HISTOCHEMICAL CHANGES IN MELOLONTHA MELOLONTHA (LINNAEUS) (COLEOPTERA) INFECTED BY A NEW VIRUS

1966 ◽  
Vol 12 (5) ◽  
pp. 965-971 ◽  
Author(s):  
Oswald N. Morris
Keyword(s):  
Protein Content ◽  
Nuclear Protein ◽  
Fat Body ◽  
Disease Process ◽  
Cytoplasmic Inclusions ◽  
Virus Particles ◽  
Melolontha Melolontha ◽  
Cytoplasmic Rna ◽  
Different Types ◽  
Histochemical Changes

Changes in DNA, RNA, protein, and glycogen in the fat body of a beetle, Melolontha melolontha (Linnaeus), were studied histochemically at intervals of 15, 23, 75, and 195 days after intrahemocoelic injection of a cytoplasmic polyhedrosis virus, Vagoiavirus melolonthae. As the disease progressed, the average nuclear diameter increased considerably without any apparent change in DNA content. Cytoplasmic RNA increased progressively for about 75 days and then decreased slightly. Nuclear protein content increased during the first 23 days after virus inoculation. Cytoplasmic protein content progressively increased throughout the disease process. There was no significant change in glycogen reserves 23 days after inoculation; thereafter, glycogen was drastically reduced.Three morphologically different types of cytoplasmic inclusions all staining intensely with naphthol yellow S (thus establishing their proteinaceous nature) were observed. The pyroninophilic "round" type is considered to be "mature" inclusions containing the virus particles demonstrated by electron microscopy. The resemblances between this virus and some viruses of higher animals are discussed.

scholarly journals Cardiac Amyloidosis with Discordant QRS Voltage between Frontal and Precordial Leads

Medicina ◽  
2021 ◽  
Vol 57 (7) ◽  
pp. 660
Author(s):  
Csilla-Andrea Eötvös ◽  
Roxana-Daiana Lazar ◽  
Iulia-Georgiana Zehan ◽  
Erna-Brigitta Lévay-Hail ◽  
Giorgia Pastiu ◽  
...  
Keyword(s):  
Left Ventricular Hypertrophy ◽  
Cardiac Amyloidosis ◽  
Ventricular Hypertrophy ◽  
Low Voltage ◽  
Disease Process ◽  
Left Ventricular ◽  
Clinical Suspicion ◽  
Immunoglobulin Light Chain ◽  
Different Types

Among the different types, immunoglobulin light chain (AL) cardiac amyloidosis is associated with the highest morbidity and mortality. The outcome, however, is significantly better when an early diagnosis is made and treatment initiated promptly. We present a case of cardiac amyloidosis with left ventricular hypertrophy criteria on the electrocardiogram. After 9 months of follow-up, the patient developed low voltage in the limb leads, while still maintaining the Cornell criteria for left ventricular hypertrophy as well. The relative apical sparing by the disease process, as well as decreased cancellation of the opposing left ventricular walls could be responsible for this phenomenon. The discordance between the voltage in the frontal leads and precordial leads, when present in conjunction with other findings, may be helpful in raising the clinical suspicion of cardiac amyloidosis.

scholarly journals Different mRNAs have different nuclear transit times in Dictyostelium discoideum aggregates.

1983 ◽  
Vol 3 (8) ◽  
pp. 1511-1517 ◽  
Author(s):  
G Mangiarotti ◽  
C Zuker ◽  
R L Chisholm ◽  
H F Lodish
Keyword(s):  
Dictyostelium Discoideum ◽  
Repetitive Dna ◽  
Mrna Species ◽  
Processing Times ◽  
Cytoplasmic Rna ◽  
Transit Times ◽  
Different Types ◽  
Nuclear Processing

Nuclear processing of mRNA precursors in differentiating multicellular Dictyostelium discoideum aggregates is markedly slower than in growing amoebae. Thus, we have been able to determine the time of nuclear processing of individual mRNA species in postaggregating cells by following the incorporation of 32PO4 into nuclear and cytoplasmic RNA complementary to cloned cDNAs. Precursors of mRNAs synthesized during both growth and differentiation remain in the nucleus for about 25 to 60 min. By contrast, typical mRNAs which are synthesized only by postaggregative cells have nuclear processing times between 50 and 100 min. Depending on the particular mRNA, between 20 and 60% of nuclear transcripts are converted into cytoplasmic mRNA. A third class of mRNAs are transcribed from a set of repetitive DNA segments and are expressed predominantly during differentiation. Nuclear precursors of these mRNAs are extensively degraded within the nucleus or very rapidly after transport to the cytoplasm. Those sequences that are stable in the cytoplasm exit from the nucleus only after a lag of over 2 h. Thus, mRNAs encoded by different genes that are subject to different types of developmental controls display different times of transit to the cytoplasm and different efficiencies of nuclear processing. Differential nuclear processing may contribute to the regulation of the level of individual cytoplasmic mRNAs.

Analysis of the Protein Content of Five Different Types of Kidney Stones

1994 ◽  
pp. 363-364
Author(s):  
B. Dussol ◽  
M. Daudon ◽  
P. Dupuy ◽  
R. Michel ◽  
Y. Berland ◽  
...  
Keyword(s):  
Protein Content ◽  
Kidney Stones ◽  
Different Types

Changes in protein during development of Triturus embryos

Development ◽  
1973 ◽  
Vol 30 (3) ◽  
pp. 647-659
Author(s):  
Hiroshi Imoh ◽  
Tsutomu Minamidani
Keyword(s):  
Protein Synthesis ◽  
Protein Content ◽  
Sodium Carbonate ◽  
Dna Content ◽  
Total Protein ◽  
Soluble Protein ◽  
Nuclear Protein ◽  
Polyacrylamide Gel Electrophoresis ◽  
Tail Bud ◽  
Stage Of Development

The present paper reports basic data on DNA content, protein content, and protein synthesis in Triturus pyrrhogaster embryos during development from cleavage to the hatching stage. Except for measurements of DNA and total protein contents, embryos were labeled with sodium carbonate-14C for 10 h and fractionated into embryonic cell components, i.e. cytoplasmic mass, yolk and pigment granules, and nuclei, in a discontinuous density gradient of sucrose. The protein content and the radioactivity incorporated into protein were measured in each fraction. Those fractions combining protein soluble in buffer at pH 8·3 and in 0·25 N-HCl were further studied with polyacrylamide gel electrophoresis. In the newt embryo, four stages of active DNA increase were observed when cultured at constant temperature; they were gastrula, neurula, late tail-bud, and before-hatching stages. Total protein per embryo decreased from 3 to 2 mg during the development studied. The content of cytoplasmic soluble protein per embryo was low and constant throughout development. Synthesis of the fraction was observed at the earliest stage of development studied though the rate was not high and specific activity of the soluble protein increased during development. Qualitative changes in the newly synthesized protein were observed. With the yolk fraction, synthesis of protein, other than from probable contamination with the cytoplasmic fraction, was not detected and a detailed description was omitted. Changes were observed at two stages of development in the synthesis of nuclear protein soluble in buffer at pH 8·3, the first at gastrulation and the second at late tail-bud stage. The change at gastrulation seemed to be the start of syntheses of the nuclear soluble proteins, while quantitative enhancement rather than qualitative change was noticed at late tail-bud stage. Most of the nuclear protein soluble in 0·25 N-HCI was histone. The histone content increased in accordance with increase in the DNA content and the rate of DNA accumulation was accompanied by proportionate incorporation of radioactivity into histone. Among histone fractions, unique behaviour of the very lysine-rich histone was observed. The availability of [14C]sodium carbonate in rough estimations of protein synthesis in embryos and significance of the data obtained have been discussed.

Peculiarities of extraction of β-lactoglobuline in protein mineral concentrates at electroactivation of whey

2020 ◽  
Vol 2 (1) ◽  
pp. 52-68
Author(s):  
Mircea BOLOGA ◽  
Elvira VRABIE ◽  
Irina PALADII ◽  
Olga ILIASENCO ◽  
Tatiana STEPURINA ◽  
...  
Keyword(s):  
Protein Content ◽  
Whey Proteins ◽  
Sodium Dodecyl ◽  
Total Protein Content ◽  
Treatment Regimens ◽  
Sds Page ◽  
Different Types ◽  
Lower Protein ◽  
Β Lactoglobulin ◽  
Excellent Source

Introduction. Whey is a by-product and an excellent source of proteins that is rather aggressive due to a large amount of organic substances it contains. The electro-activation of whey applied in the experiments is a wasteless method that allows the va-lorification of all whey components. β-lactoglobulin (β-Lg) makes up 50% of the whey proteins and 12% of the total protein content in milk. Material and methods. The recovery of β-Lg in protein-mineral concentrates (PMC) by electro-activation processing of different types of whey with different initial protein content was investigated in seven configurations. The recovery of protein fractions in the PMCs were analyzed via electrophoresis with sodium dodecyl sulfate (SDS-PAGE) and 15% non-denaturing polyacrylamide gel (PAAG).      Results. Whey electro-fractionation and the obtaining of PMCs with predetermined protein content, namely of β-Lg, were studied on three whey types, processed at different treatment regimens and in seven configurations. The proper management of electroactivation by varying the treatment regimens will allow the electro-fractionation of different types of dairy by-products. Conclusions. The maximum amount of β-Lg recovered in PMCs on electroactivation is  66-71% depending on the processed whey and on the treatment regimens. Obviously, the extraction of β-Lg from initially lower protein content shows a higher recovery degree of β-Lg. The registered temperatures allows formation of PMCs without thermal denaturation.

PCNA and total nuclear protein content as markers of cell proliferation in pea tissue

1992 ◽  
Vol 102 (1) ◽  
pp. 71-78 ◽  
Author(s):  
SANDRA CITTERIO ◽  
SERGIO SGORBATI ◽  
MARISA LEVI ◽  
BRUNO MARIA COLOMBO ◽  
ELIO SPARVOLI
Keyword(s):  
Cell Cycle ◽  
Cell Proliferation ◽  
Protein Content ◽  
Time Course ◽  
Nuclear Protein ◽  
Flow Cytometric Analysis ◽  
Nuclear Antigen ◽  
Cycle Phase ◽  
Proliferating Cells ◽  
Embryo Cells

The identification of cell proliferation markers has been shown to be a useful tool with which to study basic mechanisms of cell cycle progression. The use of immunofluorescence techniques revealed the presence of the proliferating cell nuclear antigen (PCNA) in pea tissue, where we observed a high PCNA expression in proliferating cells of the root meristem compared to noncycling cells of the differentiated leaf. The presence of PCNA was monitored also during the time-course of seed germination, before, during and after the cell cycle resumption of the embryo cells. PCNA is present in embryo cells not only during and after resumption of the cell cycle but also before, when cells have not yet begun replicating their genome. A bivariate flow cytometric analysis of DNA and nuclear protein content was used to localize precisely the cells of the examined pea tissues in different cell cycle phase subcompartments. A high correlation was found between the degree of cell proliferation and the protein content of G1 nuclei, on the one hand, and the percentage of PCNA positive cells on the other.

scholarly journals Interactions between a luteovirus and the GroEL chaperonin protein of the symbiotic bacterium Buchnera aphidicola of aphids

2011 ◽  
Vol 92 (6) ◽  
pp. 1467-1474 ◽  
Author(s):  
Sophie Bouvaine ◽  
Neil Boonham ◽  
Angela E. Douglas
Keyword(s):  
Binding Site ◽  
Barley Yellow Dwarf Virus ◽  
Fat Body ◽  
Symbiotic Bacterium ◽  
Plant Viruses ◽  
Virus Binding ◽  
Buchnera Aphidicola ◽  
Virus Particles ◽  
Groel Protein ◽  
Virus Interactions

Luteoviruses and poleroviruses are important plant viruses transmitted exclusively by aphids in a circulative manner via the aphid haemolymph. A chaperonin protein, GroEL, synthesized in aphids by a symbiotic bacterium, Buchnera aphidicola, is hypothesized to bind to virus particles in the haemolymph, thereby promoting transmission. To investigate this hypothesis, the GroEL-binding site for barley yellow dwarf virus (BYDV) was determined in vitro, and the abundance of GroEL protein in different aphid tissues was investigated. Virus binding to a peptide library representing the full GroEL molecule revealed a single binding site that coincides with the site that anchors two GroEL rings to form the native GroEL tetradecamer. In the functional form of the GroEL protein, virus binding would compete with the formation of the two GroEL rings. Using a mAb raised against a Buchnera-specific GroEL epitope, GroEL was detected in Buchnera cells by immunoblotting and immunocytochemistry, but not in the aphid haemolymph, fat body or gut. From the prediction here that GroEL–virus interactions are probably severely limited by competition with other GroEL molecules, and the evidence that GroEL is not available to interact with virus particles in vivo, it is concluded that GroEL–virus interactions are unlikely to contribute to virus transmission by aphids.

THE EFFECT OF COOKED POTATO IN CONJUNCTION WITH FERMENTABLE CARBOHYDRATE IN BREADMAKING

1932 ◽  
Vol 6 (5) ◽  
pp. 548-559
Author(s):  
R. H. Harris
Keyword(s):  
Protein Content ◽  
Sweet Potato ◽  
Significant Relationship ◽  
Simple Formula ◽  
Potassium Bromate ◽  
Loaf Volume ◽  
Fermentable Sugar ◽  
White Potato ◽  
Different Types ◽  
Diastatic Activity

A series of 11 flours of different types and baking strengths were baked by a variety of methods in order to determine the effect of adding fermentable sugar to the dough in conjunction with cooked white and sweet potato. Preliminary bakings using a simple formula of flour, water, yeast, and salt, with and without sucrose indicated the value of sucrose in flours of low diastatic power.The addition of cooked white potato in the absence of sucrose gave still poorer results with these low diastatic flours, but improved the better flours. The addition of sucrose increased the response of all flours, the maximum stimulation being obtained when both malt and sucrose were added. Evidently, cooked white potato is not a satisfactory substitute for fermentable sugars.It was found that cooked sweet potato not only supported yeast activity, but also stimulated it. However, it also imparted a deleterious dark tint to the loaf, thus lowering the color score.The addition of potassium bromate without sucrose resulted in a greater loaf volume than that obtained by the use of the simple formula with sucrose, except in the case of two flours, particularly low in diastatic activity. The inclusion of diastatic malt increased the loaf volumes of these two flours.No significant relationship was found between protein content and loaf volume, in the absence of added fermentable carbohydrate. The addition of sucrose and malt to bakings with potato extract resulted in correlations equal to those obtained with other flour improvers.

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