Light-independent and dependent phases of proplastid development in Euglena gracilis W3BUL

Cells of Euglena gracilis Klebs var. bacillaris Cori mutant W3BUL grown in darkness on Hutner's pH 3.5 medium without agitation accumulate wax ester. These cells have undeveloped proplastid remnants characteristic of this mutant. If these cells are transferred to an inorganic medium and bubbled with 2-3% CO2 in air, the wax disappears and the proplastid expands and develops in darkness to form prolamellar bodies and membrane vessicles within 96 h. No further development takes place in darkness, but if these cultures are illuminated at 96 h formation of prothylakoids is observed. Thus the wax ester accumulated during growth can be used subsequently to support proplastid development up to the prolamellar body stage, but the formation of prothylakoids is strictly light-dependent. Development in this system takes place at a slower rate than in cells grown with shaking and lacking wax which are transferred to resting medium. As previously shown, all of proplastid development requires light under these conditions. It is suggested that the oxygen-requiring utilization of wax in darkness can provide energy and metabolites for a part of proplastid development but the later steps in these cells, or the entire development in cells lacking wax is supported by paramylum degradation which is strictly light-dependent. However, a specific light reaction required for prothylakoid organization is not ruled out.     

Regulation of Protochlorophyll(ide) Levels in Dark-Grown Non-Dividing Euglena 3. Proplastid Structure during Loss and Regeneration of Protochlorophyll(ide)

Cells of Euglena gracilis Klebs var. bacillaris Cori growingin darkness on a complete medium have small undifferentiatedproplastids. On transfer to an incomplete (resting) medium indarkness, the cells cease division within 72 h. During thistime the proplastid expands and several prothylakoids and prolamellarbodies develop even though phototransformable protochlorophyll(ide)[PT-Pchl(ide)] is decreasing. As PT-Pchl(ide) decreases furtherand reaches a stable plateau after 4–5 more days in darkness,the proplastid structure becomes highly reduced. Forty minutesof light plus a one h dark period, or addition of glutamateor malate for 7 h does not change the proplastid structure significantlyeven though PT-Pchl(ide) returns to the level found in growingcells. Upon prolonged incubation in darkness after light treatment(72 h) an expanded proplastid containing prothylakoids, prolamellarbodies and membrane whorls with mitochondria in close associationis seen; most of the cellular paramylum is lost during thisperiod leaving cavities in the cytoplasm. Without light, prolongedincubation in darkness (72 h) with malate leads to accumulationof cellular paramylum but no change in proplastid structurewhile prolonged treatment with glutamate (72 h) allows the formationof a few prothylakoids but no prolamellar bodies. ¹Supported by Grants GM 14595 from the National Institutes ofHealth. ²Permanent address: Department of Microbiology, Tokyo MedicalCollege, 6-1-1 Shinjuku, Tokyo 160, Japan. ³Abraham and Etta Goodman Professor of Biology. (Received July 23, 1983; Accepted September 22, 1983)     

EFFECT OF LIGHT INTENSITY AND GLYCEROL ON THE GROWTH,PIGMENT COMPOSITION,AND ULTRASTRUCTURE OF CHROOMONAS SP.1,2,3

Growth of Chroomonas sp. increased with light intensity (100, 1800, and 2700 μW/cm²) with a fivefold increase from the lowest to the highest intensity. Chlorophyll and phycocyanin content per cell were greater in cells grown at low light intensity, but the ratio of chlorophyll a and c did not vary appreciably. Cells grown at low light intensity had 30% more phycocyanin than cells grown at high intensities of light. The chloroplast of cells with the higher phycocyanin content had average intrathyla-koidal widths of 300 Å, whereas those cells with the lower phycocyanin content had average intrathylakoidal widths of 200 Å. This result is compatible with the hypothesis that phycocyanin is located in the intrathylakoidal space in the cryptophyte algae. Of the various energy sources tested, only glycerol was able to support limited growth tinder nonphotosynthetic conditions. Under no condition was the chloroplast reduced to an elioplast or proplastid state. Starch accumulation was greatest in cells grown in continuous while light in glycerol. Eye-spots were commonest in cells grown in darkness and interrupted every 24 hr by a few seconds of white light. It was concluded that this organism is an obligate phototroph.     

Stimulation of Plastidogenesis Induced by 5-Azacytidine in Euglena gracilis Klebs

When etiolated Euglena gracilis was treated with 10 mM 5-azacytidine (5-azaC), an inhibitor of DNA methylation, stimulation of plastidogenesis in both dark and light conditions was observed. The phenomenon occurred in 10–15% of the cells possibly due to the asynchronicity of the cultures. The main features of this sub-population, as evaluated by electron and fluorescence microscopy, were the following: 1. the presence in darkness of differentiating proplastids that were red fluorescent under UV, positive to TCNBT cytochemical reaction (specific for PSII) and negative to DAB (specific for PSI); 2. the acceleration of proplastid differentiation during the first 20–30 h of illumination; 3. the occurrence in both culture conditions of concentric lamellar bodies (LB_S). These structures were considered to be proplastids blocked in the first step of evolution, since they emitted a red fluorescence, were contained within compartments limited by a triple-layered envelope, were reactive to TCNBT in darkness and to both TCNBT and DAB in light conditions. Even if the action mechanism of 5-azaC on plastidogenesis in Euglena remains to be defined, the induced stimulatory effect on plastid differentiation pointed to a relationship between DNA methylation and plastid development. Furthermore, the presence of LB_S opens the possibility of studying early aspects of plastid development in Euglena.     

Inhibition of Etiolation in Spirogyra by Phytochrome

Cells of Spirogyra filaments grown in darkness become longer than light grown cells. This elongation can be prevented by a few minutes of red light given with intervals of 24 h under the dark period. Far-red light given after the red light pulse counteracts the red light effect. Cells which have finished their elongation in light do not elongate further in darkness. Along with the cell elongation the chloroplasts become less spirally wound and ultimately shortened to straight bands.     

PHYSIOLOGICAL RESPONSES DURING DARK SURVIVAL AND RECOVERY IN AUREOCOCCUS ANOPHAGEFFERENS (PELAGOPHYCEAE)1

The harmful bloom alga Aureococcus anophagefferens Hargraves et Sieburth can survive prolonged darkness, which could facilitate overwinter survival and dispersal by anthropogenic vectors such as ballast water. Experiments were conducted to examine the biochemical and photosynthetic changes in cells during dark storage. Cells were stored in the dark for periods from 2 to 14 days and were sampled at days 0, 1, 2, 4, 7, 10, and 14. Samples from days 2, 7, and 14 were monitored during a recovery period of 4–5 days. Physiological and photosynthetic parameters were measured during the dark storage and recovery periods. Cultures resumed growth quickly when returned to light, and bacterial counts remained constant during the dark storage period but increased rapidly during recovery periods. Cellular protein, carbohydrate, and lipid concentrations declined slightly during the dark period. There were no changes in chl a per cell or in RUBISCO per cell during 14 days of darkness. The data therefore suggest that A. anophagefferens is able to maintain its photosynthetic apparatus during dark storage periods of at least 2 weeks and relies on cellular reserves until it is returned to light to resume photosynthesis. During the recovery period in the light, the cells are able to acclimate rapidly to current light levels and resume growth.     

Ornithine cycle inNostoc PCC 73102: Stimulation of in vitro ornithine carbamoyl transferase activity by addition of arginine

Cells ofNostoc PCC 73102, a free-living cyanobacterium originally isolated from the cycadMacrozamia, were cultured under different conditions and examined for the presence ofin vitro active ornithine carbamoyl transferase (OCT). Cells grown in darkness showed a significant increase ofin vitro OCT activity compared with the activity when grown in light. Addition of external arginine in the growth medium increasedin vitro OCT activity both in light and in darkness. Moreover, the highestin vitro OCT activity was observed in cells grown in darkness and with the addition of external arginine, a sevenfold increase compared with cells grown in light. Native-PAGE in combination with on gel OCT activity stain demonstrated that external arginine induced the presence of twoin vitro active OCT. In addition to the previously described 80 kDa OCT [Physiol Plant 84:275–282, 1992], a secondin vitro active enzyme with a molecular weight of approximately 118 kDa appeared. Western immunoblots, with native cell-free extracts and antibodies directed either against native or denatured OCT purified fromPisum sativum, confirmed that both enzymes were OCT. Moreover, with a denatured cell-free extract only one polypeptide, with a molecular weight of about 40 kDa, was recognized, indicating that the secondin vitro active OCT might be a trimer with three identical subunits.     

Phototransformation of protochlorophyll(ide) by a proplastid fraction from Euglena

The phototransformation of protochlorophyll(ide) (Pchl(ide)) to chlorophyll(ide) (Chl(ide)) can be demonstrated in a proplastid fraction from Euglena gracilis Klebs var. bacillaris Cori if appropriate conditions are employed. Pigments were measured fluorometrically in acetone extracts of cell or organelles. Pchl(ide) and the phototransformation to Chl(ide) are at their highest levels in cells grown in darkness on normal or low vitamin B₁₂-containing medium (pH 3.5) to the late exponential phase (1.2–1.4 × 10⁶ cells ml^?1). Late exponential cells on low B¹² medium yield a proplastid fraction that contains Pchl(ide) which is phototransformed to Chl(ide) when illuminated with red light (5.6 W m^?2 for 4 min) in the presence of 10 mM Hepes, 20 mM TES, 0.5 mM potassium phosphate (pH 7.4), 70 mM sorbitol, 5 mM DTT, 5 mM ATP, 5 mM fructose-1, 6-bisphosphate, 10 mM malate and 2 mM MgCl²; intact organelles appear to be involved since deletion of osmoticum gives a lower activity, and addition of NAD(P)H is without effect. Phototransformation of Pchl(ide) to Chl(ide) in red light shows Bunsen-Roscoe reciprocity between fluence rate and duration of illumination. Although mitochondria are present, they do not appear to be involved since inhibitors of respiration and uncouplers of oxidative phosphorylation fail to block the phototransformation. The percentage phototransformation of Pchl(ide) to Chl(ide) in late exponential normal B¹² cells is 61 ± 10, and is 52 ± 3 in low B¹² cells. About 67% of the activity in low B¹² cells is recovered in the proplastid fraction incubated with the complete incubation mixture in saturating light. In both types of cells and in the proplastid fraction, the stoichiometry of conversion of Pchl(ide) to Chl(ide) is about 1:1 (mol/mol).     

THE HETEROTROPHIC CAPABILITIES OF CYCLOTELLA MENEGHINIANA1

Cyclotella meneghiniana grew heterotrophically in darkness when glucose in concentrations from 5 mg/liter to 10 g/liter was provided. The other compounds tested did not support growth. However, in continuous light (300 ft-c) growth wax not enhanced if glucose wax provided. Under diurnal conditions of light (300 ft-c) approximately 12–14 hr of darkness were required to observe the enhancement effects of glucose. Uptake studies with labeled glucose indicated that uptake is not dependent on glucose, but that it occurs only at low light intensities. Cells required 12–14 hr of darkness to develop the uptake system.     

Ornithine cycle in Nostoc PCC 73102. Arginase,OCT and arginine deiminase,and the effects of addition of external arginine,ornithine, or citrulline

Arginase, ornithine carbamoyl transferase (OCT) and arginine deiminase activities were found in cell-free extracts of Nostoc PCC 73102, a free-living cyanobacterium originally isolated from the cycad Macrozamia. Addition of either arginine, ornithine or citrulline to the growth medium induced significant changes in their in vitro activities. Moreover, growth in darkness, compared to in light, induced higher in vitro activities. The in vitro activities of arginase and arginine deiminase, two catabolic enzymes primarily involved in the breakdown of arginine, increased substantially by a combination of growth in darkness and addition of either arginine, or ornithine, to the growth medium. The most significant effects on the in vitro OCT activities where observed in cells grown with the addition of ornithine. Cells grown in darkness exhibited about 6% of the in vivo nitrogenase activity observed in cells grown in light. However, addition of external carbon (glucose and fructose) to cells grown in darkness resulted in in vivo nitrogenase activity levels similar to, or even higher than, cells grown in light. Growth with high in vivo nitrogenase activity or in darkness with the addition of external carbon, resulted in repressed levels of in vitro arginase and arginine deiminase activities. It is suggested that nitrogen starvation induces a mobilization of the stored nitrogen, internal release of the amino compound arginine, and an induction of two catabolic enzymes arginase and arginine deiminase. A similar and even more pronunced induction can be observed by addition of external arginine to the growth medium.     

Light-dependent PER-like proteins in the cephalic ganglia of an apterygote and a pterygote insect species

Antibodies targeted to a highly conserved tetradecapeptide region of the pivotal biological clock protein PER detect in the firebrat Thermobia domestica a 115-kDa protein and in the cockroach Periplaneta americana a 110-kDa protein that are present in the cytoplasm of a small set of brain cells. A similar cytoplasmic reaction occurs with antisera to the whole PER protein of Drosophila melanogaster, but these antisera also react with numerous cell nuclei. On western blots, they detect an 80-kDa antigen in T. domestica and 70- and 80-kDa antigens in P. americana. No indication of antigen translocation between cell nuclei and cytoplasm was found. Nuclear staining is maintained at a high constant level in T. domestica held at a 12:12 h light:dark photoperiod (LD) or in continuous light, but disappears rapidly in response to extended darkness. In P. americana under LD conditions, the number of immunoreactive nuclei and their staining intensity fluctuate in parallel, with maximal staining late in the day. The circadian changes are maintained in continuous light but all staining vanishes in continuous darkness. A 6-h light pulse in early night of an LD cycle induces maximal staining after about 10 h, suggesting that the effect of light on nuclear PER-like expression is indirect. The behaviour of nuclear antigens is opposite to that of the cytoplasmic PER-like proteins that persist in constant darkness and disappear in constant light. Under LD conditions, the cytoplasmic PER-like antigen cycles in T. domestica but remains at a steady level in P. americana. The sensitivity to photoregime suggests that both the nuclear and the cytoplasmic PER-like antigens are components of the biological clock.R. Závodská and H. Sehadová contributed equally to this work     

The "Point of no Return" Concept in Cell Division. The Effects of Some Metabolic Inhibitors on Synchronized Chlorella pyrenoidosa

The coarse of growth and cell division in synchronized cultures of Chlorella pyrenoidosa was studied after the addition of metabolic inhibitors at differing times during the cell cycle (14 h light - 10 h darkness with nitrate as nitrogen source. 12 h light: 12 h darkness with urea as nitrogen source). Dinitrophenol (DNP) added to a final concentration of 0.3 mM at any time in the synchronization cycle, the compound remaining in the suspension from the time of addition to the end of the dark period, inhibited spore formation completely. Growth measured as increase in cell volume was less sensitive to the action of the inhibitor. Chloramphenicol (CAP) added dining the 0–5 h interval to a final concentration of 0.1 mM resulted in 80 per cent inhibition of cell division. Similar treatment started at successive times thereafter resulted in a gradual decrease of the inhibition. Treatment at the 14th hour and during the dark period did not affect the sporulation. Similar experiments with 0.9 mM puromycin added at various times during the illumination period gave almost complete inhibition of cell division, while the growth was reduced by only 25 per cent. para-Fluorophenylalanine (p-FPhe) at 3.3 × 10^?2 mM stopped cell division nearly completely irrespective of addition time in the light period. Addition during the dark period also prevented an increase in the number of tree cells. In this case about half of the cells produced spores which were not released. It is concluded that DNP inhibits all stages of preparation for cell division, as well as the division process itself. With CAP a genuine transition point of preparation for cell division was observed, although its interpretation as related to protein synthesis is somewhat uncertain. With puromycin and p-FPhe no transitions were observed.     

N‐ASSIMILATION IN THE NOXIOUS FLAGELLATE HETEROSIGMA CARTERAE (RAPHIDOPHYCEAE): DEPENDENCE ON LIGHT,N‐SOURCE,AND PHYSIOLOGICAL STATE1

The capabilities of the diel vertically migrating flagellate Heterosigma carterae Hulburt for assimilating ammonium and nitrate into cell‐N in light and in darkness were studied using cells of different N‐status. Ammonium utilization in darkness, except by N‐replete cells, attained>50% of use in the light. However, the capacity to use nitrate was poor in darkness, and less than 20% of nitrate‐N that was taken up in darkness was then actually incorporated into cell‐N. The ability to assimilate N in darkness improved as N‐status (N:C) declined, concurrent with an increasing content of water‐soluble carbohydrate. This carbohydrate was used to support dark N‐assimilation. Cells held in darkness for over a day and that had halted nitrate‐uptake were still capable of taking up ammonium. Furthermore, the act of taking up ammonium appeared to make available a source of C to support nitrate uptake that was previously unavailable. The implications of these results for the ecophysiology of this organism and for the construction of mathematical models of algal growth are considered.     

Photosynthetic membrane development inRhodopseudomonas spheroides

Cells ofRhodopseudomonas spheroides were depigmented by aerobic growth in the light and then transferred to 4% oxygen in the dark to induce pigment synthesis. Pigment synthesis and photochemical activity were measured fluorometrically. In conjunction with the fluorescence studies, thylakoid morphogenesis was followed by electron microscopy of thin sections of cells fixed during the repigmentation process.Both bacteriochlorophyli and the onset of photochemical activity were detected before distinct thylakoids were observed. Subsequent bacteriochlorophyll synthesis was associated with a gradual increase in the thylakoid content throughout the developmental process.The results obtained strongly indicate that initially the cytoplasmic membrane is modified by pigment incorporation, possibly at specific sites, and that the bacteriochlorophyll is photochemically active in the pigmented cytoplasmic membrane or in the early stages of invagination.Finally, in a confirmation of previous hypotheses, these studies provide evidence for the origin of the thylakoids as a protrusion and invagination of the cytoplasmic membrane. This is followed by constriction and subsequent proliferation and branching to form a continuous membrane system which gives rise to chromatophores upon cellular disruption.Extracted in part from the doctoral thesis of G. A. Peters submitted to the University of Michigan in partial fulfillment of the requirements for the Ph.D. degree. For paper I of this series see reference [3].     

Development of chloroplast structure and photosynthetic competence in dark-adapted moss protonemata after exposure to light

Summary Sporelings and protonemata ofCeratodon purpureus were grown in darkness for one to two months. On their exposure to light, starch was observed after 30 minutes but only minor changes occurred in the chloroplast structure during the first hours. After one day in light, the chloroplasts had a structure similar to that of the chloroplasts of light-grown material. The dark-grown material evolved oxygen and assimilated CO₂ readily after exposure to light. Nevertheless, maximization of the photosynthetic rate was not achieved until the second day in light, coinciding with the development of light-type chloroplasts. The ultrastructural localization of photosystems I and II revealed much higher activity of PS I in dark-adapted material than in material grown in light, whereas the activity of PS II appeared to be greater in light-grown material.     

Influence of continuous light and darkness on the secretory pinealocytes of<Emphasis Type="Italic">Heteropneustes fossilis</Emphasis>

In an earlier study onHeteropneustes fossilis, evidence of secretory activity in the pinealocytes had been demonstrated at the electron microscopic (EM) level and it was found to exist in two phases: a secretory phase (light cells) and a storage phase (dark cells). In the present investigation,H. fossilis was subjected to artificial photoperiods of continuous illumination and continuous darkness for a period of ten days and the effect on the secretory pinealocytes was studied at the EM level. Marked results were observed within the short period of ten days emphasizing the role of environmental photoperiod on the secretory activity of the pinealocytes. During continuous illuminated phase, both light and dark cells were observed: the light cells showed intense secretory activity and dark cells a storage one. During the dark phase both types of cells were present but in different metabolic states and neither of the cells demonstrated synthetic nor storage activity. Light cells were metabolically active but not secretory active and dark cells showed a necrotic condition. Phagocytotic activity of the dark cells was also seen. Intense neural activity was also observed during exposure to both the artificial photoperiods. The results highlight the role of light on the secretory activities of the pinealocytes of the catfish pineal organ.     

Effect of continuous darkness on circadian morphological rhythms in pinealocytes of the Chinese hamster,Cricetulus griseus

Summary Effects of a short-term exposure to continuous darkness on 24-h morphological variations in pinealocytes in the superficial pineal of the Chinese hamster (Cricetulus griseus) were examined. Pinealocytes contained type-1, -2 and -3 synaptic ribbons (SR), which had a central dense structure showing rod-like, various and ring-like profiles, respectively, and the quantity of each type of SR was expressed by SR index. 24-h changes in the type-1 and type-3 SR indices persisted in darkness and thus may be endogenous in nature. As under alternating light and dark (LD) conditions, the type-2 SR indices were almost constant over a 24-h period under continuous darkness, but the indices were larger in animals under darkness than in those under LD conditions. The 24-h variations in the nuclear and cytoplasmic volumes were abolished after exposing animals to darkness for 7 days, suggesting that these rhythms may be regulated exogenously. The amount of condensed chromatin exhibited a circadian change; this rhythm persisted under darkness. The results suggest that 24-h variations in the nuclear and cytoplasmic volumes in pinealocytes of the Chinese hamster are regulated by mechanisms different from those controlling the rhythms in SR and chromatin, and that the changes in the nuclear and cytoplasmic volumes and chromatin are related to the change in synthetic activity of pinealocytes.     

A light-regulated pool of phytochrome and rudimentary high-irradiance responses under far-red light in Pinus elliottii and Pseudotsuga menziesii

The presence of a phytochrome pool down-regulated by light and the occurrence of high-irradiance responses to far-red light are well documented in angiosperms but not in gymnosperms. A pool of phytochrome was identified in Pinus elliottii and Pseudotsuga menziesii seedlings grown in darkness with a monoclonal antibody developed against oat phytochrome A. This pool was barely detectable in light-grown tissues. Dark-grown conifer seedlings transferred to continuous red light showed a gradual decrease of the levels of immunodetectable phytochrome. This decrease was significantly slower in gymnosperms than in angiosperms. Dark-grown seedlings of P. elliottii and P. menziesii showed enhanced growth of the cotyledonary whorl and increased anthocyanin pigmentation of the hypocotyl, but no hypocotyl-growth inhibition in response to continuous far-red light. Hourly pulses were significantly less effective than continuos far-red light. The response to far-red light was not observed in seedlings pretreated with red light to reduce the levels of immunodetectable phytochrome. Rudiments of phytochrome A-like function and kinetics are present in P. elliottii and P. menziesii.     

Light dependence of sexual agglutinability in Chlamydomonas eugametos

The mating activity of mating-type plus gametes of Chlamydomonas eugametos depends on light. Cells lost their ability to agglutinate with mating-type minus gametes after a dark period of 30 min. They regained their agglutinability after 10 min exposure to light. Other mating reactions, such as tipping and flagellar tip activation, were not dependent upon light. Since cycloheximide and tunicamycin did not affect the light-induced activation of flagellar agglutinability, no protein synthesis or glycosylation is involved in this process. Equal amounts of biologically active agglutination factor could be extracted from cells placed either in light or in darkness. A minor portion of the active material was found to be located on the flagellar surface of illuminated cells. No active material was found on the flagellar surface of dark-exposed cells, whereas their cell bodies contained the same amount of active material as the cell bodies of illuminated cells. Since a light-induced flow of agglutination factors from the cell body to the flagella could not be detected and dark-exposed cells could be slightly activated by amputation or fixation by glutaraldehyde, we propose that light affects flagellar agglutinability by an in-situ modification of the agglutination factor on the flagella. When mt ⁺ and mt ^- strains were crossed and the progeny examined for light-sensitivity, it was apparent that this phenomenon is not mating type-linked.Abbreviations and symbols FTA flagellar tip activation - mt ^+/- mating type plus or minus - WGA wheat-germ agglutinin     

INCOMPLETENESS OF THE COCCOSPHERE AS A POSSIBLE STIMULUS FOR COCCOLITH FORMATION IN PLEUROCHRYSIS CARTERAE(PRYMNESIOPHYCEAE)1

Pleurochrysis carterae is a marine biflagellate that produces calcified structures called coccoliths. The coccoliths are formed inside the cells and released from the latter after formation. The light dependence of calcium incorporation in this species was studied using⁴⁵Ca as a tracer. Cells exposed to a repeating cycle of 16 h of light and 8 h of darkness incorporated calcium in extracellular coccoliths at a more or less constant rate throughout a cycle. The cells divided during the dark periods with a concomitant decrease in size. Their size increased during the light periods Coccolith formation in cells incubated in continuous darkness was greatly reduced and finally ceased. These cells did not divide and did not increase in size. Removal of extracellular coccoliths prior to the calcium incorporation experiments stimulated coccolith formation both in dark-incubated cells and in cells exposed to a repeating light-dark cycle. Cells in the stationary phase of growth ceased producing coccoliths. Calcification could be induced in these cells by removal of the extracellular coccoliths. Based on these findings we suggest that cells of Pleurochrysis carterae tend to produce a complete cover of coccoliths and that the available cell surface is a factor controlling coccolith formation.