Association of polyphosphate with protein in freeze-substituted sclerotia ofSclerotinia minor

Summary In freeze-substituted sclerotia stained with aqueous toluidine blue O, metachromatic material was found throughout the cytoplasm in discrete granules. It was also distributed evenly throughout spherical and elongate protein bodies. This material stained at low pH and was extracted by cold acid, indicating that it was polyphosphate. Retention of metachromatic material was much greater than previously reported in chemically fixed, conventionally processed sclerotia. X-ray microanalysis of dry-cut, unstained sections of freeze-substituted sclerotia confirmed that phosphorus was distributed evenly throughout the protein bodies and was not localised in discrete granules but phosphorus levels in the cytoplasm were very low. It is concluded that polyphosphate is lost during conventional preparation procedures but retained in dry-cut, unstained sections of freeze-substituted material. However, when freeze-substituted sections were stained with toluidine blue O, water soluble polyphosphate was extracted and subsequently precipitated in the cytoplasm as polyphosphate granules. Therefore it is considered that polyphosphate granules are an artefact, and that protein bodies are the major site for storage of phosphorus in this fungus.Abbreviations STEM scanning transmission electron microscope - ER endoplasmic reticulum     

PHOSPHORUS STATUS AND CYTOPLASMIC STRUCTURES IN SCENEDESMUS (CHLOROPHYCEAE) UNDER DIFFERENT METABOLIC REGIMES1

Phosphorus deficiency affects the anatomy of the unicellular green alga Scenedesmus obtusiusculus Chad. and influences the distribution of other inorganic elements in the cell in addition to phosphorus. Scenedesmus was grown under standard conditions with or without phosphorus. Cells were then cultured with phosphorus under conditions favouring glycolysis, respiration, or photophosphorylation for 2 h or photosynthesis for up to 8 h. The dominating features of phosphorus starvation, were loss of phosphorus and coions from polyphosphate bodies, accumulation of starch, decrease in the volume density of ribosomes both in the chloroplast and cytoplasm, and an increase in wall thickness. Under conditions favoring photosynthesis the mass fraction for phosphorus is low after 1 h, exceptionally high by 2 h, and diminishes by 8 h. High amounts of phosphorus are also regained under conditions favoring glycolysis and photophosphorylation but not respiration. After 2 h under photosynthetic conditions the volume densities of the chloroplast, cytoplasmic ribosomes, the vacuole, and the mitochondrion increased over controls. By 8 h the relative volume of the single ramified mitochondrion had decreased slightly and recognizable segments of it were sequestered within the vacuome. The autophagic nature of the vacuole was further evidenced by the presence of ribosomes and whorls of lamellae within it. Serial sections showed that all polyphosphate granules and sequestered materials were located within a continuous vacuolar cisterna.     

The elemental composition dynamics of large polyphosphate granules in Acinetobacter strain 210A

Electron microscopy and energy dispersive X-ray micro-analysis were used to examine the elemental composition of large polyphosphate granules in unfixed and unstained intact cells of Acinetobacter strain 210A. When grown in medium with butyrate, Acinetobacter strain 210A possessed 1 or 2 large granules with a diameter of 0.4 m besides a relatively large number of small granules. The large granules were composed of phosphorus, magnesium and potassium. A decrease in the Mg/Ca-ratio of the medium from 5.95 to 0.0073 resulted in a decline in the intracellular Mg/Ca-ratio from 15 to 0.56. At a high intracellular Mg/Ca-ratio, magnesium was the dominant counterion in the polyphosphate granule. Calcium became the major cation in the polyphosphate bodies at a low intracellular Mg/Ca-ratio. Omission of Ca²⁺ or modification of the K/Mg ratio in the medium did not significantly affect the cation composition of the polyphosphate granules. The dissociation constants for Mg- and Ca-polyphosphate were 9.3×10^-2 mol/l and 1.5×10^-1 mol/l, respectively.     

Localization of divalent cations in phosphate-rich cytoplasmic granules in yeast

Phosphate-rich yeast cells (Saccharomyces cerevisiae) take up more calcium and strontium than phosphate-deficient cells. The divalent cations appear to be tightly bound in phosphate-rich cells. Electron microscopical investigations, combined with energy-dispersive X-ray microanalysis, showed that divalent cations were sequestered in cytoplasmic granules, together with a large amount of phosphorus. The major part of the divalent cations is retrieved in the polyphosphate fraction, a minor part is bound to lipids. The results suggest that polyphosphate granules may serve as an important store for divalent cations.     

EFFECT OF PHOSPHATE CONCENTRATION ON THE FINE STRUCTURE OF THE CYANOBACTERIUM,MICROCYSTIS AERUGINOSA KÜTZ. EMEND. ELENKIN

SUMMARY

Microcystis aeruginosa toxic strain UV-006 stored a fixed amount of polyphosphate in spherical granules located in the centroplasm. Twenty four hours of phosphate starvation induced use of stored polyphosphate, manifested by reduction in granule numbers. Reintroduction of 2, 4 or 8 mg l^?1 K₂HPO₄ resulted in redeposition of polyphosphate in a critical number of centroplasmic polyphosphate granules. Growth rate was unaffected by phosphate concentrations, although the final cell yield was slightly lower at 8 mg l ^?1

Continued starvation decreased photosynthetic rate and growth ceased. Cells appeared senescent. Cyanophycin and polyglucoside reserves apparently increased in these cells, whilst thylakoids were reduced in number and reorientated away from. the cell wall and polyhedral bodies were lost. After the initial decrease, centroplasmic polyphosphate bodies increased to about half of the maximum numbers stored in cells grown in the presence of phosphate, suggesting that translocation of phosphorus from other areas in the phosphate-starved cell occurred.

Two further polyphosphate deposition areas were observed. DNA fibrils may have represented nucleation sites for developing polyphosphate granules. Intrathylakoidal deposits were rare.     

Phosphorus distribution in perichromatin granules and surrounding nucleoplasm as visualized by electron spectroscopic imaging

Summary— The in situ distribution of phosphorus in perichromatin granules (PCGs), and in the surrounding nucleoplasm was investigated in rat liver cells by means of electron spectroscopic imaging of unstained preparations. A 2–3 nm fibril containing high concentration of phosphorus was found to be the main substructural feature of the PCGs revealed in the maps of phosphorus. This fibril is folded within the PCG with no apparent order. Fibrils of similar diameter and phosphorus content were also found in both the halo surrounding the PCG and dispersed in the nucleoplasm. Some of such fibrils are in continuity with those occurring within PCGs. Sometimes these fibrils are grouped forming a stalk connecting the PCG to chromatin. Some stalked PCGs are U-shaped or kidneyshaped, resembling Balbiani ring granules in the process of formation as observed in Chironomus salivary gland cell nuclei. The external fibrils are interpreted as perichromatin fibrils considered to be precursors of PCGs.     

31P-NMR STUDIES ON INORGANIC POLYPHOSPHATES IN MICROALGAE1

Using “P nuclear magnetic resonance analysis, total inorganic polyphosphate in algae could be quantitatively estimated, For this purpose the algal suspension, which had been kept in cold trichloroacetic acid, was further treated with 6 mM EDTA, or the cells were kept in 2 N KOH containing 100 mM EDTA for 18 h at 37°C. These simple methods avoid hydrolysis of cellular inorganic polyphosphate and, therefore, are useful for the study of phosphorus metabolism in algae. The effects of these treatments on visualization of the signal for inorganic polyphosphate in nuclear magnetic resonance spectra were discussed in comparison with in vivo, ‘P nuclear magnetic resonance spectra of algae.     

Sub-Cellular Element Analysis of a Cyanobacterium (Nostoc sp.) in Symbiosis with Gunnera manicata by ESI and EELS

Element analysis using electron spectroscopic imaging (ESI) and electron energy loss spectroscopy (EELS) was performed in a symbiotic Nostoc sp. strain found in the upper stem tissue of Gunnera manicata, and in Nostoc PCC 9229, a free-living heterocyst-forming cyanobacterium able to enter into symbiosis with the angiosperm Gunnera in reconstitution experiments. ESI and EELS unequivocally identified the four elements nitrogen (N), sulphur (S), phosphorus (P) and oxygen (O) in different inclusion bodies of these biological specimens. High amounts of nitrogen were solely detected in huge cyanophycin granules in vegetative cells of the symbiotic Nostoc strain, whereas large polyphosphate bodies, containing high amounts of phosphorus, sulphur and oxygen, could be seen in the free-living Nostoc PCC 9229. The latter were usually not present or, when found, very small in vegetative cells of the cyanobiont.     

Dispersed polyphosphate in fungal vacuoles in Eucalyptus pilularis/Pisolithus tinctorius ectomycorrhizas.

Ectomycorrhizas produced between Pisolithus tinctorius and Eucalyptus pilularis under axenic conditions were rapidly frozen, freeze-substituted in tetrahydrofuran and embedded anhydrously, and dry-sectioned for X-ray microanalysis. The vacuoles of the sheath and Hartig net hyphae were rich in phosphorus and potassium. They also contained sulfur and variable amounts of chlorine. In anhydrously processed freeze-substituted mycorrhizas, dispersed electron-opaque material filled the fungal vacuoles. X-ray maps indicated that P was distributed evenly throughout the entire vacuole profile and was not concentrated in spherical bodies or subregions of the vacuole. There were no electron-opaque granules surrounded by electron-lucent areas, such as are commonly seen in chemically fixed material. The fungal vacuoles were also rich in K, which similarly gave a signal from the entire vacuolar profile. Such P-rich vacuoles occurred in both the mycorrhizal sheath and Hartig net hyphae. Stained sections of ether-acrolein freeze-substituted mycorrhizas also showed only dispersed material in the fungal vacuoles as, in most cases, did acetone-osmium freeze-substituted material. Precipitation of metachromatic granules by ethanol suggested that large amounts of polyphosphate are stored in these regions under the conditions of our experiments, as well as in the tips of actively growing hyphae of the same fungus. The higher plant vacuoles of ectomycorrhizas gave a much lower signal for K, and P was barely detectable. Much more K was located in the vacuoles of the root exodermal cells than in epidermal cells. The analysis of element distribution between the vacuole and cytoplasm in root cells agrees well with that found for other plant species using other techniques. We conclude that polyphosphate is indeed present in the vacuoles of the fungal cells of these ectomycorrhizas, but that in vivo it is in a dispersed form, not in granules.     

Polyphosphate metabolism in the blue-green alga Microcystis aeru-ginosa

The uptake of inorganic phosphorus was studied in an axenicstrain of phosphorus-starved cells of the blue-green alga Microcystisaeruginosa, an organism often causing blooms in freshwater bodies.Rates of growth and of cellular polyphosphate content as a functionof initial orthophosphate in the medium indicate the operationof the ‘phosphorus overplus’ phenomenon in M. aeruginosa,accompanied by formation of volutin granules. The granules wereisolated by a non-aqueous centrifugation method, and identifiedas polyphosphate bodies.     

Concentric Layers in the Granules of Human Nervous Lipofuscin Demonstrated by Silver Impregnation

Representative pieces of human brain were fixed in 10% formalin, embedded in paraffin and sectioned at 5 μ. Paired sections were used, one of which was oxidized in equal parts of 0.5% potassium permanganate and 0.5% sulfuric acid for 1-2 min, while the other was left unoxidized. Both the oxidized and unoxidized sections were impregnated with silver diamine. The lipofuscin granules in the nerve cells appeared as small intensely stained black dots, surrounded by a clear unstained zone, in the unoxidized sections, while in the oxidized sections there was an outer ring of intensely blackened material surrounding a central unstained dot.     

Polyphosphate granules are an artefact of specimen preparation in the ectomycorrhizal fungusPisolithus tinctorius

Summary Polyphosphate granules are precipitated in the vacuoles of the ectomycorrhizal fungusPisolithus tinctorius (Pers.) Coker & Couch by various treatments, including conventional specimen preparation. Granules are not produced by glutaraldehyde fixation but appear at early stages of ethanol dehydration and are visible with Nomarski DIC microscopy. They show -metachromasy with toluidine blue O at low pH, are extracted by cold trichloroacetic acid and contain phosphorus and calcium as demonstrated by X-ray microanalysis. The granules are surrounded by electron-lucent areas that do not contain these elements at detectable levels. In contrast, vacuoles of freeze-substituted hyphae contain evenly dispersed flocculent material. Phosphorus and potassium are distributed more or less uniformly throughout, but calcium is not detected. This indicates that polyphosphate is present in the vacuole of living hyphae in soluble form and is precipitated to form granules by various treatments. It is thought that granules form when membranes, including the tonoplast, become leaky and there is an influx of precipitating ions such as calcium.Abbreviations DIC differential interference contrast - GMA glycol methacrylate - MMN modified Melin Norkrans - NMR nuclear magnetic resonance - P_i inorganic phosphate - STEM scanning transmission electron microscope     

Extraction and detection methods for polyphosphate storage in autotrophic planktonic organisms

Different extraction procedures were employed to characterise the polyphosphate granules in autotrophic planktonic organisms, the green microalgae Chlorella vulgaris and the cyanobacterium Synechocystis sp. strain PPC 6803. The effectiveness of these methods was assessed using epifluorescence microscopic analysis of DAPI stained specimens as well as by electron spectroscopic imaging. The results clearly indicate that NaOH and hot water treatment followed by filtration of the extracts are suitable to obtain a cell free suspension of intact polyphosphate granules without hydrolysing the polymers. The methods described are useful to gain physiological information on the phosphorus status of autotrophic planktonic organisms.     

Immuno-gold localization of glutamine synthetase in a nitrogen-fixing cyanobacterium (Anabaena cylindrica)

Localization of glutamine synthetase in thin sections of nitrogen-fixing Anabaena cylindrica was performed using immuno-gold/transmission electronmicroscopy. The enzyme was present in all of the three cell types possible; vegetative cells, heterocysts and akinetes. The specific gold label was always more pronounced in heterocysts compared with vegetative cells, and showed a uniform distribution in all three types. No specific label was associated with subcellular inclusions such as carboxysomes, cyanophycin granules and polyphosphate granules. When anti-glutamine synthetase antiserum was omitted, no label was observed.Abbreviation GS glutamine synthetase     

Effects of Ph on Post-Mortem Retention of Trypan Blue Vital Staining in Tissues of Mice

Vital staining of aortas from mice injected subcutaneously (daily for 5 days) with trypan blue was studied. In routine paraffin sections elastic membranes were observed to be well stained and other medial elements unstained following fixation in 10% formaldehyde (25% formalin) at pH 7-9. An identical pattern of vital staining was observed in specimens that had been immersed for 48 hr in saline solutions at pH 7-11. Elastic membranes were not stained, but intermembranous connective tissue was stained after the following: (1) fixation in 10% formaldehyde at pH 1-4 and in Lavdowsky's solution (ethanol, formaldehyde, water and glacial acetic acid), pH 2.3-2.8; and (2) immersion in saline for 48 hr at pH 14. Aortic elastic membranes were vitally stained after fixation by intracardiac perfusion with 10% formaldehyde (pH 7-8) but not after perhion with Lavdowsky's fixative (pH 2.3-2.8). Vital staining was limited to medial elastic membranes in sections of fresh aorta made in a cryostat or by a regular freezing microtome. The vital staining (coarse cytoplasmic granules of dye) within macrophages (Kupffer cells and others) and in cytoplasm of renal tubular epithelium was well demonstrated following use of all methods discussed above     

Changes in polyphosphate composition and localization in Propionibacterium acnes after near-ultraviolet irradiation.

Electron microscopy showed that electron-dense granules accumulated in Propionibacterium acnes in larger amounts when the bacteria were grown on a phosphate-rich medium. X-ray microanalysis demonstrated that the granules contained mostly phosphorus and potassium, indicating that the cells contained polyphosphate granules. When cells were grown on a complex Bacto-agar medium, the amount and the size of the polyphosphate granules were reduced. Polyphosphate was also detected with 31P nuclear magnetic resonance (31P-NMR). Of the polyphosphates observed with 31P-NMR, 20% seemed to be located outside the cell membrane. Broad-band near-ultraviolet irradiation (emission maximum 366 nm) corresponding to doses that killed 37% of the cells increased the amount of polyphosphate in cells grown on the phosphate-rich medium. The fluorescent chromophore 4',6-diamidino-2-phenylindole (DAPI) shifted the fluorescence emission from 478 to 538 nm when bound to polyphosphate and excited at 340 nm. DAPI was used to detect polyphosphates generated after near-ultraviolet irradiation of the cells. Nonirradiated cells showed no increased fluorescence at 538 nm, indicating no polyphosphate is presented in the cells. We conclude that DAPI did not have "access" to the intracellular polyphosphate as long as the cells were not light damaged. This observation is important for the interpretation of near-UV damage to cells.     

Quantitative Struktur-Funktions-Korrelation an BiomembranenQuantitative Correlation of Structure and Function on Biomembranes

Microscopical studies on cells or tissues vitally stained with Neutral red (NR) were hitherto almost invariably confined to a few objects that could be investigated without tissue sectioning, for instance tissue culture. For NR, a cationic dye (molecular weight 289, PK 6,75) is easily soluble in water and organic solvents and diffuses during histological preparation for paraffin sectioning and even from cryostat sections. Thus comprehensive studies of vital staining of laboratory animals such as mouse and rat don't exist yet.This explains why it still remains doubtful, wether NR stains ‘preexisting’ or ‘newly formed’ granules, ‘paraplasmic’ cytoplasmic inclusion bodies or - complete or only partially - lysosomes and why it does so. We tried to solve these problems. Moreover we found that after intravital injection of the dye NR ‘stained’ the cells of the APUD-series (PEARSE) rather selectively as do catecholamines or catecholamine precursors. So it was to follow up wether NR could serve as a model for distribution studies of biogenic amines, too.The histological method that allows the localization of intravitally injected NR in tissue sections is freeze-drying. We applied freeze-drying to cryostat sections. The main advantages of this modiftcation are both the short time needed for the drying procedure and the large number of different tissues that can be cut and frozen-dried in the same time. In this way nearly all organs and tissues of the rat could be investigated.1 min after the intravenous injection of the dye NR has disappeared from the blood - at least in concentrations that are demonstrable in tissue sections. By using fluorescence microscopy the dye instead can be localized in all tissues being investigated mainly intracellularly. Apart from the diffuse staining of the cytoplasm in some tissues stained cell nuclei are observed. Intensely coloured nuclei together with a diffuse to scattered staining of the cytoplasm are signs of cell death.In some endocrine cells - mostly belonging to the APUD-series - a strong, often granular, reddening of the cytoplasm is seen; the nuclei are not stained. While the dosis and the form of application necessary to stain these endocrine cells, the intracellular localization and even the reactive groups (presumably carboxylic groups of the granule matrix) to which NR and catecholamines and their precursors are bound seem to be rather identic, some essential differences do exist: NR is easily and rapidly taken up and stored for a relatively short period, whereas biogenic amines accumulate in APUD - cells by active transport in a time - consuming process; their precursors are only stored following decarboxylation. - Secretory granules of some exocrine gland cells, too, may be vitally stained by NR.NR-staining of lysosomes is a well-known fact. We can add some details: a) There are-very characteristic for each of the tissues investigateddifferences in the time needed to stain lysosomes as well as in the duration of lysosomal staining: For instance lysosomes in the kidney proximal convolution are stained very rapidly directly after the injection of the dye and are destained in about 24 h, lysosomes in the thyroid epithelium are rapidly stained and destained, lysosomes in other organs need 45 to 60 min to get stained. c) There is no correlation between the vital staining of lysosomes and the characteristics lysosomes exhibit when stained by histologicalhistochemical methods in tissue sections. This may be due to the extraction from the tissue section of that particular component that, intravitally, binds the dye to lysosomes. - Differences in the composition of the lysosomal matrix in various organs are discussed as one major point of the heterogeneity of lysosomal vital staining with cationic dyes. d) NR vital staining of lysosomes of younger animals is less, that of older animals much more pronounced; lipopigment may, but must not neccessarily do so, exhibit a strong binding capacity for the cationic dye. e) In dehydration experiments the binding capacity oflysosomes is stronger, after premedication with reserpine less pronounced than normally. Desmethylimipramin has no effect at all.The so-called NR-crinom appears only in a few organs, resulting from autophagic as well as from heterophagic cell activity.Following albumin injection enlarged lysesomes are stained vitally in the renal proximal convolution. ‘Vacuoles’ induced by premedication with Macrodex® and glycerol remain unstained.NR is concentrated in the urine of the distal nephron and in the gastric lumen. Reabsorbtion occurs in the distal intestine.Essentially two factors are believed to be responsible for the pattern of NR vital staining: a) Its solubility that explains the distribution of the dye all over the organism, its diffusion through cell membranes and its elimination from the organism by ‘Non-ionic diffusion’. b) Its qualities as a light cationic dye that cause its - electrostatical - binding (‘storage’) to anionic sites of the tissue, for instance to carboxylic groups of the secretory granules of the APUDcells and carboxylic and/or phosphate groups of the lysosomal matrix.     

Electron spectroscopic imaging for high-resolution immunocytochemistry: use of boronated protein A

In the present study we adapted electron spectroscopic imaging (ESI) for high-resolution immunocytochemistry. To accomplish this, we applied boronated protein A (B-pA) for indirect detection of specific antigenic sites using pre-embedding and post-embedding protocols. Isolated acinar cells were exposed to wheat germ agglutinin (WGA) and anti-WGA, followed by B-pA, to reveal WGA binding sites at the level of the plasma membrane. The cells were then embedded in Epon and unstained ultra-thin sections were examined by electron microscopy using the ESI mode. For post-embedding, ultra-thin sections of glutaraldehyde-fixed, Lowicryl-embedded pancreatic tissue were exposed to specific antibodies (anti-insulin or anti-amylase), followed by B-pA. The unstained sections were examined using the ESI mode. In both cases, boron was detected with high resolution either at the level of the plasma membrane of acinar cells, demonstrating WGA binding sites, or over secretory granules in pancreatic insulin-secreting cells or acinar cells, demonstrating insulin and amylase, respectively. These findings were compared to those obtained with the protein A-gold technique, and have demonstrated the analogy of both types of labeling. In addition, several control experiments assessed this novel approach. They have demonstrated the specificity of labeling and the high reactivity of B-pA, as well as its antibody-binding properties. Finally, electron energy loss spectral analysis confirmed the presence of boron in the tissue sections at sites where immunolabeling was detected. These results demonstrate that ESI is an appropriate approach for cytochemistry. Since the technique is based on detection of elements, spatial resolution is considered to be in the magnitude of 0.5 nm, which represents a major improvement in resolution over actual electron microscopic cytochemical techniques.     

The binding of epidermolytic toxin from Staphylococcus aureus to mouse epidermal tissue

Summary Fluorescein-labelled epidermolytic toxin (FTC-toxin) ofStaphylococcus aureus and ferritin—toxin conjugate have been prepared and purified. FTC-toxin bound selectively to cryostat and resin-impregnated sections of neonatal mouse skin. Binding was localized at the keratohyalin granules and in the stratum corneum. In an epidermal cell (granular, spinous and basal) preparation, only keratohyalin granules of the granular cells bound FTC-toxin. Ferritin—toxin conjugate bound to skin sections at the same two sites as FTC-toxin and was competitive with the binding of free toxin. Keratohyalin granules in unstained sections had a novel patched appearance under the electron microscope, and the ferritin—toxin conjugate bound preferentially to the electron-lucent areas. In the stratum corneum it was shown by quantitative estimation that the target density decreased as the surface of the tissue was approached.