No description available.

Acute effects of repeated sprinting upon serum creatine kinase (CK), lactic dehydrogenase (LDH), and isozymal activities were studied in five collegiate runners (R_s) and six non-runners (NR_s ). After an intermittent running treadmill test, blood sampling showed three-fold mean increases in CK with no change in LDH in both groups; group differences were insignificant (p>.05). Results suggest (1) intense anaerobic exercise produces moderate enzyme elevations; (2) relatively equivalent exercise intensities are critical to enzyme responses in exercising individuals of varying fitness levels; and (3) exercise-induced enzyme release may be consequential to muscle cell membrane permeability changes from decreased intracellular high-energy phosphates.

A study of the adaptive changes of some enzyme activities to the dietary protein intake was made in the liver, kidney, and pancreas of rats and serum of humans. The rats fed the 40 per cent casein diet had a higher rate of weight gain and the weights of the liver and kidney were higher than in the rats fed the 10 per cent casein diet. Three enzymes involved in the elimination of excess nitrogen from the body were found to show a similar response to increased dietary protein intake. These enzymes were: D-amino acid oxidase in the kidneys, arginase in the liver and kidneys, and glutamic-pyruvic transaminase in the liver of rats. The rate of enzyme induction was detectable the second day, being high during the first four days and reaching the maximum value on the fourth day. Thereafter, the enzymatic activity did not change much. The alkaline phosphatase activities in the liver and kidneys of the rats did not show significant change during consumption of the diets containing 10 per cent or 40 per cent casein. Samples of pancreatic trypsinogen and chymotrypsinogen of the rats were not collected during the appropriate time to note any significant changes caused by the diets . A more appropriate experimental design, including proper timing for feedings and dissections, for the study of the adaptation of the proteolytic enzymes in the pancreas of the rats is desirable and recommended. The values for the circulating enzymes of the human serum, 0-amino acid oxidase, glutamic-pyruvic transaminase, and alkaline phosphatase were not found to be affected significantly by the diets containing 12 per cent and 30 per cent protein calories.

In this study, effect of cold stress on physiology and biochemistry of two Turkish barley cultivars, winter type Tarm-92 and spring type Zafer-160, was studied. For chilling stress treatment, cultivars were exposed to +4 &ordm / C for 1, 3 and 7 days, and for freezing stress application acclimated cultivars (+4 &ordm / C for 3 days) were treated with -3 &ordm / C and -7 &ordm / C. After freezing stress treatment, a recovery period was applied for 4 days at 4 &ordm / C. Following analyses were performed on leaf and root tissues: growth parameters (length, wet-dry weights), malondialdehyde (MDA) content, proline content, hydrogen peroxide content (H2O2) electrolyte leakage, PS II fluorescence (Fv/Fm), antioxidant enzyme activities such as catalase (CAT: EC 1.11.1.6), ascorbate peroxidase (APX: EC 1.11.1.11) and glutathione reductase (GR: EC 1.6.4.2). It was observed that effect of cold was more at freezing temperatures than chilling temperature. Cold dependent damage was more obvious as the duration of chilling temperature increased. Growth retardation, membrane damage, leaf catalase deactivation were more apparent and leaf glutathione reductase activity increase was less in spring type cultivar Zafer than in winter type Tarm. These results indicated that winter type barley cultivar is more cold tolerant than spring type barley.

Thesis (M. Sc. Agriculture (Soil Science)) -- University of Limpopo, 2015 / The activity and functional diversity of micro-organisms contribute to the stability and productivity of agro-ecosystems. Soil micro-organisms and enzyme activities have been suggested as potential indicators of soil quality. Hence, management practices that can enhance microbial diversity and enzyme activities are essential for improving soil health and soil fertility status. The aim of the study was to assess the effects of compost maturity age on the change in bio-quality indicators of compost and compost amended soil. Cattle manure-rich compost was prepared through thermophilic windrow composting using cattle manure and wood chips mixed at a proportion of 4:1 (w/w) to achieve a C:N ratio of 30:1. This compost was sampled at regular intervals of 30 days after the initiation of the composting process until 150 days when it was finally cured. Compost samples of varying degrees of maturity age were air-dried, pulverised and mixed with 1.2 kg surface soil at an equivalent rate of 100 kg P ha-1. Each compost amended soil was transferred into well labelled plastic pots for incubation. Sampling of incubated amended soils was performed at 7 days interval until 42 days; and the samples were used for microbial count, enzyme activity, and mineralisation assessments. Data generated were analysed as factorial experiment using SYSTAT package. Treatment and interaction effects were evaluated using Fisher protected least significant difference at probability level of 5%. Results of the chemical composition of the different composts are similar and comparable. Variation in compost maturity date, incubation time and their interaction exerted significant effects on the measured microbial counts and enzyme activities as bio-quality indicators. The content of bacteriameasured was consistently highest at each sampling date followed by the actinomycetes while fungi population count remained persistently lowest. Bacteria and β-glucosidase represent the dominant microbe and enzyme, respectively in all compost samples taken at different maturity age.The highest count of actinomycetes (6.18 CFU g-1), bacterial (6.73 CFU g-1) and fungi (3.06 CFU g-1) were obtained during the 42-day incubation period.Of all the enzyme activities studied, β-glucosidase content was consistently highest in all compost samples across the sampling dates. Similarly, the highest concentration of ß-glucosidase (3076 mg kg-1 hr-1), phosphatase (1480 mg kg-1 hr-1), dehydrogenase iv (120.07 μg INF g-1 2hr-1) and urease (26.15 mg kg-1 2hr-1) were obtained during the 42-day incubation period. The highest microbial counts and enzyme activities were reached beyond 19 days after incubation. Maximum Bray P1 (20.10 mg kg-1), ammonium N (108 mg kg-1) and nitrate N (189 mg kg-1) were obtained at 42, 14 and 42 days after incubation, respectively. The measured temporal change in the concentrations of bio-quality parameters in the compost-amended soils were highest in compost sampled at 90 days, except for phosphatase, indicating the peak of the thermophilic process. The bio-quality parameters of these composts and the compost amended soil were influenced by compost maturity and incubation time. The uses of mature compost with desirable level of bio-quality indicators are crucial for fertility management and improved soil health. Keywords: Compost maturity, enzyme activities, microbial count, nutrient release, soil fertility

Yeasts form significant and important part of pedosphere microbiota. They keep nature balance, participate in cycles of elements and nutrients, are antagonists of various pathogens and as important decomposers, they produce the whole spectrum of different extracellular enzymes. The aim of this study was to determine the ability of yeasts, isolated from the soil adjacent to the fruit trees in Southwest Slovakia as well as from the contaminated soil (Pernek area, Slovakia), to produce extracellular enzymes. In total, 68 strains belonging to 45 different species were tested for the production of starch-like polysaccharide and for extracellular enzyme activities: polygalacturonases, lipases, proteases, cellulases, chitinases, -glucosidases and -amylases. This work was also focused on optimization of method for the yeast chitinase assay. Four methods were proved; two of them utilized liquid medium with chitin (colloidal and insoluble) as the sole carbon source and two others used solid plate methods with agar medium containing chitin. Based on results, cultivation in colloidal liquid chitin medium, terminated by the chitinase assay according to Ehrlich, was evaluated as the best method for detection of predominant exochitinase activity of yeasts. More than 75 % of tested yeasts exhibited some extracellular activity. Generally, the yeasts isolated from the soil under the fruit trees showed broader spectrum of enzyme activities than those originated from contaminated soils. Lipases, proteases and -glucosidases were found to be the most common activities. Only small proportion of yeasts was able to produce chitinases and/or cellulases. Aureobasidium pullulans, CCY 27-1-134, from the soil adjacent to the apple tree, showed the widest range of activities from all tested strains and it possessed all examined activities. On the other side, it did not produce starch-like polysaccharide. Tausonia (Trichosporon) pullulans and Cystofilobasidium macerans were the second most active producers of extracellular enzymes with variations in production of cellulases and -amylases. Representatives of the former polyphyletic genus Cryptococcus exhibited lipases, -glucosidases, -amylases and they were producers of the starch, but the interspecies differences were also noted. All strains of the genus Galactomyces were positive for polygalacturonases and the genera Candida and Cyberlindnera were positive for -glucosidases. All strains of Galactomyces candidum were tested for the production of polygalacturonases during 168 hours long cultivation on pectin media. Strain CCY 16-3-4 showed very stable growth on this medium and simultaneously exhibited significant amount of extracellular polygalactouronases. It has a potential to be very suitable producer of these enzymes but particular characterization of properties is necessary for its future use. Results of the screening showed that the production of extracellular enzymes is mostly strain-dependent and not species-dependent.

The effects of diabetes on cytochrome P450 dependent drug metabolizing enzymes have not to be clarified yet. The most widely used animals in these studies have been rats, and information regarding the effects of diabetes on cytochrome P450 dependent procarcinogen/carcinogen metabolism in rabbits is limited. In the present study, we investigated, for the first time, the influence of benzene on liver, kidney and lung microsomal cytochrome P450 dependent drug metabolizing enzyme activities, protein and mRNA levels in diabetic and non-diabetic rabbits. Male New Zealand rabbits were made diabetic by a single dose of alloxan treatment in this study. AST, ALT and LDH enzyme activities in the blood serum and lipid peroxidation in liver microsomes were found to increase in diabetic, benzene treated and benzene treated diabetic rabbits. Besides these, CYP2E1 dependent NDMA N-demethylase and p-nitrophenol hydroxylase activities and CYP2E1 protein level were found to increase in liver and kidney of diabetic and benzene-treated rabbits. The combined effects of benzene and diabetes on these activities and protein level were found to be additive. Although diabetes caused induction of pulmonary CYP2E1 protein level and associated enzyme activities, benzene treatment of rabbits resulted in no change in enzyme activities and protein level in lung. The level of mRNA was investigated by Real-Time PCR. Accordingly, hepatic CYP2E1 mRNA level was increased 6.71-, 10.53- and 12.93-fold in diabetic, benzene treated and benzene treated diabetic rabbits with respect to the control animals. Similarly, renal CYP2E1 mRNA level was found in increase in these rabbits. In addition to CYP2E1, CYP3A6 associated enzyme activity, erythromycin N-demethylase, CYP3A6 protein and mRNA level were found to increase in diabetic rabbit liver and lung. Unlike diabetes, benzene treatment caused suppression of CYP3A6 protein and inhibition of associated enzyme activity in liver. There was no significant change in the erythromycin N-demethylase activity and CYP3A6 level of liver and lung as a result of benzene treatment of diabetic rabbits. Moreover, diabetes induced CYP1A2 protein and mRNA level and CYP1A associated enzyme activities in the rabbit liver. On the other hand, benzene caused statistically insignificant decreases in CYP1A dependent enzyme activities and CYP1A2 protein level in liver. CYP1A associated enzyme activities, CYP1A2 protein and mRNA levels were not changed in the liver of benzene treated diabetics. The results of the present work indicate that both diabetes and benzene stimulate metabolic activation toxic chemicals metabolized by CYP2E1 such as NDMA and benzene by inducing CYP2E1 which results in the formation of increased amounts of reactive metabolites. Application of benzene to diabetic rabbits further elevates expression and activities of the CYP2E1. As a result of additive induction of the CYP2E1 in benzene treated diabetics, further increase the risk of hepatotoxicity produced by toxins may be observed when compared to the separate treatments. This may in turn further potentiate the risk of organ toxicity and mutagenesis in liver and kidney of these subjects. As in the case of CYP2E1, the risk of carcinogenesis due to induction of CYP1A may be increased in diabetic subjects. Moreover, in diabetic and benzene exposed subjects, alteration of drug clearance and clinical drug toxicity may be observed due to induction or suppression of CYP3A.

No description available.

The incomplete degradation of bio-based and biodegradable plastics (BBPs) in soils causes multiple threats to soil quality, human health, and food security. Plastic residuals can interact with soil microbial communities. We aimed to link the structure and enzyme-mediated functional traits of a microbial community composition that were present during poly (butylene succinate-co-butylene adipate (PBSA) decomposition in soil with (PSN) and without (PS) the addition of nitrogen fertilizer ((NH4 )2SO4 ). We identified bacterial (Achromobacter, Luteimonas, Rhodanobacter, and Lysobacter) and fungal (Fusarium, Chaetomium, Clonostachys, Fusicolla, and Acremonium) taxa that were linked to the activities of ß-glucosidase, chitinase, phosphatase, and lipase in plastic-amended soils. Fungal biomass increased by 1.7 and 4 times in PS and PSN treatment, respectively, as compared to nonplastic amended soil. PBSA significantly changed the relationships between soil properties (C: N ratio, TN, and pH) and microbial community structure; however, the relationships between fungal biomass and soil enzyme activities remained constant. PBSA significantly altered the relationship between fungal biomass and acid phosphatase. We demonstrated that although the soil functions related to nutrient cycling were not negatively affected in PSN treatment, potential negative effects are reasoned by the enrichment of plant pathogens. We concluded that in comparison to fungi, the bacteria demonstrated a broader functional spectrum in the BBP degradation process

No description available.