Nitrogen Fixation Dynamics of Two Diazotrophic Communities in Mono Lake, California.
[This corrects the article on p. 614 in vol. 56.].
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[This corrects the article on p. 614 in vol. 56.].
Both the wild type and an isogenic hydrogenase-negative mutant of Azorhizobium caulinodans growing ex planta on N(2) as the N source were studied in succinate-limited steady-state chemostat cultures under 0.2 to 3.0% dissolved O(2) tension. Production or consumption of O(2), H(2), and CO(2) was measured with an on-line-connected mass spectrometer. In the range of 0.2 to 3.0%, growth of both the wild type and the mutant was equally dependent on the dissolved O(2) tension: the growth yield decreased, and the specific O(2) consumption and CO(2) production increased. A similar dependency on the dissolved O(2) tension was found for the mutant with 2.5% H(2) in the influent gas. The H(2)/N(2) ratio (moles of H(2) evolved per mole of N(2) consumed via nitrogenase) of the mutant, growing with or without 2.5% H(2), increased with increasing dissolved O(2) tensions. This increase in the H(2)/N(2) ratio was small but significant. The dependencies of the ATP/N(2) ratio (moles of ATP consumed per mole of N(2) fixed) and the ATP/2e ratio [moles of ATP consumed per mole of electron pairs transferred from NAD(P)H to nitrogenase] on the dissolved O(2) tension were estimated. These dependencies were interpreted in terms of the physiological concepts of respiratory protection and autoprotection.
Simultaneous measurements of photosynthesis (both oxygenic and anoxygenic) and N(inf2) fixation were conducted to discern the relationships between photosynthesis, N(inf2) fixation, and environmental factors potentially regulating these processes in microbial mats in a tropical hypersaline lagoon (Salt Pond, San Salvador Island, Bahamas). Major photoautotrophs included cyanobacteria, purple phototrophic bacteria, and diatoms. Chemosystematic photopigments were used as indicators of the relative abundance of mat phototrophs. Experimental manipulations consisted of light and dark incubations of intact mat samples exposed to the photosystem II inhibitor DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea], a dissolved organic carbon source (D-glucose), and normal seawater (37(permil)). Photosynthetic rates were measured by both O(inf2) and (sup14)C methods, and nitrogenase activity (NA) was estimated by the acetylene reduction assay. Moderate reductions in salinity (from 74 to 37(permil)) had no measurable effect on photosynthesis, O(inf2) consumption, or NA. CO(inf2) fixation in DCMU-amended samples was (symbl)25% of that in the control (nonamended) samples and demonstrated photosynthetic activity by anoxygenic phototrophs. NA in DCMU-amended samples, which was consistently higher (by a factor of 2 to 3) than the other (light and dark) treatments, was also attributed to purple phototrophic bacteria. The ecological implication is that N(inf2) fixation by anoxygenic phototrophs (purple phototrophic bacteria and possibly cyanobacteria) may be regulated by the activity of oxygenic phototrophs (cyanobacteria and diatoms). Consortial interactions that enhance the physiological plasticity of the mat community may be a key for optimizing production, N(inf2) fixation, and persistence in these extreme environments.
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[This corrects the article on p. 494 in vol. 44.][This corrects the article on p. 496 in vol. 44.][This corrects the article on p. 498 in vol. 44.][This corrects the article on p. 499 in vol. 44.][This corrects the article on p. 503 in vol. 44.][This corrects the article on p. 506 in vol. 44.][This corrects the article on p. 507 in vol. 44.][This corrects the article on p. 512 in vol. 44.][This corrects the article on p. 513 in vol. 44.][This corrects the article on p. 517 in vol. 44.].
The addition of molybdate in presence of uranyl acetate causes a considerable increase in nitrogen fixation in all the species of nitrogen-fixing Azotobacter, studied in this paper, as compared to the case in which these ions are taken separately (4, 3).
The effect of lanthanum sulphate on five Azotobacter strains (4A7, 10, 5A2, 5A1, and 3A3) isolated from Allahabad soil consists in a considerable increase in the nitrogen fixation, carbon consumption and in the amount of nitrogen fixed in mg per g of carbon consumed. The presence of 200 microM, 300 microM and 400 microM lanthanum sulphate in culture media increases the fixation of nitrogen by all the nitrogen fixers significantly.
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The rate of biological nitrogen fixation was determined by the acetylene technique in soils and on the roots of orange, mandarin and lemon trees growing in red, yellow, podzolic, alluvial brown forest, and humus-calcareous soils. The minimum nitrogen fixation in podzolic soils was 3--8 kg of nitrogen per hectare per vegetative period. The maximum nitrogen fixation (48--51 kg N per hectare) was found in red and humus-calcareous soils of orange plantations. One dose of nitrogen fertilizers with liming increased the nitrogen fixing activity of subtropic podzolic soils of mandarin plantations whereas a triple dose inhibited the activity. The rate of nitrogen fixation by the root microflora was 3--4 times higher than that by the soil microflora.
The rate of molecular nitrogen fixation was determined in bottom grounds of three Estonian lakes and the Rybinsk water reservoir in the summer of 1977--1978. Certain species of nitrogen fixing bacteria were found to be confined to lakes of certain trophic type. Ecological niches with the mass growth of Clostridium pasteurianum, Azomonas agilis and Clostridium butyricum were detected in the sediments of eutrophic lakes. Ecological niches of Az. insignis and Cl. acetobutylicum occur in polyhumic lakes. Ecological niches for the nitrogen fixing microaerophilic organisms Methylosinus trichosporium, M. sporium and Mycobacterium flavum can be found in the sediments of water reservoirs of any trophic type. The important ecological factors which favour the growth of microflora with a high rate of molecular nitrogen fixation in bottom grounds are as follows: a sufficiently high temperature, a weakly alkaline reaction, the presence of oxygen in the water near the bottom, and the ratio of organic carbon to total nitrogen about 10--11. The destruction of organic substances in such sediments involves both aerobic and anaerobic microflora, and Cl. butyricum is abundant among nitrogen fixing microorganisms.
The activity of nitrogen fixation by the museum strains of sulfate reducing bacteria isolated from oil deposits was studied using the acetylene technique. The mesophilic sulpfate reducing bacteria belonging to the species Desulfovibrio africanus 2372 and D. baculatus X were found to have a high nitrogenase activity. D desulfuricans subsp. aestuarii 2198 reduced acetylene at a low rate. The thermophilic sulfate reducing cultures of D. thermophilus 7, Desulfotomaculum nigrificans 781 and Dm. nigrificans subsp. salinus 435 produced only small quantities of ethylene. Apparently, nitrogen fixation by sulfate reducing bacteria can be considerable in oil strata whose temperature does not exceed 35--40 degrees C.
The validity of seed bacterization with Azotobacter chroococcum in soils of variable densities of naturally present azotobacters was studied. Inoculation of barley grains had no effect on counts of total microflora, neither in rhizosphere nor in root-free soil, but significantly increased Azotobacter population, especially in the rhizosphere. The rate of colonization in the root region was much higher when soil initially harboured low Azotobacter densities. Bacterization improved plant growth and increased soil nitrogen through nitrogen fixation. Nitrogen balance in soils showed higher gains in the inoculated treatments over the uninoculated analogues of 30--98 ppm.
The effects of 32 pesticides at two concentrations on acetylene reduction (non-symbiotic nitrogen fixation), nitrogen fixers, bacteria and fungi in an organic soil were assessed. None of the pesticide treatments suppressed C2H2 reduction as compared to controls. No significant inhibition of the population of non-symbiotic nitrogen fixers occurred. However, stimulatory effects were observed with treatments of fensulfothion, fonofos, oxamyl, DDR, TeloneR and Telone CR. Bacterial and fungal populations showed temporary declines but all recovered within 7 days to levels similar to or higher than those in the controls.