Nitrogen Fixation by the Blue-green Alga Anabaena flos-aquae A-37

Nitrogen fixation has been demonstrated in a bacteria-free culture of a semithermophilic blue-green alga, Anabaena flos aquae A-37, employing the criterion of an increase in cellular nitrogen as a basis for determining nitrogen fixation. This is apparently the first time that nitrogen fixation has been demonstrated in a pure culture of a blue-green alga which grows at 40 C and which produces abundant quantities of an extracellular heteropolysaccharide.     

The Effect of Various Nitrogen Sources upon Heterocyst Formation in Anabaena Flos-Aquae A-37

Heterocysts are formed abundantly in cultures of Anabaena flos-aquaeA-37 which are fixing nitrogen. Fewer are formed in the presenceof NO₃^– ions, whereas none occurred in the presence ofNH₄⁺ ions. The results indicate that heterocysts may have arole in nitrogen metabolism.     

Some Observations on the Sodium and Potassium Interactions in the Blue-green Alga Anabaena flos-aquae A-37

The growth of Anabaena flos-aquae A-37 has been shown to be severely limited by the absence of either sodium or potassium from the culture medium. Neither element is capable of replacing the other. The addition of sodium to sodium-starved cells restores growth while potassium-starved cells are not affected by the addition of potassium.     

Study of the extracellular polysaccharides produced by a blue-green alga,Anabaena flos-aquae A-37

Summary Two types of polysaccharides were separated from the extracellular polysaccharide produced by Anabaena flos-aquae A-37 by ion exchange chromatography. The neutral polysaccharide is composed of mainly glucose with minor amounts of xylose in a molar ratio of 8:1. Glucose is believed to constitute the polysaccharide core to which xylose is attached. The acidic polysaccharide is composed of glucose and uronic acid as the major monomers with equal amounts of xylose and ribose as the minor constituents. The molar ratio of the monomers found in the acidic polymer is 6:1:1:10 as glucose: xylose: ribose: uronic acid. Chemical analyses showed that the extracellular polysaccharide consists of more neutral polymer (62%) than the acidic polymer (38%).     

Effect of Monochromatic Light on Proton Efflux of the Blue-Green Alga Anabaena variabilis

Light-induced proton efflux of Anabaena variabilis was found to be biphasic, the second phase being inhibited by the ATPase inhibitor nitrofen (2,4-dichloro-1-[4-nitrophenoxy]benzene). The first, fast phase was triggered by monochromatic light of 707 nanometers, whereas the second, slower phase was not. With 707 nanometers, light, respiratory O₂ uptake was inhibited. Using light composed of two wavelengths (616 and 707 nanometers) a marked enhancement of both O₂ evolution as well as the second phase of proton efflux was observed. The first phase was not enhanced. Thus, phase II is driven by both photosystems. As concluded from the action spectrum phase I is markedly determined by photosystem-I activity. Altogether the data show that two different mechanisms of light-induced proton efflux exist on the cytoplasmic membrane of Anabaena, the slower one being dependent on ATP and linear photosynthetic electron flow.     

A Mutational Study of the Nitrogen-fixing Blue-Green Alga Anabaena doliolum

A heterocystous, non-nitrogen-fixing mutant of the nitrogen-fixingblue-green alga Anabaena doliolum has been isolated followingtreatment with nitrosoguanidine and UV radiation. Some reversiblevariations in the habit and morphology of the alga were inducedfollowing its treatment with nitrosoguanidine.     

Anaerobic and Aerobic Hydrogen Gas Formation by the Blue-Green Alga Anabaena cylindrica

An investigation was made of certain factors involved in the formation of hydrogen gas, both in an anaerobic environment (argon) and in air, by the blue-green alga Anabaena cylindrica. The alga had not been previously adapted under hydrogen gas and hence the hydrogen evolution occurred entirely within the nitrogen-fixing heterocyst cells; organisms grown in a fixed nitrogen source, and which were therefore devoid of heterocysts, did not produce hydrogen under these conditions. Use of the inhibitor dichlorophenyl-dimethyl urea showed that hydrogen formation was directly dependent on photosystem I and only indirectly dependent on photosystem II, consistent with heterocysts being the site of hydrogen formation. The uncouplers carbonyl cyanide chlorophenyl hydrazone and dinitrophenol almost completely inhibited hydrogen formation, indicating that the process occurs almost entirely via the adenosine 5′-triphosphate-dependent nitrogenase. Salicylaldoxime also inhibited hydrogen formation, again illustrating the necessity of photophosphorylation. Whereas hydrogen formation could usually only be observed in anaerobic, dinitrogen-free environments, incubation in the presence of the dinitrogen-fixing inhibitor carbon monoxide plus the hydrogenase inhibitor acetylene resulted in significant formation of hydrogen even in air. Hydrogen formation was studied in batch cultures as a function of age of the cultures and also as a function of culture concentration, in both cases the cultures being harvested in logarithmic growth. Hydrogen evolution (and acetylene-reducing activity) exhibited a distinct maximum with respect to the age of the cultures. Finally, the levels of the protective enzyme, superoxide dismutase, were measured in heterocyst and vegetative cell fractions of the organism; the level was twice as high in heterocyst cells (2.3 units/mg of protein) as in vegetative cells (1.1 units/mg of protein). A simple procedure for isolating heterocyst cells is described.     

Nitrogenase Activity in Cell-Free Extracts of the Blue-Green Alga, Anabaena cylindrica

Cell-free extracts with high nitrogenase activity were prepared by sonic oscillation and French press treatment from the blue-gree alga Anabaena cylindrica. Extracts were prepared from cells grown on a 95% N(2)-5% CO(2) gas mixture followed by a period of nitrogen starvation under an atmosphere of 95% argon-5% CO(2). No increase in the specific activity of extracts was achieved by breaking heterocysts. Activity (assayed by acetylene reduction) was found to be dependent on adenosine triphosphate (ATP), an ATP-generating system, and a low-potential reductant. Na(2)S(2)O(2) employed as reductant supports higher rates of nitrogenase activity than reduced ferredoxin. The activity is associated with a small-particle fraction that can be sedimented by ultracentrifugation. In contrast to the particulate nitrogenase of Azotobacter, which is stable in air, the A. cylindrica nitrogenase is an oxygen sensitive as nitrogenase prepared from anaerobic bacteria.     

5-Aminolevulinate Synthesis in Permeabilized Filaments of the Blue-Green Alga Anabaena variabilis

Filaments of the blue-green alga Anabaena variabilis permeabilized by dimethylsulfoxide (DMSO) produce increased amounts of 5-aminolevulinate in the presence of levulinic acid. The metabolic activity of the filaments remains unperturbed in the presence of up to 7.5% (v/v) DMSO. Studies utilizing DMSO-permeabilized filaments confirm that 5-aminolevulinate is synthesized preferably from glutamate and, to a lesser extent, from α-ketoglutarate in this organism.     

Measurement of the Cyanophycin Granule Polypeptide Contained in the Blue-Green Alga Anabaena cylindrica

An assay was developed to determine the amount of cyanophycin granules in blue-green algae. The amount of this polypeptide in cells of Anabaena cylindrica was measured as a function of culture age and was compared with changes in other proteinaceous cellular components. The data presented support the notion that the cyanophycin granule is a cellular nitrogen reserve.     

The Contribution of Photosynthate to Turgor Pressure Rise in the Planktonic Blue-green Alga Anabaena flos-aquae

The turgor pressure of the cells of the planktonic blue-greenalga Anabaena flos-aquae increases following transfer of thealga from low light intensity to high light intensity. Up tohalf of this rise in turgor pressure may be due to the accumulationof soluble photosynthate. This estimate is based on direct measurementof cell water, extraction and fractionation of ¹⁴C-labelledsoluble products of photosynthesis, and simultaneous measurementof turgor pressure rise.     

Production of Extracellular Polysaccharide by Zoogloea ramigera

In batch cultures of Zoogloea ramigera the maximum rate of exopolysaccharide synthesis occurred in a partly growth-linked process. The exopolysaccharide was attached to the cells as a capsule. The capsules were released from the cell walls after 150 h of cultivation, which caused the fermentation broth to be highly viscous. Ultrasonication could be used to release capsular polysaccharide from the microbial cell walls. Treatment performed after 48 to 66 h of cultivation revealed exopolysaccharide concentration and apparent viscosity values in accordance with values of untreated samples withdrawn after 161 h of cultivation. The yield coefficient of exopolysaccharide on the basis of consumed glucose was in the range of 55 to 60% for batch cultivations with an initial glucose concentration of 25 g liter⁻¹. An exopolysaccharide concentration of up to 38 g liter⁻¹ could be attained if glucose, nitrogen, and growth factors were fed into the batch culture. The oxygen consumption rate in batch fermentations reached 25 mmol of O₂ liter⁻¹ h⁻¹ during the exopolysaccharide synthesis phase and then decreased to values below 5 mmol of O₂ liter⁻¹ h⁻¹ during the release phase. The fermentation broth showed pseudoplastic flow behavior, and the polysaccharide was not degraded when growth had ceased.     

Anaerobic ATP Levels in the Blue-Green Alga Anabaena: Dark-Light Transients and Effects of Light Intensity

An enzymatic method was used to determine ATP extracted from anaerobically incubated samples of the blue-green alga Anabaena variabilis. The dark-light-dark transients of the ATP level in the whole cells were studied in the presence and in the absence of 3 (p-chlorophenyl)-l.l-dimethylurea (CMU). When O₂ evolution was completely inhibited by CMU, there was no significant difference between the transient under illumination of a low intensity and that of fourfold intensity. On the other hand in the absence of CMU, the ATP level decreased more rapidly after high intensity illumination than after low intensity one. The increase in ATP content during the first 5 s illumination was smaller in the absence of CMU than in the presence of CMU. With or without CMU the increase was saturated at the vicinity of the intensity at which photosynthetic O₂ evolution compensates for respiratory O₂ consumption. The calculated quantum requirement of cyclic photophosphorylation in vivo was 2.2 quanta per ATP.     

Production of Extracellular Polysaccharide Matrix by Zoogloea ramigera

Zoogloea ramigera 115 synthesized large amounts of matrix polymer from fructose, galactose, glucose, lactose, mannose, soluble starch, and sucrose when these carbohydrates were used as supplements to a chemically defined medium. All of them supported polymer synthesis to the extent that cultures thickened to a gel. Concentration of carbohydrate nutrients in the range 0.5 to 2.0% was not a critical factor in determining eventual total thickening to a gel, except in relation to the incubation time required. Glucose disappeared from the growth medium rapidly and correlated with increasing cell growth and poly-beta-hydroxybutyrate (PHB) accumulation. PHB concentration decreased as extracellular polymer was synthesized, suggesting a link between PHB and extracellular polymer production.     

Production of an Extracellular Polysaccharide by Haloferax mediterranei

The extremely halophilic archaebacterium Haloferax mediterranei produces an exocellular polymeric substance that gives the colonies a typical mucous character and is responsible for the appearance of a superficial layer in unshaken liquid medium. This exocellular polymeric substance can be obtained from the supernatant of shaken liquid cultures by cold ethanol precipitation, and yields as high as 3 mg/ml have been detected. The substance was produced under all the conditions tested and with all substrates assayed, although higher yields were obtained with sugars, particularly glucose, as carbon and energy source. The total exocellular polymeric substance produced was proportional to the total biomass. The polymer is a heteropolysaccharide containing mannose as the major component. Glucose, galactose, and another unidentified sugar were also present, as well as amino sugars, uronic acids, and a considerable amount of sulfate, which accounts for the acidic nature of the polymer. The infrared spectrum and specific assays showed the absence of acyl groups. The rheological properties of polymer solutions were studied, showing a pseudoplastic behavior and a high apparent viscosity at relatively low concentrations. Viscosity was remarkably resistant to extremes of pH, temperature, or salinity. These characteristics make this polymer interesting for enhanced oil recovery and other applications for which a very resistant thickening agent is required.     

Anaerobic Production of Extracellular Polysaccharide by Butyrivibrio fibrisolvens nyx

Anaerobic production of extracellular polysaccharide (EP) was examined, using a previously uncharacterized, obligately anaerobic rumen isolate, Butyrivibrio fibrisolvens nyx, which produced an EP that was rheologically similar to xanthan gum. The main objectives were to determine the nutritional requirements and conditions which promoted EP production by strain nyx. Strain nyx was grown anaerobically in defined and semidefined media. In addition to carbohydrate and nitrogen sources, strain nyx required acetic acid, folic acid, biotin, and pyridoxamine. Strain nyx produced similar amounts of EP at 35 to 40°C. Conditions that improved growth usually improved EP production. Of the carbohydrates tested, glucose supported the fastest growth and most EP production, followed by sucrose, xylose, and lactose. Strain nyx utilized ammonium sulfate, urea, or vitamin-free casein hydrolysate as nitrogen sources for growth and EP production. At 2 and 20 g/liter, respectively, ammonium sulfate and vitamin-free casein hydrolysate supported about the same rates of growth and EP production. EP was not produced in the lag or stationary phases, and EP production was exponential during exponential cell growth. Based on the results of this work, anaerobic EP production with B. fibrisolvens nyx could reduce energy costs for industrial EP production compared with the cost of aerated systems. Finally, this work demonstrated that, under appropriate growth conditions, a gastrointestinal tract (ruminal) microorganism produced high levels of EP.     

Evidence for the production of extracellular herbivore deterrents by Anabaena flos-aquae

SUMMARY. 1. Daphnia pulex grown in the cell-free filtrate of a log phase culture of Anabaena flos-aquae showed lower fitness as measured by filtering rate, survivorship and reproduction than did individuals in a control treatment. This suggests that the extracellular metabolites of some algae may have considerable adaptive value as a herbivore deterrent.
2. Heating of the cell-free filtrate neutralized the inhibitory effect on filtering rate, but increased the depression of reproduetive rate. This suggests the presence of a variety of bioactive compounds which may inhibit specific herbivore functions.     

Changes in Net O(2) Exchange Induced by Inorganic Nitrogen in the Blue-Green Alga Anacystis nidulans

The response of net O₂ exchange to light intensity by intact Anacystis nidulans cells in the presence of saturating NaHCO₃ concentrations followed a curve with an inflection near the light-compensation point. Addition of either KNO₃ or NH₄Cl stimulated O₂ uptake in the dark and at light intensities below the light-compensation point. This resulted in steeper slopes of the curve calculated below and above the light-compensation point. At O₂ concentrations limiting dark respiration, addition of inorganic nitrogen had no effect on either dark respiration or O₂ exchange in the light. The apparent changes in photosynthetic yield observed under normal O₂ concentration disappeared when respiration was limited by O₂ availability, indicating that the effects of inorganic nitrogen on O₂ exchange at low light intensities are due to stimulation of respiration rather than to increases in photosynthetic yield.