Spd缓解低温胁迫的效应。结果表明:(1)低温胁迫显著抑制甜瓜幼苗的生长及其光合作用,降低幼苗叶绿素含量,显著增强抗氧化酶活性及相关基因表达水平,且对品种‘GL-1’影响大于‘世纪蜜’。(2)外源Spd处理可以有效促进甜瓜幼苗的生长,提高叶片叶绿素含量、净光合速率(Pn)、气孔导度(Gs)、蒸腾速率(Tr)、气孔限制值(Ls)、水分利用效率(WUE),以及最大光化学效率(Fv/Fm)、光系统Ⅱ光能捕获效率(Fv′/Fm′)和表观光合电子传递速率(ETR),降低胞间CO2浓度(Ci)和初始荧光(Fo)。(3)外源Spd可诱导低温胁迫下甜瓜抗氧化酶活性和基因表达量发生改变,并提高了低温胁迫下甜瓜幼苗叶片超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)和抗坏血酸过氧化酶(APX)基因的表达,从而增强这些抗氧化酶活性,有效缓解低温胁迫造成的氧化胁迫伤害。(4)与对照相比,外源Spd对低温胁迫下品种‘GL-1’各指标降低或升高的幅度大于品种‘世纪蜜’。研究发现,Spd有利于甜瓜幼苗在低温胁迫下光合作用的维持,提高光合电子传递效率、光能的捕获与转换,并提高抗氧化酶活性和相关基因表达水平,促进甜瓜幼苗的生长,有效缓解低温胁迫对甜瓜幼苗生长的抑制作用,且Spd对低温敏感品种‘GL-1’缓解效果优于耐低温品种‘世纪蜜’。     

NaCl胁迫对醋栗番茄、樱桃番茄和番茄幼苗生长、叶片气体交换和离子平衡的影响

以醋栗番茄( Solanum pimpinellifolium Linn.)、樱桃番茄品种‘秦皇贵妃红’( S. lycopersicum var. cerasiforme‘Qinhuangguifeihong’)和番茄品种‘浙粉202’(S. lycopersicum‘Zhefen 202’)幼苗为材料,研究了0(对照)、100、200 mmol·L-1 NaCl胁迫对其生长、叶片气体交换参数和离子平衡的影响。结果表明：在100和200 mmol·L-1 NaCl胁迫下,‘秦皇贵妃红’和‘浙粉202’幼苗单株总干质量的降幅较大,醋栗番茄的降幅较小。 NaCl胁迫明显增加醋栗番茄幼苗的根冠比,但不同胁迫条件下‘秦皇贵妃红’和‘浙粉202’幼苗的根冠比差异不显著。与对照相比,在100 mmol·L-1 NaCl胁迫下,醋栗番茄幼苗叶片的净光合速率( Pn)、胞间CO2浓度( Ci)和蒸腾速率( Tr)的降幅明显低于‘秦皇贵妃红’和‘浙粉202’,而醋栗番茄幼苗叶片气孔导度(Gs)的降幅明显高于后二者;在200 mmol·L-1 NaCl胁迫下,三者叶片Pn、Gs、Ci和Tr值的降幅接近。在100和200 mmol·L-1 NaCl胁迫下,醋栗番茄、‘秦皇贵妃红’和‘浙粉202’幼苗叶片的水分利用效率和气孔限制值均较各自对照显著升高,其中‘秦皇贵妃红’的增幅最大。在100和200 mmol·L-1 NaCl胁迫下,醋栗番茄、‘秦皇贵妃红’和‘浙粉202’幼苗根、茎和叶中Na+含量均较各自对照显著升高,而K+含量和K+/Na+比总体上较各自对照显著降低。与对照相比,经不同浓度NaCl处理后醋栗番茄幼苗根、茎和叶的Na+含量增幅以及K+含量降幅在供试3种植物中均最小,而其不同部位的K+/ Na+比总体上较高。上述研究结果表明：醋栗番茄的耐盐性较强,‘秦皇贵妃红’次之,‘浙粉202’较弱。 NaCl胁迫显著抑制‘秦皇贵妃红’和‘浙粉202’幼苗根的生长,但显著促进醋栗番茄幼苗根的生长,使其维持较强的耐盐性,且NaCl胁迫下醋栗番茄对Na+的吸收和运输减少,以维持体内的离子平衡及较强的光合作用。     

云杉幼苗对气候变暖和UV-B辐射增强的光合响应

采用开顶式有机玻璃罩(OTCs)及紫外灯分别模拟气候变暖和紫外辐射B(UV-B)增强,对位于气候变暖和UV-B增强突出的青藏高原东缘、高山峡谷地云杉(Picea asperata)幼苗的光合气体交换和叶绿素荧光参数进行测定分析,探讨云杉幼苗对气候变暖和UV-B增强的光合响应特性。结果显示:(1)UV-B辐射增强显著抑制了云杉幼苗茎和根的伸长生长以及生物量的累积,显著降低了云杉幼苗的净光合速率(Pn)、最大光合速率(Pmax)和表观量子产量(Φ),但是提高了光补偿点(LCP);UV-B辐射增强导致了云杉幼苗光合系统Ⅱ(PSⅡ)的光抑制,使PSⅡ有效量子产量(ΦPSⅡ)显著降低。(2)单纯OTC模拟增温显著提高了云杉幼苗的Pn和Pmax,而对气孔导度(Gs)、蒸腾速率(Tr)和Φ无显著影响。(3)模拟增温缓解了UV-B增强对云杉幼苗光合作用的抑制作用,显著提高了UV-B胁迫下幼苗的Pn、Pmax、PSⅡ的潜在量子效率(Fv/Fm)和有效量子产量(ΦPSⅡ),并且提高了UV-B胁迫下幼苗茎、根的生长以及生物量的累积。研究表明,在未来气候变暖和UV-B辐射增强同时存在时,气候变暖能够在一定程度上缓解UV-B增强对云杉林光合作用的抑制作用。     

Characterization of Arabidopsis photolyase enzymes and analysis of their role in protection from ultraviolet-B radiation

DNA photolyases are enzymes which mediate the light-dependent repair (photoreactivation) of UV-induced damage products in DNA by direct reversal of base damage rather than via excision repair pathways. Arabidopsis thaliana contains two photolyases specific for photoreactivation of either cyclobutane pyrimidine dimers (CPDs) or pyrimidine (6-4)pyrimidones (6-4PPs), the two major UV-B-induced photoproducts in DNA. Reduced FADH and a reduced pterin were identified as cofactors of the native Arabidopsis CPD photolyase protein. This is the first report of the chromophore composition of any native class II CPD photolyase protein to our knowledge. CPD photolyase protein levels vary between tissues and with leaf age and are highest in flowers and leaves of 3-5-week-old Arabidopsis plants. White light or UV-B irradiation induces CPD photolyase expression in Arabidopsis tissues. This contrasts with the 6-4PP photolyase protein which is constitutively expressed and not regulated by either white or UV-B light. Arabidopsis CPD and 6-4PP photolyase enzymes can remove UV-B-induced photoproducts from DNA in planta even when plants are grown under enhanced levels of UV-B irradiation and at elevated temperatures although the rate of removal of CPDs is slower at high growth temperatures. These studies indicate that Arabidopsis possesses the photorepair capacity to respond effectively to increased UV-B-induced DNA damage under conditions predicted to be representative of increases in UV-B irradiation levels at the Earth's surface and global warming in the twenty-first century.     

Ultraviolet-B-induced DNA damage and ultraviolet-B tolerance mechanisms in species with different functional groups coexisting in subalpine moorlands

High doses of ultraviolet-B (UV-B; 280–315 nm) radiation can have detrimental effects on plants, and especially damage their DNA. Plants have DNA repair and protection mechanisms to prevent UV-B damage. However, it remains unclear how DNA damage and tolerance mechanisms vary among field species. We studied DNA damage and tolerance mechanisms in 26 species with different functional groups coexisting in two moorlands at two elevations. We collected current-year leaves in July and August, and determined accumulation of cyclobutane pyrimidine dimer (CPD) as UV-B damage and photorepair activity (PRA) and concentrations of UV-absorbing compounds (UACs) and carotenoids (CARs) as UV-B tolerance mechanisms. DNA damage was greater in dicot than in monocot species, and higher in herbaceous than in woody species. Evergreen species accumulated more CPDs than deciduous species. PRA was higher in Poaceae than in species of other families. UACs were significantly higher in woody than in herbaceous species. The CPD level was not explained by the mechanisms across species, but was significantly related to PRA and UACs when we ignored species with low CPD, PRA and UACs, implying the presence of another effective tolerance mechanism. UACs were correlated negatively with PRA and positively with CARs. Our results revealed that UV-induced DNA damage significantly varies among native species, and this variation is related to functional groups. DNA repair, rather than UV-B protection, dominates in UV-B tolerance in the field. Our findings also suggest that UV-B tolerance mechanisms vary among species under evolutionary trade-off and synergism.     

UV—B诱导水稻叶片DNA形成CPD的研究

采用单克隆抗ELISA检测了UV－B对水稻叶片CPD的诱导形成及温度的影响,水稻叶片中CPD的积累随UV－B处理时间的延长而增加;UV－B诱导的CPD形成具有温度依赖性,在0－30℃的不范围内,较低温度下UV－B诱导的CPD较少。     

Strategies of ultraviolet-B protection in microscopic algae

Different species of microalgae show a wide range of susceptibility to ultraviolet-B (UV-B) radiation. To identify factors responsible for the UV-B tolerance of some of the algae, we compared 8 species that are highly tolerant to UV-B to 8 species that are highly susceptible. The tolerant species contained substantial amounts of an acetolysis-resistant residue. The residue consists of sporopollenin, a biopolymer of variable chemical composition that occurs in the algal cell walls and absorbs UV-B radiation. The susceptible species contained little or no sporopollenin. We propose that sporopollenin provides protection to the tolerant species by screening the incident UV-B radiation. Previous studies showed that the mycosporine-like amino acids (MAA) also act as effective UV-B screens. Our data indicate that sporopollenin provides a constant protection while MAA are induced by radiation stress and occur with some delay. The tolerant species also differ from the susceptible species in their capacity to repair the reaction centers damaged by UV-B. The tolerant algae became vulnerable to UV-B when protein synthesis needed for repair was blocked by streptomycin. In the susceptible species, streptomycin had no effect during the UV-B stress. The repair deficiency in the susceptible species can be explained either by relatively less effective protein synthesis or by an inhibition of the protein synthesis by UV-B. In the tolerant species, the structures needed for protein synthesis are protected by UV-B screening of sporopollenin and MAA.     

Marine Bacterial Isolates Display Diverse Responses to UV-B Radiation

The molecular and biological consequences of UV-B radiation were investigated by studying five species of marine bacteria and one enteric bacterium. Laboratory cultures were exposed to an artificial UV-B source and subjected to various post-UV irradiation treatments. Significant differences in survival subsequent to UV-B radiation were observed among the isolates, as measured by culturable counts. UV-B-induced DNA photodamage was investigated by using a highly specific radioimmunoassay to measure cyclobutane pyrimidine dimers (CPDs). The CPDs determined following UV-B exposure were comparable for all of the organisms except Sphingomonas sp. strain RB2256, a facultatively oligotrophic ultramicrobacterium. This organism exhibited little DNA damage and a high level of UV-B resistance. Physiological conditioning by growth phase and starvation did not change the UV-B sensitivity of marine bacteria. The rates of photoreactivation following exposure to UV-B were investigated by using different light sources (UV-A and cool white light). The rates of photoreactivation were greatest during UV-A exposure, although diverse responses were observed. The differences in sensitivity to UV-B radiation between strains were reduced after photoreactivation. The survival and CPD data obtained for Vibrio natriegens when we used two UV-B exposure periods interrupted by a repair period (photoreactivation plus dark repair) suggested that photoadaptation could occur. Our results revealed that there are wide variations in marine bacteria in their responses to UV radiation and subsequent repair strategies, suggesting that UV-B radiation may affect the microbial community structure in surface water.     

Intraspecific responses of <Emphasis Type="Italic">Fagopyrum esculentum</Emphasis> to enhanced ultraviolet B radiation

The effects of supplemental UV-B radiation on crop growth, morphology, reproduction and physiology were studied in three cultivars of Fagopyrum esculentum Moench (buckwheat) originating from high elevation (Qinghai-Tibet plateau) and lower altitudes (The Sichuan Basin). Our results showed that common buckwheat was sensitive to UV-B stress. Plant growth, development, and reproduction were inhibited by elevated UV-B radiation. Plant lipid oxidation and polyphenol oxidase (PPO) activity increased with increasing UV-B radiation, along with the concentration of phenylpropanoid compounds, superoxide dismutase (SOD) activity and ascorbic acid (Asa) concentration were also enhanced at the lowest level of supplemental UV-B radiation but decreased at the higher level of enhanced UV-B. While, a cultivar originating from elevated locations had lower dry matter accumulation and was more tolerant to UV-B radiation than cultivars originating from lower elevations. The effects on leaf thickness and increased antioxidant capacity could be linked with the improved performance of cultivar originating from high elevation when exposed to enhanced UV-B radiation. We conclude that UV-B tolerance should be considered prior to introducing or breeding common buckwheat cultivars from lowland cultivation to regions at high elevation such as the Qinghai-Tibet plateau.