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Toxicological information

Genetic toxicity: in vitro

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Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Publication used for read-across purposes

Data source

Reference
Reference Type:
publication
Title:
A survey of chemicals for mutagenic action on E. coli.
Author:
Demerec, M., Bertani, G. and Flint., J.
Year:
1951
Bibliographic source:
The American Naturalist, Vol. 85: 119-136

Materials and methods

Principles of method if other than guideline:
Strains B/Sd-4/1,3,4,5 and B/Sd-4/3,4 of E. Coli were used throughout this work. For every experiment, bacteria were grown for 24 hours at 37 deg C in an aerated broth culture containing 10 micrograms of streptomycin per milliliter. They reached a saturation titer of approximately 2 to 3 x 10^9 cells per milliliter. Each culture was started from an inoculum, usually large, taken from streptomycin-agar slants kept in a refrigerator. Before treatment the bacteria were washed in saline and resuspended in distilled water. A sample of the new suspension was added to the desired solution of chemical in distilled water, and incubated at 37 deg C for a certain period of time; no growth occurs under these conditions. Another sample of the same suspension was added to an equal amount of distilled water and incubated for the same period of time, as a control. At the end of the treatment period, both treated and control suspensions were assayed by plating suitable dilutions on streptomycin-agar plates. At the same time they were plated (0.1 ml per Petri dish), either undiluted or diluted not more than 1: 10 in plain broth, onto a number of streptomycin-free plates, using a glass spreader and a turntable. The assay plates were incubated for 48 hour, after which it was possible to count the colonies and calculate the titers of the two suspensions at the end of treatment, and the percentage of survivors. The streptomycin-free plates (mutant plates) were incubated for at least six days. After this time the colonies were scored, and the frequency of mutants calculated by dividing the number of colonies by the number of (viable) bacteria plated.
GLP compliance:
no
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
L-(+)-lactic acid
EC Number:
201-196-2
EC Name:
L-(+)-lactic acid
Cas Number:
79-33-4
IUPAC Name:
2-hydroxypropanoic acid

Method

Target gene:
Sd-4
Species / strain
Species / strain / cell type:
other: Streptomycine-dependent E. coli strains B/Sd-4/1,3,4,5 and B/Sd-4/3,4
Metabolic activation:
without
Test concentrations with justification for top dose:
0.01%, 0.02%
Details on test system and experimental conditions:
IUCLID4 Type: Escherichia coli reverse mutation assay

Results and discussion

Test results
Metabolic activation:
without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
other: 0.02%
Additional information on results:
Some of the experiments with lactic acid indicated a weak mutagenic effect; but this is rendered doubtful by the fact that experiments wIth sodium lactate consistently gave negative results.
Remarks on result:
other: other: Streptomycine-dependent E. coli strains B/Sd-4/1,3,4,5 and B/Sd-4/3,4
Remarks:
Migrated from field 'Test system'.

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

Lactic acid is not mutagenic
Executive summary:

Thirty-one chemicals, representing various organic and inorganic groups, were tested for ability to induce back-mutations from streptomycin dependence (Sd-4) to nondependence in E. coli. Nineteen were found to be mutagens. It was demonstrated that mutagenicity is not a specific property of anyone group of chemicals, but appears among widely different groups. Chemicals having such different properties as boric acid, ammonia, hydrogen peroxide, copper sulfite, acetic acid, formaldehyde, and phenol were found to be mutagenic, indicating that genetic changes may be induced by many agents that are able to enter the living cell and upset its metabolic functions.

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