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Wyświetlanie 1-4 z 4
Tytuł:
Additivity interactions between fluconazole and citrus essential oils to Aspergillus fumigatus
Autorzy:
Wroblewska-Luczka, P.
Luszczki, J.
Powiązania:
https://bibliotekanauki.pl/articles/2098525.pdf
Data publikacji:
2021
Wydawca:
Instytut Medycyny Wsi
Tematy:
Aspergillus fumigatus
mycosis
mould
interaction
fluconazole
essential oil
antifungal property
antibacterial property
antiinflammatory property
isobolographic analysis
Opis:
Introduction. Aspergillus fumigatus is the most common pathogen causing allergic bronchopulmonary mycosis. The pathogenic capacity of Aspergillus fumigatus is related to its thermal tolerance and the small size of the spores which enables transfer to the respiratory tract. In the case of fungal diseases, their treatment is based on fungicidal antibiotics, such as fluconazole. Due to the growing problem of drug resistance, new therapeutic solutions are sought, especially of natural origin. Essential oils, due to their anti-bacterial, anti-fungal, anti-inflammatory and immunostimulatory properties, constitute interesting research material in the fight against mould. Objective. The aim of the study was to assess the type of pharmacodynamic interactions between fluconazole and selected essential oils: lemon, orange, tangerine, and grapefruit in an in vitro study against Aspergillus fumigatus. Isobolographic analysis of the results allowed determining the type of interactions between fluconazole and the tested essential oils. Results. According to the research results, a IC50 dose of fluconazole versus Aspergillus fumigatus IC50 = 1.87±0.88mg/ml. The most active essential oil was lemon oil, which at the concentration of 4% in medium completely inhibited the growth of Aspergillus fumigatus. Tangerine essential oil is the least active against A. fumigatus. Isobolographic analysis of the interactions between fluconazole and essential oils showed additive interactions for the combination of fluconazole with lemon, orange and grapefruit ols, and an additive interaction with a tendency to synergism for the combination of fluconazole with tangerine oil. Conclusions. Isobographic analysis can contribute to the introduction of natural substances into the therapy of many diseases.
Źródło:
Journal of Pre-Clinical and Clinical Research; 2021, 15, 3; 116-120
1898-2395
Pojawia się w:
Journal of Pre-Clinical and Clinical Research
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Manipulation of vanillin synthesis genes in flax
Autorzy:
Pastor, M.
Boba, A.
Zuk, M.
Szopa-Skorkowski, J.
Powiązania:
https://bibliotekanauki.pl/articles/951296.pdf
Data publikacji:
2015
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
vanillin synthesis
flax
secondary metabolite
antifungal property
antibacterial property
antiinflammatory property
antioxidant property
oligonucleotide synthesis
DNA fragment
homologous gene
Źródło:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology; 2015, 96, 1
0860-7796
Pojawia się w:
BioTechnologia. Journal of Biotechnology Computational Biology and Bionanotechnology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Anti-pathogenic properties of plant peptide hormone phytosulfokines [PSKs] and its selected analogues
Autorzy:
Bahyrycz, A.
Saniewska, A.
Konopinska, D.
Powiązania:
https://bibliotekanauki.pl/articles/55358.pdf
Data publikacji:
2008
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
antipathogenic property
Botrytis tulipae
antifungal activity
Phoma narcissi
phytosulphokine-alpha
plant peptide hormone
phytosulphokine-beta analogue
Opis:

Phytosulfokine-α (PSK-α) (H-Tyr(SO3H)-Ile-Tyr(SO3H)-Thr-Gln- OH) (I), a sulfated growth factor universally found in both monocotyledons and dicotyledons, strongly promotes proliferation of plant cells in culture. The C-terminal truncated analog named PSK-β (Tyr(SO3H)-Ile-Tyr(SO3H)-Thr) (II) showed a 10-fold lower activity than that of the parent pentapeptide. Because PSK-α promotes proliferation and differentiation during the plant growth we undertook the studies on the influence of PSK-α on plant defense mechanisms in that period. In present studies on PSK-α (I), PSK-β (II), and its analogues, we performed a search of another biological properties. The aim of our investigation was evaluation of PSK-α, PSK-β and their selected analogues in relation to growth and development of plant pathogens, such as Phoma narcissi and Botrytis tulipae. In these studies we elaborated the synthesis of PSK-α or PSK-β and their 22 analogues modified by natural and non-natural amino acid residues. Peptides were synthesized by the solid phase method according to the Fmoc procedure on a Wang-resin. Free peptides were released from the resin by 95% TFA in the presence of EDT. Biological effect of these peptides was evaluated by test on the growth and development of pathogens of P. narcissi and B. tulipae.

Źródło:
Pestycydy; 2008, 1-2; 109-117
0208-8703
Pojawia się w:
Pestycydy
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The search for new biological activities for selected insect peptides
Autorzy:
Kuczer, M.
Dziubasik, K.
Luczak, M.
Majewska, A.
Kamysz, W.
Saniewska, A.
Konopinska, D.
Powiązania:
https://bibliotekanauki.pl/articles/55140.pdf
Data publikacji:
2008
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
antitumour peptide
antifungal activity
antiviral peptide
oostatic peptide
antiviral activity
Phoma narcissi
Botrytis tulipae
colony growth
biological property
antimicrobial activity
insect peptide
biological activity
insect
peptide
Opis:
New biological properties of selected insect peptides are presented. The subjects of the investigation included insect oostatic peptides, like Neb-colloostatin (I) and Neb-TMOF(II), and/or insect peptides with antiviral or antitumor activity, such as alloferon (III) and its analogues modified at position 1 of the peptide chain. In the study was also included the oligopeptide Any-GS (VII) and its truncated analogues. The peptides were tested for antimicrobial activity on a series of bacterial species, antiviral activity against Human Herpes Virus type 1 (HHV-1) in vitro using a Vero cell line, and the growth and development of plant pathogens Phoma narcissi and Botrytis tulipae. The results of the biological investigations indicate that among the peptides investigated, compounds VII and IX inhibit the growth of plant pathogens P. narcissi and B. tulipae, whereas compounds I and II stimulate the mycelium growth of the aforementioned pathogens. Other peptides show slow antimicrobial activity but do not inhibit the replication of HHV-1 in Vero cells.
Źródło:
Pestycydy; 2008, 1-2; 5-11
0208-8703
Pojawia się w:
Pestycydy
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

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