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Microbiology Lab Techniques: Safety, Sterilization, and Aseptic Practices, Exams of Microbiology

A comprehensive overview of microbiology lab techniques, focusing on safety protocols, waste disposal, and sterilization methods. It covers essential procedures such as handwashing, aseptic techniques, and the preparation and handling of culture media. The document also includes detailed descriptions of various sterilization methods, including autoclaving, dry heat sterilization, and filtration. It is designed to help students understand and apply these techniques in a laboratory setting, ensuring accurate and safe experimentation. It also includes key concepts such as colony morphology, selective and differential media, and the identification of common resident microbes. Useful for students to prepare for microbiology lab exams and understand the practical aspects of microbiology.

Typology: Exams

2024/2025

Available from 06/06/2025

LennieDavis
LennieDavis 🇺🇸

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BIO 205L MIDTERM 2025/2026 LAB QUESTIONS
AND ANSWERS/MICROBIOLOGY GRADED A+
Why do transient microbiota (flora) not become entrenched?
Come into contact with skin constantly, but most are unable to multiply there and
will die. pH of skin is usually acidic (ranging from 4-6). The epidermis (outer layer
of skin) has a low water content and is frequently dry, so normal skin flora is
associated with the apocrine and sebaceous glands in the skin which provide not
only moisture, but also other nutrients for microbial growth. Washing skin with
soap and water sloughs off dead outermost layers of skin and may expose normal
flora.
Person safety
Ø Lab coat or apron
Ø Gloves
Ø Safety glasses
Ø Closed toe and covered heel shoes
Ø Hair should be tied up
disposal - Microscope slides
white paper biohazard discard pouches or the red plastic biohazard boxes
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BIO 205L MIDTERM 2025/2026 LAB QUESTIONS

AND ANSWERS/MICROBIOLOGY GRADED A+

Why do transient microbiota (flora) not become entrenched?

Come into contact with skin constantly, but most are unable to multiply there and will die. pH of skin is usually acidic (ranging from 4-6). The epidermis (outer layer of skin) has a low water content and is frequently dry, so normal skin flora is associated with the apocrine and sebaceous glands in the skin which provide not only moisture, but also other nutrients for microbial growth. Washing skin with soap and water sloughs off dead outermost layers of skin and may expose normal flora.

Person safety

Ø Lab coat or apron

Ø Gloves

Ø Safety glasses

Ø Closed toe and covered heel shoes

Ø Hair should be tied up

disposal - Microscope slides

white paper biohazard discard pouches or the red plastic biohazard boxes

disposal - broken glass

white paper biohazard discard pouches or the red plastic biohazard boxes

disposal - petri dishes

orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - plastic tubes

orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - paper trash contaminated with microbial culture

orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - tube and flask media

plastic discard tubs on the bottom of the cart, use racks for tubes, remove all labels

disease-causing for humans

pathogenic

diphtheroid Corynebacterium and Propionibacterium, species of Staphylococcus such as Staphylococcus aureus and Staphylococcus epidermis, and Malassezia yeast

Common resident microbes of the skin include...

may be present on the body temporarily but do not become firmly entrenched

Transient microbiota (flora)

the top 2 reasons for nosocomial infections in the US

Staphylococcus aureus and Pseudomonas aeruginosa

disposal - micropipette tips

plastic discard beakers on the bench tops or in the orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - swabs

plastic discard beakers on the bench tops or in the orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - tongue depressors

plastic discard beakers on the bench tops or in the orange/red biohazard trash bags in the white metal cans with foot pedal to open

disposal - glass serological pipettes

long plastic discard tubs on the bench tops provided only when needed

disposal - gloves

tall boxes labeled for glove discard only

disposal - non-contaminated paper trash

regular trash cans

disposal - unused media

do not discard; return to top of cart

Rhodophyta (red algae)

solid media in Petri dishes; the surface is used for isolation and growth of microorganisms

Plates

test tubes containing solid medium, which has been allowed to solidify in an upright position, and are usually used for anaerobic growth

Deeps

test tubes containing solid medium that has been allowed to solidify at an angle and the surface of the agar is used for the maintenance of stock cultures of microorganisms

Slants

nutrient medium designed to favor the growth of certain microbes and to inhibit undesirable competitors

Selective medium

selective only; it selects for Gram-positive organisms but tells nothing of the physiology of the organism growing on it

Phenyl ethyl alcohol agar (PEA)

medium which provides a visible indication of a physiological characteristic of a microorganism

Differential medium

both selective and differential; selects for growth of salt-tolerant organisms and differentiates mannitol fermenters (change agar from red to yellow) from non- mannitol fermenters (don't change color of agar)

Mannitol salt agar (MSA)

both selective and differential; selects for Gram-negative bacteria and differentiates lactose fermenters from non-lactose fermenters

Eosin methylene blue agar (EMB)

used when using a sample of a population to estimate or generalize to a population

Sample standard deviation

dry heat sterilization method; inoculating loops/needles are held in the flame of a Bunsen burner until flowing red hot. It is important to flame the entire wire loop/needle to minimize contamination.

Flaming

dry heat sterilization method; items to be sterilized like glassware are placed in an oven and heated to 170*C for 2 hours.

Hot-air sterilization

how heat sensitive liquids or gasses are sterilized; the surface of the filter traps particles while allowed the liquid to pass through, this is a physical removal of bacteria or other contaminants.

Filtration

widely used gas for gas chemo-sterilization; toxic and explosive and is released into a chamber where it circulates for up to 4 hours with the items to be sterilized; type of cold-sterilization

Ethylene oxide

no heat is used

Cold-sterilization

includes microwaves, ultraviolet radiation, X-rays, gamma rays, and electrons

Electromagnetic radiation

causes damage to the DNA leading to the death of exposed organisms; cannot penetrate solid, opaque, light-absorbing surfaces and is useful only to sterilize exposed surfaces

Ultraviolet (UV) radiation

causes ions and other reactive molecules to be produced and these reactive molecules can degrade or alter biopolymers such as DNA and proteins

Ionizing radiation

minute living cells that are too small to be seen with the naked eye; they are widespread in our environment and can be found on almost any surface; growing on a solid culture medium (i.e. agar plate) will form colonies if the cells used to inoculate the plate are separated from each other on the surface of the medium

Microorganisms

the nutrients on which microorganisms are grown

Medium

Whole colony shape:

round; irregular; rhizoid

Margin shape:

Smooth, entire; lobate; filamentous

Elevation:

Convex; umbonate (button-like); flat

Optical properties:

Opaque (can NOT see through it); semi-translucent (can see through edges of the colony but not the center); translucent (can see through it)

Surface characteristics:

Dull; shiny; wrinkled; concentric; pigmentation (color)

How to handle media aseptically

  • Upon entering the lab, lab bench must be wiped with disinfectant and a clean paper towel to eliminate any contaminates on the surface. Wash hands. Wear gloves. Tie back long hair.
  1. Gently shake culture tube to suspend microorganisms.

  2. Heat loop and wire to red-hot.

  3. Remove cap and flame neck of tube. Do not put down cap.

  4. After allowing loop to cool for at least 5 seconds, remove a loopful of microorganisms. Avoid touching the sides of the tube.

  5. Flame the mouth of the culture tube again.

  6. Replace cap. Place tube in test-tube rack.

  7. Flame mouth of the tube of broth or agar in which the sample will be placed. Place the loopful of microorganism on a slide for a smear or onto an agar plate, or into a tube of broth/slant/deep.

  8. Flame loop again before removing another loopful from culture or setting the inoculating loop aside.

refers to a procedure performed under sterile conditions

Aseptic technique

dry heat sterilization

one containing a single kind of organism; rarely exist in the natural world, but are useful in the lab to study cellular processes without influence from other

Pure culture

pure cultures of this were used to determine the roles of DNA polymerases involved in replication and DNA repair

Escherichia coli

a population of cells which arise from a single cell growing on a solid medium; all of the cells should be genetically identical but for a few (if any) that may have mutated

Colony

an example of a pure culture

Isolated colony

Another way of determining the purity of a broth culture is by ______ the sample. A ______ stain can reveal the different cellular morphologies (shape and/or

arrangement) of the microorganisms present, while a ______ stain like a ______ stain can reveal structural differences.

staining; simple; differential; Gram

transferring the colony to a new plate; commonly used to maintain cultures; this second plating will also allow any hidden cells of a different species to be diluted with streaking the plate for isolation

Subculturing

Adequate magnification must be used when viewing prokaryotic cells because of their small size; most are ____ μm to ____ μm. In general, the oil-immersion objective must be used to observe microorganisms and the total magnification achieved is _____.

0.2; 10; 1000X

Because cells consist mostly of ______ , even under adequate magnification unstained cells may be difficult to see because of lack of ______.

water; contrast

makes cells more visible by providing contrast

Staining

  • Coccus, rod/bacillus, and spiral
  • Diplo (pairs), strepto (chains), staphylo (clusters), or randomly

round

Cocci

Types of cocci

  • Diplococci - cocci that remain in paids
  • Streptococci - cocci that remain in chains
  • Tetrads - groups of four cocci
  • Staphylococci - grapelike clusters

rod-shaped cells that divide only across the short axis

Bacilli

Types of bacilli

§ Diplobacilli - pairs

§ Streptobacilli - chains

short oval cells that resemble cocci; can be induced by less than ideal environmental growth conditions, or simply by the genetic makeup of the cell

Coccobacilli

have one or more twists

Spiral

Types of spiral

§ Vibrios - curved rods

§ Spirilla - helical shape that is rigid

§ Spirochetes - helical, flexible, and resemble a corkscrew (could put a rod through the center)

irregular or variable shape

Pleomorphic

some actinomycete bacteria, e.g., Streptomyces coelicolor, produce filaments of hyphae that form a mycelium (network of hyphae)

Filamentous growth