Xanthophyll Cycle and Inactivation of Photosystem Ⅱ Reaction Centers Alleviating Reducing Pressure to Photosystem Ⅰ in Morning Glory Leaves under Short-term High Irradiance

Under 30-min high irradiance （1500μmol m^-2 s^-1）, the roles of the xanthophyll cycle and D1 protein turnover were investigated through chlorophyll fluorescence parameters in morning glory （Ipomoea setosa） leaves, which were dipped into water, dithiothreitol （DTT） and lincomycin （LM）, respectively. During the stress, both the xanthophyll cycle and D1 protein turnover could protect PSI from photoinhibition. In DTT leaves, non-photochemical quenching （NPQ） was inhibited greatly and the oxidation level of P700 （P700^＋） was the lowest one. However, the maximal photochemical efficiency of PSII （Fv/Fm） in DTT leaves was higher than that of LM leaves and was lower than that of control leaves. These results suggested that PSI was more sensitive to the loss of the xanthophyll cycle than PSII under high irradiance. In LM leaves, NPQ was partly inhibited, Fv/Fm was the lowest one among three treatments under high irradiance and P700^＋ was at a similar level as that of control leaves. These results implied that inactivation of PSII reaction centers could protect PSI from further photoinhibition. Additionally, the lowest of the number of active reaction centers to one inactive reaction center for a PSII cross-section （RC/CSo）, maximal trapping rate in a PSll cross-section （TRo/CSo）, electron transport in a PSll cross-section （ETo/CSo） and the highest of 1-qP in LM leaves further indicated that severe photoinhibition of PSII in LM leaves was mainly induced by inactivation of PSII reaction centers, which limited electrons transporting to PSh However, relative to the LM leaves the higher level of RC/CSo, TRo/CSo, Fv/Fm and the lower level of 1-qP in DTT leaves indicated that PSI photoinhibition was mainly induced by the electron accumulation at the PSI acceptor side, which induced the decrease of P700^＋ under high irradiance.     

Xanthophyll Cycle and Inactivation of Photosystem Ⅱ Reaction Centers Alleviating Reducing Pressure to Photosystem Ⅰ in Morning Glory Leaves under Short-term High Irradiance

investigated through chlorophyll fluorescence parameters in morning glory (Ipomoea setosa) leaves, which were dipped into water, dithiothreitol (DTT) and lincomycin (LM), respectively. During the stress, both the xanthophyll cycle and D1 protein turnover could protect PSI from photoinhibition. In DTT leaves, non-photochemical quenching (NPQ) was inhibited greatly and the oxidation level of P700 (P700+) was the lowest one. However, the maximal photochemical efficiency of PSII (Fv/Fm) in DTT leaves was higher than that of LM leaves and was lower than that of control leaves. These results suggested that PSI was more sensitive to the loss of the xanthophyll cycle than PSII under high irradiance. In LM leaves, NPQ was partly inhibited, Fv/Fm was the lowest one among three treatments under high irradiance and P700+ was at a similar level as that of control leaves. These results implied that inactivation of PSII reaction centers could protect PSI from further photoinhibition. Additionally, the lowest of the number of active reaction centers to one inactive reaction center for a PSII cross-section (RC/CSo), maximal trapping rate in a PSII cross-section (TRo/CSo), electron transport in a PSII cross-section (ETo/CSo) and the highest of 1-qP in LM leaves further indicated that severe photoinhibition of PSII in LM leaves was mainly induced by inactivation of PSII reaction centers, which limited electrons transporting to PSI. However, relative to the LM leaves the higher level of RC/CSo, TRo/CSo, Fv/Fm and the lower level of 1-qP in DTT leaves indicated that PSI photoinhibition was mainly induced by the electron accumulation at the PSI acceptor side, which induced the decrease of P700+ under high irradiance.     

Light inactivation of functional photosystem II in leaves of peas grown in moderate light depends on photon exposure

To determine the dependence of in vivo photosystem (PS) II function on photon exposure and to assign the relative importance of some photoprotective strategies of PSII against excess light, the maximal photochemical efficiency of PSII (Fv/Fm) and the content of functional PSII complexes (measured by repetitive flash yield of oxygen evolution) were determined in leaves of pea (Pisum satlvum L.) grown in moderate light. The modulation of PSII functionality in vivo was induced by varying either the duration (from 0 to 3 h) of light treatment (fixed at 1200 or 1800 mol photons · m^-2 · s^-1) or irradiance (from 0 to 3000 mol photons · m^-2 · s^-1) at a fixed duration (1 h) after infiltration of leaves with water (control), lincomycin (an inhibitor of chloroplast-encoded protein synthesis), nigericin (an uncoupler), or dithiothreitol (an inhibitor of the xanthophyll cycle) through the cut petioles of leaves of 22 to 24-day-old plants. We observed a reciprocity of irradiance and duration of illumination for PSII function, demonstrating that inactivation of functional PSII depends on the total number of photons absorbed, not on the rate of photon absorption. The Fv/Fm ratios from photoinhibitory light-treated leaves, with or without inhibitors, declined pseudo-linearly with photon exposure. The number of functional PSII complexes declined multiphasically with increasing photon exposure, in the following decreasing order of inhibitor effect: lincomycin > nigericin > DTT, indicating the central role of D1 protein turnover. While functional PSII and Fv/Fm ratio showed a linear relationship under high photon exposure conditions, in inhibitor-treated leaves the Fv/Fm ratio failed to reveal the loss of up to 25% of the total functional PSII under low photon exposure. The loss of this 25% of less-stable functional PSII was accompanied by a decrease of excitation-energy trapping capacity at the reaction centre of PSII (revealed by the fluorescence parameter, 1/Fo-1/Fm, where Fo and Fm stand for chlorophyll fluorescence when PSII reaction centres are open and closed, respectively), but not by a loss of excitation energy at the antenna (revealed by the fluorescence parameter, 1/Fm). We conclude that (i) PSII is an intrinsic photon counter under photoinhibitory conditions, (ii) PSII functionality is mainly regulated by D1 protein turnover, and to a lesser extent, by events mediated via the transthylakoid pH gradient, and (iii) peas exhibit PSII heterogeneity in terms of functional stability during photon exposure.Abbreviations D1 protein psbA gene product - DTT dithiothreitol - Fo chlorophyll fluorescence corresponding to open PSII reaction centres - Fv, Fm variable and maximum fluorescence after dark incubation, respectively - Fs, Fm steady-state and maximum fluorescence during illumination, respectively - P680 reactioncentre chlorophyll and primary electron donor of PSII - PS photosystem Financial support of this work by Department of Employment, Education and Training/Australian Research Council International Research Fellowships Program (Korea) is gratefully acknowledged.     

A comparative analysis of wild and laboratory grown Laminaria abyssalis (Phaeophyta) using modulated fluorescence

Laminaria abyssalis fronds were either collected at the Brazilian costal area - 40 meters below sea level - or grown in the laboratory. The photochemical yield as defined by the Fv/Fm and the Fo - the dark fluorescence level when all PSII centers are open - varied with the distance from the stipe to the tip of the blade in wild grown fronds while it stayed constant in the laboratory grown plants. The chlorophyll a/c ratio levels decreased in the wild fronds from 12 (near the stipe) to 6 near the top. The chlorophyll c content increased from 0.8 to near 1.7 mg cm^–2 in the wild fronds. The laboratory fronds did not show variations in their chlorophyll contents. The wild fronds pattern changed after 2 months kept in the laboratory, producing similar results to those grown in the laboratory. The results indicate that the levels of the antenna complex in the wild fronds increase from the stipe to the top of the blade, in a fashion similar of the sun/shade leaves. Also, results show, that this alga is able to adapt itself to new light conditions, possibly increasing its level of antenna complex and photosynthetic units.Abbreviations PSII Photosystem II - Fo Chlorophyll fluorescence when all PSII are opened - Fm Chlorophyll Fluorescence when all PSII are closed - Fv Variable Fluorescence (Fm-Fo) - Fv/Fm Quantum Yield for Photochemistry     

草莓叶片光合作用对强光的响应及其机理研究

用便携式调制叶绿素荧光仪和光合仪研究了强光下草莓叶片荧光参数及表观量子效率的变化.结果表明,Fm、Fv/Fm、PSⅡ无活性反应中心数量和Q_A的还原速率在强光下降低,在暗恢复时升高;而PSⅡ反应中心非还原性Q_B的比例在强光下增加,在暗恢复时降低.上述荧光参数的变化幅度均以强光胁迫或暗恢复的前10 min最大.强光下Φ_PSII、ETR和qP先升高后降低,但qN先大幅度降低,然后小幅回升.强光处理4 h后,丰香和宝交早生的表观量子效率(AQY)分别降低了20.9%和37.5%;qE(能量依赖的非光化学猝灭)为NPQ(非光化学猝灭)的最主要成分.强光胁迫下丰香的Fo、Fm、Fv/Fm、Φ_PSII、ETR和AQY的变化幅度均明显比宝交早生小.DTT处理后,草莓叶片的Fm和Fv/Fm明显降低,Fo显著升高.可以认为,依赖叶黄素循环和类囊体膜质子梯度两种非辐射能量耗散在草莓叶片防御光损伤方面起着重要作用,丰香的光合机构比宝交早生更耐强光.     

高温胁迫对柑橘光合速率和光系统Ⅱ活性的影响

用红外CO2分析仪和叶绿素荧光仪测定了温州蜜柑和脐橙叶片的净光合速率(Pn)、初始荧光(Fo)、最大光能转换效率(Fv／Fm)及电子传递速率(ETR)．结果表明,与常温(25℃)相比,高温胁迫(38～40℃)使温州蜜柑和脐橙叶片的Pn、Fv／Fm及ETR下降,Fo升高．胁迫25d后温州蜜柑和脐橙叶片的Pn分别下降55．6％和39．8％．Fv／Fm下降22．0％和6．7％,ETR下降55．0％和41．5％,Fo分别上升了113．8％和14．9％．柑橘经高温胁迫后,在25℃下处理10d,叶片的Pn、Fv／Fm、Fo及ETR恢复明显．这些结果说明柑橘的光合速率下降与PSⅡ反应中心失活有关．     

Effects of Strong Light and Active Oxygen on Photosynthesis in Soybean

With the use of chlorophyll fluorescence technique, it was found that the net photosynthetic oxygen evolution rate decreased after strong light (2 000 μmol· m-2·2-1 ) treatment for two hours in soybean ( Glycine max L. ) leaves. The chlorophyll fluorescence parameters, Fm/Fo, Fv/Fm, ФPSII, qp and qN decreased along with the increase of light intensity. In strong light, exogenous active oxygen H202、·OH and 'O2 were harmful to soybean leaves. The destruction of 'O2 and·OH to leaves was most evident, as was shown that Fv/Fm and PS H decreased significantly. The antioxidants DABCO, mannitol, ascorbate and histidine protected the leaves, but weakly, from strong light. In darkness, the SOD inhibitor sodium diethyldithiocar- bamate (DDC) had no significant effect on Fm/Fo and Fv/Fm, but NAN,, the ascorbate peroxidase (APX)inhibitor, significantly decreased Fm/Fo, Fv/Fm and ФPS II. In strong light, however, beth DDC and NaN3 reduced the above-mentioned fluorescence parameters, but NaN3 was more effective than DDC. The results suggested that photoinhibition did take place in soybean leaves under strong light, and it was related to active oxygen in vivo.     

高温强光下水杨酸对黄瓜叶片叶绿素荧光和叶黄素循环的影响

在高温强光条件下,研究了外源水杨酸对黄瓜叶片叶绿素荧光参数和叶黄素循环的影响.结果表明,在高温强光胁迫前2 d用50～400 μmol·L^-1水杨酸处理叶片,抑制了高温强光下原初光能转换效率(F_v/F_m)、光合电子传递量子效率(ΦPSⅡ)、最大荧光(F_m)和光化学猝灭系数(qP)的下降,分别比对照提高了16.1%～30.2%、11.9%～33.0%、7.2%～41.0%和27.2%～160.8%,促进了非光化学猝灭系数(NPQ)的升高,比对照提高了13.1%～62.9%,而对初始荧光(F_o)影响不大.水杨酸处理可减小高温强光下叶黄素循环库的下降幅度,使(A+Z)/(V+A+Z)升高,分别比对照高29.5%和24.6%.这些结果说明,水杨酸可通过提高非辐射能量耗散,对高温强光引起的黄瓜叶片光合机构的破坏具有保护作用.     

柑橘叶片中叶黄素循环对PSII反应中心D1蛋白的保护效应

用叶黄素循环抑制剂二硫苏糖醇（DTT）处理7h的柑橘离体叶片,其非光化学猝灭系数NPQ大幅度下降;在中等强度光（500μmol·m^-2·s^-1）和高强度光（1500μmol·m^-2·s^-1）下,DTT处理的叶片光化学效率（Fv/Fm）分别下降3．8％和39．7％,光合电子传递速率（ETR）分别下降12％和49．5％,D1蛋白含量也分别下降87％和92.3％;黑暗对DTT处理叶片的各种荧光参数和D1蛋白的影响不大。显示叶黄素循环在保护光系统（PS）II反应中心、抵御光抑制中有一定的积极效应,可能影响了D1蛋白周转。     

外源Ca2＋对高温强光胁迫下灌浆期小麦叶片光合机构运转的影响

灌浆期叶面喷施10mmol·L-1 CaCl2对高温强光胁迫下小麦叶片光合电子传递、放氧速率、叶绿素荧光参数和D1蛋白的影响结果表明,Ca2＋预处理可保护D1蛋白,削弱其降解,提高光系统I（PSI）和光系统Ⅱ（PSⅡ）子传递速率、全链电子传递速率、净光合速率（Pn）、PSII最大光化学效率（Fv/Fm）、PSII实际光化学效率（ΦPSⅡ）和光化学猝灭（qp）,维持较低的Fo,最终导致小麦适应高温强光的能力提高。     

运用叶绿素a荧光诱导动力学技术检测水稻生产潜力

运用叶绿素a荧光诱导动力学技术,检测水稻叶片和叶绿体的PSII原初光转化效率(F_v/F_m)或与此相关可代表PSII潜在活性(F_v/F_o)的参数,结果表明,不同产量水平的水稻品种之间,其叶片和叶绿体的F_v/F_m(或F_v/F_o)的比值,以及光合电子传递速率均有明显差异.此外,在外源Mg~(2+)的存在下,高产水稻品种叶绿体有更高的原初光能转化效率,同时Mg~(2+)对高产品种叶绿体PSII和PSI之间激发能分配的调节能力也较低产品种者高.实验说明Chl a荧光诱导动力学的技术,能够作为一种快速、灵敏和简便的有效方法用于早期检测水稻(或其他作物)的生产潜力.     

Photoinhibition of Photosynthesis Without Net Loss of D1 Protein in Wheat Leaves Under Field Conditions

To determine whether the net loss of D1 protein is the main cause of photoinhibition of photosynthesis in wheat leaves under field conditions in the absence of any environmental stress other than strong sunlight, the D1 protein content, photosynthetic evolution of oxygen and chlorophyll a fluorescence parameters were measured in field grown wheat leaves. After exposure to midday strong light for about 3 h, apparent photosynthetic quantum efficiency (Φ), Fv/Fm and Fo in wheat leaves declined, and these parameters recovered almost completely 1 h after transfer to the weak light of 30~40 ttmol photons · m-2 · s-1. No evident change in the D1 protein content was observed in the leaves after exposure to midday strong light for 3 h. After 3 hours exposure to strong light, the slow-relaxed fluorescence quenching in the leaves treated with streptomycin (SM) increased much more than that in the control leaves, but there was no effect SM on the recovery of Fv/Fm and F0; dithiothretol (DTT) treatment enhanced photoinhibition of photosynthesis and reduced the D1 protein content in the leaves after exposure to midday strong light. These results indicated that under field conditions with no environmental stress other than strong sunlight, photoinhibition of photosynthesis in wheat leaves was not due to the net loss of D1 protein, and it could be attributed mainly by the increased nonradiative energy dissipation.     

Development of photosynthetic apparatus and respiration in pea seedlings during greening as influenced by toxic concentration of lead

Detached leaves of 14 day-old dark-grown pea seedlings were immersed with their cut ends either in water (control) or in 20 mM Pb(NO₃)₂ solution. They were exposed to continuous illumination during 24 and 48 h. The formation of PSII primary photochemistry in thylakoids was determined in vivo by measuring changes in values of parameters of chlorophyll a fast fluorescence kinetics: Fo, Fm, Fv, Fv/Fm and t 1/2. The amount of lead accumulation in leaves, content of chlorophylls and carotenoids and rates of CO₂ uptake in light and evolution in darkness (Pn-net photosynthesis and DR - dark respiration respectively) were determined. It has been found that with the exception of Fo, values of Fv, Fm and Fv/Fm were reduced by Pb²⁺. The values of t 1/2 were significantly larger in Pb²⁺ treated leaves. Decrease in the chlorophyll a fluorescence parameters was paralleled with the strong inhibition by this metal the biosynthesis of chlorophyll a and b but less of the carotenoids. Pb²⁺ drastically reduced Pn but had a stimulatory action on DR after 24 h and small inhibition of DR after 48 h exposure of leaves to this metal. As a consequence, after 48 h of greening the ratio of DR/Pn of control leaves was 0.45 whereas in Pb²⁺ treated leaves 2.7. It is proposed that DR in leaves plays a protective role against damage of Pn by Pb²⁺. Protection can be due to the supply the respiratory derived reductant and ATP to carry out cell metabolism upon reduced photosynthesis.     

不同剂量^137Cs-γ辐射对毛竹幼苗叶片叶绿素荧光参数的影响

利用不同剂量的137Cs-γ射线对毛竹（Phyllostachys heterocycla ‘Pubescens’）种子进行辐射, 测定实生苗叶片中的光合色素含量和叶绿素荧光参数等指标, 探讨辐射对毛竹幼苗生长的影响, 为筛选有利的突变单株奠定良好基础。结果表明：30或60 Gy的137Cs-γ射线辐射后, 毛竹幼苗的光合色素含量以及最大荧光强度（Fm）、可变荧光强度（Fv）、PSII最大光化学效率（Fv/Fm）、PSII的潜在活性（Fv/Fo）、PSII实际光化学效率（Yield）和表观光合电子传递速率（ETR）等荧光参数值均高于90 Gy辐射处理, 说明较低剂量辐射后PSII反应中心的能量捕获效率高, 且具有较强的光合能力; 而90 Gy的137Cs-γ射线辐射对毛竹的影响则与之相反。不同处理剂量之间叶片光能耗散程度以及表观光合电子传递速率-光合有效辐射（ETR-PAR）响应曲线的分析结果也进一步证实了以上结论。     

Photoinhibition in cork-oak leaves under stress: influence of the bark-stripping on the chlorophyll fluorescence emission inQuercus suber L.

Quercus suber is the primary source for industrial cork and becomes bark-stripped every 9–10 years. Recurring cork extraction is a major stress factor and the large water loss from the stripped trunk surface may affect the water balance and tree productivity. To evaluate the effect of bark-stripping, fluorescence emission and stomatal conductance of leaves were determined in groups of bark-stripped and control trees. Fv/Fm ratio was found to be significantly lower in bark-stripped trees indicating a reduced photosynthetic efficiency of PSII. Photosynthesis was not found to be stomata limited. The reduction in Fv/Fm resulted from a decline in maximum and variable fluorescence while the initial fluorescence of the dark-adapted state (Fo) remained constant. A general decline in photosynthetic efficiency of PSII was found in all trees during the summer, probably reflecting the prolonged environmental stresses during a hot and dry season. Additional stress caused by the bark-stripping seems to enhance the susceptibility to photoinhibition of the trees.     

Arbuscular mycorrhizae improves low temperature stress in maize via alterations in host water status and photosynthesis

The effect of arbuscular mycorrhizal (AM) fungus, Glomus etunicatum, on growth, water status, chlorophyll concentration and photosynthesis in maize (Zea mays L.) plants was investigated in pot culture under low temperature stress. The maize plants were placed in a sand and soil mixture at 25°C for 7 weeks, and then subjected to 5°C, 15°C and 25°C for 1 week. Low temperature stress decreased AM root colonization. AM symbiosis stimulated plant growth and had higher root dry weight at all temperature treatments. Mycorrhizal plants had better water status than corresponding non-mycorrhizal plants, and significant differences were found in water conservation (WC) and water use efficiency (WUE) regardless of temperature treatments. AM colonization increased the concentrations of chlorophyll a, chlorophyll b and chlorophyll a + b. The maximal fluorescence (Fm), maximum quantum efficiency of PSII primary photochemistry (Fv/Fm) and potential photochemical efficiency (Fv/Fo) were higher, but primary fluorescence (Fo) was lower in AM plants compared with non-AM plants. AM inoculation notably increased net photosynthetic rate (Pn) and transpiration rate (E) of maize plants. Mycorrhizal plants had higher stomatal conductance (g_s) than non-mycorrhizal plants with significant difference only at 5°C. Intercellular CO₂ concentration (Ci) was lower in mycorrhizal than that in non-mycorrhizal plants, especially under low temperature stress. The results indicated that AM symbiosis protect maize plants against low temperature stress through improving the water status and photosynthetic capacity.     

微量元素营养对桉树无性系苗木叶绿素及荧光参数影响

研究了不同微量元素营养液,对栽培的三种桉树无性系苗木叶绿素及荧光参数变化。结果表明:各无性系苗木在全部测试性状的差异表现出极显著。在六个测试的微量元素因子中,Fe(B)显著地影响苗木的Fo、Fm、Fv/Fo、Fv/Fm,Zn(C)显著地影响Fo、Fv/Fm,Mn(D)显著地影响叶绿素含量(SPAD值),Mo(F)显著地影响叶绿素含量、Fo,B(G)显著地影响叶绿素含量Fo、Fv/Fo、Fv/Fm。相关分析表明Fm与Fo、Fv/Fo与Fo、叶绿素含量与Fo、Fm、Fv/Fm与Fv/Fo均存在显著的相关性。随着微量元素Fe、Zn、Cu、Mo、B浓度增大,Fo、Fv/Fm均呈增大趋势,但在不利的高浓度环境下,Fv/Fm降低。对三个无性系叶绿素荧光比较,U₆与DH_32-29具有高的Fo、Fm和低的Fv/Fm、Fv/Fo,DH_201-2却具有低的Fo、Fm和高的Fv/Fm、Fv/Fo。对微量元素浓度变化,DH_32-29较敏感。因此,叶绿素荧光参数可作为诊断植物微量元素营养状况的指标之一。     

Thermostability and photostability of photosystem II of the resurrection plant Haberlea rhodopensis studied by chlorophyll fluorescence

The stability of PSII in leaves of the resurrection plant Haberlea rhodopensis to high temperature and high light intensities was studied by means of chlorophyll fluorescence measurements. The photochemical efficiency of PSII in well-hydrated Haberlea leaves was not significantly influenced by temperatures up to 40 degrees C. Fo reached a maximum at 50 degrees C, which is connected with blocking of electron transport in reaction center II. The intrinsic efficiency of PSII photochemistry, monitored as Fv/Fm was less vulnerable to heat stress than the quantum yield of PSII electron transport under illumination (phiPSII). The reduction of phiPSII values was mainly due to a decrease in the proportion of open PSII centers (qP). Haberlea rhodopensis was very sensitive to photoinhibition. The light intensity of 120 micromol m(-2) s(-1) sharply decreased the quantum yield of PSII photochemistry and it was almost fully inhibited at 350 micromol m(-2) s(-1). As could be expected decreased photochemical efficiency of PSII was accompanied by increased proportion of thermal energy dissipation, which is considered as a protective effect regulating the light energy distribution in PSII. When differentiating between the three components of qN it was evident that the energy-dependent quenching, qE, was prevailing over photoinhibitory quenching, qI, and the quenching related to state 1-state 2 transitions, qT, at all light intensities at 25 degrees C. However, the qE values declined with increasing temperature and light intensities. The qI was higher than qE at 40 degrees C and it was the major part of qN at 45 degrees C, indicating a progressing photoinhibition of the photosynthetic apparatus.     

水分胁迫对牛心朴子叶片光合色素及叶绿素荧光的影响

研究了水分胁迫对牛心朴子叶片光合色素及叶绿素荧光动力学参数的影响。结果表明,在长期的水分胁迫中,牛心朴子叶片的叶绿素a(Chl a)、叶绿素b(Chl b)和类胡萝卜素(Car)含量没有下降或下降不明显。直到处理末期才显著下降;叶片叶绿素荧光动力学参数Fo、Fm、Fv、Fv／Fm变化不大,在处理末期各处理Fo降低,轻度、重度水分胁迫的Fm、Fv、Fv／Fm升高。说明K期水分胁迫后牛心朴子的光合功能受到影响,但牛心朴子仍表现出较强的适应干旱的能力。     

外源一氧化氮对干旱胁迫下杨树光合作用的影响

NO是生物体中一种自由基分子,其NO对树木叶片光合作用的影响研究未见报道.本文研究了外源NO对杨树叶片水分状况、光合作用和抗氧化物酶活力的调节作用.不同浓度SNP处理对杨树叶片含水量具有显著影响,杨树叶片含水率随着SNP浓度的提高而增加.当SNP浓度增加到00μmol·L^-1后各处理杨树叶片含水率变化趋于稳定.外源NO能提高水分胁迫下杨树叶片的光合、原初光能转化率Fv/Fm、Fm/Fo和Fv/Fo等的比值.其效果随水分胁迫时间的延长而降低.与此对应的是,短时间水分处理(1 h)的杨树叶片SOD和POD抗氧化物酶的活性显著高于长时间(3h)水分胁迫处理.SNP能显著提高不同干旱时间处理组的POD活性,而对SOD活性影响不明显.同时,随SNP浓度的增加,POD和SOD活性呈现先升后降的趋势.因此,干旱胁迫可引起杨树叶片光合效率降低,出现氧化伤害症状,外源NO可诱导抗氧化物酶POD和SOD活性的升高,缓解原初光能转化率Fv/Fm、Fm/Fo和Fv/Fo等值的降低,从而延缓活性氧积累,减轻水分胁迫对杨树叶片光合作用的影响.