Studies on the dependence of chlorophyll synthesis on protein synthesis in Euglena gracilis,together with a nomogram for determination of chlorophyll concentration

Summary Experiments have been carried out to determine the basis for the dependence of chloroplast pigment synthesis on protein synthesis in dark-grown cells of Euglena gracilis greening in the light. The complete inhibition of chlorophyll synthesis brought about by actidione (10 g/ml) when added half way through the greening process was not relieved, even to the slightest extent, when 0.01 M -aminolaevulinic acid (ALA) was also present. The much smaller inhibition of chlorophyll synthesis brought about by chloramphenicol (2 mg/ml) was also relieved little, if at all, by the addition of ALA. It is concluded that the inhibition of chlorophyll synthesis by actidione can not be solely or primarily due to lack of ALA resulting from the decay of possibly labile enzymes of ALA synthesis, but could be due to inhibition of synthesis of the thylakoid structural protein. The results obtained with chloramphenicol are difficult to interpret because of the possibility that the drug, at high concentration, directly inhibits processes other than protein synthesis.Chlorophyll and carotenoid synthesis by E. gracilis were both markedly stimulated by the addition of ALA. It is suggested that the rate of chlorophyll synthesis in the greening cells is limited by the rate of formation of ALA. The stimulation of formation of carotenoids as well as chlorophyll may indicate that the cells have a mechanism for ensuring that the rate of carotenoid synthesis does not fall below a certain proportion of the rate of chlorophyll synthesis.A nomogram has been devised from which the concentrations of chlorophylls a and b, and total chlorophyll can be read off once the absorbances of an 80% acetone extract at 663 and 645 m have been determined.     

The Effect of Colored Light on Pigment Synthesis in Cultured Fern Leaf Primordia

The effect of white, blue, yellow, red and far-red light on the quantitative synthesis of the primary and auxilliary photosynthetic pigments in cultured leaf primordia of Osmunda cinnamomea L. is reported. The P₆₆₀ form of the now classical photoreceptor pigment system, phytochrome, has been demonstrated to be active in chlorophyll synthesis in cultured cinnamon fern leaf primordia as shown by red/far-red reversibility of chlorophyll synthesis. Also, it is apparent from the data presented that a blue absorbing pigment (P₄₂₀) is responsible for the extensive accumulation of chlorophylls and carotenoids in these cultured leaves.     

Änderungen der Ultrastrukturen in den Grünalgen Ankistrodesmus braunii und Chlorella fusca var. rubescens bei Stickstoffmangel

Summary Ultrastructural changes as well as changes in pigment and lipid content induced by nitrogen deficiency in the green algae Ankistrodesmus braunii and Chlorella fusca var. rubescens have been studied. Electron micrographs (freezeetching technique) and analyses show that the content of chlorophylls and the number of thylakoids decrease under these conditions synchronously with the increase of secondary carotenoids (astaxanthin-like type) and lipid vacuoles. However, there is no change, as compared with the green control, in the number and structure of the plastoglobuli localized in the chloroplasts. After addition of nitrogen, synthesis of the thylakoids and chlorophylls begins. The lipid vacuoles and secondary carotenoids disappear gradually. These extraplastidic lipid vacuoles do not correspond with the intraplastidic plastoglobuli (lipid globuli) found in higher plants and in Acetabularia.     

Regulation of Prenyl Chain Synthesis in Etiolated Hordeum Seedlings by Far-Red and White Light

The kinetics of prenyl chain formation (C₂₀ phytyl in chlorophylls, vitamin K_I and α-tocopherol; C₄₀ carotenoids and C₄₅ in plastoquinone-9) in plastids of etiolated Hordeum seedlings was compared in continuous darkness and after far-red and white light treatments:

• 1 Continuous far-red (via phytochrome Pfr) enhances the synthesis rate of all prenyl chains, but does practically not change the dark pattern of prenyl chain accumulation. Free C₂₀ phytyl chains could not be detected by means of thin layer chromatography.
• 2 White light induces a much stronger enhancement of prenyl chain formation than does far-red. It also changes the pattern of prenyl chain synthesis by a particularly strong promotion of the synthesis of phytyl chains, which get bound to chlorophyll a. The rate of chlorophyllide formation seems to determine the rate of enhanced phytyl formation.
• 3 It is assumed that the enzyme, which esterifies chlorophyllide a with the phytyl chain, is formed or activated by far-red treatment, but only starts working in white light, when the protochlorophyllide holochrome is re-arranged to the chlorophyllide holochrome.

     

Pigment profiles and bacterial communities from Thailand thermal mats

Differently colored layers of freshwater hot spring mats at Boekleung (Western Thailand) were studied. Temperatures ranged from over 50 up to 57°C. Two mats were characterized: a laminated mat with a green and a red layers, and a monolayer, greenish-yellow mat. Bacterial communities in green, red, and yellow layers were investigated using molecular, culturing and pigment analysis methods. Pigment profiles covered a wide spectrum from chlorophylls to carotenoids. A green mat layer showed higher relative content of chlorophyll than yellow and red layers which presented higher proportion of carotenoids. Cyanobacterial isolates grow up to 55–56°C and their pigment profiles showed a relatively high content of chlorophylls suggesting the importance of other bacterial groups in the mat pigment profiles. Bacterial communities were analyzed by 16S rDNA surveys showing Cyanobacteria and Chloroflexi as the mayor components of the community. Other significant members were Candidate Division OP10, Bacteroidetes, Planctomycetes and Actinobacteria. These results highlight a major participation of Cyanobacteria and Chloroflexi in thermal mat communities, and the preferential presence of Candidate Division OP10 in green mat layers. Differently colored mat layers showed characteristic bacterial communities which could be discriminated from pigment profiles and molecular surveys.     

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.     

LIPOPHILIC PIGMENTS FROM CYANOBACTERIAL (BLUE-GREEN ALGAL) AND DIATOM MATS IN HAMELIN POOL,SHARK BAY,WESTERN AUSTRALIA1

Lipophilic pigments were examined in microbial mat communities dominated by cyanobacteria in the intertidal zone and by diatoms in the subtidal and sublittoral zones of Hamelin Pool, Shark Bay, Western Australia. These microbial mats have evolutionary significance because of their similarity to lithified stromatolites from the Proterozoic and Early Paleozoic eras. Fucoxanthin, diatoxanthin, diadinoxanthin, β-carotene, and chlorophylls a and c characterized the diatom mats, whereas cyanobacterial mats contained myxoxanthophyll zeaxanthin, echinenone, β-carotene, chlorophyll a and, in some cases, sheath pigment. The presence of bacteriochlorophyll a with in the mats suggest a close association of photosynthetic bacteria with diatoms and cyanobacteria. The high carotenoids: chlorophyll a ratios (0.84–2.44 wt/wt) in the diatom mats suggest that carotenoids served a photoprotective function in this high light environment. By contrast, cyanobacterial sheath pigment may have largely supplanted the photoprotective role of carotenoids in the intertidal mats.     

Effects of chlorophyll a, chlorophyll b, and xanthophylls on the in vitro assembly kinetics of the major light-harvesting chlorophyll a/b complex, LHCIIb

The major light-harvesting chlorophyll a/b complex (LHCIIb) of photosystem II in higher plants can be reconstituted with pigments in lipid-detergent micelles. The pigment-protein complexes formed are functional in that they perform efficient internal energy transfer from chlorophyll b to chlorophyll a. LHCIIb formation in vitro, can be monitored by the appearance of energy transfer from chlorophyll b to chlorophyll a in time-resolved fluorescence measurements. LHCIIb is found to form in two apparent kinetic steps with time constants of about 30 and 200 seconds. Here we report on the dependence of the LHCIIb formation kinetics on the composition of the pigment mixture used in the reconstitution. Both kinetic steps slow down when the concentration of either chlorophylls or carotenoids is reduced. This suggests that the slower 200 seconds formation of functional LHCIIb still includes binding of both chlorophylls and carotenoids. LHCIIb formation is accelerated when the chlorophylls in the reconstitution mixture consist predominantly of chlorophyll a although the complexes formed are thermally less stable than those reconstituted with a chlorophyll a:b ratio < or = 1. This indicates that although chlorophyll a binding is more dominant in the observed rate of LHCIIb formation, the occupation of (some) chlorophyll binding sites with chlorophyll b is essential for complex stability. The accelerating effect of various carotenoids (lutein, zeaxanthin, violaxanthin, neoxanthin) on LHCIIb formation correlates with their affinity to two lutein-specific binding sites. We conclude that the occupation of these two carotenoid binding sites but not of the third (neoxanthin-specific) binding site is an essential step in the assembly of LHCIIb in vitro.     

Rapid colour changes in Euglena sanguinea (Euglenophyceae) caused by internal lipid globule migration

The accumulation of red pigments, frequently carotenoids, under chronic stress is a response observed in diverse kinds of eukaryotic photoautotrophs. It is thought that red pigments protect the chlorophyll located underneath by a light-shielding mechanism. However, the synthesis or degradation of carotenoids is a slow process and this response is usually only observed when the stress is maintained over long periods of time. In contrast, rapid colour changes have been reported in the euglenophyte Euglena sanguinea. Here we study the ecophysiological process behind this phenomenon through chlorophyll fluorescence, and pigment, colour and ultrastructural analyses. Reddening in E. sanguinea was due to the presence of a large amount of free and esterified astaxanthin (representing 80% of the carotenoid pool). The process was highly dynamic, shifting from green to red in 8 min (and vice-versa in 20 min). This change was not due to de novo carotenogenesis, but to the relocation of cytoplasmic lipid globules where astaxanthin accumulates. Thus, red globules were observed to migrate from the centre of the cell to peripheral locations when exposed to high light. Globule migration seems to be so efficient that other classical photoprotective mechanisms are not operative in this species. Despite the presence and operation of the diadino-diatoxanthin cycle, non-photochemical quenching was almost undetectable. Since E. sanguinea forms extensive floating colonies, reddening can be observed at a much greater scale than at the cellular level and the mechanism described here is one of the fastest and most dramatic colour changes attributable to photosynthetic organisms at cell and landscape level. In conclusion E. sanguinea shows an extremely dynamic and efficient photoprotective mechanism, based more on organelle migration than on carotenoid biosynthesis, which prevents excess light absorption by chlorophylls reducing the need for other protective processes related to energy dissipation.     

Untersuchungen über die lichtabhängige Carotinoidsynthese

Summary Under anaerobic conditions Fusarium aquaeductuum is able to synthesize carotenogenic enzymes but does not produce pigments. If illumination of the mycelia in the presence of oxygen is followed by an incubation in the dark under N₂ atmosphere, the strictly concurrent formation of the different carotenoids sets off as soon as aerobic conditions are restored. The paraboloidal increase of pigment production possibly indicates that synthesis of carotenogenic enzymes is also resumed. Blocking this enzyme synthesis by addition of cycloheximide leads to a simultaneous and linear increase of each carotenoid portion as soon as oxygen is replenished. This is interpreted to mean that light induces carotenogenic enzymes in a coupled group. On the other hand, our present and earlier results do not support any hypothesis on the existence of a carotenogenic multienzyme complex. The composition of the pigment after carotenoid production has ceased provides evidence for a selective inhibition of the synthesis of individual carotenogenic enzymes. Changes in pigment composition caused by an incubation of the mycelia for 12 h under anaerobic conditions are also reported.     

Untersuchungen über die lichtabhängige Carotinoidsynthese

Summary Anaerobic conditions completely block the synthesis of carotenoids in Fusarium aquaeduciuum or Neurospora crassa. Even after sufficient illumination of the mycelia in the presence of air, the subsequent production of carotenoids in the dark is suppressed entirely when the fungi are transferred to an oxygen-free atmosphere. In turn, restoring aerobic conditions sets off the pigment synthesis in the dark without renewed photoinduction at any time within 48 hours, although the yields of carotenoids decrease. Thus the photo-induced state appears to be fairly stable. In order to locate this state the sequence of light-induced reactions was specifically blocked before and after the synthesis of carotenogenic enzymes.Cycloheximide is a potent inhibitor of protein synthesis in fungi. When applied prior to illumination to either of the two molds it suppresses the photo-induced carotenoid formation, apparently by blocking the production of carotenogenic enzymes. This inhibition can be overcome by removing cycloheximide (e.g. by rinsing the mycelium with buffer) at any time (up to 30 h) during the dark period following illumination; however, gradually declining quantities of pigment are produced. These results provide evidence for the formation of a remarkably lasting induction product which can clearly be distinguished from the photooxidative product and from the carotenogenic enzymes.Under anaerobic conditions Fusarium is capable of producing plentiful amounts of carotenogenic enzymes, while Neurospora crassa forms only small quantities. In order to test the stability of these enzymes in vivo the following experimental setting was employed: in the presence of air the fungi were illuminated and subsequently kept in the dark for a period as long as the absolute lag phase of the pigment synthesis. Then cycloheximide was added to block any further protein synthesis, and at the same time the mycelia were transferred to a nitrogen atmosphere. Returning the fungi to aerobic conditions after various incubation periods resulted in a successively reduced pigment production. It thus appears that the activity of the photo-induced carotenogenic enzymes diminishes only slowly in vivo. These enzymes somehow seem to be stabilized as long as carotenogenesis is blocked.     

Chloroplast to chromoplast transition in tomato fruit: spectral confocal microscopy analyses of carotenoids and chlorophylls in isolated plastids and time-lapse recording on intact live tissue

Background and Aims

There are several studies suggesting that tomato (Solanum lycopersicum) chromoplasts arise from chloroplasts, but there is still no report showing the fluorescence of both chlorophylls and carotenoids in an intermediate plastid, and no video showing this transition phase.

Methods

Pigment fluorescence within individual plastids, isolated from tomato fruit using sucrose gradients, was observed at different ripening stages, and an in situ real-time recording of pigment fluorescence was performed on live tomato fruit slices.

Key results

At the mature green and red stages, homogenous fractions of chloroplasts and chromoplasts were obtained, respectively. At the breaker stage, spectral confocal microscopy showed that intermediate plastids contained both chlorophylls and carotenoids. Furthermore, an in situ real-time recording (a) showed that the chloroplast to chromoplast transition was synchronous for all plastids of a single cell; and (b) confirmed that all chromoplasts derived from pre-existing chloroplasts.

Conclusions

These results give details of the early steps of tomato chromoplast biogenesis from chloroplasts, with the formation of intermediate plastids containing both carotenoids and chlorophylls. They provide information at the sub-cellular level on the synchronism of plastid transition and pigment changes.     

Heliothrix oregonensis,gen. nov., sp. nov., a phototrophic filamentous gliding bacterium containing bacteriochlorophyll a

An unusual filamentous, gliding bacterium was found in a few hot springs in Oregon where it formed a nearly unispecific top layer of microbial mats. It contained a bacteriochlorophyll a-like pigment and an abundance of carotenoids. There were no chlorosomes or additional chlorophylls. The organism was aerotolerant and appeared to be photoheterotrophic. It was successfully co-cultured with an aerobic chemoheterotroph in a medium containing glucose and casamino acids. Although it has many characteristics in common with the genus Chloroflexus, the lack of chlorosomes and bacteriochlorophyll c and the aerobic nature of this organism indicate that it should be placed in a new genus. This conclusion is supported by 5S rRNA nucleotide sequence data.     

CHLOROPHYLL FORMATION IN ISOLATED PUMPKIN COTYLEDONS IN THE PRESENCE OF KINETIN AND CHLORAMPHENICOL

Investigations have been made on the changes in the levels ofprotochlorophyll, chlorophyll a and chlorophyll b in relationto the kinetin induced expansion of isolated pumpkin cotyledonsin the presence and absence of chloramphenicol. It has been shown that rise in pigment level keeps pace withexpansion growth of the cotyledons. Kinetin markedly promotes the synthesis of protochlorphyll withoutmuch affecting the rate of its photoreduction to chlorophyll. Chloramphenicol strongly inhibits the development of both chlorophylla and b. The inhibition seems to be due to its interferenceboth with the synthesis of protochlorophyll and its subsequentconversion to chlorophyll. The inhibitory effect of chloramphenicol on the formation ofchlorophyll a is greater than on that of chlorophyll b, suggestingthereby the probability of divergent pathways for the formationof the two chlorophylls. (Received December 21, 1966; )     

Isolation of chlorophylls and carotenoids from freshwater algae using different extraction methods

Usually marine algae are an excellent source of pigments for different commercial sectors. Freshwater macroalgae can be exploited as a good source of biologically active compounds provided an appropriate extraction method is developed. The efficiency of four methods, like microwave‐assisted (MAE), ultrasound‐assisted extraction (UAE), supercritical fluid extraction (SFE) with ethanol as a co‐solvent, as well as conventional Soxhlet extraction were studied in the same conditions (time, solvent and temperature) for the recovery of chlorophylls and carotenoids from three freshwater green algae species: Cladophora glomerata, Cladophora rivularis and Ulva flexuosa. UV‐Vis spectrophotometry was used to determine chlorophyll a, chlorophyll b and total carotenoid content in obtained extracts. The results of this study showed that the advantages of novel extraction techniques (MAE and UAE) include higher yield and, in consequence, lower costs compared to traditional solvent extraction techniques. These methods were much more efficient in freshwater green algae pigment recovery than the classic Soxhlet extraction as well as SFE.     

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.     

Studio sui pigmenti liposolubili di Sternbergia lutea Ker-Gawl durante alcune fasi del suo ciclo biologico

Abstract

A study of Sternbergia lutea Ker-Gawl lipidsoluble pigments during some phases of its biological cycle. — In the present paper we have examined the pigments of Sternbergia lutea and their variations during some particular phases of its biological cycle in order to obtain useful information on their probable function in the plant. Therefore, we have analyzed the pigments of the leaves, floral scape, tepals and anthers. The results obtained show that Sternbergia lutea is characterized by the same pigment composition as that of the other higher plants. In addition to this, three further carotenoids have been observed (mainly in the tepals and anthers). Chromatographic and spectrophotometric properties of these new pigments indicate their relationship with carotene isomers that have already been examined. During the phases of vegetative cycle of Sternbergia lutea chlorophylls and carotenoids increase concomitantly with the growth of the plant. Carotenes reach a significant maximum value only in anthers. In the course of the necrosis (that obviously occurs in different stages for the various organs) is observed a higher decrease of chlorophylls (in the green tissues) and of the carotenes (in the anthers) while lutein and violaxanthin increase greatly (in the tepals).     

PHOTOSYNTHETIC PIGMENTS IN FIFTY-ONE SPECIES OF MARINE DIATOMS1

The photosynthetic pigments of 51 species (71 isolates) of tropical and sub-tropical diatoms from 13 out of 22 families were examined. These were the Thalassiosiraceae, Melosiraceae, Coscinodiscaceae, Rhizosoleniaceae, Biddulphiaceae, Chaetoceraceae, Lithodesmiaceae, Eupodiscaceae, Cymatosiraceae, Diatomaceae, Naviculaceae, Nitzschiaceae and Phaeodactylinaceae. Pigments were analyzed by cellulose and polyethylene thin-layer chromatography (TLC) and reverse-phase high-performance thin-layer chromatography (HPTLC). All species contained chlorophylls a and c₂ and the carotenoids carotene, fucoxanthin, diatoxanthin and diadinoxanthin. In addition, 14 species (20 isolates) contained one or more of four minor carotenoids, which were not identified further. One species, Thalassiothrix heteromorpha, contained small amounts of a 19′-butanoyloxyfucoxanthin-like pigment, in addition to fucoxanthin. Chlorophyll c₂ was present in all the diatoms tested and occurred together with chlorophyll c₁ in 88% of them. The presence of both chlorophylls c₁ and c₂ therefore can no longer be considered a universal characteristic of the diatom class. Where chlorophyll c₁ was absent or occurred in trace amounts only (8 species, 11 isolates), it was usually replaced by a new chlorophyll c pigment designated chlorophyll c₃, recently characterized from several prymnesiophytes and one chrysophyte. Exceptions were Nitzschia closterium (CS-114), which contained only chlorophyll c₂, and Nitzschia bilobata (CS-47), which contained all three chlorophylls (c₁, c₂ and c₃) in approximately equal amounts. Five species that contained chlorophylls c₁ and c₂ also contained chlorophyll c₃ in trace quantities Quantitative pigment analyses of the 71 isolates showed that chlorophyll concentrations ranged from 0.02 μg. 10⁶ cells^?1 in the smallest diatom, Extubocellulus spinifer, to 174.4 μg. 10⁶ cells^?1 in one of the largest diatoms, Coscinodiscus sp. under the standard growth conditions used. The mean molar ratio of chlorophyll a:c in the 72 isolates was 3.33, with a range of 1.65–7.25. The close similarity between diatom and prymnesiophyte pigmentation was confirmed. Each class has three patterns of pigmentation: viz species with chlorophylls c₁ and c₂ and‘true’fucoxanthin, species with chlorophylls c₃ and c₂ and‘true’fucoxanthin, and species with chlorophylls c₃ and c₂ and fucoxanthin derivatives.     

Role of inorganic nitrogen in the synthesis and degradation of chlorophyll and carotenoids in maize leaves

Supply of KNO₃, NH₄Cl or NH₄NO₃ to the maize seedlings increased total chlorophyll and carotenoids (over zero nitrogen control) amounts per fresh matter unit of the primary leaves. The increase was most apparent when the pigment level in control plants started declining,i.e. between days 14 and 16. Supply of inorganic nitrogen increased pigment synthesis in excised leaf segments from dark grown seedlings, although the increase during a 24 h incubation was not as high as with either glycine or glutamine. Salicylic acid at 0.01 to 1 mM concentration increased and at 10 mM lowered the pigment biosynthesis. The increase at lower concentrations of salicylic acid was unaffected by KNO₃ but it was suppressed by NH₄Cl. When 12-day seedlings were transferred to the dark, total chlorophyll and carotenoids declined appreciably, but the supply of inorganic nitrogen protected them from decline to same extent. Thus inorganic nitrogen, especially the nitrate, is more important in protecting from degradation of chlorophyll and carotenoids than in increasing their biosyntheses.     

Die Hemmung der Carotinoidsynthese im Stickstoffmangel

Summary The ability to synthesize carotenoids during normal or strongly reduced nitrogen supply was tested in a higher plant (Hordeum vulgare L.) and in a green alga (Scenedesmus obliquus). Though carotenoids are nitrogenfree, their synthesis is strongly inhibited during nitrogen deficiency. The formation of secondary carotenoids, which apparently proceeds at the expense of the primary carotenoid components, occurs in Scenedesmus but not in Hordeum plants. It is concluded that the dimerisation of geranly-geranyl-pyrophosphate is the limiting step in the carotenoid synthesis during nitrogen deficiency. The synthesis of prenyl chains is less affected by nitrogen deficiency.