A Demineralization Procedure for Enzymatic Histochemical Use: A Quantitative Succinic Dehydrogenase Assay

Thinnest practical slices of bones or teeth are suspended at 4 C in a 10% solution of EDTA in 0.1 M tris buffer brought to pH 6.95 with KOH pellets. The solution is stirred moderately and continuously with a magnetic stirrer until specimens are demineralized. Unwashed specimens, taken directly from the demineralizing fluid, are frozen on a block of CO₂ ice, mounted on a tissue carrier and sectioned at 6 μ in a cryostat. Histochemical stains conducted on sections stored in a slide holder enclosed in a plastic bag in a refrigerator for as long as 2 wk were successful. Quantitative studies on the preservation of succinic dehydrogenase showed nearly all of it present in specimens demineralized for 2 days, and approximately 50% remaining in specimens demineralized for 7 days. Qualitative studies with other dehydrogenases indicate that several may be similarly affected.     

Multinuclear magnetic resonance studies of collagen molecular structure and dynamics

We have measured the percentages of cis and trans Gly-Pro and X-Hyp peptide bonds in thermally unfolded type I collagen. ¹³C-nmr solution spectra show that 16% of the Gly-Pro and 8% of the X-Hyp bonds are cis in unfolded chick calvaria collagen. These results support the hypothesis that cis–trans isomerization is that rate-limiting step in the propagation of the collagen triple helix. We have used multinuclear solid-state nmr to study the molecular dynamics of the collagen backbone in tendon, demineralized bone, and intact bone as a function of temperature, hydration, and pH. These studies show that collagen backbone motions are characterized by a broad distribution of correlation times, τ, covering the range from 10^?4 to 10^?9 s. In the case of nonmineralized collagen, the root-mean-square fluctuations in azimuthal angle, γ_rms, range from ca. 10° when τ ～ 10^?9 s to ca. 30° when τ < 10^?4 s; in the case of bone collagen, γ_rms values are about half as large as those found in nonmineralized collagen. Backbone motions are negligible at temperatures below ?25°C. This is also the case at 22°C when demineralized bone collagen is lyophilized. In contrast, flexibility of hydrated demineralized bone collagen greatly increases as pH is lowered from 7 to 2. The more limited flexibility observed at neutral pH is a consequence of the intermolecular interactions that contribute to fibril organization and strength. However, the fibrils retain significant flexibility at physiological pH, enabling them to distribute stress and dissipate mechanical energy.     

Growth of Euglena gracilis on whey

Summary To extend the use of industrial wastes, we have studied the growth of Euglena cells on demineralized whey powder, an industrial dairy waste from cheese making. The demineralized whey powder was solubilized (15 g/l) in 0.04 N HCl and autoclaved for two hours at 120°C. The solution was then brought to pH 3.5 with NH₄OH and tested for its ability to support Euglena growth. In the dark, cell densities of 4.5 to 5.5×10⁶ cells/ml were obtained when vitamin B₁₂, thiamine and minerals were added to the hydrolyzed whey solution. Although growth of Euglena is possible on whey, the industrial application may be limited due to the need to hydrolyze the whey and to the low utilization of carbon (20%) as the glucose, but not the galactose, released during hydrolysis is used.     

In vitro recalcification of the demineralized shell-repair membrane of the snail,Helix pomatia L.

Summary The role of the amoebocytes in the calcification process of the shell-repair membrane of the snail, Helix pomatia, was investigated in vitro. The shell-repair membranes were demineralized with 0.5 M EDTA at pH 7.4. For the recalcification of the demineralized membranes two substrates were chosen: (i) Tris-buffered Helix pomatia-saline, pH 7.4, and (ii) Helix pomatia-saline supplemented with 5 mM CaCl₂ and 5 mM NaHCO₃. The membranes were incubated in 2 ml substrate at 37° C and examined after 2 h, 24 h, and 3, 5 and 7 days. Calcium deposition and crystal formation were observed within the membrane incubated in the salt-supplemented substrate. The control membranes were either heat-inactivated or deprived of lipids. No calcium precipitation was observed in control membranes. The experiments show that the recalcification of the shell-repair membrane is under strict cellular control and that the granules released from the amoebocytes serve as sites for calcium deposition. The role of phospholipids in the calcification process is discussed.     

The effect of adenosine triphosphate,magnesium chloride and phospholipids on crystal formation in the demineralized shell-repair membrane of the snail,Helix pomatia L.

Summary The effect of adenosine triphosphate (ATP), magnesium chloride (MgCl₂) and phospholipids on the calcium-binding activity and crystal formation within the decalcified shell-repair membrane of the snail, Helix pomatia, was studied in vitro. The application of ATP produced a characteristic dual effect on calcification: (1) It strongly inhibited the formation of inorganic calcium carbonate (CaCO₃) crystals. (2) It stimulated the development of organic crystalline bodies and induced deposition of amorphous calcium carbonate. The demineralized shell-repair membranes became white and rigid after incubation for 7 days in the medium containing 1.0mM ATP. The inhibitory effect of Mg²⁺ on CaCO₃ crystal formation was diminished by reduction of the concentration of MgCl₂ in the incubation solution. Thus, after incubation for only 24h, 1.0mM MgCl₂ promoted the formation of birefringent CaCO₃ crystals within the repair membranes. The principal effect of phospholipids on the demineralized shell-repair membrane was stimulatory, but after application of phospholipids to the medium, the formation of crystals proceeded slowly. The very large, composite crystals that were formed within the repair membranes showed strong birefringence. In all cases the development of the crystals and the organic crystalline bodies occurred in close vicinity to the amoebocytes. The role of ATP, MgCl₂ and phospholipids in the recalcification of shell-repair membrane is discussed.The author wishes to thank Mrs. E. Hellmén for valuable technical assistance     

Selective and Differential Media for Isolation and Tentative Identification of Each Species of Pityrosporum Residing on Normal or Diseased Human Skin

Selective and differential media were designed for each species of Pityrosporum; P. pachydermatis, P. ovale, and P. orbiculare in order to make feasible a quantitative cultivation. Medium for P. pachydermatis (medium A) was composed of 1% trypticase peptone (BBL), 0.5% yeast extract (BBL), 0.3% glucose, 0.2% NaCl, 1.2% KH₂ PO₄ (anhydrous), 1.5% agar, 0.01% ampicillin, and 0.025% cycloheximide with a pH of 5.5. Medium for P. ovale (medium B) was medium A supplemented with 0.05% sodium acetate (anhydrous), 0.2% Tween 80, and 0.025% (selective medium) or 0.075% (differential medium) sodium laurate. Medium for P. orbiculare was medium B (devoid of laurate) supplemented with 2% olive oil, 0.25% glycerol, 0.25% gall powder, 0.05% sodium palmitate, 0.05% sodium stearate, 0.05% sodium oleate and 8% (selective medium) or 10% (differential medium) sodium lactate and an increase in Tween to 1%. For isolation of Pityrosporum, specimens were suspended in 0.1% Tween 80 solution and inoculated onto agar plates of three selective media. The plates were incubated aerobically at 37 C for 8–10 days under conditions of prevention of water loss from the media. The plating efficiency of each selective medium, expressed as a ratio of cultural counts to microscopic counts was generally over 70%. Species of Pityrosporum could also be identified when we inoculated the cell suspension onto differential agar plates and incubated the preparations at 37 C for 7 days.     

Comparison of different trapping methods for surveillance of mosquito vectors of West Nile virus in Rhône Delta,France

Five trapping methods were compared for monitoring potential vectors of the West Nile virus in four areas in the Camargue Plain of France: carbon dioxide traps, bird‐baited traps, gravid traps, resting boxes, and human landing catches. A total of 73,721 specimens, representing 14 species, was trapped in 2006. Results showed significant differences in species and abundance between the type of traps. Many more specimens were collected using CO₂ traps than any other method, with an average of 212 specimens per night per trap (p<0.05). Culex pipiens was the most abundant species collected (36.8% of total with CO₂ traps), followed by Aedes caspius (22.7%), Anopheles hyrcanus (18.3%), Culex modestus (18.3%), and Aedes detritus (3.2%). Bird‐baited traps captured only eight specimens per night per trap on average, mainly Cx. pipiens (89.9%). The species collected and their abundance are influenced by the trap location, at ground or canopy level. Culex pipiens was twice as abundant in the canopy as on the ground, whereas it was the opposite for Ae. caspius, An. hyrcanus, and Ae. detritus. Culex modestus was equally abundant at both levels. Resting boxes and gravid traps were much less efficient, capturing around 0.3 specimens per night per trap. Results are discussed in relation to West Nile virus surveillance.     

Notes of Technic

The leaching of water-soluble and exchangeable calcium in histoautoradiog-raphy of oat tissue can be prevented by using acetone as the dehydration fluid (freeze substitution technique) and by keeping the tissue sections, while stretching on water, embedded in the methacrylate matrix. Ca⁴⁵ was either added to the mineral solution on which the oat plants were grown (75 μc), or applied on the leaf surface (8 μc). After freezing in melting isopentane, specimens of 1-2 mm dimensions are fixed for 24 hr in an acetone-OsO₄ (1%) solution at—80 C. Dehydration is obtained by transferring the material every day for 6 successive days to a fresh acetone solution at—80 C. The material is infiltrated by a three-time renewed monomer methacrylate mixture (methylmethacrylate I, butylmethacrylate 4) at—50 C. The specimens are embedded in the polymerizing methacrylate mixture at room temperature. Sections of 4-8 μ are easily cut with a rotating microtome. If the methacrylate is not removed from the sections, they can be stretched on water without leaching of calcium. The presence of methacrylate in no way hinders microscopic observation nor effective histoautoradiography.     

Induction of Growth Increase and Systemic Resistance to Exserohilum turcicum in Maize by Foliar Spray of Phosphates

A single foliar spray of 0.1 M solution of phosphate salts on the upper side of maize (cv. ‘jubilee') leaves 1, 2 and 3 at the 5–6 fully–expanded leaf-stage, 2-4 h before inoculation induced systemic resistance to northern leaf blight caused by Exserohilum turcicum. Nine days after challenge, protection was demonstrated by 91% reduction in the size and 69% in the number of E. turcicum lesions developing on leaves 4, 5, 6 and 7. Appropriate mixing of phosphate solution with KOH revealed that the level of protection was not necessarily dependent on the pH of the solution. The size and number of lesions decreased to 62% and 56%, respectively, 12 days after challenge. There was no damage or chlorotic stipling on the induced leaves (1, 2, and 3) as a result of the phosphate spray. There were no significant differences in the reduction in the number or size of the lesions obtained when the foliar spray was applied 2-4 h or 1, 3, 6, 8, or 10 days before inoculation. One foliar spray ofK₂HPO₄ on leaves 1, 2 and 3 in these intervals before inoculation, remarkably stimulated growth of inoculated plants, which was expressed by several parameters. The possible dual use of phosphate salts as foliar fertilizers and as resistance-inducing agents is discussed     

Storage of Shredded Cabbage under a Dynamically Controlled Atmosphere of High O2 and High CO2

Shredded cabbage (Brassica oleracea L., Capitata group) was stored under a dynamically controlled atmosphere (DCA) and modified atmosphere (MA) at 5°C. Quality factors were measured every 2 days. Browning was suppressed as the CO₂ concentration was increased (0% to 15%), with no influence from O₂ concentration (2.5% to 10%). The development of an off-odor was markedly delayed with an increase in O₂ concentration, such an odor being detected after 6 days at 2.5% O₂,8 to 10 days at 5% to 7.5% O₂, and not at all above 10 days at 10% O₂, while the off-odor development was little affected by CO₂ concentration (5% to 15%). Total sugar, polyphenolics, total ascorbate, and total microbial count were little influenced by O₂ and CO₂. These results show that shredded cabbage can be kept in good condition with a combined high O₂ and high CO₂ atmosphere. These findings are largely different from those for MA storage.     

Overexpression of the Escherichia coli catalase gene, katE, enhances tolerance to salinity stress in the transgenic indica rice cultivar, BR5

Salinity stress is a major limiting factor in cereal productivity. Many studies report improvements in salt tolerance using model plants, such as Arabidopsis thaliana or standard varieties of rice, e.g., the japonica rice cultivar Nipponbare. However, there are few reports on the enhancement of salt tolerance in local rice cultivars. In this work, we used the indica rice (Oryza sativa) cultivar BR5, which is a local cultivar in Bangladesh. To improve salt tolerance in BR5, we introduced the Escherichia coli catalase gene, katE. We integrated the katE gene into BR5 plants using an Agrobacterium tumefaciens-mediated method. The introduced katE gene was actively expressed in the transgenic BR5 rice plants, and catalase activity in T₁ and T₂ transgenic rice was approximately 150% higher than in nontransgenic plants. Under NaCl stress conditions, the transgenic rice plants exhibited high tolerance compared with nontransgenic rice plants. T₂ transgenic plants survived in a 200 mM NaCl solution for 2 weeks, whereas nontransgenic plants were scorched after 4 days soaking in the same NaCl solution. Our results indicate that the katE gene can confer salt tolerance to BR5 rice plants. Enhancement of salt tolerance in a local rice cultivar, such as BR5, will provide a powerful and useful tool for overcoming food shortage problems.     

Factors Affecting Germination of Oospores of Phytophthora infestans

When oospores from the pairing between A¹ and A² mating types of Phytophthora infestans were treated with 0.25 % KMnO₄ solution for 15 min and incubated at 19 °C under light on a modified S+L medium, germination commenced within 4 days and reached about 70 % after 20 days. Under these conditions, more than 25 % of oospores obtained from a 4-day-old culture germinated. To obtain a high germination rate of P. infestans oospores, light was essential during germination but not during growth and oospore formation. The optimum time for activation of oospores with 0.25 % KMnO₄ was 15 to 30 min and a suitable concentration of KMnO₄ for 15 min activation was 0.25 to 0.45 %.     

The relationship between the entry of isoproturon into Alopecurus myosuroides and its effect on growth and CO2 fixation

Alopecurus myosuroides (blackgrass) was grown in nutrient and with isoproturon added to the solution when plants had three leaves. The transpiration stream coefficient factor was calculated over a period of 96h after treatment to be approximately 1. On this basis isoproturon entry into A. myosuroides was estimated using data for water loss through plants and there was a linear relationship between herbicide entry and plant weight 14 days after treatment. Treatment for at least 7 days with isoproturon at a dose of 1 μg a.i./15 ml nutrient solution (≡ 0.32 × 10^-6M) before returning plants to fresh nutrient was necessary for damage to be still evident after 14 days. This time period corresponded with the reduction of CO₂ exchange to zero as measured by infra-red gas analysis. Some recovery occurred from 6 h treatment with 120 μg a.i. isoproturon/15 ml nutrient solution when assessed after returning plants to untreated nutrient for 14 days. A quicker depletion in CO₂ uptake by blackgrass occurred when both the primary and secondary roots were treated compared with secondary alone but eventually the levels reached were similar. The ‘CALF’ model predicted much higher concentrations of isoproturon than appeared necessary to damage A. myosuroides. This suggests a major influence of climate on the plant and this and other interactions are discussed.     

The effect of extractants on degradation of L-glutamate and L-arginine in the course of shaking and filtration at low temperature

Summary. The effects of demineralized water (DEMI H₂O) and 0.5 M ammonium acetate (0.5 M AAc) on losses of L-glutamic acid and L-arginine in the course of shaking and filtration at low temperature (6 °C) were tested. The concentration of L-glutamic acid decreased by 6.3% in DEMI H₂O and by 4.9% in 0.5 M AAc, whereas the L-arginine concentration decreased by 6.0% (DEMI H₂O) and 10.7% (0.5 M AAc). We found a significantly (P < 0.05) higher degradation of L-arginine in 0.5 M AAc compared with that of DEMI H₂O.     

Effects of Foliar Sprays of Phosphates on Powdery Mildew (Sphaerotheca pannosa) of Roses

Powdery mildew on plants of a local clone of Rosa indica Major was significantly controlled by a single spray of 25 mM aqueous solutions of K₂HPO₄, KH₂PO₄ plus KOH, or NaHCO₃, all plus Tween 20 (0.5 ml/l) or bupirimate (Nimrod) at 0.5 ml/l, which was applied 4 days before inoculation with conidial suspension of Sphaerotheca pannosa var. rosae. Disease incidence was reduced by 79, 71, 54 and 50%, as compared to controls on plants sprayed with KH₂PO₄ plus KOH, K₂HPO₄, NaHCO₃ or bupirimate, respectively. Phosphates were suppressive and expressed by disappearance of 99% of the pustules and conidia, as early as 2 days after a single spray on mildewed foliage. This treatment was efficient for at least 9 days after the first application when large infected greenhouse-grown plants were used. Re-application of these salts on the same plants reduced the lesion area by about 90% from that recorded before the application. Phosphate and bicarbonate were more suppressive than the systemic fungicide bupirimate in the early period (up to 2 days). The suppresion effects of bicarbonate and bupirimate, however, were short-term and not persistent, while the phosphate treatments remained significantly suppressive for up to 23 days, when the experiment was terminated. The inhibitory and suppressive effectiveness of phosphate salts is discussed in the light of their possible acceptance as ideal foliar fertilizers which should be considered for use in the field for disease control.     

Effects of aluminium on growth and root reactions of phosphorus stressed Betula pendula seedlings

The impact of two constant non-toxic levels of Al stress (0.2 and 0.4 mM) on growth and ³²P uptake capacity on sub-optimal (P-limited) Betula pendula seedlings grown in sand culture was examined.Seedling growth was under optimum controlled conditions in a growth chamber where nutrient additions were made at a predetermined relative addition rate (R_A) of 10% day^-1. Three treatment groups of seedlings 0, 0.2 and 0.4 mM Al were harvested at 15, 29 and 42 days. The excised roots were exposed to a ³²P-labelled solution for 15 minutes to measure their capacity for P uptake. Growth was determined by weighing the roots, stems and leaves of the seedlings.Growth data showed that relative growth rate (R_G) should equal the R_A of P the most limiting nutrient, which was supplied at P/N 3% instead of an optimal 15%. Therefore, Ingestad's theory can also be used succesfully in sand culture and this may be particularly important for future studies of root and rhizosphere exudates. Low levels of Al (< 0.2 mM) in combination with low P supply significantly lowered the R_G of the birch seedlings by further reducing P supply. However, previous studies of birch seedling growth and nutrient uptake using Ingestad's solution culture technique with optimumal P supply did not show any effect of Al on growth untill the Al was in excess of 3 mM. Aluminium was not directly toxic to the plants and therefore roots could respond to the ³²P bioassay.     

Differential protein synthesis during differentiation (spherulation) of Physarum polycephalum: Lack of synthesis of glucose-6-phosphate dehydrogenase

Summary In the neutral lipid fraction of Hydrogenomonas eutrapha strain H 16, two esters of phthalic acid were found and separated by column chromatography.By totally labelling chemolithotrophically growing bacteria with ¹⁴CO₂ it was demonstrated that these phthalic acid esters are not genuine bacterial products but of exogenous origin.It is supposed that these esters which are used as plasticizers for various plastics originate from such materials used in the preparation and storage of demineralized water.     

Effects of Foliar Sprays of Phosphates on Powdery Mildew (Sphaerotheca pannosa) of Roses

Powdery mildew on plants of a local clone of Rosa indica Major was significantly controlled by a single spray of 25 mM aqueous solutions of K₂HPO₄, KH₂PO₄ plus KOH, or NaHCO₃, all plus Tween 20 (0.5 ml/l) or bupirimate (Nimrod) at 0.5 ml/l, which was applied 4 days before inoculation with conidial suspension of Sphaerotheca pannosa var. rosae. Disease incidence was reduced by 79, 71, 54 and 50%, as compared to controls on plants sprayed with KH₂PO₄ plus KOH, K₂HPO₄, NaHCO₃ or bupirimate, respectively. Phosphates were suppressive and expressed by disappearance of 99% of the pustules and conidia, as early as 2 days after a single spray on mildewed foliage. This treatment was efficient for at least 9 days after the first application when large infected greenhouse-grown plants were used. Re-application of these salts on the same plants reduced the lesion area by about 90% from that recorded before the application. Phosphate and bicarbonate were more suppressive than the systemic fungicide bupirimate in the early period (up to 2 days). The suppresion effects of bicarbonate and bupirimate, however, were short-term and not persistent, while the phosphate treatments remained significantly suppressive for up to 23 days, when the experiment was terminated. The inhibitory and suppressive effectiveness of phosphate salts is discussed in the light of their possible acceptance as ideal foliar fertilizers which should be considered for use in the field for disease control.     

Reduced Methylene Blue as a Stain for Crustacean Nerves

Effective in situ staining of crustacean nerves was achieved with leuco methylene blue reduced with either ascorbic acid or sodium hydrosulfite (Na₂S₂O₄). A stock solution of methylene blue, 0.4% (ca. 0.001 M), and the reductants, ascorbic acid or sodium hydrosulfite (0.01 M), were prepared in van Harreveld's crayfish physiological solution. Methylene blue stock solution was mixed with either of the reductants in the approximate ratio of 1:10, v/v, and titrated to the end point. Ascorbic acid reduction is light catalyzed and requires intense illumination during titration. The cleared or leucomethylene blue stock solution is suitable for immediate use as a working nerve stain. With either reductant, the working solution oxidizes on standing in air, but can be titrated repeatedly without loss of staining properties. Dissected nerve trunks or tissue were immersed in the working stain for 20 min at room temperature and the staining process observed until suitable contrast developed. Excess dye was decanted and the tissues flooded with crayfish physiological solution. Contrast could sometimes be enhanced by flooding the stained area with 1% hydrogen peroxide in van Harreveld's solution. When permanent mounts were prepared, tissues were dehydrated with tertiary butyl alcohol in preference to ethyl alcohol series. For anatomical and neurophysiological studies of nerve distribution in crustaceans, the alternative use of either ascorbic acid or sodium hydrosulfite, as reductants for methylene blue, was preferable to the more complicated rongalit-technique and characterization of neural elements was fully as satisfactory.     

High-efficiency vitrification protocols for cryopreservation of in vitro grown shoot tips of rare and endangered plant <Emphasis Type="Italic">Emmenopterys henryi</Emphasis> Oliv.

In vitro-grown shoot tips of Emmenopterys henryi Oliv. were successfully cryopreserved by vitrification. Shoot tips excised from 3-month old plantlets were precultured in a liquid hormone-free Murashige and Skoog (MS) medium supplemented with 0.5 M sucrose for 3 days at 25°C and then treated with a mixture of 2 M glycerol plus 0.4 M sucrose (LS solution) for 40 min at 25°C. Osmo-protected shoot tips were first dehydrated with 60% vitrification solution (PVS₂) for 30 min at 0°C and followed by 100% PVS₂ for 40 min at 0°C. After changing the solution with fresh 100% PVS₂, the shoot tips were directly plunged into liquid nitrogen. After rapid warming in a water-bath at 40°C for 2 min, the shoot tips were washed for 20 min at 25°C with liquid MS medium containing 1.2 M sucrose and then transferred onto solid MS medium supplemented with kinetin 2 mg l⁻¹, α-naphthaleneacetic acid 0.1 mg l⁻¹, 3% (w/v) sucrose and 0.75% (w/v) agar. The shoot tips were kept in the dark for 7 days prior to exposure to the light (12 h photoperiod cycle). Direct shoot elongation was observed in approximately 12 days. The regeneration rate was approximately 75–85%. This method appears to be a promising technique for cryopreserving shoot tips of Emmenopterys henryi Oliv. germplasm.