Aesculin

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Aesculin
IUPAC name 7-hydroxy-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy- 6-(hydroxymethyl)-2-tetrahydropyranyl]oxy}-2-chromenone
Identifiers
CAS number 531-75-9
PubChem 5281417
SMILES
Properties
Molecular formula C15H16O9
Molar mass 340.282 g/mol
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Aesculin is a glucoside that naturally occurs in the horse chestnut (Aesculus hippocastanum),1 California Buckeye (Aesculus californica)2 and in daphnin (the dark green resin of Daphne mezereum).

Contents

Medical uses

Aesculin is used in a microbiology laboratory to aid in the identification of bacterial species (especially Enterococci).

Aesculin hydrolysis test

Aesculin is incorporated into agar with ferric citrate and bile salts (bile aesculin agar).3 Hydrolysis of the aesculin forms aesculetin (6,7-dihydroxycoumarin) and glucose. The aesculetin forms dark brown or black complexes with ferric citrate, allowing the test to be read.

The bile aesculin agar is streaked and incubated at 37°C for 24 hours. The presence of a dark brown or black halo indicates that the test is positive. A positive test can occur with Enterococcus, Aerococcus and Leuconostoc. Aesculin will fluoresce under long wave ultraviolet light (360 nm): hydrolysis of aesculin results in loss of this fluorescence.

Enterococcus will often flag positive within four hours of the agar being inoculated.

Line notes

  1. ^ Plant poisons: Aesculin
  2. ^ C. Michael Hogan, 2008
  3. ^ National Standard Methods (UK)

References


Wikipedia content modification information:

  • This page was last modified on 4 December 2008, at 23:58.

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