• Vancomycin packaged and labeled.

click on thumbnail to zoom
SKU: V010

Size  
Quantity:
  Click 'Bulk Order' for 10 or more
Price: make selection(s)
Description

Vancomycin is a glycopeptide antibiotic derived from Streptomyces orientalis that was discovered in 1953 from a soil sample found in Borneo. It is effective against gram-positive bacteria such as Staphylococcus aureus and is used in studies of nanoparticle transport and antibiotic resistance studies.

Vancomycin acts as a cell wall synthesis inhibitor in bacteria by preventing the transfer and addition of NAM/NAG-peptides that make up the peptidoglycan cell wall structure. 

Vancomycin has low cell toxicity in plant cells and has been used in conjunction with Cefotaxime or Carbenicillin to stop the growth of agrobacterium in plant cell culture and transformation.

Click here for more vancomycin products.

    CAS Number

    1404-90-6

    Molecular Formula

    C66H75Cl2N9O24

    Molecular Weight

    1449.25

    Mechanism of Action

    Vancomycin prevents cell wall synthesis by two separate mechanisms. One mechanism prevents N-acetylmuramic acid (NAM) and N-acetylglucosamine (NAG) peptides from linking together forming the peptidoglycan backbone through the incorporation of the vancomycin molecule to the D-alanyl-D-alanine terminal. The second mechanism prevents crosslinking between amino acid residues in the peptidoglycan chain altering bacterial cell membrane permeability as well as RNA synthesis.

    Storage Conditions

    2-8°C

    Tariff Code

    2941.90.1010

    Spectrum

    Vancomycin inhibits growth of many gram-positive bacteria including the antibiotic resistant superbug, MRSA (Methicillin resistant Staphylococcus aureus). Vancomycin is effective for treating MRSA infections because it inhibits cell wall synthesis through a different mechanism than β-lactam antibiotics.

    Over the years gram-positive bacteria have emerged that are resistant to vancomycin, such as vancomycin resistant staphylococcus aureus (VRSA) and vancomycin-resistant enterococci (VRE).

Applications

    Eukaryotic Cell Culture Applications

    Vancomycin can be used to select for cells containing the pcDNA3.1 resistance plasmid in 293 cell lines at an effective concentration of 400 µg/mL. For additional information on your cell culture needs, please visit our cell-culture database.

    Microbiology Applications

    Vancomycin inhibits the growth of most gram-positive bacteria including the MRSA.  It is usually only indicated for the treatment of serious or life-threatening bacterial infections like those caused by β-lactam-resistant staphylococci bacterial infections.  There are now vancomycin resistant bacteria, primarily, vancomycin resistant staph aureus (VRSA), and vancomycin resistant enterococci (VRE).

    Vancomycin (V010) and Vancomycin HCl, USP (V001) are commonly used in selective media for isolation of Gram-negative pathogens including Campylobacter jejuniEscherichia coliHaemophilus influenzaeHelicobacter pylori, and Neisseria gonorrhoeae.  superbug vancomycin resistant enterococcus (VRE) detection.

    Representative MIC values include:

    • Methicillin resistant Staphylococcus aureus (MRSA) 0.25 µg/mL - 2 µg/mL
    • Clostridium difficile 0.06 µg/mL - 4 µg/mL
    • For a complete list of vancomycin HCl MIC values, click here.

    Pryjma et al. used TOKU-E vancomycin in Mueller Hinton (MH) medium to isolate Campylobacter jejuni: "FdhTU-Modulated Formate Dehydrogenase Expression and Electron Donor Availability Enhance Recovery of Campylobacter jejuni following Host Cell Infection"

    Plant Biology Applications

    Vancomycin has low toxicity to Plant cells and is often used in Agrobacterium tumefaciens mediated transformations as a method to control its growth in plant cell culture media.  Vancomycin is also suitable for bacterial contamination control in plant cell culture media and is sometimes used in combination with cefotaxime due to greater synergistic effects. Most studies do not describe any negative effects to the plant by using vancomycin, however, in a study done by Silva and Fukai (2001), lower efficiency of transformation was found at concentrations of 500 µg/ml.

Specifications

    Form

    Powder

    Appearance

    White to off-white powder

    Source

    Streptomyces orientalis

    Impurity Profile

    Individual Impurity: Not more than 3.0%
    Related Substances: Not more than 7.0%
    Content of EDTA: Not more than 120 ppm

    Water Content (Karl Fischer)

    Not more than 20.0%

    Absorbance

    (465nm): Not more than 0.1

    Assay

    (As Is): Not less than 850 µg/mg
    (Dried Basis): Not less than 950 µg/mg

    Residue On Ignition

    Not more than 1.0%

    Heavy Metals

    Not more than 20 ppm

References

    References

    Courvalin, Patrice. "Vancomycin Resistance in Gram-Positive Cocci." Oxford Journals(2006): 25-34. Clinical Infectious Diseaes. Web. 21 Aug. 2012.

    Pollock, H.M., Holt J., and Murray C., Comparison of susceptibilities of anaerobic bacteria to cefemenoxime, ceftriaxone and other antimicrobial compounds, Antimicrob. Agents Chemother., Vol. 23, pp.780-783, 1983

    Silva J.A. and Fukai S., The impact of carbenicillin, cefotaxime and vancomycin on chrysanthemum and tobacco TCL morphogenesis and Agrobacterium growth, J. Appl. Hort., Vol. 3(1), pp. 3-12, 2001.

    Joshi, S., Ray, P., Manchanda, V., Bajaj, J., Chitnis, D. S., Gautam, V., &...Balaji, V. (2013). Methicillin resistant Staphylococcus aureus (MRSA) in India: Prevalence & susceptibility pattern. Indian Journal Of Medical Research, 137(2), 363-369

Other Items In This Category