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22B: G - Unknown Bacterium

  • Page ID
    3643
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    Objectives

    • Maintain a pure culture of the unknown organism provided
    • Determine physical characteristics of the organism provided
    • Inoculate various biochemical tests and be able to read and understand the significance of each test, whether positive or negative
    • Use the information generated by testing, along with the given reference flow chart and identification texts, to deduce the Genus and Species designation of the unknown organism provided
    • Hand in a report of the testing performed (Unknown identification sheet), a journal of how you arrived at the identification you indicated and a TSA plate containing the unknown organism streaked to demonstrate isolated colonies

    It is virtually impossible to identify bacteria based on physical characteristics alone.  This is due to the fact that there are only a few basic shapes and physical features commonly seen in the prokaryotic world. Instead, biochemical testing has been used to make bacterial identification down to the “species” level. These schemes are based on creating and matching biochemical profiles of the production of enzymes, acids and gases by isolated pure cultures of a given microorganism. Identification schemes and flow charts can be found in reference texts such as “Bergey’s Manual of Determinative Bacteriology” or “The Prokaryotes”.

    Each group of students will receive a TSA slant or broth containing a pure culture of an unknown bacterium belonging to the Family Enterobacteriaceae.  It is the responsibility of the group to maintain stock cultures of the organism provided.  Working stock cultures will be used to inoculate the various biochemical test media over the next several weeks and should be fresh and free from contaminants.  A reserve stock culture should be made and after incubation and comparison with the original slant, kept with the original slant in the refrigerator.  

    It is critically important that aseptic techniques are used during transfers and inoculations to prevent contamination of your cultures.  If contamination is suspected, you will be able to fall back to your reserve stock.  If you fail to maintain a reserve stock you will not be able to recover your organism if disaster strikes.  The instructor will not provide a new culture for you to start with in the middle of the unknown exercises.

    Student Responsibility

    It is your responsibility to:

    • keep your organisms alive and fresh to run tests
    • check with us if you question purity of your organism or your test results
    • appropriately select media to identifying unknowns
    • ask for help
    • keep your bacteria in pure culture
    • check your results in a timely fashion (which may be CRITICAL for certain tests)
    • ask for ID books when you cannot find them (the Bergey’s Manual chapter is in eCampus)
    • put everything back where you found it
    • ask for media and/or test materials
    • come to lab prepared to run tests (your lab exercises, notebook, etc.)
    • NOT write in the above ID books

    Note

    • Each student will hand in their own separate report even though you have performed the work together as a group.
    • Remember it is import to keep your own journal and not to plagiarize other students in the group.

    MATERIALS NEEDED 

    • TSA plates
    • TSA slants
    • TSB broths
    • Clean glass slides
    • Gram stain reagents
    • Oxidase strips and reagent
    • Various biochemical media (distributed in sets during subsequent lab periods)

    THE PROCEDURES

    Schematic of identification procedure

     

    1st session  ⇒        2nd session  ⇒        3rd session  ⇒        4th session  ⇒        5th session

    Gram stain                oxidase test         Decarboxylase broths     Casein hydrolysis         optional tests

    Streak plate              catalase test        Deaminase agar              Lipid hydrolysis

    TSA slant/TSB          O-F glucose         Gelatin hydrolysis            starch hydrolysis

    SIM                           O2 tests

    TTC motility              Carbohydrates

    IMViC tests               nitrate test

              Urea hydrolysis

    1st Session

    1. Inoculate a TSA slant using an inoculum from the original culture you have been given.
    2. Inoculate a TSB broth from the original culture.
    3. Streak a TSA plate for isolated colonies using the 3 section method, using the original agar slant culture.   You will check for purity of the culture with this plate as well as use it to characterize the colony structure.
    4. Run tests listed in schematic above (see individual exercises for specifics on each test).
    5. Incubate all cultures at 25º C or 37º C as directed by your instructor.
    6. Gram stain your unknown organism using the TSB broth culture.  Note the shape, arrangement and Gram reaction of your organism.
    7. Place the original stock slant labeled with your group names and instructor in the refrigerator. Inoculate a new working culture each week to have a fresh culture to inoculate new media.

    2nd Session

    1. Observe your new slants looking carefully for signs of contamination. Compare to the original slant noting the color (note pigmentation), texture, opacity and odor.
    2. Describe the colony morphology displayed by isolated colonies observed on the streaked plate (refer back to the Colony Morphology experiment).
    3. Observe the biochemical reactions and record the results on your unknown identification sheet. Make any additional notes in your journal.
    4. Run tests listed in schematic above (see individual exercises for specifics on each test).
    5. Incubate at temperature recommended by instructor.

    3rd Session

    1. Observe the biochemical reactions and record the results on your unknown identification sheet. Make any additional notes in your journal.
    2. Run tests listed in schematic above (see individual exercises for specifics on each test).
    3. Incubate at temperature recommended by instructor.

    4th Session

    1. Observe the biochemical reactions and record the results on your unknown identification sheet. Make any additional notes in your journal.
    2. Run tests listed in schematic above (see individual exercises for specifics on each test).
    3. Incubate at temperature recommended by instructor.

    5th Session

    1. Observe the biochemical reactions and record the results on your unknown identification sheet. Make any additional notes in your journal.
    2. Run tests listed in schematic above (see individual exercises for specifics on each test).
    3. Incubate at temperature recommended by instructor.

    6th Session

    1. Read and record final tests results according to each separate procedure in the laboratory manual.  Review the resources available in the laboratory (Bergey’s Manual and other reference textbooks). If you are still unsure of the identity of your unknown, inoculate other tests as suggested  in the reference texts for next class.

    IT IS YOUR DECISION ABOUT WHAT OTHER TESTS SHOULD BE RUN FOR THE IDENTIFICATION OF YOUR BACTERIUM.  This decision should be made with the identification tables in mind, identifying which tests might further identify your organism.

    1. Streak a fresh TSA plate for isolated colonies.  This plate will be handed in with the final identification report.

    7th Session

    Hand in your:

    1. Unknown identification sheet (per table)
    2. Your journal (per table)
    3. The streaked plate of the unknown (1 per group)

    MEDIA LIST for unknown bacterial identifications

    Ask for the medium. Most of this media is available presently. If out, fresh media can be made upon request.

    Gelatin deep                                                            DNAse agar plate

    MacConkey or EMB agar plate                                EMB agar plate

    Methylene blue lipid agar plate                                Thioglycolate broth

    MRVP broth                                                             Litmus milk

    Nitrate broth                                                             Blood agar plate

    Uni-OF glucose                                                        Malonate (discs)

    ONPG discs                                                             Mannitol salt agar plate

    pH media (3, 5, 10)                                                  Starch agar

    Phenylalanine deaminase agar slant                       Skim milk agar plate

    Decarboxylase (Moeller's) broths:                            SIM

    arginine decarboxylase (ADC) broth            Simmon citrate agar slant

    lysine decarboxylase (LDC) broth                TTC motility MRVP broth TSIA slant

    ornithine decarboxylase (ODC) broth           Urea broth

    Sugars

    ASK for a sugar ……

    adonitol                                                 maltose                                        xylose

    arabinose                                              mannitol                                       cellibiose

    dextrose/glucose                                   mannose                                     malonate

    dulcitol                                                   melibiose                                     lactose

    esculin                                                   raffinose                                      inulin

    fructose/levulose                                   rhamnose                                    trehalose

    galactose                                              salicin                                           inositol

     sorbitol                                          sucrose

    BACTERIAL UNKNOWN SHEET

    Note

    • Tests that are italicized and in bold MUST be run, and reactions reported. All other tests performed must be reported as + or if run.
    • Tests NOT RUN do not have to be reported.

     

    GRAM REACTION ___________________                                                  DNAse __________

               Casein hydrolysis __________

    MICROSCOPIC MORPHOLOGY AND                                                          Starch hydrolysis __________

    ARRANGEMENT ___________________                                                     Urea hydrolysis __________

    Gelatin hydrolysis __________

    Lipid hydrolysis __________

    DESCRIPTION OF COLONY:                                                                        ONPG __________

    Color (clear, white, pigmented (if so, what color?)                                          TSIA __________

    Nitrate reduction __________

    Distinctive colony characteristics:                                                                   Phenol red sugars:

    colony shape/ type of margin  __________                                                    Glucose (no gas)_________

    elevation of colony  __________                                                                    Glucose (with gas)________

    other? __________                                                                                         Lactose __________

    Sucrose __________

    Mannitol __________

                                        Other sugars? __________

    GROWTH CHARACTERISTICS: Circle one for each

    O2 needs:  aerobe or facultative anaerobe? __________

    Optimal growth T:  25o C     30o C   37º C __________

    O-F glucose: oxidative, fermentative, or nonfermenter? __________

    Other tests run (names + reactions)? ____________________

     

    BIOCHEMICAL TESTS (+ or -?):

    Oxidase __________

    Catalase __________

    Indole __________

    Methyl red __________

    Voges-Proskauer __________

    Citrate __________

    Motility __________

    H2S __________

    Phenylalanine deaminase __________

    Decarboxylase tests:

    Arginine __________

    Ornithine __________

    Lysine __________

     

    THE BACTERIUM WAS IDENTIFIED AS :    _________________  __________________

    (genus)                     (species)

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