Effects of Light Quality and Norflurazon on the Formation of Plastid Pigments in Cotyledons of Pinus sylvestris

The effects of different light qualities and a special inhibitor of carotenoid biosynthesis on formation of plastid pigments of cotyledons of Pinus sylvestris were studied. The experimental results indicate: 1. The rate of synthesis of carotenoids in far-red light is relatively higher than that of chlorophylls, on the contrary in red light the rate of chlorophyll synthesis is higher. 2. When biosynthesis of carotenoids is inhibited, in white light the rate of total chlorophyll synthesis reduced with similar proportion. Accumulation of chlorophyll, however, is relatively much more than that of carotenoids. The highest molar ratio of chlorophyll/carotenoids is approximately 10.0. This implicates that chlorophyll and carotenoid synthesis proceed with certain independence. 3. After 4h exposure of strong white light of 9 day-old pine seedlings grown with 10-5 mol 1-1 norflurazon in farred light, contents of carotenoids and total, chlorophyll of cotyledons increase. Chlorophyll a biosynthesis promoted by light is higher than photooxidation of the pigment.     

光质和除草剂norflurazon对欧洲赤松子叶质体色素形成的影响

本文研究了不同光质和类胡萝卜素专一抑制剂 norflurazon 对欧洲赤松(Pinussylvestris)子叶叶绿体色素形成的影响,所得结果如下:1.在远红光下,类胡萝卜素相对合成速率大于叶绿素的合成速率,而在红光下恰恰相反。2.在白光下,当类胡萝卜素合成受抑制时,叶绿素的合成速率也有所降低。但是叶绿素相对积累量比类胡萝卜素大得多,叶绿素与类胡萝卜素的分子比增大到10:1,说明这两种色素的合成与积累有相当大的独立性。3.把连续在远红光下类胡萝卜素合成受抑制(含量为正常幼苗的30%)的松苗,移入强白光下4小时后,其总叶绿素和类胡萝卜素都有增加,表明只要有少量类胡萝卜素存在,光对色素合成的促进仍大于光氧化破坏。     

Changes in ultrastructure and photosynthetic capacity withinScenedesmus obliquus mutants C-2 A′, C-6 D,and C-6 E on transfer from dark grown to illuminated conditions

Summary The ultrastructure, pigments and photosynthetic capacities of 3 X-ray induced mutants (C-2 A, C-6 D, and C-6 E) ofScenedesmus obliquus were studied whilst growing heterotrophically in the dark and upon transfer into the light (10,000 lux).Dark grown C-2 A, having no photosynthetic capacity and sparse amounts of chlorophylls a and b, greened at a faster rate than mutant C-6 D which already had photosystem I activity and chlorophyll a in the dark. Ultrastructural development to the wild-type situation was similar in both, but again much faster in C-2 A (24 hours) than in C-6 D (48 hours). In the dark grown C-2 A mutant the single lamellae differed from C-6 D in that they were already perforated. In the light, membrane overlapping took place in both to form first double, and later triple, thylakoid bands. A distinct phase of association of plastid ribosomes in a whorl-like arrangement with the developing thylakoids was shown by both only during the greening process. Over a similar period, mitochondrial appressions to these plastids were observed.In the dark, mutant C-6 E resembled dark grown C-6 D and possessed considerable photosystem I activity but no carotenoids. In the light it did not green, no ultrastructural changes were apparent and the unprotected chlorophyll a was photo-oxidized.All mutants in the dark showed tubular connections, resembling but not identical with the prolamellar bodies of higher plant etioplasts. Occasionally tubular connections similar to those in the dark-grown mutants were also found in the light.     

Inhibition of Accumulation of Bacteriochlorophyll and Carotenoids by Blue Light in an Aerobic Photosynthetic Bacterium, Roseobacter denitrificans, during Anaerobic Respiration

The effects of light on the accumulation of bacteriochlorophylland carotenoids were investigated in an aerobic photosyntheticbacterium, Roseobacter denitrificans during anaerobic respiration.Accumulation of pigments occurred in darkness but not in whitelight, with the growth rate being similar under both dark andlight conditions. Once pigments had accumulated during growthin darkness, subsequent irradiation with white light did notresult in degradation of the accumulated pigments, an indicationthat the pigments were stabilized in the membranes. The presentresults, therefore, exclude the possibility of inhibition ofthe accumulation of the photosynthetic pigments by the photochemicaldegradation of the pigments in the presence of molecular oxygenand light (blue light). The action spectrum for the inhibitionof the accumulation of the pigments showed that light at 470nm was the most effective and light at wavelengths longer than500 nm had little inhibitory effect. Together with previousresults [Shimada et al. (1992) Plant Cell Physiol. 33: 471],the present data suggest that a signal-transduction system associatedwith an unidentified blue pigment(s) is involved in the inhibitionof the accumulation of the photosynthetic pigments in R. denitrificans. (Received May 6, 1992; Accepted September 21, 1992)     

Leaf senescence in a non-yellowing mutant of Festuca pratensis: Degradation of carotenoids

The loss of pigments was assessed in detached leaves of Festuca pratensis Huds. kept in permanent darkness. Two genotypes, a normal yellowing cultivar Rossa and a non-yellowing mutant Bf 993 were compared with each other. Analysis of individual pigments, chlorophylls. β-carotene, lutein, violaxanthin and neoxanthin was performed using HPLC. In the non-yellowing genotype the high retention of chlorophylls was associated with an equally high retention of total carotenoids. Although the two genotypes differ markedly with regard to the rate of pigment loss, the ratios of yellow to green pigments did not change significantly during dark-induced senescence. At the end of the senescence period β-carotene was retained to a higher degree than the xanthophylls, particularly in the yellowing genotype. In the mutant leaves the ratio of chlorophyll a to b remained nearly constant, whereas in leaves of the normal genotype a preferential retention of chlorophyll b was observed towards the end of the senescence period. It is concluded that the thylakoids of the non-yellowing genotype retain all the principal components of protein-pigment complexes, i.e. chlorophylls, carotenoids and apoproteins. Possible explanations for the stability of these complexes in the mutant are discussed.     

Chromatic adaptation in lichen phyco- and photobionts

The effect of light quality on the photosynthetic pigments as chromatic adaptation in 8 species of lichens were examined. The chlorophylls, carotenoids in 5 species with green algae as phycobionts (Cladonia mitis, Hypogymnia physodes, H. tubulosa var. tubulosa and subtilis, Flavoparmelia caperata, Xanthoria parietina) and the chlorophyll a, carotenoids and phycobiliprotein pigments in 3 species with cyanobacteria as photobionts (Peltigera canina, P. polydactyla, P. rufescens) were determined. The total content of photosynthetic pigments was calculated according to the formule and particular pigments were determined by means CC, TLC, HPLC and IEC chromatography. The total content of the photosynthetic pigments (chlorophylls, carotenoids) in the thalli was highest in red light (genus Peltigera), yellow light (Xanthoria parietina), green light (Cladonia mitis) and at blue light (Flavoparmelia caperata and both species of Hypogymnia). The biggest content of the biliprotein pigments at red and blue lights was observed. The concentration of C-phycocyanin increased at red light, whereas C-phycoerythrin at green light.     

Efficiency of the photosynthetic apparatus in developing needles of Norway spruce (Picea abies L. Karst.)

The photosynthetic performance of developing spruce (Picea abies L. Karst.) needles was investigated. As revealed by previous reports, the biosynthesis of chlorophylls and carotenoids was not following the characteristic chloroplast ultrastructure building up during needle elongation process. The aim of our study was to investigate photosynthetic capability (evaluated by oxygen evolution and chlorophyll a fluorescence kinetics measurements), the dynamics of chloroplast pigments biosynthesis and the expression of major photosynthetic proteins as well as to find out possible correlation between components of issue. Low amounts of chlorophylls and carotenoids, LHC II and Rubisco LSU were detected in the embryonic shoot of vegetative buds. Although PS II was functional, oxygen production was not sufficient to compensate for respiration in the same developmental stage. The light compensation point of respiration was successively lowered during the needle elongation. Nevertheless the significant increase in photosynthetic pigments as well as the high level of expression of LHC II and Rubisco LSU proteins was observed in the later stages of needle development. Our results suggest that, besides light, some other environmental factors could be critical for producing fully functional chloroplasts in rapidly growing young needles.     

Effect of Temperature on Photosynthetic Activities of Senescing Detached Wheat Leaves

Changes in various components of photosynthetic activity duringthe dark induced senescence of detached wheat leaves, maintainedat 25°C (control) and 35°C (mildly elevated temperaturetreatment), were examined. Senescence-associated decline measuredup to 96 h, in photosynthetic activity was appreciably hastenedat 35°C, than at 25°C as evident by the relative higherlosses of chlorophyll, photosystem (PS) II and PS I catalyzedphotochemical activities and ribulose-1,5-bisphosphate (RuBP)carboxylase activity. In addition, a comparatively higher risein light scattering profile of isolated chloroplasts was notedat 35°C than at 25°C. Senescence-induced degradationof chlorophyll was faster at 35°C than at 25°C; on theother hand, the degradation of carotenoids was faster at 25°Cthan at 35°C. Furthermore, the ratio of carotenoids to chlorophyllincreased with senescence up to 96 hours, higher ratio beingobtained at 35°C than at 25°C. Both PS II and PS I activitiesshowed a transient rise in the beginning phase of dark incubation,whereas loss in chlorophyll was continuous throughout the periodof senescence. The initial rise observed in photochemical activitieswas attributable to the uncoupling of electron transport fromphotophosphorylation. Elevated temperature treatment resultedin greater inactivation of RuBP carboxylase than control. Itappears that during senescence the loss in chlorophyll and RuBPcarboxylase activity are triggered simultaneously. (Received June 7, 1985; Accepted October 30, 1985)     

The xanthophyll cycle is induced by light irrespective of water status in field-grown lavender (Lavandula stoechas) plants

The water relations, the photosynthetic capacity and the pigment content of leaves, i.e. chlorophylls, carotenes and xanthophylls, were analysed during the summer drought and recovery after autumn rainfalls in lavender ( Lavandula stoechas L.) plants grown in Mediterranean field conditions. Summer drought caused photoinhibition of photosynthesis and significant decreases in chlorophylls (by ca 75%), β -carotene (by ca 65%), and lutein and neoxanthin (by ca 50%), although their contents remained unaltered between predawn and midday, suggesting a progressive decrease in response to drought. In contrast, the levels of violaxanthin decreased from predawn to midday, giving rise to enhanced formation of zeaxanthin and antheraxanthin in high light. Zeaxanthin and antheraxanthin formation was not induced by water deficit. Although the levels of photosynthetic pigments were severely affected by water deficit, carotenoids decreased less than chlorophylls, which resulted in increased levels of carotenoids per unit of chlorophyll. We conclude that the enhanced formation of zeaxanthin in high light and the increased levels of carotenoids per unit of chlorophyll observed in water-stressed plants may help to avoid photoinhibitory damage to the photosynthetic apparatus.     

Die Hemmung der lichtinduzierten Chlorophyll-, Carotinoid- und Anthocyansynthese durch Äthanol

The Inhibition of the Light Induced Chlorophyll, Carotenoid and Anthocyan Synthesis by Ethanol. It is shown that already low concentrations of ethanol inhibit the light induced formation of pigments (chlorophylls, carotenoids, anthocyanins) in Raphanus-seedlings. The degree of inhibition depends on the ethanol concentration and rises with increasing incubation period. The inhibition of pigment synthesis is reversible, and immediately ceases when ethanol is removed. The formation of chlorophylls and anthocyanin is more repressed than that of carotenoids, and the formation of β-carotene to a higher extent than that of xanthophylls. It is concluded that ethanol inhibits pigment formation by inhibition of protein synthesis. These results indicate that ethanol and other lower alcohols cannot be used for the solubilizing of organic compounds when these are applied to plant tissues.     

Photosystem II efficiency in low chlorophyll,iron-deficient leaves

Iron deficiency (iron chlorosis) is the major nutritional stress affecting fruit tree crops in calcareous soils in the Mediterranean area. This work reviews the changes in PS II efficiency in iron-deficient leaves. The iron deficiency-induced leaf yellowing is due to decreases in the leaf concentrations of photosynthetic pigments, chlorophylls and carotenoids. However, carotenoids, and more specifically lutein and the xanthophylls of the V+A+Z (Violaxanthin+ Antheraxanthin+Zeaxanthin) cycle are less affected than chlorophylls. Therefore, iron-chlorotic leaves grown in either growth chambers or field conditions have increases in the molar ratios lutein/chlorophyll a and (V+A+Z)/chlorophyll a. These pigment changes are associated to changes in leaf absorptance and reflectance. In the chlorotic leaves the amount of light absorbed per unit chlorophyll increases. The low chlorophyll, iron-deficient leaves showed no sustained decreases in PS II efficiency, measured after dark adaptation, except when the deficiency was very severe. This occurred when plants were grown in growth chambers or in field conditions. However, iron-deficient leaves showed decreases in the actual PS II efficiency at steady-state photosynthesis, due to decreases in photochemical quenching and intrinsic PS II efficiency. Iron-chlorotic leaves were protected not only by the decrease in leaf absorptance, but also by down-regulation mechanisms enhancing non-photochemical quenching and thermal dissipation of the light absorbed by PS II within the antenna pigment bed. This revised version was published online in June 2006 with corrections to the Cover Date.     

Separation and quantification of pigments from natural phototrophic microbial populations

Abstract A simple high-performance liquid chromatography (HPLC) method is described for the rapid (approx. 20 min) simultaneous separation and identification of the major chlorophylls and carotenoids from phytoplankton cells and phototrophic sulfur bacteria. Lyophilized samples were extracted with acetone in the dark at room temperature. Pigments were eluted from a silica column with a hexane-acetone mixture (80: 20, v/v). About 20 algal and bacterial chlorophyll and carotenoid pigments could be separated in one run. The method allowed for the detection of trace amounts of major carotenoids (> approx. 6 ng · 1⁻¹) and of chlorophylls and pheophytins (> approx. 200 ng · 1⁻¹) in natural samples. The method has been applied to samples from the metalimnion of Lake Vechten (The Netherlands) and has proved very useful in estimating algal and bacterial pigments simultaneously with respect to depth distribution and biomass changes of the microbial populations.     

ELIPs – Light-induced stress proteins

Exposure of plants to light intensities higher than those required to saturate photosynthesis leads to a reduction in photosynthetic capacity. This effect is known as photoinhibition. Photoinhibition is followed by destruction of carotenoids, bleaching of chlorophylls and increased lipid peroxidation due to damage by oxygen-derivatives. The oxygen concentration in chloroplasts in the light is high because of oxygen production by photosystem II (PSII). This can result in the release of reactive intermediates of reduced dioxygen such as superoxide radicals, hydroxyl radicals, hydrogen peroxide or singlet oxygen. In order to maintain their normal function under light stress conditions, chloroplasts have developed multiple repair and protection systems. The induction of specific light stress proteins, the ELIPs (for early light-induced proteins) can be considered to be part of these protective responses. The accumulation of ELIPs under light stress conditions is correlated with the photoinactivation of PSII, degradation of the D_l-protein of PSII reaction centre and changes in the level of pigments. Futhermore, the accumulation of ELIPs in the thylakoids is strictly controlled by the pigment content, especially by chlorophylls. Isolation of ELIPs in a native form and analysis of pigments bound to these proteins revealed that ELIPs can bind chlorophyll a and lutein. These data indicate that ELIPs might represent unique chlorophyll-binding proteins which have a transient function(s) during light stress. A transient 'pigment-carrier' function is postulated for ELIPs.     

Loss of chlorophylls, cessation of photosynthetic CO2 assimilation and respiration in the poikilochlorophyllous plant Xerophyta scabrida during desiccation

During a slow desiccation in photosynthetically fully active leaves of the poikilochlorophyllous desiccation-tolerant (PDT) monocotyledon Xerophyta scabrida (Pax) Th. Dur. et Schinz (Velloziaceae), thylakoid activity, CO₂ assimilation and respiration decline and chlorophylls and carotenoids are successively broken down. The initially slow rate of leaf water loss is related to the large reduction in leaf area which is reflected in the decrease of specific leaf area. Chlorophylls are broken down faster than carotenoids. The ratio of the variable chlorophyll fluorescence, an indicator of photosynthetic activity (Rfd690-values), shows that the functionality of thylakoids and chlorophylls is successively lost during desiccation. The decline in net CO₂ assimilation in desiccating leaves is largely caused by stomatal closure. The complete cessation of CO₂ assimilation, however, is due to the breakdown of chlorophylls and thylakoids. Respiration continued during desiccation and remained active far below -3.2 MPa leaf water potential. The differences during desiccation of the photosynthetic apparatus between poikilochlorophyllous and homoiochlorophyllous desiccation-tolerant plants are discussed.     

不产氧光合细菌光合色素的光氧调控机制

[目的]为不产氧光合细菌光合色素研究提供可行的较系统规范的研究方法和数据,揭示固氮红细菌(Rhodobacter azotoformans 134K20)光合色素光氧适应性机制.[方法]采用光谱法和色谱法对光和氧调控下的类胡萝卜素和细菌叶绿素合成代谢进行了研究.[结果]134K20菌株光照好氧时细胞得率最高.光照厌氧时主要合成3黄、1红、1紫、2绿、2蓝9种色素,黄色素大量表达.有氧时红色素大量表达,且启动2种新的红色素和1种新的紫色素表达,而黄色和蓝绿色素则受氧抑制.黑暗好氧主要合成2黄、3红、2紫、1绿、1蓝9种色素,但不同于光照厌氧.光照好氧时黄色素减少到1种,紫色素含量增加,其余同黑暗好氧.[结论]固氮红细菌(Rhodobacter azotoformans 134K20)是通过PpsR调节途径来调节光合基因表达的.黄色和红色素属于类胡萝卜素.黄色素1属于球形烯系列,其余两种黄色素是新的类胡萝卜素组分.红色素为新的球形烯酮组分,3种红色素极性、峰形和峰位差别显著,正己烷能显示其精细结构.紫色为极性较大的细菌脱镁叶绿素,绿色和蓝色为4种极性不同的细菌叶绿素a中间产物.乙醚甲醇法适合类胡萝卜素的提取,丙酮甲醇冰冻研磨法能快速有效完全提取光合色素.溶剂效应可有效鉴别细菌叶绿素a中间产物.     

Photobleaching in the unicellular green alga Dunaliella parva 19/9

The change in the pigment composition of the unicellular alga Dunaliella parva 19/9 during exposure to high light (4000 mol m^-2 s^-1) has been investigated. During photobleaching the carotenoids were lost at a greater rate than the chlorophylls. In these photoinhibitory conditions, -carotene and especially the minor carotenes, - and -carotene, were more susceptible to oxidative destriction than the xanthophylls. Lutein, the major carotenoid present, was the most stable of the carotenoids in these conditions. In addition to the direct photobleaching of carotenoids and chlorophylls, high light treatment induced the de-epoxidation of violaxanthin to antheraxantin and zeaxanthin. Small amounts of zeaxanthin were present in cells prior to illumination but the amount increased 2.4 fold following high light treatment. The effects of extremes of temperature during exposure to high light intensities were also investigated. The destruction of chlorophylls was found to be more temperature sensitive than that of the carotenoids. The general pattern of loss for the individual carotenoids was similar to that found at 25°C, i.e., the carotenes were more readily degraded than the xanthophylls.     

Morphophysiological and biochemical characteristics of potato plants with various expression rates of the Δ12 acyl-lipid desaturase gene

This paper reports on morphophysiological and biochemical characteristics of control and potato plants (Solarium tuberosum L., Skoroplodnyi cultivar) transformed with the Δ12 acyl-lipid desaturase gene (desA) grown long-term in vitro. The transformed plants showed faster growth and faster ontogenesis as compared to controls, which was accompanied with changes in the accumulation of photosynthetic pigments (chlorophylls a and b, carotenoids) and phenolic compounds, including flavonoids in the leaves. These characteristics were pronounced to a high degree in Line II plants with high expression rates of the desA gene, whereas Line I plants (moderate expression rate) were similar to control plants in many parameters.     

Molecular adaptation of photoprotection: triplet states in light-harvesting proteins

The photosynthetic light-harvesting systems of purple bacteria and plants both utilize specific carotenoids as quenchers of the harmful (bacterio)chlorophyll triplet states via triplet-triplet energy transfer. Here, we explore how the binding of carotenoids to the different types of light-harvesting proteins found in plants and purple bacteria provides adaptation in this vital photoprotective function. We show that the creation of the carotenoid triplet states in the light-harvesting complexes may occur without detectable conformational changes, in contrast to that found for carotenoids in solution. However, in plant light-harvesting complexes, the triplet wavefunction is shared between the carotenoids and their adjacent chlorophylls. This is not observed for the antenna proteins of purple bacteria, where the triplet is virtually fully located on the carotenoid molecule. These results explain the faster triplet-triplet transfer times in plant light-harvesting complexes. We show that this molecular mechanism, which spreads the location of the triplet wavefunction through the pigments of plant light-harvesting complexes, results in the absence of any detectable chlorophyll triplet in these complexes upon excitation, and we propose that it emerged as a photoprotective adaptation during the evolution of oxygenic photosynthesis.     

干旱胁迫下石灰花楸幼苗叶片的解剖结构和光合生理响应

采用盆栽控水设置4种水分梯度,研究1年生石灰花楸幼苗叶片解剖结构和光合生理指标对干旱胁迫的响应。结果显示:(1)干旱胁迫下,石灰花楸叶片逐渐变薄,轻度和中度胁迫下栅海比显著升高,而重度胁迫下显著降低。(2)干旱胁迫抑制了光合色素合成,降低了叶绿素和类胡萝卜素含量,同时使叶绿素a/b和叶绿素/类胡萝卜素值升高。(3)随干旱程度加剧,净光合速率、蒸腾速率和气孔导度日变化整体下降,胞间CO2浓度整体上升,光合限制以非气孔因素为主。研究表明,石灰花楸能根据水分亏缺程度调整叶片结构和光合生理特征以维持生存和生长,具有较强的耐旱性。