Molybdenum nutrition of isolates of four Aspergillus species

1986 ◽  
Vol 32 (7) ◽  
pp. 557-561 ◽  
Author(s):  
S. C. Agarwala ◽  
C. Chatterjee ◽  
N. Nautiyal ◽  
C. P. Sharma
Keyword(s):  
Acid Phosphatase ◽  
Nitrate Reductase ◽  
Aspergillus Flavus ◽  
Soluble Protein ◽  
Specific Activity ◽  
Succinic Dehydrogenase ◽  
Dry Weight ◽  
Catalase Peroxidase ◽  
Conidial Formation ◽  
Specific Activities

The molybdenum requirement for growth and conidial formation by Aspergillus flavus, A. terreus, and A. sulphureus was found to be 0.2 ppb, which was one-fifth that of an A. niger isolate. Molybdenum deficiency depressed growth, conidial formation, dry weight, soluble protein, and the specific activities of nitrate reductase, succinic dehydrogenase, and aconitase in all the isolates of Aspergillus studied, but the specific activities of catalase and peroxidase were depressed only in isolates of A. niger, A. terreus, and A. flavus. Also, molybdenum deficiency stimulated the specific activities of acid phosphatase and ribonuclease in the A. flavus isolate, although the specific activities of these enzymes decreased in other isolates. Eighteen hours after the addition of molybdenum (5 ppb) to molybdenum-deficient (0.02 ppb) cultures of A. niger, the specific activities of catalase, peroxidase and succinic dehydrogenase were restored in the absence of cycloheximide, while the specific activity of nitrate reductase was recovered even in the presence of the inhibitor. There was no effect on the specific activities of aconitase and acid phosphatase following the addition of molybdenum to molybdenum-deficient cultures of A. niger.

THE PHYSIOLOGY OF HOST-PARASITE RELATIONS: IX. FURTHER OBSERVATIONS ON THE ACCUMULATION OF RADIOACTIVE SUBSTANCES AT RUST INFECTIONS

1961 ◽  
Vol 39 (6) ◽  
pp. 1393-1407 ◽  
Author(s):  
Michael Shaw
Keyword(s):  
Specific Activity ◽  
Dry Weight ◽  
Insoluble Fraction ◽  
Pentose Phosphate ◽  
Accumulation Ratio ◽  
X Ray ◽  
Specific Activities ◽  
Leaf Segments ◽  
Wheat Leaves ◽  
Host Parasite

Wang (Can. J. Botany, 38, 635–642 (1960)) concluded that the accumulation of radioactivity observed on radioautographs at infection sites on rusted leaves fed with C14-labelled substances was 'apparent' rather than real. The ‘accumulation ratio’ is defined as the ratio of the specific activities (c.p.m./mg dry weight of intact tissue) of rust-infected to uninfected areas of infected leaves. Theoretical considerations relating to the radioautography of leaves labelled with C14 and to the measurement of ‘accumulation ratios’ by extraction of C14-labelled substances from rusted and uninfected segments of infected leaves, as well as experimental data, show that Wang's conclusion is not generally applicable.Experimentally, it was shown using polymethacrylate C14 sources that differences in distance between sources and X-ray film of the order of 100 μ had no effect on the intensity of autoradiographs. Rust-infected leaves, fed with radioactive glucose, were radiographed between X-ray plates. Localization of radioactivity at infection sites was observed on both ‘dorsal’ and ‘ventral’ radiographs, indicating a real accumulation per unit area. Ventral were more radioactive than dorsal surfaces. The main development of the fungus occurred on the former. Radioautography revealed that C14 from glucose-1-C14, glucose-6-C14, and uniformly labelled glucose fed to excised wheat leaves became localized at 10-day-old rust infections in 2 hours. ‘Accumulation ratios’ calculated from the specific activity of leaf segments remained close to 1.0 for at least 6 hours after introduction of the tracer, but increased to more than 2 after 24 hours. When ‘accumulation ratios’ were calculated from the specific activities of individual pustules (excised with a punch 1 mm in diameter) and interpustular disks, values greater than 1 were observed in 2 hours, thus confirming the results of autoradiography. Differences between the ‘accumulation ratios’ observed with glucose-6-C14 and glucose-1-C14 were consistent with an increased role of the pentose phosphate pathway at infection sites. Incorporation of C14 from uniformly labelled glucose into the alcohol-insoluble fraction of rusted leaf segments was 2.5-fold that in uninfected segments in 6 hours and 3.65-fold in 24 hours. The humin formed during hydrochloric acid hydrolysis accounted for approximately 50% of the activity of the alcohol-insoluble material. The ‘accumulation ratio’ for the alcohol-soluble material was only 1.56 after 24 hours.All the results support the view (Shaw and Samborski, Can. J. Botany, 34, 389–405 (1956)) that there is a quantitative, metabolically dependent accumulation of C14 from radioactive glucose at vigorous rust infections. The relative roles of fungus and host in this process are discussed briefly.

Isolation and characterization of electrophoretic variants of human prostatic acid phosphatase.

1983 ◽  
Vol 29 (11) ◽  
pp. 1886-1889 ◽  
Author(s):  
M D Hibbard ◽  
R C McCarthy ◽  
H Markowitz
Keyword(s):  
Enzyme Activity ◽  
Acid Phosphatase ◽  
Specific Activity ◽  
Prostatic Acid Phosphatase ◽  
Ph Gradient ◽  
Electrophoretic Variants ◽  
Isolation And Characterization ◽  
Immunochemical Determination ◽  
Km Value ◽  
Specific Activities

Abstract Prostatic acid phosphatase (EC 3.1.3.2) purified from benign hypertrophic prostate tissue was fractionated by preparative slab isoelectric focusing over a pH gradient of 3.16 to 7.16. Twenty-two of 29 fractions contained enzyme activity. We further examined each active fraction by determining the Michaelis-Menten constant and specific activity. The protein concentration used in the latter determination was estimated either spectrophotometrically or immunochemically by three different radioimmunoassays for the enzyme. Determination of specific activities for each fraction directly correlated enzyme activity with an immunochemical determination, which indicated the immunochemical relationships among different molecular species of the enzyme. We found that the Michaelis-Menten constants for the isolated fractions were similar to the Km value for purified, unfractionated enzyme. Most fractions analyzed by each immunoassay had similar specific activities; the few fractions with discrepant specific activities were found at either end of the pH gradient. The similarity in specific activities among the fractions indicates that RIAs involving polyclonal antisera detect all of the electrophoretic variants of the enzyme.

Water availability affects extracellular hydrolytic enzyme production by Aspergillus flavus and Aspergillus parasiticus

2009 ◽  
Vol 2 (3) ◽  
pp. 313-322 ◽  
Author(s):  
S. Alam ◽  
H. Shah ◽  
N. Magan
Keyword(s):  
Acid Phosphatase ◽  
Aspergillus Flavus ◽  
Enzyme Production ◽  
Specific Activity ◽  
Hydrolytic Enzyme ◽  
Hydrolytic Enzymes ◽  
Aflatoxin Production ◽  
Initial Growth ◽  
Wide Range ◽  
Microtitre Plate Assay

The objectives of this study were to examine the effect of different water activities (aw; 0.99, 0.96 and 0.94) and time (up to 120 h) on quantitative and specific enzyme production during germination and initial growth of Aspergillus flavus and A. parasiticus strains at 25 °C. This is an important early indicator of potential for aflatoxin production under conducive conditions. Qualitative API ZYM generic enzyme strips were used to identify key hydrolytic enzymes produced. Subsequently, the temporal effects of aw on the total/specific activity of the key 4-5 hydrolytic enzymes were determined using 4-nitrophenyl substrates in a 96-well microtitre plate assay. The main enzymes produced by germinating conidia of A. flavus were esterase, lipase, acid phosphatase, β-glucosidase and N-acetyl-β-D-glucosaminidase, while for A. parasiticus these were alkaline phosphatase, lipase, acid phosphatase and β-fucosidase for both total (µmol 4-nitrophenol/min/g) and specific activity (nmol 4-nitrophenol/min/µg protein). There were significant increases in the specific activity of all these enzymes of germinating spores of A. flavus (0-120 h) except for β-glucosidase which was maximum at 72 h. The total/specific activities of the enzymes produced by A. flavus were maximum at 0.99 aw, with the exception of acid phosphatase and N-acetyl-β-D-glucosaminidase at 0.94 aw. For A. parasiticus, maximum total activity occurred at 0.99 aw for fucosidase activity, while specific activity was found to be higher at lower aw levels. These enzymes are important in early colonisation of food matrices by these species and single factors (aw, time) and two-way interactions were all statistically significant for the enzymes assayed for both species. These enzymes could be used as an early and rapid indicator of the activity of Aspergillus section flavi species and suggests that rapid infection may occur over a wide range of aw conditions.

scholarly journals Foliar Application of Potassium Nitrate Affects the Growth and Nitrate Reductase Activity in Sunflower and Safflower Leaves under Salinity

2011 ◽  
Vol 39 (2) ◽  
pp. 172 ◽  
Author(s):  
Nusrat JABEEN ◽  
Rafiq AHMAD
Keyword(s):  
Nitrate Reductase ◽  
Leaf Area ◽  
Soluble Protein ◽  
Protein Concentration ◽  
Foliar Application ◽  
Saline Water ◽  
Tap Water ◽  
Reductase Activity ◽  
Dry Weight ◽  
Potassium Nitrate

Effect of foliar application of KNO3 on growth and the activity of nitrate reductase were studied in the leaves of sunflower (Helianthus annuus L.) and safflower (Carthamus tinctorius L.) plants growing under different levels of salinity. The seeds were sown in pots under non saline condition and saline water irrigation was started at three leaf stage after germination. Different concentration of saline water (i.e. 0.3% and 0.6%, equivalent to an EC of 4.8 and 8.6 dS/m respectively) were made by dissolving sea salt per litre of tap water. Nutrient solution of KNO3 was sprayed at the rate of 250 ppm. The concentration of Na+ and Cl- rapidly increased in the leaves of both the plants under salinity stress. In contrast the nitrate (NO3-) and soluble protein concentration were decreased with the increasing salinity. Salinity reduced leaf area, its fresh and dry weight per plant and also inhibited the activity of Nitrate reductase (NRA) enzyme. The application of KNO3 significantly reduced the increasing tendency of Na+ and Cl- and increased leaf area, its fresh and dry weight per plant, NO3- and soluble protein concentration and NR activity in leaves irrespective to the growth of plant under non saline or saline conditions.

The Effect of Cortisone Acetate on Lysosomal Enzyme Levels In Rat Liver

1972 ◽  
Vol 50 (1) ◽  
pp. 20-24 ◽  
Author(s):  
A. Kyaw ◽  
A. Mellors
Keyword(s):  
Acid Phosphatase ◽  
Rat Liver ◽  
Lysosomal Enzyme ◽  
Lysosomal Enzymes ◽  
Specific Activity ◽  
Cortisone Acetate ◽  
Maximum Increase ◽  
Tyrosine Transaminase ◽  
Specific Activities

Increases in the levels of four lysosomal enzymes were measured during the induction of tyrosine transaminase in rat liver by cortisone acetate. Tyrosine transaminase showed a maximum specific activity 2 h after the injection of the steroid hormone whereas lysosomal enzyme levels reached a maximum specific activity at 4 h. The maximum increase in specific activity for 15 injected animals compared to 15 controls was 100% for tyrosine transaminase; 40% for cathepsin A, cathepsin D, and β-N-acetylglucosaminidase; and 10% for acid phosphatase. Increased specific activities from livers of cortisone-acetate-treated rats were observed when lysosomal enzymes were released both by detergent treatment and by freezing and thawing.The increased specific activities were found in the readily solubilized lysosomal enzyme fractions and not in those lysosomal enzyme fractions which remain associated with particulate matter after lysosomal disruption. Similar increased specific activities for acid phosphatase and β-N-acetylglucosaminidase were observed in cultures of Morris hepatoma cells from rat liver when incubated with cortisone acetate in vitro. Thus the response appears to be typical of single cell types.

An International Collaborative Study to Investigate Standardisation of Hirudin Potency

1993 ◽  
Vol 69 (05) ◽  
pp. 430-435 ◽  
Author(s):  
Colin Longstaff ◽  
Man-Yu Wong ◽  
Patrick J Gaffney
Keyword(s):  
Specific Activity ◽  
Collaborative Study ◽  
Residual Activity ◽  
Quality Standard ◽  
Upper Limit ◽  
Assay Procedure ◽  
Specific Activities ◽  
International Collaborative ◽  
Range Of Values ◽  
International Collaborative Study

SummaryAn international collaborative study has been carried out to investigate the reproducibility of hirudin assays in 13 laboratories using four recombinant hirudins and one natural, sulphated product. A simple assay procedure was proposed involving the titration of α-thrombin with inhibitor and measurement of residual activity using a chromogenic substrate. A standard α-thrombin preparation was supplied to ensure that this reagent was of uniform quality throughout the study. The method appeared to present no difficulties and laboratories reported similar potencies for the 5 hirudin samples, in line with expected values. This gave 200–222 Thrombin Inhibitory Units/ampoule (TIU/ampoule) of lyophilised hirudin, with geometric coefficient of variation (gcv) values ranging from 10.15–15.97%. This corresponds to specific activities of approximately 14,300–15,900 TIU/mg protein. This is close to the upper limit of previously reported values of specific activity. We conclude that the precision of this determination compared with the wider range of values in the literature (8,000–16,000 thrombin inhibitory units [TIU]/mg) results from the use of good quality standard α-thrombin by all laboratories. This study has important implications for hirudin standardisation.

STUDIES ON THYROIDAL COLLOID PINOCYTOSIS USING A DOUBLE ISOTOPE TECHNIQUE

1972 ◽  
Vol 70 (1) ◽  
pp. 48-55 ◽  
Author(s):  
Mario A. Pisarev ◽  
Noe Altschuler ◽  
Leslie J. DeGroot
Keyword(s):  
Acid Phosphatase ◽  
Thyroid Hormone ◽  
Trichloroacetic Acid ◽  
Specific Activity ◽  
Acid Precipitation ◽  
Solvent System ◽  
Blood Stream ◽  
Radioactive Materials ◽  
Isotope Technique ◽  
Double Isotope

ABSTRACT The process of secretion of the thyroid hormone involves several steps: pinocytosis of thyroglobulin, fusion of the colloid droplets with the lysosomes, digestion of thyroglobulin by a cathepsin, dehalogenation of tyrosines and release of thyronines into the blood stream. The present paper describes a double isotope technique for studying the first two steps. Thyrotrophin (TSH) administration to rats increased the radioactivity present in all fractions, specially in the 15 000 × g pellet. When the subcellular distribution of acid phosphatase was determined, the highest specific activity was found in this fraction, thus indicating the presence of lysosomes. The content of radioactive materials in the 15 000 × g pellet was analyzed by trichloroacetic acid precipitation and by ascending paper chromatography using n-butanol:ethanol:ammonium hydroxide (5:1:2;v/v) as solvent system. The results obtained showed that 90% of the radioactivity was protein bound and strongly suggest that this material is thyroglobulin.

scholarly journals Gibberellic acid and nitrogen efficiently protect early seedlings growth stage from salt stress damage in Sorghum

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Adam Yousif Adam Ali ◽  
Muhi Eldeen Hussien Ibrahim ◽  
Guisheng Zhou ◽  
Nimir Eltyb Ahmed Nimir ◽  
Aboagla Mohammed Ibrahim Elsiddig ◽  
...  
Keyword(s):  
Chlorophyll Content ◽  
Seedling Growth ◽  
Soluble Protein ◽  
Dry Weight ◽  
Sod Activity ◽  
Seedling Length ◽  
Relative Water ◽  
Emergence Percentage ◽  
Negative Impacts ◽  
Stress Damage

AbstractSalinity one of environmental factor that limits the growth and productivity of crops. This research was done to investigate whether GA3 (0, 144.3, 288.7 and 577.5 μM) and nitrogen fertilizer (0, 90 and 135 kg N ha−1) could mitigate the negative impacts of NaCl (0, 100, and 200 mM NaCl) on emergence percentage, seedling growth and some biochemical parameters. The results showed that high salinity level decreased emergence percentage, seedling growth, relative water content, chlorophyll content (SPAD reading), catalase (CAT) and peroxide (POD), but increased soluble protein content, superoxide dismutase (SOD) activity and malondialdehyde (MDA) content. The SOD activity was decreased by nitrogen. However, the other measurements were increased by nitrogen. The interactive impact between nitrogen and salinity was significant in most parameters except EP, CAT and POD. The seedling length, dry weight, fresh weight, emergence percentage, POD, soluble protein and chlorophyll content were significantly affected by the interaction between GA3 and salinity. The GA3 and nitrogen application was successful mitigating the adverse effects of salinity. The level of 144.3 and 288.7 μm GA3 and the rate of 90 and 135 kg N ha−1 were most effective on many of the attributes studied. Our study suggested that GA3 and nitrogen could efficiently protect early seedlings growth from salinity damage.

scholarly journals Gut Digestive Function and Microbiome after Correction of Experimental Dysbiosis in Rats by Indigenous Bifidobacteria

2021 ◽  
Vol 9 (3) ◽  
pp. 522
Author(s):  
Lyudmila V. Gromova ◽  
Elena I. Ermolenko ◽  
Anastasiya L. Sepp ◽  
Yulia V. Dmitrieva ◽  
Anna S. Alekseeva ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Digestive Enzymes ◽  
Specific Activity ◽  
Control Group ◽  
Enteropathogenic Escherichia Coli ◽  
Beneficial Bacteria ◽  
Opportunistic Bacteria ◽  
Dyspeptic Symptoms ◽  
Specific Activities ◽  
Impaired Motor Function

In recent years, great interest has arisen in the use of autoprobiotics (indigenous bacteria isolated from the organism and introduced into the same organism after growing). This study aimed to evaluate the effects of indigenous bifidobacteria on intestinal microbiota and digestive enzymes in a rat model of antibiotic-associated dysbiosis. Our results showed that indigenous bifidobacteria (the Bf group) accelerate the disappearance of dyspeptic symptoms in rats and prevent an increase in chyme mass in the upper intestine compared to the group without autoprobiotics (the C1 group), but significantly increase the mass of chyme in the colon compared to the C1 group and the control group (healthy animals). In the Bf group in the gut microbiota, the content of opportunistic bacteria (Proteus spp., enteropathogenic Escherichia coli) decreased, and the content of some beneficial bacteria (Bifidobacterium spp., Dorea spp., Blautia spp., the genus Ruminococcus, Prevotella, Oscillospira) changed compared to the control group. Unlike the C1 group, in the Bf group there was no decrease in the specific activities of maltase and alkaline phosphatase in the mucosa of the upper intestine, but the specific activity of maltase was decreased in the colon chyme compared to the control and C1 groups. In the Bf group, the specific activity of aminopeptidase N was reduced in the duodenum mucosa and the colon chyme compared to the control group. We concluded that indigenous bifidobacteria can protect the microbiota and intestinal digestive enzymes in the intestine from disorders caused by dysbiosis; however, there may be impaired motor function of the colon.

scholarly journals THE Ah PHENOTYPE. SURVEY OF FORTY-EIGHT RAT STRAINS AND TWENTY INBRED MOUSE STRAINS

Genetics ◽  
1982 ◽  
Vol 100 (1) ◽  
pp. 79-87
Author(s):  
Daniel W Nebert ◽  
Nancy M Jensen ◽  
Hisashi Shinozuka ◽  
Heinz W Kunz ◽  
Thomas J Gill
Keyword(s):  
Specific Activity ◽  
Inbred Mouse ◽  
Inbred Mouse Strain ◽  
Mouse Strains ◽  
Ah Receptor ◽  
Inbred Mouse Strains ◽  
Sprague Dawley ◽  
Rat Strains ◽  
Specific Activities ◽  
Inbred Rat

ABSTRACT Forty-four inbred and four randombred rat strains and 20 inbred mouse strains were examined for their Ah phenotype by determining the induction of liver microsomal aryl hydrocarbon (benzo[a]pyrene) hydroxylase activity (EC 1.14.14.1) by intraperitoneal treatment with either β-naphthoflavone or 3-methylcholanthrene. All 48 rat strains were found to be Ah-responsive. The maximally induced hydroxylase specific activities of the ALB/Pit, MNR/Pit, MR/Pit, SHR/Pit, and Sprague-Dawley strains were of the same order of magnitude as the basal hydroxylase specific activities of the ACI/Pit, F344/Pit, OKA/Pit, and MNR/N strains. Six of the 20 mouse strains were Ah-nonresponsive (i.e. lacking the normal induction response and presumably lacking detectable amounts of the Ah receptor). The basal hydroxylase specific activities of the BDL/N, NFS/N, STAR/N, and ST/JN mouse strains were more than twice as high as the maximally induced hydroxylase specific activity of the CBA/HT strain.——To date, 24 Ah-nonresponsive mouse strains have been identified, out of a total of 68 known to have been characterized. The reasons for not finding a single Ah-nonresponsive inbred rat strain—as compared with about one Ah-nonresponsive inbred mouse strain found for every three examined—remain unknown.

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