Antifungal Polyamides of Hydroxycinnamic Acids from Sunflower Bee Pollen
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F18%3A43916666" target="_blank" >RIV/60461373:22310/18:43916666 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/60461373:22330/18:43916666 RIV/60461373:22340/18:43916666 RIV/60461373:22810/18:43916666
Výsledek na webu
<a href="http://dx.doi.org/10.1021/acs.jafc.8b03976" target="_blank" >http://dx.doi.org/10.1021/acs.jafc.8b03976</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.jafc.8b03976" target="_blank" >10.1021/acs.jafc.8b03976</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Antifungal Polyamides of Hydroxycinnamic Acids from Sunflower Bee Pollen
Popis výsledku v původním jazyce
The aim of the bioassay-guided fractionation was the selection of the most potent group of compounds responsible for the protection of sunflower bee pollen grains. Synthesis of prospective antifungal polyamides of hydroxycinnamic acids was based on previous structural elucidation of ethanol soluble fraction by H-1,H-1-PFG-COSY, H-1,C-13-HSQC, FT-IR, FT-Raman, and LC-MS experiments. The main compounds found were tri-p-coumaroylspermidines accompanied by other HCAA of spermidine and putrescine. Several model HCAA derivatives were prepared to test their antifungal activity against widespread spoilage fungi (A. niger 42 CCM 8189, F. culmorum DMF 0103, and P. verrucosum DMF 0023). A. niger CCM 8189 and F. culmorum DMF 0103 exhibited higher resistance to the antifungal effects of hydroxycinnamic acid amides, whereas P. verrucosum DMF 0023 was the most sensitive strain. It has been discovered the effect of HCAA polarity on the role of secondary metabolites in the microbial protection of pollen grains. The combination of bioassay-guided fractionation, structural elucidation, selection of prospective compounds, and their synthesis to determine their antifungal properties could be considered as an original approach.
Název v anglickém jazyce
Antifungal Polyamides of Hydroxycinnamic Acids from Sunflower Bee Pollen
Popis výsledku anglicky
The aim of the bioassay-guided fractionation was the selection of the most potent group of compounds responsible for the protection of sunflower bee pollen grains. Synthesis of prospective antifungal polyamides of hydroxycinnamic acids was based on previous structural elucidation of ethanol soluble fraction by H-1,H-1-PFG-COSY, H-1,C-13-HSQC, FT-IR, FT-Raman, and LC-MS experiments. The main compounds found were tri-p-coumaroylspermidines accompanied by other HCAA of spermidine and putrescine. Several model HCAA derivatives were prepared to test their antifungal activity against widespread spoilage fungi (A. niger 42 CCM 8189, F. culmorum DMF 0103, and P. verrucosum DMF 0023). A. niger CCM 8189 and F. culmorum DMF 0103 exhibited higher resistance to the antifungal effects of hydroxycinnamic acid amides, whereas P. verrucosum DMF 0023 was the most sensitive strain. It has been discovered the effect of HCAA polarity on the role of secondary metabolites in the microbial protection of pollen grains. The combination of bioassay-guided fractionation, structural elucidation, selection of prospective compounds, and their synthesis to determine their antifungal properties could be considered as an original approach.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
21101 - Food and beverages
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Agricultural and Food Chemistry
ISSN
0021-8561
e-ISSN
—
Svazek periodika
66
Číslo periodika v rámci svazku
42
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
9
Strana od-do
11018-11026
Kód UT WoS článku
000448754600009
EID výsledku v databázi Scopus
2-s2.0-85055093412