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Micro Lab Exercise 4
| Question | Answer |
|---|---|
| Bacteria that are introduced into various forms of culture media to keep them alive and to study their growth without introducing unwanted microbes. | Inoculated |
| Unwanted microbes | Contaminants |
| Technique used in microbiology to exclude contaminants. | Aseptic Technique |
| Rendered free of all life | Sterilized |
| Test tubes containing solid culture media that were left at an angle while the agar solidified. Easier to store and transport. | Agar Slants |
| Agar is allowed to solidify in the bottom of a test tube. Often used to grow bacteria that require less oxygen than is present on the surface of the medium. | Agar deep |
| A sterile, heat-resistant, noncorroding Nichrome wire attached to an insulated handle. When the end is bent into a loop it's called? | Inoculating loop |
| A sterile, heat-resistant, noncorroding Nichrome wire attached to an insulated handle. When it's straight it's called? | Inoculating needle |
| For special purposes, sterile swabs, pipettes, glass rods, or syringes may be used to transfer cultures. | True |
| What is the purpose of flaming the mouth of the tube? | Convection. To prevent airborne contamination. |
| What other methods can be used to determine motility? | A flagella stain. A microscope. Motility agar. |
| What is the primary use of slants? | Long-term storage. Pure cultures. |
| What is the primary use of deeps? | To store anaerobic bacteria. To test oxygen requirements. |
| What is the primary use of broths? | To grow large amounts of bacteria. |
| What is the purpose of flaming the loop before and after use? | To sanitize the loop. To incinerate anything that is on the loop. |
| Why must the loop be cool before you touch it to a culture? | To avoid killing the organisms. |
| Should you set down the loop to let it cool? | No. It will get contaminated. |
| How do you determine when the loop is cool? | You will hear a sizzle if it is not. Trial and error. Practice. |
| When is a loop preferable for transferring bacteria? | When you are transferring bacteria to a plate, a slant, or broth. |
| When is a needle preferable? | When you are transferring bacteria to a deep. |
| Why is aseptic technique important? | To prevent contamination and disease. |
| For a bacterium, what evolutionary advantage is associated with forming a pellicle in a liquid medium? | If the bacteria is aerobic, it floats to the top. |
| How can you tell that the media provided for these exercises were sterile? | No turbidity, clear. |