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Dwa chińskie preparaty bionawożeniowe Juwei i C. B. I. uruchamiające K i P z minerałów glebowych przebadano pod względem przeżywalności zawartych w nich aktywnych mikroorganizmów podczas przechowywania i po wprowadzeniu do gleby opłaszczonych C. B. I. nasion. Po 10 miesięcznym okresie przechowywania liczebność aktywnych bakterii w Juwei obniżyła się o 1 rząd wielkości. Nie stwierdzono zmian w liczebności bakterii rozpuszczających fosforany wapnia i potasu w glebie po wprowadzeniu opłaszczonych biopreparatem nasion rzodkiewki. Liczebność bakterii uruchamiających fosfor i potas stwierdzona na jednym ziarnie kukurydzy opłaszczonym preparatem C. B. I., była 10-krotnie wyższa niż liczebność takich bakterii występująca w 1 gramie suchej gleby użytej w doświadczeniu. Badane biopreparaty były barwy czarnej, wyglądem przypominały mursz i wykazywały lekko kwaśny odczyn. Pod względem składu chemicznego biopreparat C. B. I. zawierał więcej materii organicznej, ogólnego potasu, magnezu i wapnia i mniej przyswajalnego i ogólnego fosforu niż preparat Juwei. Nie stwierdzono w nich natomiast substancji szkodliwych (metale ciężkie, pestycydy chloroorganiczne i PCB) w ilościach zagrażających funkcjonowaniu środowiska glebowego.
Background. Microbial and fungal cellulases are known to hydrolyse cellulose, which is ingested as plant material by herbivorous/omnivorous fishes. Microbial enzymes have enormous advantage of being produced in large quantities by established fermentation techniques. The present investigation aims to optimize the environmental and nutritional parameters for fermentation to enhance cellulase production by two bacterial strains isolated from fish gastrointestinal tracts. Materials and Methods. Two bacterial strains, Bacillus subtilis CY5 and Bacillus circulans TP3, isolated from the gastrointestinal tracts of common carp, Cyprinus carpio L., and Mozambique tilapia, Oreochromis mossambicus (Peters, 1852), respectively were identified as potent cellulase producers. Both strains were cultured in tryptone soya broth for 24 h at 32 ± 2°C, when average viable count of 9.75 • 107 cells • mL-1 culture broth was obtained. This was used as the inoculum for the production medium. The fermentation medium was seeded with 1.0%, 2.0%, 3.0%, 4.0%, and 5.0% inoculum (tryptone soya broth) and incubated in static culture at 40°C to standardize the inoculum size for fermentation. The effect of different production parameters, such as fermentation condition, moisture, pH, temperature, inoculum size, and nitrogen sources on cellulase production by the isolated bacterial strains were studied. Results. Cellulase yield was highest (26 U in B. subtilis and 20.2 U in B. circulans) in solid-state fermentation (SSF). Enzyme production in both the isolates increased in an optimum pH range of 7.0 to 7.5. Minimum cellulase production was observed at 45°C, while maximum production was obtained at 40°C. To standardize the fermentation period for cellulase production, production rate was measured at 12-h intervals up to 120 h. Enzyme production increased for 96 h of fermentation in both strains, and decreased thereafter. The enzyme production increased with increased inoculum size up to 3.0 percentage points. Asparagine as the nitrogen source was most effective in B. subtilis CY5, while beef extract proved useful in optimizing enzyme production by B. circulans TP3. Conclusion. The results of this study will help to standardize the requirements for optimum production of cellulase by cellulase-producing fish gut bacteria and might contribute towards better fish feed formulation incorporating plant ingredients, especially in the larval stages when the enzyme system is not efficient.
Regulation and production of Fibrinolytic enzymes from bacterial sources especially from Bacillus strains has taken a leading role in the medical sciences for the treatment of cardiovascular disorders as it removes thrombus or clots adding to its significant role in curing human health issues saving millions. Significant progress has been made during the last few years on the studies of fibrinolytic enzymes in identifying, cloning, purification, characterization and overproduction of these for commercialization in medical sciences and in fields like detergents development. Production of fibrinolytic enzyme from Bacillus circulans was done using Nutrient broth medium. In addition, a strong fibrinolytic enzyme was purified from the cultivation media. The purified enzyme was almost homogeneous with other species of same genus, as examined by SDS−PAGE and sephadex G-75 column chromatography. The enzyme had an optimal pH of 7-12, an optimal temperature of 50 °C, for fibrin hydrolysis. The molecular mass estimated by gel filtration was 24 to36 KDa. Further studies for characterization and structural elucidation are necessary for their medicinal applications and molecular biological characteristics.
Background. Because of the advancement of multiple spawning of carps, the importance of a quality larval diet is increasing day by day. The larval fish do not have the necessary enzyme or the amount of digestive enzymes to digest feed at optimum level. Therefore, fermentation of feed ingredients and/or formulated diets by bacterial enzymes to produce simpler forms of nutrients may be beneficial for them. Materials and Methods. Five isocaloric (4.38 kcalּg-1) and isonitrogenous (35% crude protein approximately) experimental diets (D1-D5) containing 32% fish meal, 34% mustard oil cake, 30% rice bran, and 2% cod liver oil, were fermented in vitro with Bacillus circulans cells (at the rate of 108 bacterial cells per g) at 37oC for 1-5 day duration (1 day: D1, 2 days: D2, 3 days: D3, 4 days: D4, and 5 days: D5). The bacterial strain [extracellular enzyme producer Bacillus circulans (Lr 1.1)] used for fermentation was isolated from the intestine of rohu, Labeo rohita fingerlings. The reference diet (RD), containing same ingredients, was not fermented with bacterial cells. Rohu spawn (av. wt. 0.35 Âą 0.01 mg) were fed ad libitum for 21 days in the laboratory condition at 30 minutes interval starting from 0900 h to 1600 h. Results. Fermentation of diets resulted in an increase in crude protein and free amino acid contents and decrease in crude fibre content. Diets D4 and D5 resulted in best growth and survival (98% and 98.33%, respectively) of rohu spawn compared to those fed with the reference diet (RD) and other experimental groups. A significant positive correlation was obtained between RNA : DNA ratio and specific growth rate (SGR) of 18 dietary groups (6 groups in triplicate). Conclusion. Fermentation of feed ingredients may be practiced as a tool for starter diet formulation to obtain better growth and survival of rohu spawn. The enzyme-producing strain, Bacillus circulans could be used to ferment diets for 4 to 5 days to increase the bioavailability of nutrients.
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