ENNIATIN B Property

storage temp. 

-20°C

solubility 

DMSO: soluble10mg/mL

form 

White to off-white crystalline solid.

Boiling point:

827.0±65.0 °C(Predicted)

Density 

1.036±0.06 g/cm3(Predicted)

Melting point:

229 °C

pka

-1.08±0.70(Predicted)

Safety

Hazard Codes 

T

Risk Statements 

23/24/25

Safety Statements 

45

RIDADR 

2811

WGK Germany 

3

HazardClass 

6.1(a)

PackingGroup 

I

HS Code 

29419000

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

ENNIATIN B Chemical Properties,Usage,Production

Uses

Enniatins are a family of depsipeptide ionophores, produced several Fusarium species. More recently, the effects of the ennitins on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumour action have received more focus. Enniatin B is the most studied of four major analogues of the enniatin complex.

Uses

Enniatins are a family of depsipeptide ionophores produced by several Fusarium species. Recently, the effects of the enniatins on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin B is the most studied of four major analogues of the enniatin complex.

Definition

ChEBI: An enniatin obtained from formal cyclocondensation of three N-[(2R)-2-hydroxy-3-methylbutanoyl]-N-methyl-L-valine units.

Biological Activity

enniatin b is an ionophore antibiotic.enniatins are one of the cyclohexadepsipeptides produced by various species of the genus fusarium, and are reported to have antibiotic, ionophoric, and in-vitro hypolipidaemic activities.

Biochem/physiol Actions

Enniatins are a group of cyclohexadepsipeptide mycotoxins produced by Gnomonia errabuda and several Fusaria species, with phytotoxic, antibiotic, and insecticidal activities. Enniatins function as ionophors by their incorporation into the cellular membrane to form dimeric structures that transport monovalent ions across the membrane (especially the mitochondrial membranes) affecting oxidative phosphorylation uncoupling. It has been demonstrated that enniatins have a cytotoxic effect on human cancer cells. Furthermore, incubation of H4IIE hepatoma cells with enniatins strongly diminished phosphorylation of the ERK (p44/p42). Enniatins B and B1 inhibit the multi-drug resistance transporter Pdr5p from Saccharomyces cerevisiae, indicating their beneficial potential in cases of drug resistant patients.

in vitro

a non-toxic concentration of enniatin b could strongly inhibit a pdr5p-mediated efflux of cycloheximide or cerulenin in pdr5p-overexpressing cells. the mode of pdr5p inhibition caused by enniatin b was competitive against fk506. however, enniatin b could not inhibit the function of snq2p, a homologue of pdr5p [1]. another study showed that enniatin b was a relatively poor ionophore that could facilitate import of k+ and na+ across membranes [2]. it was also found that like other enniatins, enniatin b was able to inhibit acyl-coa: cholesterol acyltransferase [3].

in vivo

after oral administration to mice, no toxicological signs or pathological changes were observed. moreover, enniatin b was found in all tissues and serum but not in urine, and the highest amounts was measured in liver and fat. three phase i metabolites of enniatin b were found in liver and colon, with dioxygenated-enniatin b being most prominent [4].

References

[1] k. hiraga, s. yamamoto, h. fukuda, et al. enniatin has a new function as an inhibitor of pdr5p, one of the abc transporters in saccharomyces cerevisiae. biochemical and biophysical research communications 328(4), 1119-1125 (2005).
[2] m. r. kamyar, p. rawnduzi, c. r. studenik, et al. investigation of the electrophysiological properties of enniatins. archives of biochemistry and biophysics429(2), 215-223 (2004).
[3] tomoda, x. h. huang, j. cao, et al. inhibition of acyl-coa: cholesterol acyltransferase activity by cyclodepsipeptide antibiotics. j.antibiot.(tokyo) 45(10),1626-1632 (1992).
[4] rodríguez-carrasco y et al. mouse tissue distribution and persistence of the food-born fusariotoxins enniatin b and beauvericin. toxicol lett. 2016 apr 15;247:35-44.