Effects of concentrating phytoplankton on the acetylene-reduction assay for nitrogenase activity

SUMMARY.

• 1 The consequences of concentrating freshwater phytoplankton communities prior to measurement of nitrogenase activity using the acetylene-reduction assay were investigated.
• 2 Retention of heterocystous blue-green algae by 10 and 45 öm plankton nets was usually much less than 100% and the percent retention differed among blue-green algal species and varied for the same species both on different sampling dates and in different lakes. Retention of heterocyst numbers and helerocyst volume during concentration differed from that of total cell volume of heterocystous blue-green algae.
• 3 Effects of concentration on specific nitrogcnase activity varied among the lakes studied. In Lake Bysjön activity decreased on all sampling occasions, in Lake Trummen there was no apparent effect, and in Lake Vaxjosjon both results were found.
• 4 Effects on nitrogenase activity of mechanical disturbance during concentration and of increased pH. reduced carbon availability. light inhibition and subsaturation. photorespiration and oxygen supersaturation in concentrated samples are discussed. Interactions between these factors are suggested to explain the varying responses in the three lakes.
• 5 It is concluded that phytoplankton should not be concentrated in the acetylene-reduction assay for nitrogenase activity, since both volumetric and cell concentration factors are inadequate and effects of concentration on specific nitrogenase activity are not predictable.

     

Site of Nitrogenase Activity in the Blue-Green Alga <Emphasis Type="Italic">Anabaena</Emphasis> sp. L-31

MANY blue-green algae fix nitrogen, assimilate carbon dioxide and evolve oxygen and as algal nitrogenase is inhibited^1–3 by high oxygen pressure, enhanced nitrogen fixation accompanying photosynthesis is surprising. Heterocysts do not contain⁴ or have comparatively less amounts^4–7 of photosystem II (PS II) pigments, which are responsible for the evolution of oxygen. This tends to favour the suggestion of Fay et al.⁸ that these cells are the sites of nitrogenase activity. Until now, however, attempts at obtaining unequivocal evidence for heterocysts as principal loci for nitrogenase activity have yielded conflicting results. Stewart et al.⁷ first demonstrated nitrogenase activity in heterocysts incubated aerobically, a finding confirmed by Wolk and Wojciuch⁹ and Van Gorkom and Donze¹⁰. By contrast, Smith and Evans^3,11 and Kurz and La Rue¹² reported results favouring vegetative cells as the major site of nitrogenase activity. Other evidence^2,13 showed high nitrogenase activity in cell-free preparations of Anabaena cylindrica and the non-heterocystous alga Plectonema boryanum strain 594.     

Nitrogen Fixation by Photosynthetic Bacteria in Lowland Rice Culture

Propanil (3′,4′-dichloropropionanilide) was a potent inhibitor of the nitrogenase activity of blue-green algae (cyanobacteria) in flooded soil, but the herbicide at comparable concentrations was not toxic to rice, protozoa, and nitrogen-fixing bacteria. Ethanol-amended flooded soils treated with propanil exhibited higher rates of nitrogenase activity than those not treated with the herbicide. The enhanced nitrogenase activity in propanil-treated soils was associated with a rise in the population of purple sulfur bacteria, especially of cells resembling Chromatium and Thiospirillum. By employing propanil and a means of excluding light from the floodwater to prevent the development of phototrophs during rice growth under lowland conditions, the relative activities of blue-green algae, photosynthetic bacteria, and the rhizosphere microflora were determined. The results suggest that the potential contribution of photosynthetic bacteria may be quite high.     

CHANGES IN EMISSION SPECTRA OF PHOTOSYNTHETIC PIGMENTS IN VIVO

1. The effects of 3-(4'-chlorophenyl)-1, 1-dimethylurea (CMU)onthe fluorescence of photosynthetic pigments in vivo wereinvestigatedin blue-green, red and brown algae and in isolatedspinach chloroplasts.CMU caused an increase in steady statelevel of fluorescenceof chlorophyll a, but did not influencethe fluorescence ofphycobilins. The spectrum of the fluorescenceincrement hada peak at 685 m/µ and a shoulder at 730–740mµ.These two bands probably arise from chlorophyll a(C_f684) belongingto pigment system II.
2. On excitation of chlorophylla in a red alga, Porphyra yezoensis,a fluorescence band witha peak at 720 mµ was observedbesides a shoulder at 685mµ. The 720 m band is inferredto arise from chlorophylla (probably, C_f-1) in pigment systemI.
3. On addition of CMUto the algal cells, the induction of fluorescencewas modifiedto take a simple time course. The induction wasobserved onlywith respect to the fluorescence of chlorophylla, but not inthe fluorescence of phycobilins. The spectrumof the "transient"fluorescence showed two emission bands ofchlorophyll a at 685mµ and 740 mµ, and was quitesimilar in form tothe spectrum of the CMU-caused increase insteady state fluorescence.
4. These facts were interpreted in terms of the correlation offluorescence of chlorophyll a and the photochemical reactionsof photosynthesis

(Received July 20, 1967; )     

Effect of Rice Plants on Nitrogenase Activity of Flooded Soils

In samples of flooded soil containing blue-green algae (cyanobacteria), the presence of rice plants did not influence the nitrogenase activity of the algae. Nitrogenase activity of heterotrophic bacteria was enhanced by the presence of rice plants, but this activity was not affected by changes in plant density. The rate of nitrogen fixation in the rhizosphere, however, varied significantly among the 16 rice varieties tested. A simple method was devised to test the nitrogen-fixing activity in the root zone of rice varieties, and data were obtained showing marked differences in the activities of the 16 varieties. In tests of two varieties with dissimilar rates of nitrogen fixation in their rhizospheres, the variety which had the greater root weight and lesser shoot weight and which supported greater methane formation had the greater nitrogenase activity.     

Ion-Exchange Properties of Isolated Cell Walls of Brown Algae: The Interstitial Solution

Kloareg, B., Demarty, M. and Mabeau, S. 1987. Ion-exchange propertiesof isolated cell walls of brown algae: the interstitial solution.—J.exp. Bot. 38: 1652–1662. Isolated cell walls of Pelvetia canaliculata (Dene) et Thur.,Laminaria digitata (L.) and other intertidal brown algae wereequilibrated in seawater and various mixtures of sodium andcalcium chlorides. After elution with distilled water, the interstitialsolution was assayed for ionic composition. With respect tothe external solution, it was less concentrated and containedlower proportions of divalent cations. Such modifications wererelated to the divalent ionic fraction and the total anion concentrationof the external solution. No significant differences were foundamong the brown algae investigated in spite of the differingcomposition of their walls. Results were analysed accordingto the polyelectrolyte condensation model. When the concentrationof the external solution was high (1000 meq dm³), experimentaldata were qualitatively in good agreement with the predictionsof the model. Key words: Cell walls, ion-exchange, Phaeophyta.     

The occurrence of the hydrogenase in some blue-green algae

Several blue-green algae were surveyed for the occurrence of the hydrogenase which was assayed by the oxyhydrogen or Knallgas reaction in the intact organisms. In aerobically grown cultures, the reaction was detectable in Anabaena cylindrica, Nostoc muscorum and in two Anabaena variabilis species, whereas virtually no activity was observed in Anacystis nidulans and Cyanophora paradoxa. In these latter two algae, the reaction was, however, found after growth under molecular hydrogen for several days, which drastically increased the activity levels with all the algae tested. In the nitrogen fixing species, the activity of the Knallgas reaction was enhanced when all combined nitrogen was omitted from the media. H₂ and hydrogenase could not significantly support the CO₂-fixation in photoreduction experiments with all blue-green algae investigated here. Hydrogenase was assayed by the dithionite and methyl viologen dependent evolution of hydrogen and was found to be present with essentially the same specific activity levels in preparations of both heterocysts and vegetative cells from Anabaena cylindrica. Na₂S₂O₄ as well as H₂ supported the C₂H₂-reduction of the isolated heterocysts. The H₂-dependent C₂H₂-reduction did not require the presence of oxygen but was strictly light-dependent where H₂ served as an electron donor to photosystem I of these cells. It is concluded that hydrogen can be utilized by two different pathways in blue-green algae.Abbreviations Chl chlrophyll - CP creatine phosphate - CP kinase creatine phosphokinase - DCMU N-(3,4-dichlorophenyl)N,N-dimethylurea     

Quantitative relationship between two reaction centersin the photosynthetic system of blue-green algae

The quantitative relationship between reaction centers I andII was studied with blue-green algae Anabaena cylindrica, Anabaenavariabilis and Anacystis nidulans grown under different lightconditions. The number of reaction centers I was estimated fromthe P700 content and that of reaction centers II, from the O₂yield of repetitive short flashes. Supplementary determinationswere done with three other blue-green algae and one red alga.The maximum number of reaction centers II counted from the O₂yield of repetitive short flashes was markedly smaller thanthe total number of P700 in all algae tested when the algaewere grown under weak light; in the extreme case (Anabaena cylindrica),the ratio was only 0.258?0.015. This ratio became larger andclose to unity when the algae were grown under stronger light.Variation in the number of reaction centers in a single cellsuggested that reaction center I was a variable component. Ourresults indicate that the proportion of the two reaction centersmay markedly vary in blue-green algae depending on the growthconditions (Received November 13, 1978; )     

The Effect of Available Nitrate and Ammonium-Nitrogen on the Growth of Two Nitrogen-Fixing Blue-Green Algae

The effect of combined nitrogen supplied as nitrate or ammonium-nitrogenon the growth of two nitrogen-fixing blue-green algae, Nostocentophytum and Calothrix scopulorum, has been studied. Thesespecies have been isolated from marine environments. Both algaegrew as vigorously on elemental nitrogen as in the presenceof combined nitrogen. Growth was equal at all levels of nitrate-nitrogenemployed but high levels of ammonium-nitrogen proved inhibitoryor even toxic to the algae. Nostoc was slightly more susceptibleto high ammonium-nitrogen levels than was Calothrix. Increasein pH of the medium from 7.2 to 8.4 increased the toxic effectof ammonium-nitrogen although relative growth at the variouslevels of nitrate-nitrogen was not affected. The results suggestthat the different effects of ammonium-nitrogen on the growthof freshwater and marine blue-green algae may be due in partat least to the different pH levels of freshwater and marineenvironments in which the algae grow, rather than to any inherentdifference between the two groups.     

Isolation and characterization of rapidly-growing,marine, nitrogen-fixing strains of blue-green algae

Five strains of heterocystous blue-green algae capable of high rates of growth and nitrogenase activity were isolated from shallow coastal environments. Growth of the organisms was characterized with respect to temperature, NaCl concentration in the medium, and nitrogen source. The temperature optima ranged from 35–42°C, and all but one of the strains displayed a requirement for added NaCl. The generation times under N₂-fixing conditions were 5.1–5.9 h, and were as low as 3.4 h for growth on NH₄Cl. Nitrogenase activity (C₂H₂ reduction) was high throughout the logarithmic growth phase of each strain. The maximum value observed for one strain was 65.5 nmoles C₂H₄ produced/mg protein x min, and the average values for the five strains ranged from 24.5–46.7 nmoles C₂H₄/mg protein x min. The organisms all belong to the genusAnabaena. The growth and nitrogenase activity of these strains are much higher than those of the heterocystous blue-green algae commonly used for investigation of nitrogen metabolism, and they thus should prove to be useful physiological tools. Their prevalence, as judged by the ease of their enrichment and isolation, in bay and estuarine environments suggests that they are important contributors of combined nitrogen.     

Resistance to blue-green algal toxins by Bosmina longirostris

Bosmina longirostris was resistant to strains of Microcysrtsaeruginosa and Anabaena flosaquae previously reported to havelethal toxic effects on cladocerans. These blue-green algaewere of poor nutritional value to B.longirostris; survivorshipwas increased when fed these algae but reproduction was negligible.Results of feeding selectivity experiments showed that B.longirostrisdid not avoid consuming these blue-green algae, indicating thatthe mechanism for resistance must be post-ingestion. These resultssuggest that, unlike the other cladocerans tested, B.longirostriscould potentially coexist with toxic blue-green algal blooms.     

White Clover N2-Fixation in Response to Root Temperature and Nitrate: II. N2-FIXATION, RESPIRATION, AND NITRATE REDUCTASE ACTIVITY

Established, nodulated white clover plants were transferredto eight tanks of a flowing culture apparatus with solutiontemperatures of 5, 11, 17, and 25 ?C (two tanks per temperature).Shoot temperature and light environment were common to all plants.After 7 d, (10 mmol m^–3) was continuouslysupplied to one tank at each temperature while in the remainingfour tanks (one at each temperature) the plants were completelydependent on nodule N₂-fixation. Plants were randomly selected at intervals during the following14 d period in order to measure root and nodule respirationand acetylene reduction activity (ARA) in a flow-through systemset at the adapted root temperature. Additional plants wereassayed for in vitro nitrate reductase activity in leaves, roots,and nodules. Apparent nitrogenase activity (ARA) and respiration associatedwith it were each markedly affected by temperature in two ways;(1) Activity per unit weight of nodule was reduced at lowertemperatures; (2) Development of the plant, and thus also nodulemass, was restricted at lower temperatures which, in turn, restrictedtotal nodule activity per plant. The presence of nitrate significantly reduced ARA of nodules,particularly at higher temperatures. However, significant discrepancieswere found when N₂-fixation rates, estimated from the acetylenereduction assay, were compared with N₂-fixation rates calculatedfrom curves fitted to N accumulation data (minus the rate of uptake in the case of nitrate-treated plants). Carbon use efficiency (CO² respired per C₂H₄ produced) was notsignificantly affected by temperature or the presence of nitrate. Nitrate reductase activity (NRA) developed in all plant partsat the three highest temperatures, but not at 5 ?C. We calculatethat leaf NRA may account for 82, 75, and 68% of total nitratereduction at 11, 17, and 25 ?C respectively. Key words: Trifolium repens, white clover, N₂ fixation, root temperature, acetylene reduction assay, nitrate, nitrate reductase     

Fine control of citrate synthase activity in blue-green algae

Summary The citrate synthases of four blue-green algae, two unicellular (Aphanocapsa spp.) and two filamentous (Nostoc sp., Phormidium sp.) were inhibited by -ketoglutarate but not by NADH. This control of citrate synthase activity reflects the lack of -ketoglutarate dehydrogenase in blue-green algae and the strictly biosynthetic role played by the glutamate branch of the tricarboxylic acid cycle. The citrate synthases were also inhibited by ATP and the enzyme of one of the unicellular organisms was also sensitive to inhibition by NADPH. These effectors may function in regulating the flow of fixed carbon into lipids rather than the glutamate family of amino acids.Contribution No. 1649 from the University of Miami, Rosenstiel School of Marine and Atmospheric Science, 10 Rickenbacker Causeway, Miami, Florida 33149, U.S.A.     

Fixation of Elemental Nitrogen by Marine Blue-green Algae

Three blue-green algae, Calothrix scopulorum, Nostoc entophytum,and Oscillatoria brevis, isolated from the upper littoral andsupralittoral fringe of the sea-shore were obtained in pureculture and tested for fixation of elemental nitrogen. Appreciablefixation by Calothrix and Nostoc was detected, a proportionof the total nitrogen fixed being liberated into the culturemedium. There was no evidence of fixation by Oscillatoria. Thisappears to be the first evidence that blue-green algae isolatedin pure culture from marine habitats fix nitrogen.     

Benthic algal populations respond to aluminum,acid, and aluminum-acid mixtures in artificial streams

Elevated aluminum (Al) concentrations are often associated with acid-stressed aquatic ecosystems, so it has been unclear whether acidic water or elevated Al is more responsible in changing community composition. Experiments were done to investigate effects of acidification and increased Al on the abundance of benthic algae in artificial streams supplied with natural water and nominal treatments of (a) pH 4.8, (b) 500 µg l^-1 Al, or (c) the mixture of pH 4.8 and 500 µg l^-1 Al compared to a control without added Al or acid. These treatments are referred to as Acid, Al-only, Acid + Al, and the control, respectively. In the Acid treatment the abundance of two diatoms, two green algae, dry weight biomass, and chlorophyll a decreased; one diatom and one filamentous blue-green alga increased. In the Al-only treatment, densities of two diatoms, one green alga, one blue-green alga, dry weight biomass, and chlorophyll a increased. In the Acid + Al treatment, abundances of one green alga, two blue-green algae, and concentrations of chlorophyll a decreased below the levels observed in the Acid treatment. Acid and Al concentrations were altered by each other and by chemical and biological processes in the stream system. Species of diatoms, green algae, and blue-green algae responded individually to treatments and mixtures of acid and Al. Shifts in the abundance of species may change food web relationships for higher-level consumers, and algae may be useful biomonitors of ecological stress.     

Nitrogen Fixation by Thermophilic Blue-Green Algae (Cyanobacteria): Temperature Characteristics and Potential Use in Biophotolysis

Thermophilic, nitrogen-fixing, blue-green algae (cyanobacteria) were investigated for use in biophotolysis. Three strains of Mastigocladus laminosus were tested and were found to be equally effective in biophotolysis as judged by nitrogenase activity. The alga, M. laminosus NZ-86-m, which was chosen for further study, grew well in the temperature range from 35 to 50°C, with optimum growth at 45°C, at which temperature acetylene reduction activity was also greatest. The maximum tolerable temperature was 55°C. Acetylene reduction activity was saturated at a light intensity of 1 × 10⁴ ergs cm⁻² s⁻¹. Atmospheric oxygen tension was found to be slightly inhibitory to acetylene reduction of both slowly growing and exponentially growing cultures. Nonsterile continuous cultures, which were conducted to test problems of culture maintenance, could be operated for 2 months without any significant decrease in nitrogenase activity or contamination by other algae. Nitrogen-starved cultures of M. laminosus NZ-86-m produced hydrogen at comparable rates to Anabaena cylindrica. The conversion efficiency of light to hydrogen energy at maximum rates of hydrogen production was 2.7%.     

Influence of Cadmium on Growth and Nitrogen Metabolism of Anabaena cylindrica Lemm

A study was made of the effects of cadmium on the Cyanobacterium(blue-green alga) Anabaena cylindrica Lemm. as part of the paddy-fieldecosystem. A simple culture vessel has been designed, which allows periodicalmeasurement of growth (optical density) and nitrogenase activity(C₂H₂-C₂H₄ method). The influence of medium renewal was checked:the renewal of the medium maintained a higher growth rate andhigher nitrogen fixation ability. The cadmium effects were studied using six concentration levelsranging from 0 (control) to 2 parts 10^–6 with renewedmedia (10% every day). No significant differences could be seen up to 1 part 10^–6for nitrogenase activity and relative percentage of heterocysts(decreasing as a function of time from ±4% to ±1.5%). Inhibition of growth (OD and dry weight) was weak at 1 part10^–6 but important at 2 parts 10^–6; at this concentrationcadmium induced morphological and physiological effects: chlorosis,cellular malformations and destruction, and increase in heterocystfrequency (up to 7.72% ±0.19). The cadmium concentration factors were much lower than thosereported for other plants like Chlorella and water pests     

N2 Fixation (C2H2-Reducing Activity) and Leghaemoglobin Content during Nitrate- and Water-Stress-Induced Senescence of Medicago sativa Root Nodules

Nitrate and water stress were used to induce senescence in rootnodules of alfalfa (Medicago sativa L. cv. Aragon). Nodule senescencewas assessed by determinations of the nitrogenase (C₂H₂-reducing)activity, and the leghaemoglobin (LHb) and total soluble proteincontents of the nodules. Nodules responded similarly to and water stress in many respects, but there was a significant difference.All parameters of nodule activity, expressed on the basis ofnodule dry weight (DW), consistently decreased following treatmentwith or during drought; there was a significant interaction (synergism) between the inhibitory effects of and water stress on nitrogenase activity, but sucheffects were merely additive in the case of LHb content or LHb/solubleprotein ratio. However, caused the selective decay of LHb with respect to other nodular soluble proteins,whereas the decrease of LHb during water stress was due to ageneral inhibition of protein synthesis and to an increasedproteolytic activity in the nodule cytosol rather than to aspecific proteolysis of LHb. Key words: Leghaemoglobin, Medicago saliva, nitrogen fixation, root nodule senescence, water stress     

Variation in Photosynthesis and Enzyme Activity in Cenchrus ciliaris L.

Populations of Cenchrus ciliaris differ significantly in relativegrowth-rate (R), net assimilation rate (E), and leaf-area ratio(F). Differences in R were related to differences in E ratherthan in F. The populations also differed in the rate of apparentphotosynthesis of individual leaves as measured by infra-redgas analysis. Warburg and ^l4CO₂ techniques. Temperature andlight-response measurements revealed optimum temperature forphotosynthesis of 35 °C and the rate in most populationscontinued to increase up to the highest levels of irradianceemployed (200 W m²). The relative order of the populations wassimilar in all methods of analysis, but there was no relationshipevident between leaf photosynthesis and E derived from growthanalysis. The activity of the enzyme PEP carboxylase, expressedin terms of unit leaf area, was correlated with photosyntheticrate of the leaf. Activities of PEP carboxylase and of proteinsynthesis in vitro expressed on a basis of soluble protein contentwere correlated with E, but no such relationship was found forthe enzymes acid phosphatase and alanine--ketoglutarate aminotransferase.     

Cyanidium caldarium as a bridge alga between Cyanophyceae and Rhodophyceae: Evidence from immunodiffusion studies

The primer-independent phosphorylase isozyme, a₂, of Cyanidiumcaldarium was used for immunization of rabbits. The immune serumwas tested against pure a₂ isozymes from blue-green, red, andgreen algae. Double immunodiffusion in agar indicated that therewas structural similarity in the isozyme from Cyanidium caldarium,the blue-green algae, Oscillaloria princeps, Pleclonema nostocorumand the red alga, Rhodymenia pertusa. Complete fusion of theprecipitin lines was obtained with these algae. However, onlypartial fusion was observed with the a₂ isozymes from Chlorophyceaesuch as Chlorella pyrenoidosa and Spirogyra setiformis. Spurformation on the precipitin lines occurred when the isozymesfrom these algae were tested against the immuneserum. The results were interpreted as indicative of the possible transitionstatus of Cyanidium caldarium between prokaryotic blue-greenalgae and eukaryotic red algae. It would appear that the Chlorophyceaeevolved along different lines from Cyanophyceae than did theRhodophyceae. (Received November 25, 1975; )