Effect of light intensity on macromolecular synthesis in cyanobacteria

The light-dependent incorporation of NaH¹⁴CO₃ into low molecular weight compounds, polysaccharide, or protein was determined in cultures of the cyanobacteriumMerismopedia tenuissima incubated at a series of light intensities. There was an inverse relationship between incorporation into polysaccharide and protein. At light intensities of 90 E/m²/sec or above, relative incorporation of radioisotope into polysaccharide was greatest and relative incorporation into protein was lowest. Optimal relative protein accumulation occurred in samples incubated at 20 E/m²/sec. A broader optimum of light intensity for maximal protein accumulation was found if ammonia rather than nitrate was the nitrogen source. Physiological adaptation of cultures to growth at a particular light intensity did not alter the pattern of macromolecular incorporation when those cultures were tested over the series of light intensities. The response of cultures ofOscillatoria rubescens to light intensity was similar to that ofM. tenuissima, although incorporation into low molecular weight compounds was significantly greater.The effect of light intensity on macromolecular synthesis in a natural population ofOscillatoria rubescens was also determined. A pattern similar to that observed in batch cultures ofO. rubescens was occasionally found, but in other experiments there was no increase in relative protein incorporation when light intensity was decreased.     

The effect of sulfide on the blue-green algae of hot springs II. Yellowstone National Park

In the Mammoth Springs (Yellowstone National Park) waters with near neutral pH and soluble sulfide (H₂S, HS^–, S^2–) of over 1–2 mg/liter (30–60M) are characterized by substrate covers of phototrophic bacteria (Chloroflexus and aChlorobium-like unicell) above 50C and by a blue-green alga (Spirulina labyrinthiformis) below this temperature.Synechococcus. Mastigocladus, and other blue-green algae typical of most hot springs of western North America are excluded, apparently by sulfide. The sulfide-adaptedSpirulina photosynthesized at maximum rates at 45C and at approximately 300 to 700Ein/m²/sec of visible radiation. Sulfide (0.6–1.2 mM) severely poisoned photosynthesis of nonadapted populations, but those continuously exposed to over 30M tolerated at least 1 mM without inhibition. A normal¹⁴C-HCO₃ photoincorporation rate was sustained with 0.6–1 mM sulfide in the presence of DCMU (7M) or NH₂OH (0.2 mM), although both of these photosystem II inhibitors prevented photoincorporation without sulfide. Other sulfur-containing compounds (S₂O₃ ^2– SO₃ ^2–, S₂O₄ ^2– thioglycolic acid cysteine) were unable to relieve DCMU inhibition. The lowering of the photoincorporation rate by preferentially irradiating photosystem I was also relieved by sulfide. The most tenable explanation of these results is that sulfide is used as a photo-reductant of CO₂, at least when photosystem II is inhibited. It is suggested that in some blue-green algae photosystem II is poisoned by a low sulfide concentration, thus making these algae sulfidedependent if they are to continue photosynthesizing in a sulfide environment. Presumably a sulfidecytochrome reductase enzyme system must be synthesized for sulfide to be used as a photo-reductant.     

Caffeine inhibition of postreplication repair of UV-damaged DNA in mouse epidermal cells

The effect of caffeine (0.25–1.5 mM) on UV-irradiated (5 and 10 J/m²) primary cultures of mouse epidermal cells (EPD) and an in vitro transformed cell line (PDV) was studied at the cellular and molecular levels. A synergistic reduction in cell survival induced by caffeine with UV-irradiation was found in the PDV cells at 10 J/m² but not at 5 J/m². When conversion of low molecular weight newly-synthesized DNA to high molecular weight DNA was studied in both cell types, caffeine at 1.5 mM had no effect on this conversion in unirradiated cultures. At 5 J/m², caffeine had a transitory inhibitory effect on this conversion. However, at 10 J/m² caffeine had a strong permanent inhibitory effect on this conversion at doses higher than 0.5 mM in PDV cells and higher than 0.25 mM in EPD cells. This apparent inhibition of elongation by caffeine in irradiated cells could not be accounted for by an effect on the rate of DNA synthesis. In PDV cells there was a direct correlation in terms of effective caffeine dose level between synergistic reduction in cell survival after UV and the effect on DNA elongation. Irradiated EPD cells were more sensitive to the inhibitory effect of caffeine on DNA elongation.     

Effect of Light with Different Spectral Composition on Cell Growth and Pigment Composition of the Membranes of Purple Sulfur Bacteria <Emphasis Type="Italic">Allochromatium minutissimum</Emphasis> and <Emphasis Type="Italic">Allochromatium vinosum</Emphasis>

The effect of light with different spectral composition: white, red and blue-green (the first one is absorbed by all the pigments of the cell, and the second and the third ones are absorbed by bacteriochlorophyll and carotenoids, respectively) on culture growth, carotenoid synthesis, and assembly of the light-harvesting complexes was studied for the purple sulfur bacteria Allochromatium (Alc.) minutissimum MSU and Alc. vinosum ATCC 17899. The working hypothesis on the growth of bacteria under blue-green illumination (absorbed by carotenoids) resulting in the inhibition of cell growth was tested. When equalizing the light by luxes, the intensity of illumination for each luminous flux was 1800 lx (white and red light, 4 W/m²; bluegreen light, 0.4 W/m²). The growth of the cells was recorded in white and red light, while in blue-green light an insignificant increase was observed only for Alc. vinosum at the end of the experiment (7–9 days). Regardless of the spectral composition of the light the B800-850 type LH2 complex was always assembled in Alc. minutissimum membranes, and two short-wave LH2 complexes of В800-820 and В800-840 type were assembled in the membranes of Alc. vinosum. Upon smoothing and increasing the luminous flux up to 6 W/m² for every illumination mode, both cultures grew with approximately equal rates in blue-green light. In the membranes of Alc. minutissimum and Alc. vinosum the same types of LH2 complexes were assembled as in the case of 1800 lx illumination. It was found that blue-green light did not inhibit cell growth. At illumination of the cells collected at the end of the experiment with blue-green light for 6 h, no photooxidation of BChl850 was registered. However, in the membranes from the cells oxygen-saturated at isolation, ~50% of BChl850 was oxidized after 30 minutes of illumination. In the course of cell growth, oxygen is probably completely consumed and anaerobic conditions develop inside the cell. Under these conditions, formation of reactive oxygen species, BChl photooxidation and inhibition of the cell growth become impossible.     

Growth and energy production in Bacteroides amylophilus

The molar growth yield (Y _m) of Bacteroides amylophilus strain WP91 on maltose was 68±2 g/mol when determined from batch cultures at the peaks of maximal growth. Continued incubation led to considerable cell lysis. When calculated from batch cultures in exponential phase (specific growth rate, =0.57 h^-1) Y _m was 101 g/mol. The maximum value of Y _m in maltose-limited chemostat cultures at the maximum dilution rate (D) attainable (D==0.39 h^-1) was about 79 g/mol. Ammonia-Fmited chemostat cultures metabolized maltose with a much reduced efficiency and this was associated with a difference in morphology and chemical composition of the cells. The theoretical maximum molar growth yields (Y _m ^max ) were 55 and 114 g/mol for ammonia- and maltose-limited growth respectively. However, if account was taken of extracellular nitrogen-containing material in ammonia-limited cultures, Y _m ^max became 60. The maintenance coefficient (m _s), estimated from the lines relating the specific rate of maltose consumption (q _m) and D (where m _s=q _m at D=0), was 7.4±0.6×10^-4 mol maltose/g x h for both nutrient limitations. A difference in maintenance energy demand, independent of growth-rate, could not account, therefore, for the observed differences in Y _m between ammonia- and maltose-limited growth.     

Complex repair kinetics of DNA strand breaks induced by γ-rays or UV radiation in Ehrlich ascites tumour cells

Fluorometric analysis of DNA unwinding (FADU) – a sensitive technique for the detection of strand breaks in DNA – has been modified and used for the detailed investigation of repair kinetics of DNA-strand breaks arising under different conditions in Ehrlich ascites tumour (EAT) cells irradiated by γ-rays or ultraviolet (UV) radiation. The repair kinetics of DNA-strand breaks induced in EAT cells by γ-radiation was measured at radiation doses of 8, 20 and 50 Gy. We found complex repair curves in all cases, probably reflecting the combined processes of break rejoining and break generation during repair. In order to affect the above-mentioned processes, we have used different conditions of repair and different types of radiation. Lowering of the temperature of incubation and treating the cells by 5-fluoro-2′-deoxyuridine (FUdR) lead to complex changes of the repair curve with a reduced ``wave' pattern. In order to change the type of damage to DNA, we used UV radiation (254 nm, 10 and 20 J/m²). Detailed studies of the repair kinetics showed that the repair curve for 10 J/m² had a second maximum within 70 min after irradiation. Received: 17 May 1995 / Accepted in revised form: 15 March 1996     

Effects of UV‐A Radiation on Desmodesmus armatus: Changes in Growth Rate,Pigment Content and Morphological Appearance

Laboratory cultures of Desmodesmus armatus (R. Chod. ) Hegew. were grown under different levels of photosynthetically active radiation (PAR) supplemented with 3.75 mW · cm^–2 UV‐A radiation. Growth rate was monitored daily, chlorophyl‐a concentration, total carotenoid content, cell number and the relative abundance of different coenobial forms was determined at the end of each experiment. Exposure to UV‐A radiation resulted in an increasing inhibition of growth towards higher PAR levels, reaching 100% at 400 µmol · m^–2 · s^–1. Cellular carotenoid content was higher in the presence of UV‐A radiation, on the other hand no differences were observed in cellular chlorophyll‐a concentration. UV‐A radiation also induced changes in coenobium formation with a decreasing proportion of 4‐celled coenobia and an increase in the abundance of 2‐celled and teratologic coenobia, suggesting that high intensity UV‐A radiation may influence cell cycle events or morphology development. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

THE EFFECT OF NUTRIENT LIMITATION AND ITS INTERACTION WITH LIGHT UPON THE PRODUCTS OF PHOTOSYNTHESIS IN MERISMOPEDIA TENUISSIMA (CYANOPHYCEAE)1

The metabolic fate of photosynthetically-fixed CO₂ was determined by labeling samples of Merismopedia tenuissima Lemmerman for 30 min with NaH¹⁴CO₃ and analyzing its incorporation into low molecular weight compounds, polysaccharide and protein. In N- and P-sufficient cultures, relative incorporation into protein increased as the irradiance used during the labeling period was decreased to 20 μE · m^-2 s^-1. This pattern was found for cells grown at irradiances of either 20 or 180 μE · m^-2· s^-1, although incorporation into protein was greater in cultures grown at the higher irradiance. In N-limited continuous cultures, relative incorporation into protein was low, independent of growth rate, and the same for samples tested at 20 or 180 μE · m^-2· s^-1 irradiance. In contrast, ¹⁴C incorporation into protein by P-limited cultures increased as growth rate increased, and at relative growth rates greater than 0.25, the incorporation was greater at 20 than at 180 μE · m^-2· s^-1. However, the total RNA content and maximum photosynthetic rate of the cultures was the same at all growth rates tested. The interaction between nutrient concentration and light intensity was studied by growing-limited continuous cultures at the same dilution rate, but different irradiances. Relative incorporation into protein was highest in cultures grown at 20 μE · m^-2· s^-1, in which the relative growth rate was 0.4. These results suggest that photosynthetic carbon metabolism may respond to relative growth rate μ/μ_max rather than to growth rate directly.     

UV-induced mutagenesis at the hypoxanthine—guanine phosphoribosyl transferase locus in two L5178Y mouse lymphoma cell strains with different UV sensitivities

Two strains of L5178Y mouse lymphoma cells, L5178Y-R (LY-R) and L5178Y-S (LY-S), differ markedly in their sensitivity to 254 nm UV radiation (D₀ = 0.7 and 5.5 J/m²; n = 6.0 and 2.0 for LY-R and LY-S cells, respctively). In this study, the frequency o hypoxanthine-guanine-phosporibosyl-transferase-deficient mutants was determined, using 6-thioguanine (TG) as a selective agent, in populations of LY-R and LY-S cells exposed to various fluences of UV radiation. The spontaneous mutation frequency for LY-R cells was (3.7 ± 0.6) × 10^?5 TG^r mutants per viable cell, and the UV induction rate was (2.2 ± 0.8) × 10^?4 TG^r mutants per viable cell, per J/m². Both spontaneous and induced mutantion frequencies were much lower for LY-S cells. The sopntaneous mutation frequency for these cells were too low to make its measurement practicable ( < 0.0013 × 10^?5 TG^r mutants per viable cell). Mutation induction rate was (4.2 ± 2.2) × 10^?7 TG^r mutants per viable cell, per J/m². These differences in mutability do not appear to be due to gene duplication in LY-S cells, or to selective growth disadvantage of LY-S-derived TG-resistant mutants. Possible mechanisms underlying the differences in mutability of LY-R and LY-S cells are considered.     

UV-A mediated induction of carotenoid accumulation in Dunaliella bardawil with retention of cell viability

The effect of adding UV-A radiation (320–400 nm) to photosynthetically active radiation (PAR, 400–700 nm) during growth of the photosynthetic marine microalga Dunaliella bardawil was investigated in this work in terms of cell growth and carotenoid production. Although signs of slow cell growth (slight reduction of chlorophyll and protein content) were observed after 24 h of cell exposure to UV-A (40 mol photons m^–2 s^–1 and 70 mol photons m^–2 s^–1) plus 140 mol photons m^–2 s^–1 PAR , 84 h exposure to these UV-A conditions slightly stimulated cell growth and increased the photosynthetic efficiency of the exposed cultures. The enhanced cell growth was coupled with an increase in total carotenoid content. Besides -carotene as the major pigment, increases in the well-known antioxidants lutein and zeaxanthin of about 3-fold and 5-fold, respectively, were determined in cultures exposed to UV-A radiation of 70 mol photons m^–2 s^–1for 84 h. As a consequence, far from being negative to cell growth, low and medium UV-A radiation are stress factors that could be successfully applied to long-term processes for large scale carotenoid production using D. bardawil cultures with retention of cell viability. UV-A exposure has the advantage of being a factor either easily applied or removed as required, in contrast to other nutrient stresses, which require medium replacement for their application.     

Regeneration of NADPH by Frozen-thawed Cells of a Blue-green Alga,Synechococcus sp.

The photoreduction of NADP ⁺ and its associated reactions were studied in a blue-green algal preparation that was frozen in liquid nitrogen and thawed at room temperature. The preparation was capable of photoreducing exogeneous NADP⁺. Water was the ultimate electron donor for the reduction. The optimum pH was 7.5 ~ 8.0, and optimum temperature, around 50°C. Light saturation for NADP⁺ photoreduction was reached at 50 μEinstein/m²/sec. Factors limiting the stability of the preparation were examined and a possible application of this cofactor regeneration system is discussed.     

CHARACTERIZATION AND BIOLOGICAL IMPLICATIONS OF SCYTONEMIN,A CYANOBACTERIAL SHEATH PIGMENT1

Scytonemin, the yellow-brown pigment of cyanobacterial (blue-green algal) extracellular sheaths, was found in species thriving in habitats exposed to intense solar radiation. Scytonemin occurred predominantly in sheaths of the outermost parts or top layers of cyanobacterial mats, crusts, or colonies. Scytonemin appears to be a single compound identified in more than 30 species of cyanobacteria from cultures and natural populations. It is lipid soluble and has a prominent absorption maximum in the near-ultraviolet region of the spectrum (384 nm in acetone; ca. 370 nm in vivo) with a long tail extending to the infrared region. Microspectrophotometric measurements of the transmittance of pigmented sheaths and the quenching of ultraviolet excitation of phycocyanin fluorescence demonstrate that the pigment was effective in shielding the cells from incoming near-ultraviolet-blue radiation, but not from green or red light. High light intensity (between 99 and 250 μmol photon · m^?2· S^?1, depending on species) promoted the synthesis of scytonemin in cultures of cyanobacteria. In cultures, high light intensity caused reduction in the specific content of Chl a and phycobilins, increase in the ratio of total carotenoids to Chl a, and scytonemin increase. UV-A (320–400 nm) radiation was very effective in eliciting scytonemin synthesis. Scytonemin production was physiological and not due to a mere photochemical conversion. These results strongly suggest that scytonemin production constitutes an adaptive strategy of photoprotection against short-wavelength solar irradiance.     

Optical characteristics and parameters of the plasma of a barrier discharge excited in a mixture of mercury dibromide vapor with nitrogen and helium

Results are presented from experimental and theoretical studies of the optical characteristics and parameters of the plasma of an atmospheric-pressure barrier discharge excited in a HgBr₂: N₂: He mixture, which was used as the working medium of a small-size (with a radiation area of 8 cm²) exciplex gas-discharge radiation source. The mean radiation power of 87 mW was achieved at the radiation wavelength λ_max = 502 nm. The electron energy distribution function, the transport characteristics, the specific energy lost in the processes involving electrons, the electron temperature and density, and the rate constants of elastic and inelastic electron scattering by the components of the working mixture were calculated as functions of the reduced field E/N. The plasma of a discharge excited in a HgBr₂: N₂: He mixture can be used as the working medium of a small-size blue-green radiation source. Such a source can find application in biotechnology, photonics, and medicine and can also be used to manufacture gas-discharge display panels.     

RESPONSE OF PROROCENTRUM MARIAE-LEBOURIAE (DINOPHYCEAE) TO LIGHT OF DIFFERENT SPECTRAL QUALITIES AND IRRADIANCES: GROWTH AND PIGMENTATION1

Growth and pigment concentrations of the, estuarine dinoflagellate, Prorocentrum mariae-lebouriae (Parke and Ballantine) comb. nov., were measured in cultures grown in white, blue, green and red radiation at three different irradiances. White irradiances (400–800 nm) were 13.4, 4.0 and 1.8 W · m^?2 with photon flux densities of 58.7 ± 3.5, 17.4 ± 0.6 and 7.8 ± 0.3 μM quanta · m^?2· s^?1, respectively. All other spectral qualities had the same photon flux densities. Concentrations of chlorophyll a and chlorophyll c were inversely related to irradiance. A decrease of 7- to 8-fold in photon flux density resulted in a 2-fold increase in chlorophyll a and c and a 1.6- to 2.4-fold increase in both peridinin and total carotenoid concentrations. Cells grown in green light contained 22 to 32% more peridinin per cell and exhibited 10 to 16% higher peridinin to chlorophyll a ratios than cells grown in white light. Growth decreased as a function of irradiance in white, green and red light grown cells but was the same at all blue light irradiances. Maximum growth rates occurred at 8 μM quanta · m^?2· s^?1 in blue light, while in red and white light maximum growth rates occurred at considerably higher photon flux densities (24 to 32 μM quanta · m^?2· s^?1). The fastest growth rates occurred in blue and red radiation. White radiation producing maximum growth was only as effective as red and blue light when the photon flux density in either the red or blue portion of the white light spectrum was equivalent to that of a red or of blue light treatment which produced maximum growth rates. These differences in growth and pigmentation indicate that P. mariae-lebouriae responds to the spectral quality under which it is grown.     

Effects of UVB Radiation on the Initial Stages of Growth of Gigartina Skottsbergii, Sarcothalia Crispata and Mazzaella Laminarioides (Gigartinales, Rhodophyta)

The effects of UVB radiation on the growth of macroalgal thalli were evaluated using tetrasporophytic fronds of the Rhodophytes Gigartina skottsbergii, Sarcothalia crispata and Mazzaella laminarioides. The tetrasporophytic fronds were collected from nature and the tetrasporophyte sporelings grown in a temperature regulated chamber at 8 ± 2 ^∘C with a 12L:12D (Light: Dark) photoperiod, Photosynthetically Active Radiation (PAR) of 55 μmol photons m⁻² s⁻¹ and seawater enriched with 20 mL L⁻¹ of Provasoli medium. We exposed the thalli of these macroalgae to PAR (55 μmol photons m⁻² s⁻¹) and three treatments using a combination of PAR with three different levels of UVB radiation (0.10, 0.15 and 0.23 W m⁻² for G. skottsbergii and S. crispata and 0.02, 0.05 and 0.10 W m⁻² for M. laminarioides) during a period of 71 days. Growth of thalli was quantified by measuring their length using digitized photographs of samples.Important differences were detected in the growth of individuals cultured under the effects of UVB radiation, when compared to the control (i.e. plants exposed to PAR only). In the case of G. skottsbergii and S. crispata higher levels of UVB radiation resulted in slower growth of thalli. In nearly all measurements for the first two species, UVB radiation levels of 0.1 W m⁻² induced differences in thallus growth, while for M. laminarioides levels of UVB radiation of 0.1 W m⁻² were effective only after a prolonged period of exposure.Differential effects of UVB radiation on G. skottsbergii, S. crispata and M. laminarioides could interfere with the natural populations of these economically important macroalgal species in southern Chile, where they occur under the annual influence of the Antarctic Ozone Hole and the general thinning of the ozone layer.     

Combined influence of light and temperature on growth rates of <Emphasis Type="Italic">Nannochloropsis oceanica</Emphasis>: linking cellular responses to large-scale biomass production

The interaction effects between irradiance and temperature on growth rates ofNannochloropsis oceanicawere determined in both laboratory cultures and large-scale tubular photobioreactors. Growth responses were investigated in 48 batch cultures subjected to crossing light/temperature gradients ranging from 34–80μmol photons m⁻²s⁻¹and 14.5–35.7^∘C respectively. Comparisons were made to growth responses observed in production systems (200L biofences) operated in climate-regulated greenhouses with controlled temperature and artificial light gradients. Cellular responses showed increasing specific growth rates as a function of temperature, with a peak at 25–29^∘C, after which the growth became increasingly unstable. The optimum temperature for growth increased with higher light intensities up to approximately 28^∘C at 80μmol photons m⁻²s⁻¹. At low light intensities the specific growth rate was less affected by temperature. The maximum daily production measured in the biofence systems increased proportionally with irradiation and reached approximately 0.7gL⁻¹d⁻¹at 1030μmol photons m⁻²s⁻¹average daily radiation for a culture temperature of 24^∘C. This corresponds to a daily yield of 140g per day in a 200L biofence system. When specific growth rates for the biofence cultures were measured at different densities and plotted against temperature, results showed a peak with the 24^∘C temperature treatment. This peak became less pronounced as the density increased in the cultures. This is consistent with the laboratory results; increasing cell density in the biofence cultures resulted in less average light cell⁻¹, which produced the same temperature dependent response as seen by reducing the external irradiance exposure for the dilute laboratory cultures.     

Influence of CO2, light and watering on growth of Nostoc flagelliforme mats

The terrestrial blue-green alga (cyanobacterium), Nostoc flagelliforme, was cultured in air at variouslevels of CO₂, light and watering to see theireffects on its growth. The alga showed the highestrelative growth rate at the conditions of highCO₂ (1500 ppm), high light regime (219–414mol m^-2s^-1) and twice daily watering,but the lowest rate at the conditions of low light(58–114 mol m^-2s^-1) and daily twicewatering. Increased watering had little effect ongrowth rate at 350 ppm CO₂, but increased byabout 70% at 1500ppm CO₂ under high lightconditions. It was concluded that enriched CO₂could enhance the growth of N. flagelliformewhen sufficient light and water was supplied.     

Photosynthetic response of Nereocystis luetkeana (Phaeophyta) to high light

Photosynthetic response to high light was determined for Bull kelp, Nereocystis luetkeana (K. Mertens) Postels and Ruprecht in order to understand how this species is affected by short‐term fluctuations in irradiance. Exposure of N. luetkeana blades to high intensity photosynthetically active radiation (1000 µmol photons m^?2 s^–1) caused increased non‐photochemical quenching of fluorescence and higher de‐epoxidation ratios for xanthophyll pigments indicating that energy‐quenching xanthophylls were used to protect blades against photoinhibition. Despite initiation of these photoprotective mechanisms, maximum photochemical efficiency of photosystem II (F_v/F_m) decreased 40% in response to a 60 min exposure to 1000 µmol photons m^?2 s^–1 photosynthetically active radiation indicating that photoinhibition had occurred. Light‐saturated rates of oxygen evolution were not changed significantly by the high light treatment. Recovery of maximum photochemical efficiency of photosystem II to within 8% of initial values occurred after a 300‐min dim light period. Younger sections of the blades were slightly more susceptible to high light damage than older sections. Middle sections of the blades were more prone to light‐induced damage at water temperatures of 7°C or 18°C, as compared to 13°C. Exposure to biologically effective ultraviolet‐B radiation (UV‐B_be) (up to 4.5 kJ m^–2 day^–1) in photoinhibitory light conditions did not significantly affect light‐induced damage to photosystem II.     

Growth at low temperature causes nitrogen limitation in the cyanobacterium Synechococcus sp. PCC 7002

The coloration of cells of the cyanobacterium Synechococcus sp. PCC 7002 changed from normal blue-green to yellow-green when cells were grown at 15° C in a medium containing nitrate as the sole nitrogen source. This change of coloration was similar to a general response to nutrient deprivation (chlorosis). For the chlorotic cells at 15° C, the total amounts of phycobiliproteins and chlorophyll a decreased, high levels of glycogen accumulated, and growth was arithmetic rather than exponential. These changes in composition and growth occurred in cells grown at low (50 μE m^–2 s^–1) as well as high (250 μE m^–2 s^–1) light intensity. After a temperature shift-up to 38° C, chlorotic cells rapidly regained their normal blue-green coloration and normal exponential growth rate within 7 h. When cells were grown at 15° C in a medium containing urea as the reduced nitrogen source, cells grew exponentially and the symptoms of chlorosis were not observed. The decrease in photosynthetic oxygen evolution activity at low temperature was much smaller than the decrease in growth rate for cells grown on nitrate as the nitrogen source. These studies demonstrate that low-temperature-induced chlorosis of Synechococcus sp. PCC 7002 is caused by nitrogen limitation and is not the result of limited photosynthetic activity or photodamage to the photosynthetic apparatus, and that nitrogen assimilation is an important aspect of the low-temperature physiology of cyanobacteria. Received: 24 April 1997 / Accepted: 5 August 1997     

Comparing the response of Antarctic,tropical and temperate microalgae to ultraviolet radiation (UVR) stress

The response of Antarctic, tropical and temperate microalgae of similar taxonomic grouping to ultraviolet radiation (UVR) stress was compared based on their growth and fatty acid profiles. Microalgae of similar taxa from the Antarctic (Chlamydomonas UMACC 229, Chlorella UMACC 237 and Navicula UMACC 231), tropical (Chlamydomonas augustae UMACC 246, Chlorella vulgaris UMACC 001 and Amphiprora UMACC 259) and temperate (Chlamydomonas augustae UMACC 247, Chlorella vulgaris UMACC 248 and Navicula incerta UMACC 249) regions were exposed to different UVR conditions. The cultures were exposed to the following conditions: PAR (42 μmol photons m⁻² s⁻¹), PAR + UVA (854 μW cm⁻²) and PAR + UVA + UVB (117 μW cm⁻²). The cultures were subjected to UVA doses of 46.1, 92.2 and 184.4 J cm⁻² and UVB doses of 6.3, 12.6 and 25.2 J cm⁻² by varying the duration of their exposure (1.5, 3 and 6 h) to UVR during the light period (12:12 h light-dark cycle). UVA did not affect the growth of the microalgae, even at the highest dose. In contrast, growth was adversely affected by UVB, especially at the highest dose. The dose that caused 50% inhibition (ID₅₀) in growth was used to assess the sensitivity of the microalgae to UVB. Sensitivity of the microalgae to UVB was species-dependent and also dependent on their biogeographic origin. Of the nine microalgae, the Antarctic Chlorella was most tolerant to UVB stress (ID₅₀ = 21.0 J cm⁻²). Except for this Chlorella, the percentage of polyunsaturated fatty acids of the microalgae decreased in response to high doses of UVB. Fatty acid profile is a useful biomarker for UVB stress for some microalgae. Presented at the 6th Meeting of the Asian Pacific Society of Applied Phycology, Manila, Philippines.