A microbiology laboratory is a place for working with a variety of microorganisms.
Most microbiological laboratory procedures require the use of living organisms and the
integral part of all laboratory sessions is the use of aseptic techniques. Although the virulence
of microorganisms used in the academic laboratory environment has been greatly diminished
because of their long term maintenance on artificial media, all microorganisms should be
treated as potential pathogens (capable of causing disease). Thus microbiology students must
follow aseptic techniques (free of contaminating microorganism) in the preparation of pure
cultures that are essential in the industrial and clinical applications.
Rewarding laboratory experience demands strict adherence to prescribed rules for
personal and environmental safety. The former reflects concern for personal safety in terms
of avoiding laboratory accidents. The latter is required maintaining a scrupulously clean
laboratory setting to prevent contamination of experimental procedures by microorganisms
from exogenous sources. These techniques will thus determine the success or failure of the
scientific experiments conducted as well as protects the lab personnel from potentially
harmful microorganisms.
The following basic steps should be observed at all times to reduce the ever present
microbial flora of the laboratory environment.
1. Upon entering the laboratory, place coats, books and other paraphernalia in specified
locations and never on working bench tops. Working space should be reserved for
essential equipments and a lab book.
2. Keep doors and windows closed during laboratory sessions to prevent contamination
from air currents.
3. A lab coat or apron must be worn at all times in the laboratory to protect clothing
from contamination or accidental discoloration by staining solutions. When leaving
the laboratory, remove the coat or apron and at regular intervals, get the apron
washed.
4. Wear a paper cap or tie back long hair to minimize its exposure to open flames and
contamination with microbial cultures.
5. Wear closed shoes at all times in the laboratory.
6. Cut nails regularly and don’t put finger in eyes, ear or mouth as it can facilitate the
chance of infection by microorganisms.
7. Do not eat, drink, apply cosmetics or insert contact lenses in the laboratory.
8. Wash the hands with liquid detergent, rinse with 70% ethyl alcohol and dry them with
paper towels upon entering and prior to leaving the laboratory.
9. Wipe bench tops with disinfectant solution, at the beginning and termination of each
laboratory sessions and after every spill.
10. Carry cultures in a test tube rack when moving around the laboratory. Also keep
cultures in a test tube rack on the bench top when not in use. This helps to prevent
accidents and to avoid contamination of yourself and the environment.
11. Open the culture tubes or plates and perform the experiments near the vicinity of the
flame of the burner. The burner must be kept at a distance from organic solvents and
immediately turned off after use.
12. Always use a mechanical device for pipetting reagents or bacterial cultures. Mouth
pipetting is strictly prohibited in the microbiology laboratory.
13. Do not lick labels. Use only self stick labels for the identification of the experimental
cultures.
14. Do not place contaminated instruments such as inoculating loops, needles, pipettes
and slides on bench tops. Loops and needles should be sterilized by incineration and
pipettes and slides should be disposed off in designated receptacles.
15. On completion of the laboratory sessions, place all cultures and materials in the
disposal area
16. Rapid and efficient manipulation of fungal cultures is required to prevent
dissemination of their reproductive spores in the laboratory environment.
17. Speak quietly and avoid unnecessary movements in the laboratory so as to prevent
distractions which can lead to accidents.
18. Report accidental cuts or burns or spills immediately.
19. Spilled cultures or broken tubes must be immediately covered with paper towel and
saturated with disinfectant solutions. After 15 minutes of reaction time, the towel
should be removed and dispensed.
20. Follow strict aseptic techniques for personal safety and success of experiments
performed
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