Results 121 to 130 of about 1,569 (164)
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Enniatin A1, enniatin B1 and beauvericin on HepG2: Evaluation of toxic effects

Food and Chemical Toxicology, 2015
Hepatotoxicity of three Fusarium mycotoxins, beauvericin (BEA) and two enniatins (ENNs) ENN A1 and ENN B1, in hepatocarcinoma cells (HepG2) were evaluated and compared. Concentrations used were 1.5 and 3 μM at 24, 48 and 72 h for each mycotoxin. Flow cytometry was used to examine enniatins effects on cell proliferation, to characterize the cell cycle ...
Ana, Juan-García   +3 more
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Biosynthesis and biological activity of enniatins.

Die Pharmazie, 2007
Enniatins are N-methylated cyclohexadepsipeptides (CHDPs), composed of three units each of N-methylated branched-chain L-amino acid and D-2-hydroxy acid arranged in an alternate fashion. These low-molecular secondary metabolites are produced by Fusarium species, typical mycotoxin producing fungi. Enniatins are known for their ionophoric, phytotoxic and
Firáková, S.   +2 more
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Synthesis of enniatin B

Experientia, 1963
Die Struktur von Enniatin B, eines antimikrobiellen Wirkstoffes aus Fusarienstammen (ETH, Zurich), wird durch Synthese als die eines Cyclohexapeptolids bewiesen (vgl. X).
Pl. A. Plattner   +4 more
openaire   +1 more source

The structure of enniatins and related antibiotics

Tetrahedron, 1963
Abstract The synthesis of cyclotetradepsipeptides the structure of which has previously been assigned to antibiotics of the enniatin group is described. It was found that these antibiotics cannot be represented by the formulas (I)–(VI).
M M, Shemyakin   +3 more
openaire   +2 more sources

Stimulation of erythrocyte phospholipid scrambling by enniatin A

Molecular Nutrition and Food Research, 2011
AbstractScope: Enniatin A, a peptide antibiotic and common food contaminant, triggers mitochondrial dysfunction and apoptosis. Even though lacking mitochondria, erythrocytes may similarly undergo suicidal cell death or eryptosis. Eryptosis is characterized by cell shrinkage and cell membrane phospholipid scrambling.
Kashif Jilani, Syed M Qadri, Anand Rotte
exaly   +3 more sources

Über die Chemie des Enniatins

Experientia, 1947
Judging by the physical and chemical properties and “bacterial spectra”, the antibiotic substance, Enniatin, previously isolated from a strain ofFusarium by the authors, appears to be identical with that which was recently reported byCook et al. derived from another strain and designated by them as Lateritiin-I, although the reported empirical formulae
Pl. A. Plattner, U. Nager
openaire   +1 more source

Investigation of the electrophysiological properties of enniatins

Archives of Biochemistry and Biophysics, 2004
Enniatins are cyclohexadepsipeptides produced by various species of the genus Fusarium, and are known to have ionophoric, antibiotic, and in vitro hypolipidaemic properties. With the patch clamp technique in the inside-out mode it could be shown that enniatin easily incorporates into the cell membrane in which it forms cation-selective pores.
Kamyar, Majid-Reza   +4 more
openaire   +3 more sources

Structural studies on minor enniatins from Fusarium sp. VI 03441: Novel N-methyl-threonine containing enniatins

Toxicon, 2009
A strain of a yet unidentified Fusarium sp. produced in addition to enniatins A1, B and B1 a number of minor enniatins. The strain formed a well supported clade with strains identified as Fusarium acuminatum (Gibberella acuminata) in phylogenetic analyses using the TEF-1alpha gene sequences.
Silvio, Uhlig   +3 more
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Fate of enniatins and deoxynivalenol during pasta cooking

Food Chemistry, 2016
The fate of deoxynivalenol and enniatins was studied during cooking of commercially available dry pasta in the Netherlands in 2014. Five samples containing relatively high levels of deoxynivalenol and/or enniatins were selected for the cooking experiment.
de Nijs, Monique   +4 more
openaire   +3 more sources

Synthese von Stereoisomeren des Enniatins B

Chemische Berichte, 1968
AbstractAusgehend von der Synthese des Enniatins B wird der Aufbau seiner Stereoisomeren all‐L‐, all‐D‐Enniatin B und des Antipoden (Enantio‐Enniatin B¹) beschrieben.
Günter Losse, Hartmut Raue
openaire   +1 more source

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