Staining of Negri Bodies

The following procedure for staining Negri bodies in sections is based on methods previously described by MacNeal, by Haynes, and by Richter:

Fixation:

1. 1. Zenker's solution 4 hours at 37°C or Dominici's 3 hours.

2. 2. 70% alcohol, 12 to 18 hours at room temperature.

3. 3. 80% alcohol, about 5 to 6 hours.

4. 4. 90% alcohol, about 4 to 6 hours.

5. 5. Absolute alcohol about 16 hours.

6. 6. Ether and absolute alcohol aa, about 8 hours.

7. 7. 16 to 24 hours in the following mixture: celloidin 1 g., methyl salycilate 25 cc., abs. alcohol 25 cc., ether 25 cc.

8. 8. Chloroform and paraffin, 2 to 3 hours.

9. 10. Paraffin, 1 to 1 1/2 hours.

10. 11. Embed.

staining:

1. 1. Cut sections 4 to 5 μ.

2. 2. Bring section to water and cover with Lugol's iodine for 10 minutes.

3. 3. Decolorize with a 2% sodium thiosulfate (hypo).

4. 4. Wash thoroly with water.

5. 5. Cover with a mixture of equal parts of 0.5% phloxine and 1% eosin Y (National Aniline brand) and leave for 15 minutes.

6. 6. Wash with water and stain 2 to 5 minutes in 0.1% azure B (National Aniline).

7. 7. Wash with 96% alcohol and decolorize in a mixture of 2 parts absolute alcohol with 1 part clove oil, ordinarily for not more than 1/2 to 1 minute.

8. 8. Dehydrate rapidly, clear, and mount in Yucatan Elemi.

     

Embriologia Della “Vinca Difformis„ Pourr. (Apocinaceae)

Riassunto

L'A. ha studiato l'embriogia della Vinea difformis Pourr. ed ha potuto stabilire che:

1. l'archisporio è pluricellulare e possono svilupparis talvolta pi[ugrave] cellule madri;

2. normalmente solo una cellula madre arriva a maturità;

3. delle quattro megaspore solo una è fertile e precisamente la pi[ugrave] calazale;

4. lo sviluppo del gametofito è del tipo Normale cioè Monomegasporiale con oangio emisporiale.

Ha inoltre risontrato una anomalia di sviluppo constituita da un gametofito binucleato abnorme per ritardo delle divisioni nucleari cispetto all'acerescimento che è quello di un gametofito ottonucleato.     

Analisis de la craneometria diferencial entre la vicuña (Vicugna vicugna) y la alpaca (Lama guanicoë pacos)

Using a total of 43 craneological data obtained from any of 73 vicugna and 25 alpaca skulls, three problems were analyzed:

• Identification of skulls

• Taxonomic situation of the vicugna

• Origin of the alpaca.

For rapid identification of New World cameloid skulls it is recommended to use the condilobasal length, the length to heigth ratio and the presence of the Fissura nasolacrimalis.

Some characteristics of the skulls considered essential for the evaluation of domestication processes exclude the vicugna from the alpaca's ancestors.     

Ecological Risk Assessment and Quantitative Consequence Analysis

Ecological risk actually refers to two separate things. First, risk to the environment as a result of human activity. Contaminated sites are an example. Second, risk to the biota—flora, fauna, and people—as a result of environmental hazards. Geophysical risk arising from natural hazards is an example. Risk is a combination of likelihoods and consequences. This article examines methods used to quantify the consequences. At the general level, such methods are linked to the methods used to quantify the likelihoods and thus to quantify the risks. It is possible to use the existing frameworks of risk management, health risk assessment, and ecological risk analysis to develop a risk management framework that is suitable for ecological risk assessment. The framework consists of the following steps:

1. Determine concernsby using risk assessment techniques for various scenarios.

2. Identify the consequences by systematically identifying hazards.

3. Undertake calculations by using relevant models.

4. Evaluate certainties, uncertainties, and probabilities involved in the calculations of the vulnerability and of the exposure.

5. Compare with criteriato assess the need for further action.

6. Determine and act on options to control, mitigate, and adapt to the risk.

7. Communicatethe results to those who need to know.

     

Enzymatic synthesis of gallic acid from tannic acid with an inducible hydrolase of Enterobacter spp

Gallic acid acts as a precursor molecule to synthesize various tannin molecules. These are plant polyphenols and were proved to be good anti-oxidant, anti-cancerous, anti-inflammatory, anti-microbial compounds. In order to fully exploit prominent biological activities of specific tannins and to develop tannin-based new medicines, it is necessary to obtain their pure preparations with an aim of high yield and specificity. In the present study, gallic acid is synthesized by the hydrolysis of tannic acid using a microbial based transformation process. The microorganism was isolated and identified. The ability of the isolated microorganism to covert tannic acid into gallic acid was determined by HPLC and enzyme production.

• Highlights

• The present investigation signifies the role of Enterobacter spp. in various processes:

• ??To synthesize gallic acid (a precursor for food oxidant such as propyl gallate) and a bacteriostatic antibiotic (trimethoprim).

• ??To protect the environment from tannery’s discharge through the process of biodegradation.

• ??To reduce the toxicity of tannins in animal feed.

     

L'azione degli insetti fitofagi sulle variazioni di sostanza secca nelle foglie

Summary

The Author studies with the weighing method the action of plant-eater insects on the alteration of the substances fresch and dry in the hust leaves and he comes to the following conclusions:

1. The fresh substance stand less alterations in the leaves with the excavated border than in the sound leaves, the dry substance is less in the hust leaves than in those sound.

2. The fresh substance shows little waverigs in the leaves notched on alone side of the border, but the dry substance is always inferior in the hust leaves than in the sound half and in those entire.

3. The substances fresh and dry are less in the bored leaves than in the sound, the dry substance shows little alternations in those bored in one or the other half of the border.

This would indicate that the traumatic action of insects causes in the leaves a depresson of the cellular swuelling, whih determines a bigger mobilization of the dry substanc's elements than in the sound leaves.     

Protective Actions of l-Aspartate from Acid or Proteolytic Inactivation

1. l-Aspartate was found to replace l-asparagine in the protective action from acid inactivation of l-asparaginase (EC 3.5.1.1) produced by Escherichia coli A–1–3 and at the same time to inhibit the proteolytic inactivation by α-chymotrypsin.

2. l-Asparaginase changed in its chromatographic properties in the presence of l-aspartate and became to be absorbed on the CM Sephadex column.

3. The sedimentation patterns of l-asparaginase at pH 3.5 were identical either in the presence or absence of l-aspartate, showing partial dissociation. But the reversibility to the active state was observed only in the enzyme dissolved in the solution containing l-aspartate.

4. l-Aspartate did not prevent the enzyme either from the dissociation into subunits or from decrease in the activity by urea.

5. High concentration of l-aspartate was shown to inhibit the l-asparagine hydrolysis reaction.

6. l-Aspartate was suggested from ORD measurements to cause changes in the higher structure as well as the ionic properties or proteolytic inactivation.

     

Influence d'éclairements brefs, à différentes longeurs d'onde,sur les variations circadiennes des activités enzymatiques digestives chez Palaemon serratus (Crustacea,Natantia)

Abstract

The Influence of Short Periods of Lighting with Different Wavelengths on the Orcadian Changes of the Enzymatic Digestive Activities in Palaemon serratus (Crustacea, Natantia)

The effect of light on the circadian rhythms of digestive activities in the Shrimp Palaemon serratus have been studied.

1. Continuous darkness leads in a few days to a disappearance of the variations of the circadian rhythms of digestive enzymes while these rhythms go on in continuous light.

2. Short (1 or 2 hrs) and low intensity flashes of white light are effective in bringing on the reappearance of rhythmic variations in darkness.

3. We have been able to establish an isoquantic spectrum of action of the light. Two values of wavelength appears to account for a maximum sensibility of the shrimp: one in ultraviolet light and an other one, more important, in the green (λ=544 nm).

4. In green light it is possible to obtain the same effect of light by decreasing the time of stimulation to 5 or 10 mn and in increasing the total quantity of energy. Significant responses are obtained with total energy greater than 10000 pE. cm^‐2.

     

Status and Conservation of Prince Ruspoli's Turaco Tauraco ruspolii

Borghesio, L. & Massa, R. 2000. Status and conservation of Prince Ruspoli's Turaco Tauraco tuspolii. Ostrich 71 (1 & 2): 355–358.

Prince Ruspoli's Turaco is an Ethiopian endemic, distributed in a small region at the southern border of the Abyssinian Plateau. Owing to the difficulty of visiting its secluded range, little information is available on its current conservation status. Based on the available data, it is currently considered endangered in the IUCN criteria. In order to evaluate the conservation status of T. ruspolii, field work was carried out during spring 1995. The results of the survey were as follows:

1. the species was found in 26 localities, including all of those previously reported by other authors, and had an area of occurrence about 6 500 km²

2. the population of T. ruspolii was censused by means of linear transects, giving an estimate of about 10 000 individuals.

3. T ruspolii frequents mostly forest margins and relatively dry Acacia woodlands. These habitats are less severely threatened by human activity than true forests in present day Ethiopia.

4. since T. ruspolii and the related T. leucotis usually occur in different habitats (the latter preferring wetter forest) competition is not likely to be a severe threat for T. tuspolii.

5. the species is subject to some egg collecting by local people, but probably not to a severe extent. Other direct human persecution was not recorded.

6. although there is no hint of numerical decrease in the past, this is likely to occur in the future, as consequence of the increasing human pressure in the region.

These results are evaluated and discussed. It is consequently proposed that Prince Ruspolii's Turaco should be considered as a Vulnerable species instead of Endangered in the IUCN criteria.     

Induction of Catalase Activity by Hydrocarbons in Candida tropicalis рK 233

1. The catalase activity of Candida tropicalis pK 233 was induced by hydrocarbons but not by glucose, galactose, ethanol, acetate or lauryl alcohol.

2. The induction of the catalase activity depending upon hydrocarbons was sensitive to cycloheximide but not to chloramphenicol.

3. Glucose repressed strongly the induction of the catalase activity by hydrocarbons but galactose did not affect seriously.

4. When C. tropicalis was incubated with hydrocarbons, the appearance of microbodies was observed electronmicroscopicaliy.

     

L'azione dei raggi U.V. sul Grano

Summary

In order to study a side of the influence of ultra-violet light on plants, the A. has harvested, 10 days after fertilisation, 1040 plants of Triticum vulgare Vill. and made many groups of them; then he sheared differently the ears and screened them partially from light so as to obtain, from the same subject, treated and untreated grains. Such ears he treated for different times of exposure with the light of a quarzlamp giving almost only ultra-violet rays. For the present, are here reported only results concerning the influence of ultra-violet light upon both germinating energy and power:

• ultra-violet light stimulates the germinating power of grains, born from subjects treated no longer than 240 hours at a distance of 1 m from the lamp; longer treatments abate germinating power;

• ultra-violet light stimulates, the germinating energy of grains born from subjects treated no longer than 120 hours; treatments during 120–240 hours don't notably modify it; treatments of over 240 hours reduce it very much;

• according to the conditions in which this work has been done, a 10 days-irradiation seems to be, under every point of view, for the best. A 71/2 — days irradiation seems to be insufficient, a 121/2 — days one excessive, and hence prejudicial;

• glumes are strong screening-organ for ultra-violet light;

• ultra-violet light gives late appearing effects.

Since great difficulties usually occur whenever tests such as the present one are undertaken, the A. proposes some leading ways to previously settle the U.V.-rays dosimetry fit for every plant, in order to avoid wast of time and to get data of general value.     

Removal of Anti-complementary Material and Australia Antigen from Immunoglobulin

Inmunoglobulin isolated from human sera, be it by the cryo-alcohol, rivanol, multi membrane electrodecantation or polyethylene glycol process, alvays contains denatured material. This may result from the influence either singly or in combination, of acme of the follwing factors:

1. inefficiency of the purification procedure;

2. surface denaturation;

3. imperfect freeze-drying of the final product; and

4. factors yet unknown vhich cause alteration in the immoglobulins or other protein components not ellminated by the purification procedures.

     

Quantitative analysis of sarcosine with special emphasis on biosensors: a review

The quantitative determination of sarcosine is of great importance in clinical chemistry, food and fermentation industries. Elevated sarcosine levels are associated with Alzheimer, dementia, prostate cancer, colorectal cancer, stomach cancer and sarcosinemia. This review summarizes the various methods for quantitative analysis of sarcosine with special emphasis on various strategies of biosensors and their analytical performance. The current bio sensing methods have overcome the drawbacks of conventional methods. Sarcosine biosensors work optimally at pH 7.0 to 8.0 in the linear range of 0.1 to 100?μM within 2 to 17?s and between 25 and 37?°C, within a limit of detection (LOD) between 0.008 and 500?mM. The formulated biosensors can be reused within a stability period of 3–180?days. Future research could be focused to modify existing sarcosine biosensors, leading to simple, reliable, and economical sensors ideally suited for point-of-care treatment.

• Clinical significance

• Elevated sarcosine levels are associated with prostate and colorectal cancer, Alzheimer, dementia, stomach cancer and sarcosinemia.

• Quantitative determination of sarcosine is of great importance in clinical chemistry as well as food and fermentation industries.

• Attempts made in development of sarcosine biosensors have been reviewed with their advantages and disadvantages, so that scientist and clinicians can improvise the methods of developing more potent sarcosine biosensor applicable in multitudinous fields.

• This is the first comprehensive review which compares the various immobilization methods, sensing principles, strategies used in biosensors and their analytical performance in detail.

     

Dynamic ejection behaviour of water molecules passing through a nano-aperture nozzle

This study used molecular dynamics (MD) simulation to investigate the passage of water molecules through a composite graphene/Au nano-nozzle. Our focus was on the degree to which system temperature, extrusion speed, and nozzle diameter affect jet dynamics and the associated transient phenomena. Our findings show that high pressure and spatial confinement cause the nanojet from a small nozzle diameter (1.0?nm) to bend and twist, whereas the jets from a nozzle with a diameter of 1.5?nm present columns of greater stability. At 100?K, the H₂O nanojet froze at the outlet of the nozzle in the form of condensed icicles. At 500?K, the H₂O nanojet formed a loose spray and gaseous clusters. High extrusion speed of 55.824?m/s produced recirculating flow downstream from the nanojet with the appearance of an erupting volcano, which further prompted the jet column to thicken. Lower extrusion speeds produced jets with flow velocity insufficient to overcome the capillary force at the outlet of the nozzle, which subsequently manifests as unstable fluctuations in the flow rate.

• HIGHLIGHTS

• Water molecules through a composite graphene/Au nano-nozzle forming a nanojet is investigated.

• High pressure and spatial confinement cause the nanojet from a small nozzle diameter (≤1.0?nm) to bend and twist.

• High extrusion speed (≧55.824?m/s) produced recirculating flow downstream from the nanojet.

• Figure abstract: Schematic of the H₂O nano-jet through a nano-nozzle of graphene/Au

     

Fenomeni di Inattivazione e di Riattivazione Enzimatica in Endospermi di semi di Ricino

Abstract

Inactivation and riactivation of enzymes in endosperms of castor bean seeds. — On the basis of previous results, the possibility has been investigated of the reversible interconversion of active and inactive form of enzymes in castor bean seeds, during their development.

The results described here indicate that:

1. the activity of some glycolytic enzymes increases greatly (81% and 400% increase of, respectively, Gl-6-P-dehydrogenase and aldolase) upon incubation of dry seeds for few hours at 4 °C.

2. The decrease of enzyme activity upon dehydration of seeds and the increase during the subsequent imbibition can be shown reproducibly.

3. This same observation is made for oxygen uptake.

These results are interpreted to indicate the reversible inactivation of enzymes caused by dehydration of seeds.     

Effects of Acetylation with Acetic Anhydricle

1. L-Asparaginase (EC 3.5.1.1) from Escherichia coli A–l–3 was acetylated using acetic anhydride as a modifying chemical. The fully acetylated L-asparaginase retained 60% of the activity of the unmodified L-asparaginase.

2. The acetylated L-asparaginase hydrolyzed D-asparagine and L-glutamine as well as L-asparagine in the same ratio as the unmodified L-asparaginase did.

3. However, the effects of pH on the activity of the acetylated L-asparaginase showed very interesting differences from that of L-asparaginase. On the other hand, both L-asparaginase and the acetylated L-asparaginase exhibited similar pH activity curves on L-glutamine hydrolysis.

4. The acetylated L-asparaginase was found to become more stable against acid or heat in the presence of L-aspartate than in its absence in the same manner as L-asparaginase was.

     

Improvement of lipase activity by synergistic immobilization on polyurethane and its application for large-scale synthesizing vitamin A palmitate

Abstract

We have developed an improved and effective method to immobilize lipase on hydrophobic polyurethane foam (PUF) with different modifications. PUF was treated with hydrochloric acid to increase the active sites and then the active carboxyl groups and amino groups were exposed. Enzyme activity of lipase immobilized on PUF-HCL (8000?U/g) was 50% higher than that of lipase immobilized on PUF (5300?U/g). There is an increase in the activity of the immobilized lipase on AA/PEI-modified support (115,000?U/g), a 2.17-fold increase compared to lipase immobilized on the native support was observed. The activity of immobilized lipases was dependent on the PEI molecular weight, with best results from enzyme immobilized on PUF-HCL-AA/PEI (MW 70,000?Da, 12,800?U/g)), which was 2.41 times higher compared to that of the same enzyme immobilized on PUF. These results suggest that the activity of immobilized lipase is influenced by the support surface properties, and a moderate support surface micro-environment is crucial for improving enzyme activity. Finally, the immobilized lipase was used for the production of vitamin A palmitate. The immobilized lipase can be reused for up to 18 times with a conversion rate above 90% for 12?h in a 3?L bioreactor.

• Research highlights

• An efficient immobilization protocol on polyurethane foam was developed

• Polyethyleneimine and acetic acid were used to regulate the micro-environment concurrently

• The activity of lipase immobilized on PUF-HCL-AA/PEI was improved by 2.41 times

• Immobilized lipase exhibited excellent operational stability for vitamin A palmitate synthesis

     

Direct determination of diene conjugation and deoxyribonucleic acid (DNA) oxidative damage can explain the role of DTPA-Fe2+-O2 complex in a linoleic acid-DNA system

SUMMARY

Exposure of linoleic acid to diethylenetriminepentaacetic acid (DTPA)-Fe²⁺ complexes resulted in fast diene conjugation and peroxidized products which could further react with deoxyribonucleic acid (DNA) to cause DNA oxidative damage. In this paper, we have detected diene conjugation and DNA oxidative damage in a linoleic acid-DNA model system driven by DTPA-Fe²⁺ and found that:

• 1. in air or oxygen-saturated reaction systems, addition of hydrogen peroxide resulted in a decrease in diene conjugation and double-stranded DNA content, but had no obvious effects on the formation of DNA fluorescent products;

• 2. in anoxic conditions, addition of hydrogen peroxide had no effect on the formation of diene conjugation and fluorescent products, but resulted in a decrease of double-stranded DNA content;

• 3. in the presence of DTPA, Fe³⁺ did not stimulate the formation of diene conjugation;

• 4. the formation of diene conjugation and fluorescent products was not inhibited by superoxide dismutase, catalase, sodium benzoate, sodium azide and mannitol.

However, these ‘scavengers’ increased the percentage of double-strand DNA to different degrees. α-tocopherol, but not reduced glutathione (GSH), inhibited the formation of diene conjugates. α-tocopherol and GSH both could reduce the amounts of fluorescent products and DNA strand breaks. Taken together, these data further indicate that chelator-Fe²⁺-O₂ complex, a perferryl-type oxidant, is probably an important initiator of lipid peroxidation in the linoleic acid-DNA system.