Skip to main content

Bile Esculin Test


Bile Esculin Test 


Bile esculin agar is a selective and differential medium which is used to presumptively identify enterococci and group D streptococci based on the ability of an organism to hydrolyze esculin.
Image result for streptococcus group d
  • Esculin is a glycosidic coumarin derivative (6-beta-glucoside-7-hydroxy-coumarin). The two moieties of the molecule (glucose and 7-hydroxycoumarin) are linked together by an ester bond through oxygen.
  • Many bacteria can hydrolyze esculin, but few can do so in the presence of bile.
  • Thus the bile esculin test is based on the ability of certain bacteria, notably the group D streptococci and Enterococcus species, to hydrolyze esculin in the presence of bile (4% bile salts or 40% bile).
  • Bacteria that are bile-esculin positive are able to grow in the presence of bile salts and the hydrolysis of the esculin in the medium results in the formation of glucose and a compound called esculetin.
  • Esculetin, in turn, reacts with ferric ions (supplied by the inorganic medium component ferric citrate) to form a black diffusible complex.
Principle
Gram-positive bacteria other than some streptococci and enterococci are inhibited by the bile salts in this medium. Organisms capable of growth in the presence of 4% bile and able to hydrolyze esculin to esculetin. Esculetin reacts with Fe3+ and forms a dark brown to black precipitate. Thus the tolerance to the presence of bile and the hydrolysis of esculin provide the means to presumptively identify organisms. If an organism can hydrolyze esculin, the media will turn dark brown or black.
Image result for bile esculin testMedia:
Beef extract (11 g), enzymatic digest of gelatin (34.5 g), esculin (1 g), ox bile (2 g), ferric ammonium citrate (0.5 g), agar (15 g), per 1000 mL, pH 6.6.
Method

Image result for streaking method of tube
1.    Inoculate one to two colonies from an 18- to 24-hour culture onto the surface of the slant.
2.    Incubate at 35°-37°C in ambient air for 48 hours.
3.    Observe for growth and blackening of the medium.
 Results
Image result for bile esculin test
  • Positive: Growth and blackening of the agar slant
  • Negative: Growth and no blackening of medium ; No growth
Uses
  • This test is used for the presumptive identification of enterococci and organisms in the Streptococcus bovis group.
  • The test differentiates enterococci and group D streptococci from non–group D viridans streptococci.
Limitations
Image result for bile esculin test
  • It should be used in conjunction with other biochemical tests to identify cultures of isolated organism.
  • As a result of nutritional requirements, some organisms may grow poorly or not at all on this medium.
  • Some strains of StaphylococcusAerococcus, and Listeria monocytogenes may grow in the presence of bile and hydrolyze esculin.  monocytogenes will form minute black colonies.
  • A heavy inoculum on BEA may cause interpretation of the bile esculin test difficult to read. Excess inoculum decreases the ability of the bile to inhibit growth of other gram-positive organisms that may hydrolyze esculin.
  • There are a few streptococci that do not hydrolyze esculin but will grow in the presence of bile. Growth without blackening of this medium does not constitute a positive test.
  • BEA does not contain azide; as a result, gram-negative rods will grow on this medium. Many of these organisms may hydrolyze esculin.
References
www.time2026end.com

Comments

Popular posts from this blog

Mueller Hinton Agar

Mueller Hinton Agar (MHA)       The major use of Mueller Hinton Agar is for antimicrobial susceptibility testing. Composition of MHA Ingredients   Beef Extract                                  2.00 gm Acid Hydrolysate of Casein         17.50 gm Starch                                           1.50 gm Agar                                             17.00 gm Distilled Water                             1000 ml Final pH 7.3 ± 0.1 at 25ºC Why Mueller Hinton agar is used for antibiotic susceptibility testing? 1.     It is a non-selective, non-differential medium. This means that almost all organisms plated on here will grow. 2.     It contains starch. Starch is known to absorb toxins released from bacteria, so that they cannot interfere with the  antibiotics . It also mediates the rate of diffusion of the antibiotics through the agar. 3.     It is a loose agar. This allows for better diffusion of the antibiotics than most other plates. A bette

Urease Test

Urease Test The urease test is used to determine the ability of an organism to split urea, through the production of the enzyme urease. Principle  Urea  is the product of decarboxylation of  amino acids . Hydrolysis of  urea  produces  ammonia  and  CO2 . The formation of  ammonia  alkalinizes the medium, and the pH shift is detected by the color change of  phenol red  from  light orange  at pH 6.8 to  magenta (pink)  at pH 8.1. Rapid urease-positive organisms turn the entire medium  pink  within 24 hours. Weakly positive organisms may take several days, and negative organisms produce  no color change  or  yellow  as a result of  acid production . Uses  1.     This test is used to differentiate organisms based on their ability to hydrolyze urea with the enzyme urease. 2.     This test can be used as part of the identification of several genera and species of Enterobacteriaceae, including  Proteus, Klebsiella ,

Simmons Citrate Test

Simmons Citrate Reaction It  used to differentiate among the Gram-Negative bacilli in the family Enterobacteriaceae. Principle  Citrate agar is used to test an organism’s ability to utilize citrate as a source of energy. The medium contains  citrate  as the sole  carbon source  and  inorganic ammonium salts (NH4H2PO4)  as the sole source of  nitrogen . Bacteria that can grow on this medium produce an enzyme,  citrate-permease , capable of converting  citrate  to  pyruvate .  Pyruvate  can then enter the organism’s metabolic cycle for the production of  energy . Growth is indicative of utilization of citrate, an intermediate metabolite in the  Krebs cycle . When the bacteria metabolize  citrate , the  ammonium salts  are broken down to  ammonia , which increases  alkalinity . The shift in pH turns the  bromthymol blue  indicator in the medium from  green to blue  above pH 7.6. Christensen  developed an alternative citrate test medium that does not require the organism