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Microbial Mutagenicity Assay: Ames Test    

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The Microbial mutagenicity Ames test is a bacterial bioassay accomplished in vitro to evaluate the mutagenicity of various environmental carcinogens and toxins. While Ames test is used to identify the revert mutations which are present in strains, it can also be used to detect the mutagenicity of environmental samples such as drugs, dyes, reagents, cosmetics, waste water, pesticides and other substances which are easily solubilized in a liquid suspension. We present the protocol for conducting Ames test in the laboratory.

Keywords: Mutagenicity, Carcinogenicity, Salmonella strains, Gene mutation, Revertants


The Microbial Ames test is a simple, rapid and robust bacterial assay consisting of different strains and applications of Salmonella typhimurium/E. coli, used for ascertaining the mutagenic potential (Levin et al., 1982; Gupta et al., 2009). In 1975, Ames and his followers standardized the traditional Ames assay protocol and reappraised in 1980’s (Maron and Ames, 1983). Induction of new mutations replacing existing mutations allows restoring of gene function. The newly formed mutant cells are allowed to grow in the absence of histidine and form colonies, hence this test is also called as ‘Reversion assay’ (Ames, 1971). While traditional Ames test is quite laborious and time consuming for initial monitoring of mutagenic compounds, miniaturization of liquid suspension significantly impacted the usability by making it more convenient. The standard doses (2 µl, 5 µl, 10 µl, 50 µl and 100 µl) were set to evaluate the mutagenicity from lower to higher concentration (Hayes, 1982). Mice liver has been used as a tissue for preparing homogenate 9,000 x g (S9 hepatic fraction) whereas in S9 mix, hepatocytes are used to minimize the mammalian metabolic activation formed in the mice liver. In Ames bioassay, the sensitivity of a compound for mutagenicity is based on the knowledge that a substance which is mutagenic in the presence of liver enzymes metabolizing compound might be a carcinogen (Mathur et al., 2005).

Genetic Approach: The Salmonella/E. coli tester strains: Several strains of Salmonella typhimurium have been used in Ames assay which requires histidine synthesis to assess the mutagenicity. In the histidine operon, each tester strain contains a different mutation. In addition to the histidine mutation, the standard tester strain of Salmonella typhimurium contains other mutations that greatly enhance their ability to detect the mutations (Figure 1). One of the mutations (rfa) causes partial loss of the lipopolysaccharides barrier that coats the surface of the bacteria and increases permeability to large molecules such as benzo[a]pyrene allowing not to penetrate in the normal cell wall (Mortelman and Zeiger, 2000). The mutagens present in the tested samples give rise to induced revertants on a minimal medium (absence of histidine). They are further used to observe revertants in previously mutated strains (that are not able to grow in a medium without histidine). The other mutation (uvrB) is a deletion mutation in which deletion of a gene, coding for the DNA excision repair system, causing gradually increased sensitivity in detecting many mutagens (Ames et al., 1973a). The reason behind this mutation is the deletion excising the uvrB gene emulsifying these bacteria requiring biotin for growth. The standard strains such as TA 97, TA 98, TA 100 and TA 102 contain the R-factor plasmid, pKM101. These R-factor strains are reverted by a number of mutagens that are detected weakly or not at all with the non R-factor parent strains (Ames et al., 1975a).

Figure 1. Genetic approach for assessing the mutagenicity in Salmonella strains (modified from https://en.wikipedia.org/wiki/Ames_test)

Many studies (Ames et al., 1975b; Levin et al., 1982) revealed that development of plasmid pKM101 in TA 1535 and TA 1538 strains leads to complement other isogenic strains such as TA 98, TA 100, TA 104 and TA 102. The his G46 mutation in TA 100 and TA 1535 codes for the first enzyme of histidine biosynthesis (hisG) (Ames et al., 1975b). This mutation, determined by DNA sequence analysis, substitutes proline (-GGG-) for leucine (-GAG-) in the wild type organism (Barnes et al., 1982). The tester strains TA 1535 and its R-factor derivative present in TA 100, detect mutagens which causes base-pair substitutions generally at one of these G-C pairs. The hisD3052 mutation in TA 1538 and TA 98 is in the hisD gene coding for histodinol dehydrogenase. TA 1538 and its R-factor derivative TA 98 detect various frameshift mutagens in repetitive sequences as ‘hot spots’ resulting in a frame shift mutation (Walker and Dobson, 1979; Shanabruch and Walker, 1980) (Table 1).

Table 1. Genotype of the Salmonella strain used for mutagenesis testing

Levin et al. (1982) described a standard strain Salmonella typhimurium bacterium called TA 102 which was used to evaluate the effect of some compounds reacting with nucleotides AT. Tester strain TA102 containing nucleotides AT, present in hisG gene carrying plasmid pAQ1. There are certain mutagenic agents which are detected by TA 102 but not by TA 1535, TA 1537, TA 1538, TA 98 and TA 100 (Wilcox et al., 1990). Before performing experiment, a new set of fresh strains are prepared; and the genotypes are assessed (R-factor, His, rfa and uvrB mutations). For these, we refer readers to many excellent reviews (Walker, 1979; Czyz et al., 2002; Fluckiger-Isler et al., 2004).

Certain carcinogens present in active forms in biological reaction are easily catalyzed by cytochrome-P450. Metabolic activation system is absent in Salmonella, and in order to improve the potentiality of bacterial test systems, liver extracts of Swiss albino mice are used. This serves as a rich source in converting carcinogens to electrophilic chemicals that are incorporated to detect in vivo mutagens and carcinogens (Garner et al., 1972; Ames et al., 1973a). The crude liver homogenate as 9,000 x g S9 fraction contains free endoplasmic reticulum, microsomes, soluble enzymes and some cofactors set with S9 concentration to 10% (Franz and Malling, 1975). The oxygenase requires the reduced form of Nicotinamide Adenine Dinucleotide Phosphate (NADP) which is generally in situ by the action of glucose-6-phosphate dehydrogenase and reducing NADP both work as cofactors in assay (Prival et al., 1984; Henderson et al., 2000). While water is considered as a negative control, sodium azide, 2-nitrofluorine and mitomycin for TA 98, TA 100 and TA 102 without S9 metabolic activation and 2-anthramine with S9 hepatic fraction are used as positive controls for conducting the test (Table 2). Before performing the experiment, fresh solutions must be prepared.

Table 2. Positive controls with and without S9 metabolic activation (DeFlora et al., 1984)

Spontaneous Reversion Control: Each strain of Salmonella contains a specific mutant range. Selection of solvents shows the effect on the frequency range of spontaneous mutant (Maron and Ames, 1983) (Table 3). The range of revertants varies in research laboratories. The spontaneous revertants are visible through unaided eyes (Figure 2).

Table 3. Spontaneous revertants control values for various strain types and number of revertants (Mortelmans and Stocker, 1979)

Figure 2. Spontaneous revertants colonies obtained after addition of waste water from health center in Salmonella mutagenicity assay at different concentrations, viz. 2 µl, 10 µl, 50 µl, 100 µl (Vijay, 2014)

Materials and Reagents

  1. Materials
    1. Tips (1,000 µl, 200 µl, 10 µl) (Tarsons)
    2. Sterile Petri plates (HiMedia Laboratories, catalog number: PW001 )
    3. Erlenmeyer flask and beaker (SchottDuran,10 ml, 250 ml, 500 ml)
    4. Eppendorf tubes (Tarsons,1.5 ml, 2.0 ml)
    5. Metal loop holder (metal loop Ch-2, HiMedia Laboratories, catalog number: LA012 )
    6. L shaped spreader(HiMedia Laboratories, catalog number: PW1085 )

  2. Mutagens
    1. Sodium azide (HiMedia Laboratories, catalog number: GRM1038 )
    2. 4-Nitroquinoline N-oxide (Sigma-Aldrich, catalog number: N8141 )
    3. 2-Aminofluorene (Sigma-Aldrich, catalog number: A55500 )
    4. Benzo(a)pyrene (Sigma-Aldrich, catalog number: B1760 )
    5. Mitomycin C (Roche Diagnostics, catalog number: 10107409001 )
    6. 2,4,7-Trinitro-9-fluorenone (Accustandard, catalog number: R-033S )
    7. 4-Nitro-o-phenylenediamine (Sigma-Aldrich, catalog number: 108898 )

  3. Reagents
    1. Oxoid nutrient broth No. 2 (Sigma-Aldrich, catalog number: 70123 )
      Note: This product has been discontinued.
    2. 70% ethanol
    3. Magnesium sulphate heptahydrate (MgSO4·7H2O) (HiMedia Laboratories, catalog number: RM683 )
    4. Citric acid monohydrate (HiMedia Laboratories, catalog number: GRM1008 )
    5. Potassium phosphate, dibasic (K2HPO4) (anhydrous) (Merck, catalog number: 61788005001730 )
    6. Sodium ammonium phosphate tetrahydrate (NaNH4HPO4·4H2O) (Sigma-Aldrich, catalog number: S9506 )
    7. D-biotin (HiMedia Laboratories, catalog number: TC096 )
    8. L-histidine (HiMedia Laboratories, catalog number: TC076 )
    9. Hydrochloric acid (HCI) (HiMedia Laboratories, catalog number: AS003 )
    10. Potassium chloride (KCl) (Merck, catalog number: 61753305001730 )
    11. Magnesium chloride hexahydrate (MgCl2·6H2O) (HiMedia Laboratories, catalog number: MB040 )
    12. Sodium dihydrogen phosphate monohydrate (NaH2PO4·H2O) (Merck, catalog number: 1063700050 )
    13. Disodium hydrogen phosphate (Na2HPO4) (HiMedia Laboratories, catalog number: TC051 )
    14. NADP (sodium salt) (HiMedia Laboratories, catalog number: RM392 )
    15. D-glucose-6-phosphate (monosodium salt) (Sigma-Aldrich, catalog number: G7879 )
    16. Ampicillin trihydrate (Sigma-Aldrich, catalog number: A6140 )
    17. Sodium hydroxide (NaOH) (Merck, catalog number: 106462 )
    18. Crystal violet (Sigma-Aldrich, catalog number: C6158 )
    19. Agar-Agar (Himedia Laboratories, catalog number: RM026 )
    20. Nutrient broth (HiMedia Laboratories, catalog number: M002 )
    21. Tetracycline (Sigma-Aldrich, catalog number: 87128 )
    22. Dimethylsulfoxide (HiMedia Laboratories, catalog number: TC185 )
    23. Vogel-Bonner medium E (50x) (see Recipes)
    24. 0.5 mM histidine/biotin solution (see Recipes)
    25. Salt solution (1.65 M KCl + 0.4 M MgCl2) (see Recipes)
    26. 0.2 M sodium phosphate buffer, pH 7.4 (see Recipes)
    27. 1 M Nicotinamide Adenine Dinucleotide Phosphate (NADP) solution (see Recipes)
    28. 1 M glucose-6-phosphate (see Recipes)
    29. Ampicillin solution (4 mg/ml) (see Recipes)
    30. Crystal violet solution (0.1%) (see Recipes)
    31. Minimal glucose plates (see Recipes)
    32. Histidine/Biotin plates (see Recipes)
    33. Ampicillin and tetracycline* plates (see Recipes)
    34. Nutrient agar plates (see Recipes)
    35. S9 mix (Rat Liver Microsomal Enzymes + Cofactors) (see Recipes)
    36. Sodium azide (see Recipes)
    37. Mitomycin (see Recipes)
    38. 2-Anthramine (see Recipes)


  1. Orbital shaking incubator (Remi, model: RIS-24(BL) )
  2. Laminar Flow hood (Bio safety cabinet) (Deepak Meditech Pvt Ltd., Steri clean)
  3. Pipettes (Eppendorf, model: Research® plus, catalog number: 3120000062 , 1,000 μl; catalog number: 3120000046 , 200 μl; catalog number: 3120000020 , 10 μl)
  4. Vortex mixer (Labnet International, catalog number: S0100 )
  5. Hot water bath (Daiki Sciences, catalog number: KBLee2001 )
  6. Autoclave (TSC)
  7. Automatic Colony counter (Sonar)
  8. Refrigerator centrifuge (Thermo Fisher Scientific, Thermo ScientificTM, model: Heraeus Biofuge Primo R )
  9. pH meter (Labindia Analytical Instruments, model: PICO pH Meter , catalog number: PC13330101)
  10. Tissue tearor (Bio Spec Products, catalog number: 985370-04 )


  1. Before performing the experiment, inoculate a single fresh colony of standard strains of S. typhimurium TA 98, 100 and 102, in oxoid nutrient broth-2 and incubate for 10-12 h at 37 °C in an incubator shaker at 120 rpm to ensure sufficient aeration for 1 x 109 bacterial cells. Each strain of S. typhimurium is grown separately in Erlenmeyer flasks (10 ml).
  2. Prepare fresh mutagen for each experiment (see Recipes).
    Negative control: Autoclaved distilled water
    Positive controls for TA 98, TA 100 and TA 102 without S9 metabolic activation (S9 mix): sodium azide (1 μg/ml) 2-nitrofluorine (1 μg/ml) and mitomycin (0.125 μg/ml)
    For TA 98, TA 100 and TA 102 with S9 metabolic activation (S9 mix): 2-Anthramine (2 μg/ml)
  3. Preparation of minimal glucose agar (MGA) plates: Mix the medium of minimal glucose agar plates (Recipe 9) and pour 25 ml into each Petri dish. Prepare the plates freshly before use.
  4. Label all minimal glucose agar plates and Eppendorf tubes prior to experiment.
  5. To the 2 ml sterile Eppendorf tubes, add the following each:
    1. 0.1 ml fresh culture of Salmonella strains
    2. 0.2 ml of His/Bio solution
    3. 0.5 ml sodium phosphate buffer (absence of S9 mix) or 0.5 ml S9 (presence of S9 mix)
    4. 0.1 ml of test sample or 0.1 ml of positive or negative control
    5. Make up to 1 ml with autoclaved distilled water.
  6. Mix the contents of Eppendorf tubes and pour onto Petri plates and spread using L-shaped spreader on the surface of MGA plates. Cover the Petri plates with sterile aluminum foil to protect the testing sample from photo reactive substances.
  7. After incubation of 48 h at 37 °C, spontaneous revertants colonies appear and are clearly visible with unaided eyes. All plates are run in triplicates.
  8. Revertants form a uniform lawn of auxotrophic bacteria on the surface the background of medium.

Data analysis

Non-statistical analysis
The most widely used method for non-statistical analysis of result in Ames test is ‘two-fold rule’ described by Mortelmans and Zeiger (2000) and Morino-Caniello and Piegorsch (1996). On the basis that the increase in the number of revertant colonies, the concentration of the tested sample goes up (dose-dependent manner), mutagenicity ratio (MR) is calculated first by counting the number of revertant colonies per plate and then calculating the MR as described by Maron and Ames (1983) using the formula below (see Sample data below for results):

Sample data
Medical liquid waste was collected from different health care premises of Jaipur city. Salmonella mutagenicity test was performed on all the samples in their crude natural state using the plate incorporation procedure described by Maron and Ames, 1983. The results of Salmonella mutagenicity assay was analyzed through Mutagenicity Ratio method and shown in Table 4.

Table 4. Mutagenicity ratios of S. typhimurium strains TA98, TA100 and TA102 treated with waste water from different health premises (Vijay, 2014)

+Mutagenicity Ratio > 2.0 imply mutagenic, -Ratio < 2.0 imply non-mutagenic

The Ames test is a widely accepted bacterial assay to detect the mutagenicity in pathogenic bacteria. In this protocol, although we have shown the step wise methodology to perform Ames assay applicable for three strains, this method can be used for studying all compounds to infer mutagenicity. Whereas the Ames assay experiments involve sterile measures, care must be taken in ensuring the sample/plasmid is not contaminated. The improved methods to detect the genotoxicity of compounds help us troubleshoot methods for studying the compounds tested in clinical trials.


Sterilization (safety considerations while working with Salmonella)

  1. As S. typhimurium is a pathogenic bacterium, it is prudent to use precautionary measures every time and apply standard biosafety guidelines such as using plugged pipettes, proper sterilization by 70% ethanol and autoclaving all contaminated material.
  2. Handling of chemicals and strains should be done in biosafety cabinet. Before and after the use, cabinet must be sterilized using 70% ethanol and exposed to 15 min UV.
  3. Care must be taken to protect from chemical exposure by wearing gowns, eye glasses and gloves.
  4. Before discarding, all contaminated material (e.g., test tubes, pipettes and pipette tips, gowns and gloves) should be properly autoclaved.


Ames assay consists of Salmonella typhimurium strains and so it is not a perfect model for human. Mice liver S9 hepatic fraction is used to minimize the mammalian metabolic activations formed in the hepatic system so that the mutagenicity of metabolites can be assessed. There are several differences between human and mice metabolism which can affect the mutagenicity of testing substances. Major disadvantages of fluctuation test is slower and slightly more laborious than Ames protocol. The test is primarily used for testing aqueous samples containing low levels of mutagen and therefore, this test is well adapted for evaluating the mutagenicity of wastewater samples.


  1. Vogel-Bonner medium E (50x)
    For Minimal agar (Recipe 9)
    Per 500 ml
    Warm distilled H2O (45 °C)
    335 ml
    Magnesium sulfate (MgSO4·7H2O)
    5 g
    Citric acid monohydrate
    50 g
    Potassium phosphate, dibasic (anhydrous) (K2HPO4)
    250 g
    Sodium ammonium phosphate (NaNH4HPO4·4H2O)
    87.5 g
    1. Salts are added to the warm water in a flask. Place the flask on a hot plate
    2. After each salt dissolves entirely, transfer the solution into glass bottles and autoclave for 20 min at 121 °C
    3. When the solution gets cool, cap the bottle tightly
    4. Store the solution at 4 °C
  2. 0.5 mM histidine/biotin solution
    For mutagenic bioassay
    Per 125 ml
    D-Biotin (F.W. 247.3)
    15.45 mg
    L-Histidine·HCl (F.W. 191.7)
    12.0 mg
    Distilled H2O
    125 ml
    Dissolve the biotin in hot distilled water. The solution is autoclaved for 20 min, at 121 °C and then stored at 4 °C
  3. Salt solution (1.65 M KCl + 0.4 M MgCl2)
    For S9 hepatic fraction
    Per 250 ml
    Potassium chloride (KCl)
    30.75 g
    Magnesium chloride (MgCl2·6H2O)
    20.35 g
    Distilled H2O to final concentration of
    250 ml
    All the components are dissolved in water. The solution is autoclaved for 20 min, at 121 °C and then stored at 4 °C
  4. 0.2 M sodium phosphate buffer, pH 7.4
    For S9 hepatic fraction 
    Per 250 ml
    0.2 M sodium dihydrogen phosphate (NaH2PO4·H2O)
    30 ml (6.9 g/250 ml)
    0.2 M disodium hydrogen phosphate (Na2HPO4)
    220 ml (7.1 g/250 ml)
    Adjust pH to 7.4. Sterilize the buffer by autoclaving for 20 min at 121 °C
  5. 1 M nicotinamide adenine dinucleotide phosphate (NADP) solution
    For S9 hepatic fraction
    Per 2.5 ml
    191.5 mg
    Sterile distilled H2O
    2.5 ml
    NADP is dissolved in the distilled water and mixed by vortexing. Tubes are placed in an ice bath. The solution can be used for up to six months
  6. 1 M glucose-6-phosphate
    For S9 hepatic fraction
    Per 5 ml
    Glucose-6-phosphate (G-6-P)
    1.41 g
    Sterile distilled H2O
    5 ml
    Glucose-6-phosphate is dissolved in the 5 ml distilled water and mixed by vortexing. Tubes are placed in an ice bath. The solution can be used for up to six months
  7. Ampicillin solution (4 mg/ml)
    Used in tests of ampicillin resistance
    Master plates for R-factor strains
    Per 500 ml
    Ampicillin trihydrate
    0.4 g
    Sodium hydroxide (0.02 N)
    50 ml
    Ampicillin trihydrate is dissolved in the 50 ml of NaOH (0.02 N) and mixed by vortexing. Tubes are placed in an ice bath
  8. Crystal violet solution (0.1%)
    Used in tests for crystal violet sensitivity (to confirm rfa mutation)
    Per 500 ml
    Crystal violet
    0.05 g
    Distilled H2O
    50 ml
  9. Minimal glucose plates
    Used in Mutagenic bioassay
    Per 500 ml
    7.5 g
    Distilled H2O
    465 ml
    50x VB salts (Recipe 1)
    10 ml
    40% glucose
    25 ml
    Add agar in 465 ml of distilled water and autoclave for 20 min, at 121 °C. After cooling, add the salts and glucose gently
  10. Histidine/Biotin plates (Master plates for non R-factor strains)
    Used in tests for histidine requirement 
    Per 500 ml
    7.5 g
    Distilled H2O
    457 ml
    50x VB salts
    10 ml
    40% glucose
    25 ml
    Sterile histidine (2 g per 400 ml H2O)
    5 ml
    Sterile 0.5 mM biotin
    3 ml
    Dissolve agar in the given concentration in distilled water. Autoclave each solution separately for 20 min. After cooling of solution, add each salt gently
  11. Ampicillin and tetracycline* plates
    Master plates for the cultivation of strains containing the plasmids pKM101 and pAQ1*
    Per 500 ml
    7.5 g
    Distilled H2O
    405 ml
    50x VB salts
    10 ml
    40% glucose
    25 ml
    Sterile histidine (2 g per 400 ml H2O)
    5 ml
    Sterile 0.5 mM biotin
    3 ml
    Sterile ampicillin solution (8 mg/ml 0.02 N NaOH)
    1.58 ml
    *Sterile tetracycline solution (8 mg/ml 0.02 N HCl)
    0.125 ml
    Dissolve agar in the given concentration in distilled water. Autoclave each solution separately for 20 min. After cooling of solution, add each salt gently
    *Note: TA 102 is resistant to tetracycline. The shelf life of the plates is two weeks at 4 °C.
  12. Nutrient agar plates
    Used in tests for genotypes [Crystal violet sensitivity (rfa) and UV sensitivity (AuvrB)] and viability of bacteria
    Per 500 ml
    Nutrient agar
    7.5 g
    Distilled H2O
    500 ml
    Dissolve agar in the given concentration in distilled water. Autoclave separately for 20 min. Pour the cooled solution into the Petri plates
  13. S9 mix (Rat Liver Microsomal Enzymes + Cofactors)
    Standard S9 mix Per 25 ml
    Mice liver
    1.0 ml (2%)
    MgCl2-KCl salts
    0.5 ml
    1 M glucose-6-phosphate
    0.125 ml
    0.1 M NADP
    1.0 ml
    0.2 M phosphate buffer, pH 7.4
    12.5 ml
    Sterile distilled H2O
    9.86 ml
    Note: Add each ingredient in the reverse order listed above (First water, and then phosphate buffer…). Avoid refreezing the S9 mix.
  14. Sodium azide
    Used in Mutagenicity assay 
    Per ml
    Sodium azide
    10 µg
    Autoclave distilled H2O
    990 µl (to make a total volume of 1 ml)
    Working concentrations are prepared by taking 1, 2, 4 µl of 10 mg/ml
  15. 2-Nitrofluorine
    Used in Mutagenicity assay 
    Per ml
    10 µg
    Autoclave distilled H2O
    990 µl (to make a total volume of 1 ml)
    Working concentrations are prepared by taking 1, 2, 4 µl of 10 mg/ml
  16. Mitomycin
    Used in Mutagenicity assay 
    Per ml
    10 µg
    Autoclave distilled H2O
    990 µl (to make a total volume of 1 ml)
    Working concentrations are prepared by taking 1, 2, 4 µl of 10 mg/ml
  17. 2-Anthramine
    Used in Mutagenicity assay 
    Per ml
    10 µg
    Autoclave distilled H2O
    990 µl (to make a total volume of 1 ml)
    Working concentrations are prepared by taking 1, 2, 4 µl of 10 mg/ml


Urvashi Vijay would like to thank the Department of Zoology, The IIS University, Jaipur where the work was carried out. The financial help received by IISU Fellowship 2012/9389 to Urvashi Vijay is gratefully acknowledged.
Conflict of interests: None declared.
Authors contributions: Urvashi Vijay, Sonal Gupta, Priyanka Mathur carried out the protocol and the methods under the guidance of Pradeep Bhatnagar. Prashanth Suravajhala re-reviewed the works and proofread the manuscript before all authors approving it.


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Copyright: © 2018 The Authors; exclusive licensee Bio-protocol LLC.
How to cite: Vijay, U., Gupta, S., Mathur, P., Suravajhala, P. and Bhatnagar, P. (2018). Microbial Mutagenicity Assay: Ames Test. Bio-protocol 8(6): e2763. DOI: 10.21769/BioProtoc.2763.

If you have any questions/comments about this protocol, you are highly recommended to post here. We will invite the authors of this protocol as well as some of its users to address your questions/comments. To make it easier for them to help you, you are encouraged to post your data including images for the troubleshooting.

If you have any questions/comments about this protocol, you are highly recommended to post here. We will invite the authors of this protocol as well as some of its users to address your questions/comments. To make it easier for them to help you, you are encouraged to post your data including images for the troubleshooting.

Ajay Kumar
CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow
Dear Prashanth
Thank you for your response. Please check the Composition of Vogel Bonner Medium. The right composition is:
1. MgSo4.7h20-10.0gm
2. Citric Acid Monohydrate-100gm
3 K2HPo4-500gm
4- NaHNH4Po4.4H20-175gm

Distilled Water to make vol. one litre.

The Composition of Agar used for solidification is 1-2%, Generally 1.5%, So the Amount would be 15 Gram for 1 litre and 7.5 gm for half litre. Please check your composition.

BTW, Please let me Know this is review paper?
Please make the necessary changes.
7/13/2018 10:00:08 PM Reply
Ajay Kumar
CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow
Dear Sir/Mam
I have read your article in bio-protocol and found so many mistakes in the protocol. Please go through the composition of Vogel Bonner Medium Recipe 1 in your protocol.
1) All the constituents listed are in mg (miligram), but actually it is in grams.
2) the composition Agar mentioned in recipe 9, 10 and 11 in mg but actually it is in grams.
3) Please check all the compositions carefully.
There is so many blunder mistakes, which can make experiment non-reproducible.
Peer review is necessary.
7/9/2018 12:01:09 AM Reply
Prashanth N Suravajhala
Amrita University, Kollam

Dear Ajay

Apologies if you could not reproduce the protocol. Can you please clarify in details while our PhD fellow Urvashi who benchmarked all these recipes get back to you ASAP?

BTW, this protocol was peer-reviewed by three experts and reviewers and after careful check, it was published.

Prash for authors

7/9/2018 12:21:40 AM Reply

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