▪ Abstract New and exciting developments in boron research in the past few years greatly contributed to better understanding of the role of boron in plants. Purification and identification of the first boron-polyol transport molecules resolved much of the controversy about boron phloem mobility. Isolation and characterization of the boron-polysaccharide complex from cell walls provided the first direct evidence for boron crosslinking of pectin polymers. Inhibition and recovery of proton release upon boron withdrawal and restitution in plant culture medium demonstrated boron involvement in membrane processes. Rapid boron-induced changes in membrane function could be attributed to boron-complexing membrane constituents. Boron may affect metabolic pathways by binding apoplastic proteins to cis-hydroxyl groups of cell walls and membranes, and by interfering with manganese-dependent enzymatic reactions. In addition, boron has been implicated in counteracting toxic effects of aluminum on root growth of dicotyle...

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Boron in plant structure and function

Oxygen relations of nitrogen fixation in cyanobacteria.

Heterocysts are differentiated cells that are specialized for fixation of N2 in an aerobic environment. In heterocysts in the light, Photosystem I generates ATP, but no photosynthetic production of O2 takes place. Instead, reductant moves into heterocysts from vegetative cells. In return, fixed nitrogen moves from heterocysts to vegetative cells. In neither case is there certainty about the identity of the traffic molecules. Pathways of electron-donation to N2 have been extensively investigated, but their in-vivo importance remains to be critically tested. Nitrogenase in heterocysts is protected from inactivation by O2 by a variety of means, principally by enhanced respiration and by a barrier, the heterocyst envelope, to entry of O2. However, the respiratory apparatus and the biosynthetic processes that result in synthesis of the barrier have been little studied. The detailed mechanisms underlying metabolic, environmental, and developmental control of nitrogenase are under investigation. Studies of heterocyst development are being greatly facilitated by recent advances in the genetics of Anabaena sp. An autoregulated gene, hetR, that is activated shortly after nitrogen-stepdown is critical for the differentiation of heterocysts. Two enigmas remain to be answered: how is it determined which cells will differentiate; and, after differentiation is initiated, what intercellular interactions and intracellular mechanisms regulate the progression of the differentiation process? An evolutionary and biochemical relationship between the processes leading to the formation of heterocysts and akinetes is suggested.

Heterocyst Metabolism and Development

Planktonic nitrogen fixation in lakes is strongly related to lake trophic status, with moderate and high rates usually occurring only in eutrophic lakes. Among eutrophic lakes, nitrogen fixation is related to the ratio of nitrogen loading to phosphorus loading to the lake; significant nitrogen fixation by planktonic organisms generally occurs only when the N: P ratio of the nutrient loading is near or below the Redfield ratio of 16: 1. In contrast, nitrogen fixation by planktonic organisms is generally low in estuaries even when the N: P ratio of nutrients inputs is low.

The tendency toward less nitrogen fixation by plankton in estuaries and coastal marine ecosystems than in lakes subject to similar loadings of nitrogen and phosphorus may be due to a lower availability in oxic seawater of one or more trace elements required for nitrogen fixation, such as molybdenum and iron. Iron concentrations are generally lower in estuarine waters and seawater than in most lakes. And although molybdenum concentrations in seawater are actually higher than in lakes, molybdenum availability is probably lower, since sulfate inhibits molybdate assimilation by microbes. Molybdate is the primary form of molybdenum in oxic seawater, and the ratio of sulfate: molybdate is greater than in lakes. However, even in lakes sulfate is several orders of magnitude more abundant than molybdenum, and the ratio of dissolved sulfate to dissolved molybdenum typically is much greater than the ratio of sulfur to molybdenum apparently required by nitrogen-fixing cyanobacteria. Consequently, assimilation of molybdate by cyanobacteria is probably an energetically expensive process in all natural waters, but more so in seawater than in freshwaters. High concentrations of dissolved organic matter are known to favor blooms of cyanobacteria, perhaps by increasing iron and/or molybdenum availability through chelation.

The primary controls on nitrogen fixation in sediments, wetlands, macrophyte beds, and cyanobacterial mats may be different from those for fixation by planktonic organisms. Both molybdenum and iron are probably more available in these systems than in oxic waters, since reducing conditions and high DOC concentrations will increase iron solubility and favor the stability of reduced forms of molybdenum; sulfate should not inhibit the assimilation of these reduced molybdenum compounds. Consequently, nitrogenase synthesis (and, therefore, nitrogen fixation) in wetlands and in sediments may be less energetically expensive than in oxic water columns. A major control on nitrogen fixation in sediments may be repression of nitrogenase synthesis by high concentrations of ammonium, a factor less important to planktonic fixation because of the much lower concentrations of ammonium generally found in water columns than in sediments.

https://aslopubs.onlinelibrary.wiley.com/doi/pdf/10.4319/lo.1988.33.4part2.0688

Nitrogen fixation in freshwater, estuarine, and marine ecosystems. 2. Biogeochemical controls1

A 4 year series of field, light-microscope and ultrastructural observations is presented to illustrate biological aspects of the annual cycle of natural Microcystis populations enclosed in Lund tubes. Nine morphological stati, all referable to M. aeruginosa f. aeruginosa , feature at various stages of the cycle. Summer bloom-forming populations originate from vegetative colonial stock that overwinters on the bottom sediment each year, but there is no mass transfer of these colonies to the water column: intensive growth from individual cells in the old colonies leads to the formation of new infective colonies, being stimulated when the bottom water approaches anoxia and light penetrates to the bottom sediments. Growth is slow but the developing populations sustain only minor losses through grazing and settling out, eventually becoming dominant over other species. Allelopathy possibly contributes to this effect. In postmaximal populations, several mechanisms can contribute to net buoyancy loss and a (usually) rapid recruitment of vegetative colonies to the sediments is observed. Hypotheses are advanced to account for the observed behaviour, and some of these have been tested in the laboratory. The apparent physiological flexibility of Microcystis seems well suited to growth and survival in the microenvironments encountered in eutrophic lakes.

On the Annual Cycle of the Blue-Green Alga Microcystis Aeruginosa Kutz. Emend. Elenkin

A method involving penicillin treatment was developed to osmotically lyse the cells of the blue-green alga,Microcystis aeruginosa Kuetz. emend. Elenkin, and release the pressure-sensitive gas vacuoles intact. The gas vacuoles were purified by liquid-polymer partitioning or by macromolecular sieving and centrifugation. The degree of purification of the gas vacuoles was followed by observation in the electron microscope and by the use of C14-labeled vacuolated and nonvacuolated strains ofM. aeruginosa. The gas-vacuole membrane is composed of only protein consisting of 10% basic, 18% acidic and 52% non-polar amino acids.

Isolation and chemical characterization of gas-vacuole membranes from Microcystis aeruginosa Kuetz. emend. Elenkin.

In exponentially growing cultures of the blue-green alga Microcystis aeruginosa the number of gas vacuoles per cell decreases and reaches a value of 4.5×103 at 1.2×107 cells per ml. The assembly of gas vacuoles with respect to number and length was followed after the organelles were caused to collapse by a pulse of ultrasound. The change in the number N of gas vacuoles per cell is N=224.8×t0.757, 0<t<24 h. After 24 h 50% of the value of non-sonicated cultures is reached. The changes in the length L of the organelles is expressed by L=87.06 ×t0.4084, 0<t<24 h. After 24 h 85% of the control value is reached.

Kinetics of the assembly of gas vacuoles in the blue-green alga Microcystis aeruginosa Kuetz. emend. Elekin.

The morphological parameters of the cylindrical gas vacuoles in the blue-green alga, Microcystis aeruginosa, were investigated by quantitative electron microscopy. The gas vacuoles are made up of a...

Morphological parameters and macromolecular organization of gas vacuole membranes of Microcystis aeruginosa Kuetz. emend. Elenkin.

The purified protein which constitutes the membranes of the gas vacuoles of the the blue-green alga, Microcystis aeruginosa, was partially characterized. Gel electrophoresis and end-group analysis indicate that the protein is a single species. Strongly protic solvents such as formic acid are the only reagents causing appreciable solubilization of the membrane protein. Infrared spectroscopy shows that the membrane protein has both α-helix or random-coil conformation, and β-conformation.

Characterization of the protein from gas-vacuole membranes of the blue-green alga, Microcystis aeruginosa.

Physiological evidence was obtained for a light shielding role for gas vacuoles inMicrocystis aeruginosa Kuetz. emend. Elenkin, by comparing photosynthetic oxygen evolution, growth behaviour and pigment composition of cells with intact or collapsed gas vacuoles. The oxygen evolution rates were strongly dependent on cell concentration, a maximum rate for cells with intact gas vacuoles occurring at about 1.4×109 cells/ml and for cells with collapsed gas vacuoles at about 2.5×109 cells/ml. By using light saturation curves for oxygen evolution, it was estimated that at low light intensities up to 30% of the photosynthetically useable light was shielded at a cell concentration of 6×108 cells/ml. Collapsing the gas vacuoles twice daily did not alter the initial growth rate of the cultures, but enabled them to reach a higher final cell density. Collapsing of gas vacuoles during growth for about four generations resulted in a lower level of all acetone soluble pigments with a greater relative reduction in carotenoids than in chlorophyll a. Collapse of the gas vacuoles does not alter the cell volume. Various optical interactions which could account for light shielding are discussed.

Physiological effects of the presence and absence of gas vacuoles in the blue-green alga, Microcystis aeruginosa Kuetz. emend. Elenkin.

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