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Nitrocefin is a substrate routinely used to detect the presence of enzymes produced by various microbes. mediated resistance to antibiotics such as is a widespread mechanism of resistance for a number of including members of the family Enterobacteriaceae, a major group of enteric Gram-negative bacteria. Other methods for detection exist including PCR; however, nitrocefin allows for rapid detection using few materials and inexpensive equipment.


Structure
As a , nitrocefin contains a ring which is susceptible to mediated . Once hydrolyzed, the degraded nitrocefin compound rapidly changes color from yellow to red. Although nitrocefin is considered a , it does not appear to have antimicrobial properties.


Degradation and chromogenic properties
Intact antibiotics act by binding to penicillin binding proteins (PBPs) involved in synthesis. hydrolyze the bond between the and the in the ring of susceptible beta-lactams and members of subclasses (including certain cephalosporins). After hydrolysis of the amide bond, the antibiotic lacks the ability to bind bacterial PBPs and is rendered useless. Visual detection of this process is essentially impossible with most because the shift of absorption from the intact versus hydrolyzed product occurs outside of the . Hydrolysis of nitrocefin however, produces a shift of absorption inside the visible light spectrum from intact (yellow) nitrocefin (~380 nm) to degraded (red) nitrocefin (~500 nm) allowing visual detection of activity on a macroscopic level.


Detection assays
The following assays describe methods in which nitrocefin can be used to detect enzymes using inexpensive materials and equipment. Working solutions of nitrocefin lie within 0.5 mg/mL to 1.0 mg/mL.

Slide Surface Assay

  1. Add one drop of 0.5 mg/ml Nitrocefin to the surface of a clean glass slide.
  2. Select a colony from an agar surface using a sterile loop and mix with the drop.
  3. Appearance of red color within 20-30 min. indicates activity.

Direct Contact Assay

  1. Place one drop of 0.5 mg/ml Nitrocefin directly on the surface of an isolated colony.
  2. Appearance of red color within 20-30 min. indicates activity.

Broth Suspension Assay

  1. Add 3-5 drops of 0.5 mg/ml Nitrocefin to 1 ml of broth suspension.
  2. Appearance of red color within 20-30 min. indicates activity.

Lysed Cell Assay

  1. Lyse 1ml of cell suspension by sonication.
  2. Add 3-5 drops of 0.5 mg/ml Nitrocefin to lysed cell suspension.
  3. Appearance of red color within 20-30 min. indicates activity.

Filter Paper Assay

  1. Place a small piece of filter paper (~3 x 3 cm) in a clean petri dish or another clean isolated surface and saturate (3-5 ml) with 0.5 mg/ml Nitrocefin
  2. Select an isolated colony and smear over the surface of the impregnated filter paper.
  3. Appearance of red color within 20-30 min. indicates activity


See also

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