Behavior of filamentous cyanobacteria in laboratory culture

The observations of a laboratory culture of filamentous cyanobacteria revealed a complex of behavioral responses of their community, which maintain their activity as an integrated entity. A number of structures formed in the course of filament regrouping were revealed and described; their possible structural and functional analogues in eukaryotic organisms were determined. It is assumed that the behavioral reactions of the filaments help to maintain the integrity of the community at the stage prior to the formation of the structural bonds between its elements.     

Behavior of filamentous cyanobacteria in laboratory culture

The observations of a laboratory culture of filamentous cyanobacteria revealed a complex of behavioral responses of their community, which maintain their activity as an integrated entity. A number of structures formed in the course of filament regrouping were revealed and described; their possible structural and functional analogues in eukaryotic organisms were determined. It is assumed that the behavioral reactions of the filaments help to maintain the integrity of the community at the stage prior to the formation of the structural bonds between its elements.     

Morphogenesis in a community of filamentous cyanobacteria

Reversible differentiation was experimentally discovered in a community of modern filamentous cyanobacteria Oscillatoria terebriformis. Splitting of the initially uniform community into differentiated parts (strands, multiradiate aggregates, networks, etc.) occurs only for the duration of a function facilitating the activity of this community as an integral unit. The structures are formed as a result of regrouping of the filaments, without their specialization. A morphologically regulatory system (polygonal network) was found to develop under the impact of extreme factors. The levels of structural organization of filamentous cyanobacteria and multicellular eukaryotes were compared (individual cells in a filament—cell organelles; filaments—individual cells; community—organism), and the similarities and differences in morphogenesis of these groups were analyzed using the data on the embryonic regulation in multicellular eukaryotes. Spatial information in morphogenesis was shown to result not from direct realization of an inherited program but is created by the elements of integral organisms (cells and filaments) in the course of development.     

Polyadenylated RNA in two filamentous cyanobacteria.

Polyadenylated RNA was detected in the cyanobacteria Nostoc sp. strain MAC and Anabaena variabilis by oligodeoxythymidylic acid-cellulose chromatography and by hybridization to [3H]polyuridylic acid. Polyadenylate tracts from A. variabilis were located at the 3' end of RNA chains and had an estimated length of 15 to 22 nucleotides.     

Sodium transport in filamentous nitrogen fixing cyanobacteria

Two filamentous, nitrogen fixing cyanobacteria were examined for their salt tolerance and sodium (Na⁺) transport.Anabaena torulosa, a saline form, grew efficiently and fixed nitrogen even at 150 mM salt (NaCl) concentration while,Anabaena L-31, a fresh water cyanobacterium, failed to grow beyond 35 mM NaCl.Anabaena torulosa showed a rapidly saturating kinetics of Na⁺ transport with a high affinity for Na⁺ (K _m, 0.3 mM).Anabaena L-31 had a much lower affinity for Na⁺ (K_m, 2.8 mM) thanAnabaena torulosa and the pattern of uptake was somewhat different. BothAnabaena spp. exhibited an active Na⁺ extrusion which seems to be mediated by a Na⁺-K⁺ ATPase and aided by oxidative phosphorylation.Anabaena L-31 was found to retain much more intracellular Na⁺ thanAnabaena torulosa. The results suggest that the saline form tolerates high Na⁺ concentrations by curtailing its influx and also by an efficient Na⁺ extrusion, although these alone may not entirely account for its success in saline environment.     

Vanadate-sensitive proton efflux by filamentous cyanobacteria

Abstract Light-induced proton efflux has been investigated with intact cells of Anabaena, Nostoc, Anacystis , and Aphanocapsa . The proton efflux by filamentous blue-green algae is biphasic, strongly inhibited by ortho -vanadate and insensitive to cyanide. These data are taken as evidence for a proton-pumping ATP-hydrolase present on the cytoplasmic membrane of Anabaena and Nostoc .     

Envelope structure of four gliding filamentous cyanobacteria.

The cell walls of four gliding filamentous Oscillatoriaceae species comprising three different genera were studied by freeze substitution, freeze fracturing, and negative staining. In all species, the multilayered gram-negative cell wall is covered with a complex external double layer. The first layer is a tetragonal crystalline S-layer anchored on the outer membrane. The second array is formed by parallel, helically arranged surface fibrils with diameters of 8 to 12 nm. These fibrils have a serrated appearance in cross sections. In all cases, the orientation of the surface fibrils correlates with the sense of revolution of the filaments during gliding, i.e., clockwise in both Phormidium strains and counterclockwise in Oscillatoria princeps and Lyngbya aeruginosa. The lack of longitudinal corrugations or contractions of the surface fibrils and the identical appearances of motile and nonmotile filaments suggest that this structure plays a passive screw thread role in gliding. It is hypothesized that the necessary propulsive force is generated by shear forces between the surface fibrils and the continuing flow of secreted extracellular slime. Furthermore, the so-called junctional pores seem to be the extrusion sites of the slime. In motile cells, these pores exhibit a different staining behavior than that seen in nonmotile ones. In the former, the channels of the pores are filled with electron-dense material, whereas in the latter, the channels appear comparatively empty, highly contrasting the peptidoglycan. Finally, the presence of regular surface structures in other gliding prokaryotes is considered an indication that comparable structures are general features of the cell walls of gliding microbes.     

Undirected motility of filamentous cyanobacteria produces reticulate mats

The roles of biology in the morphogenesis of microbial mats and stromatolites remain enigmatic due to the vast array of physical and chemical influences on morphology. However, certain microbial behaviors produce complex morphological features that can be directly attributed to motility patterns. Specifically, laboratory experiments with a strain of the cyanobacteria Pseudanabaena demonstrate that distinctive morphologies arise from the undirected gliding and colliding of filaments. When filamentous cells collide, they align and clump, producing intersecting ridges surrounding areas with low cell density, i.e. reticulate structures. Cell motility is essential for the development of reticulates and associated structures: filaments organize into reticulates faster than cell division and growth, and conditions that inhibit motility also inhibit reticulate formation. Cell density of the inoculum affects the frequency of cell–cell collisions, and thus the time required for biofilm organization into reticulate structures. This also affects the specific geometry of the reticulates. These patterns are propagated into larger structures as cyanobacterial cell numbers increase and cells remain motile. Thus, cell motility is important for templating and maintaining the morphology of these microbial communities, demonstrating a direct link between a microbial behavior and a community morphology. Reticulate geometries have been identified in natural microbial mats as well as in the fossil record, and these structures can be attributed to the motility of filamentous bacteria.     

Membrane electrogenesis and sodium transport in filamentous nitrogen-fixing cyanobacteria

Transport of Na+ and its relationship with membrane potential (delta psi m) was examined in Anabaena L-31 (a fresh water cyanobacterium) and Anabaena torulosa (a brackish water cyanobacterium) which require Na+ for diazotrophic growth. The data on the effect of N,N'-dicyclohexylcarbodiimide indicated that delta psi m was generated by electrogenic proton extrusion predominantly mediated by ATPase(s). In addition, operation of a plasmalemmabound, non-ATP-requiring, H+-pumping terminal oxidase was suggested by the sensitivity of delta psi m to anaerobiosis, cyanide and azide, all of which inhibit aerobic respiration. The response of delta psi m to external pH and external Na+ or K+ concentrations indicated that a diffusion potential of Na+ or K+ may not contribute significantly to delta psi m. Kinetic studies showed that Na+ influx was unlikely to be a result of Na+/NA+ exchange but was a carrier-mediated secondary active transport insensitive to low concentrations (less than 10 mM) of external K+. There was a close correspondence between changes in delta psi m and Na+ influx; all the treatments which caused depolarisation (such as low temperature, dark, cyanide, azide, anaerobiosis, ATPase inhibitors) lowered Na+ influx whereas treatments which caused hyperpolarisation (such as 2,4-dinitrophenol, nigericin) enhanced Na+ influx. Remarkably low intracellular Na+ concentrations were maintained by these cyanobacteria by means of active efflux of the cation. The basic mechanism of Na+ transport in the fresh water and the brackish water cyanobacterium was similar but the latter demonstrated less influx, more efficient efflux, more affinity of carriers for Na+ and less accumulation of Na+, all attributes favouring salt tolerance.     

Light-induced electrical potential changes and motility in desmids

Motility of the desmid Cosmarium cucumis depends on light: switching the light on induces a large fraction of previously immotile cells to start moving, and switching it off causes many motile cells to stop. Turning light on or off causes light-induced electrical potential changes which can be measured with internal microelectrodes. The electrical gradient within the cell is not correlated with the light gradient. Consequently, the cell cannot obtain information concerning the spatial distribution of the incident light, e.g. for phototactic orientation. However, light-induced potential changes could serve as signals for photokinesis, since switching the light on causes a transient increase and switching the light off a transient decrease in the electrical potential of the front half as compared to the rear half or the extracellular space.     

Miniprep DNA isolation from unicellular and filamentous cyanobacteria

A rapid miniprep method for isolation of DNA from 12 strains of cyanobacteria belonging to groups I, III, IV and V is described. The protocol is a modification of the methods of Boyle and Lew [Boyle, J.S., Lew, A.M., 1995. An inexpensive alternative to glassmilk for DNA purification. Trends Genet. 11, 8] and the cetyltrimethyl ammonium bromide (CTAB) extraction method of Sahgai-Maroof et al. [Sahgai-Maroof, M.A., Soliman, K.M., Jorgensen, R.A., Allard, R.W., 1984. Ribosomal DNA spacer-length polymorphisms in barley: Mendelian inheritance, chromosomal location and population dynamics. Proc. Natl. Acad. Sci. USA 81, 8014-80181. The new method is especially useful for obtaining cyanobacterial DNA from unicellular, filamentous and filamentous branched species. The method does not require phenol extraction and the product can be used directly for PCR amplification and restriction digestion.     

Use of filamentous cyanobacteria for biodegradation of organic pollutants

Volume 61, no. 1, p. 234: the corresponding author footnote should read as follows: * Corresponding author. Present address: Center for Risk Management, Oak Ridge National Laboratory, Oak Ridge, TN 37830. Phone: (615) 241-6013. Fax: (615) 574-9887. [This corrects the article on p. 234 in vol. 61.].     

Re-occurrence of filamentous planktonic cyanobacteria during permanent artificial destratification

In a whole-lake long-term experiment of permanent artificialdestratification, the filamentous planktonic cyanobacterium,Limnothrix (Oscillatoria) redekei (Van Goor) Meffert (1988),re-occurred at the end of the third year, after complete absencefor 2 years. The cyanobacteria peaked at the end of the fourthyear of permanent destratification, the biomass being much higherthan during the pre-destratification period. Limnothrix (Oscillatoria)redekei is obviously a turbulence-tolerant cyanobacterial species.     

Characterization and cloning of extrachromosomal DNA from filamentous cyanobacteria

Abstract Physical maps of cryptic plasmids from the filamentous cyanobacteria Anabaena variabilis PCC7118 (pGL1: 3.6 MDa), Nostoc PCC6705 (pGL2: 2.6 MDa) and Plectonema PCC6306 (pGL3: 0.95 MDa) were generated. Selectable markers were introduced onto pGL2 and pGL3 by fusing them to the vector pBR328, using their single restriction sites for Cla I. The recombinant plasmids generated were characterised with respect to the orientation of the insert and the single sites for restriction endonucleases which they possess. The stability of pGL1 and of the two recombinant plasmids in culture was investigated and a method for isolating larger cyanobacterial plasmids (> 20 MDa) was devised.     

Evidence of electrical potential changes in photophobically reacting blue-green algae

The correlation between photophobic responses and light-induced electric potential changes has been studied in the blue-green alga Phormidium uncinatum.

1. The photophobic reaction time depends on both length of preillumination and presentation time of stimulus. Under optimal conditions a reaction time of about 10 s has been determined.
2. Light-induced potential changes can be measured by means of external electrodes with a small gap between them bridged by a population of perpendicularly oriented trichomes. These potential changes follow a light-dark cycle with a lag phase of about 10 s.
3. The amplitude of these light-induced potential changes increases with light intensity until it reaches a saturation value of about 12 mV at 10000 lx. The action spectrum resembles the photophobic action spectrum with peaks in the absorption region of C-phycoerythrin and chlorophyll a.

The significance of light-induced potential changes as a means of sensory transduction for photophobic responses in blue-green algae is being discussed.     

Competitive ability of Daphnia under dominance of non-toxic filamentous cyanobacteria

It is generally assumed that Daphnia is more susceptible to the inhibitory effects of filamentous cyanobacteria than small cladocerans since daphnids have a larger gape size and filtrate the filaments, whereas small cladocerans do not. This study addresses the question whether food limitation has the potential to modify this scenario of cladoceran response to dominance of non-toxic filamentous cyanobacteria. Daphnia galeatawas grown under limited (0.1 mg C l^–1) and unlimited concentrations (1.0 mg C l^–1) of high-quality food algae both in the absence/presence of non-toxic filamentous Aphanizomenon flexuosum. As the effects of these cyanobacteria on D. galeatawere positive under food limiting conditions and negative at the high food density, it was concluded that D. galeatawas mainly affected by nutritional quality due to its ability to ingest the filaments, while mechanical interference with food collection was not important. In competition experiments between D. galeataand Bosmina longirostris, D. galeatawas the dominant species at regular additions of food (1.0 mg C l^–1) in the absence of Aphanizomenon. In the presence of these cyanobacteria, D. galeatawas inhibited during the first days of the experimental period. However, the negative effect at the initially high food density was outweighed by nutrition at food limiting conditions and the outcome in competitive dominance was not changed. The results demonstrate that the ability of D. galeata to ingest large-sized non-toxic cyanobacteria can be considered as advantageous under food limiting conditions.     

Use of filamentous cyanobacteria for biodegradation of organic pollutants.

Biodegradation is increasingly being considered as a less expensive alternative to physical and chemical means of decomposing organic pollutants. Pathways of biodegradation have been characterized for a number of heterotrophic microorganisms, mostly soil isolates, some of which have been used for remediation of water. Because cyanobacteria are photoautotrophic and some can fix atmospheric nitrogen, their use for bioremediation of surface waters would circumvent the need to supply biodegradative heterotrophs with organic nutrients. This paper demonstrates that two filamentous cyanobacteria have a natural ability to degrade a highly chlorinated aliphatic pesticide, lindane (gamma-hexachlorocyclohexane); presents quantitative evidence that this ability can be enhanced by genetic engineering; and provides qualitative evidence that those two strains can be genetically engineered to degrade another chlorinated pollutant, 4-chlorobenzoate.     

A simplified protocol for preparing DNA from filamentous cyanobacteria

The preparation of good quality genomic DNA from microalgae and plants is often time-consuming because of the need to remove contaminants that may interfere with the downstream enzymatic manipulation of the DNA. Simpler protocols have been reported but these are applicable only to a few species and in many cases are not effective for removing trace contaminants. In this report, we describe a modification of existing protocols that significantly simplified the preparation of genomic DNA from cyanobacteria and plants. A key step in our protocol is the precipitation of DNA in a high concentration of salt (2–2.5 M NaCl) in the presence of isopropanol, immediately following phenol and chloroform extractions. The preparation and enzymatic digestion of the DNA can be performed in a single day. The DNA was easily digested in 2 h at normal restriction enzyme concentrations, and is highly suitable for PCR and Southern hybridization. We successfully used this simplified protocol to prepare genomic DNA from several filamentous cyanobacteria, such asAnabaena sp. PCC 7120,Anabaena siamensis, andSpirulina strains M2 and Kenya. This protocol may also be useful for preparing genomic DNA from other algae and from higher plants.     

Molecular cloning and characterization of hetR genes from filamentous cyanobacteria

HetR, a serine type protease, plays an important role in heterocyst differentiation in filamentous cyanobacteria. We isolated and sequenced the hetR genes from different heterocystous and filamentous nonheterocystous cyanobacteria. The hetR gene in the heterocyst forming Anabaena variabilis ATCC 29413 FD was interrupted by interposon mutagenesis (mutant strain WSIII8). This mutant does not form heterocysts and shows no diazotrophic growth under aerobic conditions. However, under anaerobic N(2)-fixing conditions, the WSIII8 cells are able to grow, and high nitrogenase (Nif2) activity is detectable. Nif2 expression was demonstrated in each vegetative cell of the filament by immunolocalization 4 h after nitrogen step-down.     

Factors affecting photobiological hydrogen production in five filamentous cyanobacteria from Thailand

Photosynthetica - We report here the screening of sixteen cyanobacterial and three green algal strains from Thailand for their potential biohydrogen production. Five filamentous cyanobacterial...