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Number of results: 8
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Abstract

The paper presents microbiological characteristic of sewage sludge composted in controlled conditions together with biowastes (wheat, maize and rapeseed straw, sawdust and refined glycerol). An experiment was carried out in which the material was mixed at appropriate weight proportions and then placed in bioreactor chambers of constant air flow (4 lźmin-1). The performed composting process aimed at determining the developmental dynamics of heterotrophic bacteria, molds, actinomycetes as well as bacteria from Salmonella genus and Enterobacteriaceae family. Microbiological analyses were performed on selective substrates using Koch's plate method. Moreover, using the floatation method, the presence of live eggs of ATT (Ascaris spp., Trichuris spp., Toxocara spp.) intestinal parasites was assessed and levels of dehydrogenase activity were determined using 1% triphenylotetrazole chloride as a substrate. It was concluded, on the basis of the obtained research results, that the composting process reduced bacterial counts of heterotrophic bacteria, molds and the activity of dehydrogenases activity in all experimental treatments. On the other hand, no reduction was observed in quantities of actinomycetes in the composted materials whose changes in numbers were found to correlate positively most strongly with levels of dehydrogenases activity. In addition, it was found that changes in numbers of the analysed groups of microorganisms depended, primarily, on the pH value and concentrations of ammonia released from the composted materials. Furthermore, the obtained research results also revealed that the sewage sludge used in the experiment did not contain Salmonella spp. bacteria and live eggs of ATT intestinal parasites, and that the composting process reduced completely numbers of bacteria from the Enterobacteriaceae family in all compost treatments. The obtained composts fulfilled all sanitary standards complying with the requirements issued by the Minister of Agriculture and Rural Development (2008) as well as with the EU regulation (EC) No. 185/2007 from February 2007 changing EEC regulations No. 809/2003 and No. 810/2003 connected with the extension of the period of transitional requirements for composting and biogas plants as provided by the EU regulation No. 1774/2002 of the European Parliament and Council.

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Authors and Affiliations

Agnieszka Wolna-Maruwka
Krzysztof Pilarski
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Abstract

The paper presents the research results for the soils sampled from the area located in the eastern part of the Chodzieskie Lakes, between the Middle Noteć River Valley and the Wełna River Valley, the right tributary of the Warta River. The research involved 7 soil samples from the surface horizons, allocated to the cultivation of various plant species (cereals and vegetable crops). The following were determined in the soil material: the content of phytoavailable forms of selected heavy metals Zn, Cu, Pb, Ni, Fe and Mn, active and available to plants phosphorus against the activity of selected oxydo-reduction and hydrolytic enzymes. The soil under the vegetable crops showed a very high richness in phosphorus available to plants, which must have been related to an intensive fertilisation. There were identified relatively low contents of the available forms of the heavy metals investigated, the fact that points to their natural content in soil, which triggered the inhibition of neither the oxydo-reduction nor hydrolytic enzymes.

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Authors and Affiliations

Joanna Lemanowicz
Agata Bartkowiak
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Abstract

This study aimed to determine the levels of milk cell total protein (TP), reduced nicotinamide adenine dinucleotide phosphate (NADPH), total glutathione (tGSH), activities of glucose-6-phos- phate dehydrogenase (G6PD) and glutathione peroxidase (GPx) in subclinical mastitic cows. Milk from each udder was collected and grouped by the California Mastitis Test. Then, a somatic cell count (SCC) was performed, and the groups were re-scored as control (5–87 × 103 cells), 1st group (154–381 × 103 cells), 2nd group (418–851 × 103 cells), 3rd group (914–1958 × 103 cells), and 4th group (2275–8528 × 103 cells). Milk cell TP, NADPH, tGSH levels, G6PD, and GPx ac- tivities were assessed. Microbiological diagnosis and aerobic mesophyle general organism (AMG, cfu/g) were also conducted. In mastitic milk, TP, NADPH, and tGSH levels, and G6PD and GPx activities were significantly reduced per cell (in samples of 106 cells). In addition, milk SCC was positively correlated with AMG (r=0.561, p<0.001), NADPH (r=0.380, p<0.01), TP (r=0.347, p<0.01) and G6PD (r=0.540, p<0.001). There was also positive correlation between NADPH (r=0.428, p<0.01), TP (r=0.638, p<0.001) and AMG. NADPH was positively correlated with TP (r=0.239, p<0.05), GPx (r=0.265, p<0.05) and G6PD (r=0.248, p=0.056). Total protein was positively correlated with tGSH (r=0.354, p<0.01) and G6PD (r=0.643, p<0.001). There was a negative correlation between tGSH and GPx activity (r=-0.306, p<0.05). The microbiological analysis showed the following ratio of pathogens: Coagulase-Negative Staphylococci 66.6%, Streptococcus spp 9.5%, Bacillus spp 9.5%, yeast 4.8%, and mixed infections 9.5%.

As a conclusion, when evaluating the enzyme and oxidative stress parameters in milk, it is more suitable to assign values based on cell count rather than ml of milk. The linear correlation between the SCC and AMG, milk cell NADPH, TP and G6PD suggests that these parameters could be used as markers of mastitis.

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Authors and Affiliations

P.P. Akalin
Y. Ergün
N. Başpinar
G. Doğruer
A. Küçükgül
Z. Cantekin
M. İşgör
M. Saribay
E. Koldaş
A. Baştan
S. Salar
S. Pehlivanlar
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Abstract

5-fluorouracil (5-FU), which is a commonly used chemotherapy agent exerts undesired cardiac toxicity. Mitochondrial dysfunction is thought to be one of potentially important mechanisms of 5-FU- induced cardiotoxicity. α-ketoglutarate dehydrogenase (α-KGDHC) is the key regulatory enzyme of TCA cycle. The complex consists of multiple copies of three catalytic subunits: α-ketoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and dihydrolipoamide dehydrogenase (E3). α-KGDHC together with branched chain α-ketoacid dehydrogenase (BCKDHC) and pyruvate dehydrogenase (PDHC), are the members of 2-oxoacid dehydrogenases family that share some structural and functional similarities. Recently, it has been found that 5-FU stimulates BCKDHC in rat’s cardiac muscle. Therefore, we hypothesize that 5-FU modifies α-KGDHC activity and affects cardiac muscle metabolism. The aim of this study was to determine the effect of 5-FU on α-KGDHC activity and protein levels of E1 and E2 subunits of the complex in rat’s cardiac muscle. Wistar male rats were administered with 4 doses of 5-FU, 150 mg/kg b.wt. each (study group) or 0.3% methylcellulose (control group). α-KGDHC activity was assayed spectrophotometrically. The E1 and E2 proteins levels were quantified by Western blot. 5-FU administration resulted in stimulation of myocardial α-KGDHC activity in rats. In addition, E2 protein level increased in response to 5-FU treatment, while the E1 protein level remained unchanged. Up- regulation of α-KGDHC appears to result from change in E2 subunit protein level. However, the effect of 5-FU on factors modifying α-KGDHC activity at post-translational level cannot be excluded.
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Authors and Affiliations

Małgorzata Knapik-Czajka
1
Anna Gawędzka
1
Michał Jurczyk
2
Jagoda Drąg
1
Małgorzata Belczyk
1
Veronika Aleksandrovych
2
Anna Gil
3
Krzysztof Gil
1

  1. Department of Biochemical Analytics, Jagiellonian University Medical College, Kraków, Poland
  2. Department of Pathophysiology, Jagiellonian University Medical College, Kraków, Poland
  3. Department of Anatomy, Jagiellonian University Medical College, Kraków, Poland
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Abstract

In the present work, the dried biomass of soil isolated fungus Eurotium cristatum was used for synthesizing silver na-noparticles (AgNPs). The synthesized AgNPs were spherical in shape with average diameter of 16.56 nm and displayed maximum absorbance at 418. Fourier transform infrared (FTIR) study indicated the presence and binding of proteins with myco-produced silver nanoparticles. The optimum conditions for AgNPs biosynthesis were found to be at temperature of 40°C, pH of 8.0, substrate concentration of 500 ppm and fungal biomass wt. of 0.8 g. The AgNPs showed antibacterial ac-tivity against Staphylococcus aureus, Listeria monocytogenes, Escherichia coli and Shigella flexneri. AgNPs was built-in thin film nanocomposite (TFNC) membrane and the impacts of nanomaterial composition on membrane properties and de-salination process were studied. The AgNPs produced membrane TFNC had better filtration performances than pure thin film composite membrane TFC. The TFNC membrane had enhanced water flux (32.0 vs. 16.5 dm3∙m–2∙h–1) and advanced NaCl rejection (91.7 vs. 89%) compared to the TFC membrane. A pot experiment was conducted to evaluate the effect of the irrigation with desalinated water on yield and productivity of essential oil of the sweet basil (Ocimum basilicum L.) and lavender (Lavandula multifida L.). The irrigation with desalinated water reduced significantly the soil reaction, soil electri-cal conductivity (EC), sodium adsorption ratio and exchangeable sodium percent in rhizospheric soil, it also enhanced the growth and oil yield of both plants compared with those irrigated with salt water.

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Authors and Affiliations

Rabaa Yaseen
Yousra Kotp
Doaa Eissa
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Abstract

White adipose tissue plays an important role in the catabolism of branched chain amino acids (BCAAs). Two initial regulatory steps in BCAAs catabolism are catalyzed by branched chain aminotrans-ferase (BCAT) and branched chain α-keto acid dehydrogenase complex (BCKDH complex), respectively. It has been demonstrated that synthetic ligands for PPARγ receptors increased mRNA levels for enzymes involved in BCAAs catabolism. We hypothesized that feeding rats with diet rich in linoleic acid (LA), a natural PPARγ agonist modifies mRNA levels for enzymes catalyzing BCAAs degradation in adipose tissue. The current pilot study was aimed at the investigation of the effect of diet rich in LA on mRNA levels for BCATm, branched chain α-keto acid dehydrogenase (E1 component of the BCKDH), and mRNA levels for the regulatory enzymes of BCKDH complex, a specific kinase (BDK) and a specific phosphatase (PPM1K) in epididymal white adipose tissue (eWAT). Wistar male rats were fed with high unsaturated fat diet containing mainly linoleic acid (study group) or with the high saturated fat diet (control group). The relative mRNA levels were quantified by reverse transcription PCR. We have found that in rats fed diet rich in LA mRNA level for BCATm decreased, while mRNA amount for BDK increased. There was no difference between mRNA levels for BCKDH E1 and PPM1K. It is con-ceivable that changes in mRNA levels for enzymes involved in BCAAs metabolism in eWAT may lead to modification of BCAAs catabolic rate. Further studies are required to fully elucidate this issue.
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Authors and Affiliations

Małgorzata Knapik-Czajka
1
Justyna Bieleń
1
Monika Zajonz
1
Anna Gawędzka
1
Jagoda Drąg
1
Małgorzata Belczyk
1

  1. Department of Biochemical Analytics, Jagiellonian University Medical College, Kraków, Poland
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Abstract

Undisturbed branched-chain amino acids (BCAA) catabolism is necessary for normal heart function. The key enzyme in BCAA catabolism is a multienzyme branched-chain α-keto acid dehydro-genase complex (BCKDH). BCKDH activity is regulated mainly by reversible dephosphorylation (activa-tion)/phosphorylation (inactivation) cycle catalyzed by regulatory enzymes, a specific phosphatase (PPM1K) and kinase (BDK). 5-fluorouracil (5-FU) is widely used in the treatment of different types of cancer. 5-FU has the potential to cause a wide spectrum of cardiotoxicity, ranging from asymptomatic electrocardiographic changes to cardiomyopathy and subsequent cardiac failure. We hypothesize that 5-FU modifies BCKDH activity and affects cardiac muscle metabolism. The current study was aimed at the investigation of the in vivo effect of 5-FU on BCKDH activity and mRNA levels for E1, PPM1K and BDK. Wistar male rats were administered with 4 doses of 5-FU, 150 mg/kg b.wt. each (study group) or 0.3% methylcellulose (control group). BCKDH activity was assayed spectrophotometrically. The mRNA levels were quantified by real-time PCR. 5-FU treatment caused an increase in BCKDH activity that appears to result mainly from increased dephosphorylation of the complex and is associated with an increase of PPM1K mRNA level and reduction of BDK and E1 mRNA levels. It is conceivable that 5-FU stimulation of BCKDH is an adaptive reaction with the purpose of enhancing the BCAA catabolism and protecting from toxic effect caused by excessive accumulation of these amino acids in heart.
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Authors and Affiliations

Małgorzata Knapik-Czajka
1
Michał Jurczyk
2
Justyna Bieleń
1
Veronika Aleksandrovych
2
Anna Gawędzka
1
Paulina Stach
2
Jagoda Drąg
1
Krzysztof Gil
3

  1. Department of Biochemical Analytics, Jagiellonian University Medical College, Kraków, Poland
  2. Department of Pathophysiology, Jagiellonian University Medical College, Kraków, Poland
  3. 2Department of Pathophysiology, Jagiellonian University Medical College, Kraków, Poland

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