Hydrocarbons in green and blue-green algae

Liquid column chromatography and thin-layer chromatography were used to determine the total content of hydrocarbons and gas chromatography was used to evaluate composition of hydrocarbons in green algae (Chlorella kessleri, C. vulgaris, Chlorella sp.,Scenedesmus acutus, S. acuminatus, S. obliquus) and the blue-green alga (Spirulina platensis) cultivated under autotrophic or heterotrophic conditions. InC. kessleri cultivated under heterotrophic conditions the content of hydrocarbons was found to be about 10^-2 % (per dry mass), whereas under autotrophic conditions it was about 10^-3 % (per dry mass). The highest content of hydrocarbons was detected in species of the genusScenedesmus cultivated autotrophically (10^-1 %). Heptadecane and hexacosane were found as major alkanes, 1-heptadecene was detected among alkenes.     

Survival of blue-green and green algae under stress conditions

Terrestrial blue-green algae Scytonema millei, Phormidium bohneri and Lyngbya mesotricha survived to 100 % at atmospheric temperatures of 5-36 degrees C and relative humidity 55-100 % in rainy, winter and spring seasons but the survival was 15-25 % in summer when atmospheric temperature reached 48 degrees C and relative humidity was < or =23 %. Microcoleus chthonoplastes maximum survival was =80 % in rainy season followed by a decrease to =1/2 and 1/4 level in winter and spring, respectively; it disappeared in summer but a few cells and/or trichomes enclosed within sheath may be surviving sticking to soil, not evident microscopically, since the population reappeared at the same place with the onset of rain. Terrestrial green alga Rhizoclonium crassipellitum survived only in spring and died at the onset of summer without forming any dormant cell and/or reproductive structure. Only P. bohneri survived better and longer under submerged conditions in liquid medium than air-exposed on moist soil surface in the culture chamber, while the other algae fared almost equally or slightly better air-exposed on moist soil surface (or even on 2 % agarized medium) than when suspended in liquid medium, indicating that air exposure rather than submerged conditions was needed for most of the terrestrial algae to survive. Water stress imposed on growing algae either on high-agar-solid media or in 0.2-0.6 mol/L NaCl liquid media in the culture chamber reduced vegetative survival in all; it resulted in death without any dormant cell remaining. When stored in desiccators over fused CaCl2, M. chthonoplastes died within 1/2 month, R. crassipellitum and L. mesotricha within 1 month, P. bohneri within 1/2 month, and S. millei not even within 1 1/2 month, indicating their survival pattern against atmospheric dryness to be wide; it also explained the M. chthonoplastes absence in summer and S. millei presence throughout the year. At increased atmospheric humidity the desiccation-sensitive algae (e.g., M. chthonoplastes) survived better than a desiccation-resistant alga (here S. millei). All algae survived considerable darkness (S. millei > 1 1/2 month; P. bohneri, M. chthonoplastes and R. crassipellitum >1 month, and L. mesotricha >1/2 month), and low light intensity of 2 and 10 micromol m(-2)s(-1) which explains their prolific growth in shady places. All algae were differently sensitive to wet heat (45 degrees C for 5-40 min) and to UV shock (0.96-3.84 kJ/m2).     

Regulation of glucose 6-phosphate dehydrogenase in blue-green algae

Glucose 6-phosphate dehydrogenase (EC 1.1.1.49) has been partially purified from Anacystis nidulans and Anabaena flos-aquae by means of ammonium sulfate fractionation and exclusion gel chromatography and the kinetic properties determined.     

The relationship between heat-stress and photobleaching in green and blue-green algae

Two characteristic temperatures were identified from measurements of the temperature dependence of O₂ evolution by Chlorella vulgaris and Anacystis nidulans: T₁, the threshold temperature for inhibition of O₂ evolution under saturating light conditions, and T₂, the upper temperature limit for O₂ evolution. Measurement of delayed light emission from photosystem II (PSII) showed that it passed through a maximum at T₁ and was virtually eliminated on heating the samples to T₂. Related changes were observed in low-temperature (77K) fluoresence emission spectra. Heat-stress had little effect on the absorption properties of the cells at temperatures below T₁ but incubation at higher temperatures, particularly under high-light conditions, resulted in extensive absorption losses. An analysis of these measurements suggests that this increased susceptibility to photobleaching is triggered by an inhibition of the flow of reducing equivalents from PSII that normally serves to protect the light-harvesting apparatus of the cells from photo-oxidation. Adaptation to higher growth temperatures resulted in increases in the values of T₁ and T₂ for Anacystis nidulans but not for Chlorella vulgaris.Abbreviations PSI photosystem I - PSII photosystem II - Chl a chlorophyll a - Chl b chlorophyll b - DCMU 3-(3 4 dichlorophenyl)-11-dimethylurea - PC plastocyanin - APC allophycocyanin CIW-DPB Publication No. 887.     

Studies with deoxyribonucleic acid from blue-green algae

Summary The total DNA in species of blue-green algae is similar to that of bacteria on an individual cell, but not on a dry weight, basis. The % G+C content of DNA from four species of blue-green algae has been determined by melting temperature measurement. An attempt tomeasure genetic homology between blue-green algae and certain bacterial species is described.     

Comparison of the long-wave chlorophyll fluorescence in various green and blue-green algae and diatoms

Two types of long-wave fluorescence bands with similar band shape occur at room temperature in various algae: F_II700 and F_I715. F_II700 occurs in a limited number of algae, follows PS II transients, increases with culture age and is moderately increased by cooling to 83 K. F_I715 occurs in most algae, especially Anabaena, but much less in most diatoms and Tribonema. It does not follow PS II transients, does not increase with culture age and is much increased by cooling to 83 K.An interpretation for the characteristics of F_II700 and F_I715 is given.     

Comparative studies on the regulation of DAHP synthetase activity in blue-green and green algae

Summary Regulation of DAHP synthetase activity was investigated in autotrophically grown blue-green and green algae. Members of the class of blue-green algae possess an enzyme, the activity of which is regulated by l-tyrosine and l-phenylalanine, whereby l-tyrosine is effective in 100 fold lower concentrations. DAHP synthetases of two organisms, Anabaena and Anacystis, were shown to belong to the V-type of allosteric enzymes.In contrast to the DAHP synthetase of blue-green algae regulation of this enzyme could not be demonstrated in two green algae, Ankistrodesmus and Maesotaenium. However, Euglena gracilis, both under conditions of mixotrophic and autotrophic growth, exhibits very effective regulation of this key enzyme; again, the inhibitors are tyrosine and phenylalanine. DAHP synthetase activity of Euglena has been purified about 40 fold; during this enrichment no separation of the enzyme activity inhibited by tyrosine and that by phenylalanine could be observed.     

Mesosomes in blue-green algae

Summary Mesosome-like, unit-membrane structures are clearly defined in the blue-green algae, Spirulina and three strains of Synechococcus, after osmium or potassium permanganate fixation and observation with the electron microscope. The membranous structures are distinct from the photosynthetic membranes and, in the case of Spirulina, are frequently observed in cells and can occur in large volume within the cell.     

Respiration of blue-green algae in the light

The CO₂ evolution in the light of Anabaena as well as several other blue-green algae is below 10% of the dark control. Addition of DCMU restores CO₂ evolution in the light almost to the dark level. Furthermore, by adding unlabeled NaHCO₃, a ¹⁴CO₂ release is observed with prelabeled algal cells attaining 15 to 100% of dark control. Analysis by double-reciprocal plots exhibits a competitive relationship between added and endogenously released carbon dioxide. We conclude that CO₂ evolved by respiration is immediately refixed in the light without being liberated.The degree of ¹⁴CO₂ release induced by unlabeled bicarbonate in the light allows to determine true photoinhibition of respiration. Anabaena variabilis Kütz. exhibits almost no inhibition while in eight other species respiration is light-inhibited between 50 and 85% of the dark control.Abbreviations CCCP carbonyl cyanide m-chlorophenylhydrazone - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - TCA trichloroacetic acid     

Fatty acid composition and physiological properties of some filamentous blue-green algae

Summary The fatty acids of 32 axenic strains of filamentous blue-green algae have been analyzed. As an aid to the interpretation of the results, the strains have been assigned to provisional typological groups based upon their morphology and certain physiological characters. The latter are the ability to grow heterotrophically in the dark with glucose as carbon and energy source, the ability to grow in the light at the expense of glucose in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), and the ability to synthesize nitrogenase under anaerobic conditions in the light. Each typological group has been given an appropriate generic name.The strains examined for fatty acid composition can be divided into groups according to the major fatty acid of highest degree of unsaturation found in each strain as was done for the unicellular strains examined previously in this laboratory. Four metabolic groups of strains of unicellular and filamentous blue-green algae can be recognized: 1. those in which there is little or no desaturation of oleate; 2. those in which linoleate is desaturated toward the -end of the molecule to give -linolenate; 3. those in which linoleate is desaturated toward the carboxyl end of the molecule to give -linolenate; 4. those in which octadecatetraenoate is synthesized. The nature of the major cellular fatty acids of two of the strains examined is the same whether growth is in the light or in the dark on glucose. All filamentous strains contain glycolipids with the properties of mono- and digalactosyldiglycerides.Abbreviation DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea     

Biosynthesis of delta-aminolevulinic acid by blue-green algae (cyanobacteria).

When levulinic acid, a competitive inhibitor of delta-aminolevulinic acid dehydratase, was added to growing cultures of blue-green algae (cyanobacteria), delta-aminolevulinic acid was excreted into the medium and cell growth was inhibited.