Lab work – Microbiology – Flashcards
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Pasuerization - 63 Autoclave - 121 Control 37 Boiling water 100 Human 37 Freezing 0 or 32 |
Agar is suitable for growing
Bacteria because it doesnt consume it Melts at 100 c and resulidifys at 45c or RT |
Handwashing
Look for a plate that has BEFORE/AFTER
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Normal Flora - Organisms that live live in or on body surfaces that do not normally cause disease, but are actually beneficial. This broken down to two groups TRANSIENT FLORA RESIDENT FLORA |
TRANSCIENT FLORA - org. that colonize the body for short periods of time due to recent environmental exposures to fomites, other people pets, etc |
RESIDENT FLORA - kind of like a microbial fingerprint that represents well-es, lifestyle. established species that thrive in or on the body. They colonize and reporduce successfully due to a person's genetic make-up, nutrition, general health. It will re establish after disruption due to hand washing, antibiotic therapy etc because they are essentially you. |
SIGNS
Objective. Things you can see. FACT.... temperture, fever |
SYMPTOMS
Subjective -You cant see Chest Pain, Headache |
Soaps - What makes them Effective?
If proper procedures are followed: First wet hands, then apply soap, Next rub your hands together vigorously, rubbing all surfaces for 20seconds. Rinse well and dry your hands. |
Plain Soaps Are:
Surfactants or Wetting agents. They remove bacteria and dirt by lowering surface tension and emulsification of fats and oils |
Why wasnt Iodine Effective?
Because of the expiration date on the bottle. |
DENTAL CARIES ; Snyder Agar; what does it contain? ; - contains sucrose and a PH indicator called Bromcresol green. ; What is Ph indicator of Snyder Agar? Bromcresol green ; |
Degree of Change - From Green to Yellow. Depends on how many orgs, how much it will FERMENT. |
Pathogens
Cause diseases
Determined by signs and symtoms |
Opportunists
Generally non-pathogenic very young, veryold, immunocompromised individuals, antibiotic therapy |
Dental Caries Org: Streptococcus mutans love sugar, particularly sucrose Convert enzymatically into long chains of sticky carbohydrate(dextrose)
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Dextran
allows adhesion, colonization, biofilm, community |
Biofilm
becomes DENTAL PLAQUE Dextran allows org to adhere, which allows colonization of the org. The colonization of this org forms BIOFILM |
Dental caries MEDIA:
Synder agar; sucrose, ph indicator (Bromcresol green) GREEN : GOOD YELLOW : acidic Value: 0-4 O= no change 4= bright yellow |
Quadrant Streak Plates
GOAL: get isolated colonies First step in getting pure colonies MOST IMP STEP: 1/2 streak Flame 1,2 quads Quad 3,4 no flame and lazy S Why turn dish upside down? avoid contamination, avoid breathing into plates condensation |
Simple Microscope vs Light or Compound Microscope
Simple: single lens system Compound: 2 lenses |
Magnification
make object appear larger, not better |
Resolution
ability to see 2 objects are separate, not blurry, have distinct outlines |
Ocular lens: binocular Objective lens: scanning: 4x Low power: 10x High Power/ high dry: 40x Oil immersion:100x |
Ocular is always : 10
X
Objective lens 10x100 = 1000. Best you can get |
How does Oil Immersion work:
it reduces the amount of scattered light because it isnt bending |
Wet Mounts; (lake, pond water)
What are the organisms:
Algae and protozoa |
Wet Mount
Benefits -
quick, easy, can view large eukarotic cells. Able to see depth of field better |
Wet Mount
CONS: drys quickly alive so could be a hazard |
What is Proto Slow?
Used in Wet mounts only to slow down org so it can be viewed better |
What is a Smear?
It is a Mono Layer |
What is the difference between plate and broth?
Only one difference. WATER |
What is a Salt? it is a chemical compound that is made of two parts, a positively charged part is called Cation CATION - positively charged part
Anion - Neg. charged part
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What is the difference between Basic and Acid?
The CHROMOPHORE
Basic has a pos. one Acid has a neg. one |
How does it affect staining? |
What dye do we use most in Lab
Basic |
Only Acidic one we use is what?
India Ink |
Why is India Ink Acidic?
because it has a neg. charge |
GRAM STAIN
The best culture (age)
is at 18 to 24 hrs. |
What Gram stain do we NEVER have in LAB?
GNC - It is rare in Nature |
What is another name for Gram Stain?
Differential Stain - the reason it is called this is you see more than one color. You are using two different ????(dyes) |
Gram Stain Procedures make a smear of the desired culture, being sure very thin smear - Place smear on the staining rack and flood w crystal violet -Leave for 1 min. -Rinse, shake off and go to next step quickly -apply mordant (Gram's Iodine) for 1min -rinse -Decolorize w ethyl alcohel for 3-5 sec. -Rinse off excess decolorizer -Counterstain w safranin, leave for 2min. rinse off for final time and allow slide to air dry fully -View under oil immersion Can be saved for 1 year
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Purpose of Each Gram Stain Step
First step Crystal violet - Primary stain.It stains all organisms
Mordant - Gram's iodine. this increase the affinity or attraction between the org. and the primary dye. ethyl alcohol- this attempts to remove the blue color from only one group of bacteria. Counterstain - Safranin. Any cells that lost their color with the decolorizing step are now clear and are counterstained w the additon of safranin. IF CELLS ARE BLUE - GRAM POSITIVE IF CELLS ARE RED - GRAM NEGATIVE
Decolorizer - eth |
Gram Stain Procedure: Make a smear of the desired culture. Make very thin smears. ; Place the smear on rack and flood w Crystal Violet for 1min. ; Rinse off excess dye using gentle stream of water. Shake off excess water ; Apply Mordant - Gram iodine for 1min. ; Rinse as before ; Decolorize w/ethyl alcohol for 3-5 sec. ; Rinse off excess decolorizer ; Counterstain w safranin, leaving on for 2 minutes. ; Rinse off for the final time and allow to air dry ; View under oil immersion. Slides can be saved for 1 year. |
What is the structure being stained in a GRAM STAIN? ; ; The structure imparting color is the cell well |
Why are Gram Pos and Gram Neg different colors ; due to chemical differences in the structure of the bacterial cell wall. ; ; ; What is the Best age of culture is ? ; ; 18-24 hrs |
Differences shown by the Gram stain are: Gram neg. - wall contains alcohol soluble lipids Producer of endotoxin Lipid A - need to give a slow dosage or endotoxin will be released and pt will go into shockk sensitive to tetracycling ; ; ; ; GRAM POS. lacks the lipids and retains crystal violet-iodine complex used; Produces exotoxins susceptible to certain antibiotics and phenol disinfectants |
Basic dye what colors will be what? ; Background Clear Org. colored |
Acidic Dyes what will be colored what? ; Background color Org. clear |
Negative Stain ; ; ACCP ; ; Acidic stain clear cell colored background Push smear NO HEAT FIXING ; |
Negative Stain ; Advantages: ; ; No heat, better look at size and shapes faster than simple,smear and staining done in one step ; Disadvantages : ; ; Because no heat fix potentially dangerous |
What is a NB made with:? ; ;water based, yeast extract, NaC1, beef pepton, phbuffer, ; ; |
If you see Malachite Green what stain is she referring too? ; ; ; Schaeffer Fulton Enpospore Stain |
If she puts out Ethyl Alcohl which stain did we use this on? ; ; Gram Stain |
What orgs were used in Acid Fast? ; ; Mycobacterium smegmatis micrococcus luteus |
What orgs were used in Endospore Stain? ; ; Bacillus subtilis old and new ; old - 3days young 24-48 |
What are the two org that endospores are made from? ; ; ; Bacillus and Clostridium |
What are procedures for Endospore? ; ; ; Stain: Malachite green Decolorizer: water Counterstain : Safranin ; What is purpose? ; ; to differentiate between orgs that can produce endospores and those that cant |
Endosopore procedures ; ; Use steam heat to allow the primary stain to penetrate the thick spore coat. Water for decolorizer Safrain used to color the vegetative cells |
Why do we have to use special Stains on the Acid Fast? ; ; Because of the thick waxy coat is resistant and impervious to decolorizing agents. so you cook in primary stain. THen the acid alcohol will strip the the primary dye from the non acid fast cellsl of the primary dye, carbolfuchsin BUT. will not penetrate the AFB. Then the Non acid fast org are counterstained w methylene blue so they can be seen under OI |
What color will the Non acid org be? ; ; Blue |
What color will the acid fast orgs be; ; ; ; PINK |
What is one of the Most Imp. environmental org from Bacillus(endospore) ; ; ; ;is B.anthracis B.cereus also causes problems as a food pathogen Clostridium contains some of the worst pathogen known to humans like Tentanus,botulism |
What is NB made out of? ; ; ; water based, yeast extract, beef peptone, NaCI,ph buffer |
What is NAP made out of ? ; ; ; same as NB, just add agar |
What color will org be on Endospore Stain? ; ; ; Endo - Green Veg - Red green and red - sporalation phase |
What is microbial growth? ; ; ; relates to an increase in the number of cells rather than in the size of individual cells |
What is Macroscopic growth? ; ; ; Is big enough to be seen or examined by the naked eye |
How are Broths asset? ; ; ; check for pellet - on bottom check for pelicle on top then resuspend then one inch from paper |
why;is Ethyol Alcolyl critical step on a Gram Stain? ; ; ; has too do w mono layer - some are thicker so would call for longer Ethyol Alcohol time |
Trouble shooting for Gram Stains ; Org is not blue enough??? ; Inc. the timing of the primary dye, crystal violet or Iodine not left on long enough |
Gram Positive orgs appear negative? over decolorizing on alcohl step. Decrease the time |
Gram neg appear gram Pos.? ; ; ; Under - decolorzing. This usually happens when smears are too thick. You can try decolorzing longer but best thing is too make new smear |
Orgs are not red eough and are very difficult to see? ; ; ; Safranin not lft on long enough. inc the time on safranin |
Org stains unevened on a gram stain due to the state of the cell wall? Why? ; ; Org are too old, young or are sporulating |
If it is not a baccillus or cocci what is it? ; ; ; ; Most likely, GNR |
What is Parocal ? ; ; This is the quality of the microscope that allows you to change obj. lenses w/o greatly altering the focus. ; EQUAL FOCUS |
What is Depth of field? as one layer is being veiwed, other layers fade out and get blurry. |
Refractive Index? ; ; ; the degree that light bends is indicated by the refractive index. ; Refractive index and OI is the same as glass |
Working distance? ; ; space between glass slide and the objective lens in position |
Base and Body of m.scope? ; ; ; ; Supports all of the working parts |
Arm? what is purpose ; ; ; ; to connect the base to the part of scope that houses the various lenses. Used to grab scope to move from oneplace to another. |
Lamp ; ; ; ; Provides illumination |
Voltage Regulator ; ; Used to vary the voltage going to the lamp |
What is Menisus? ; ; Causes a concave and adheres to side of the tubes ; ; ; ; |
Oil Immersion - ; ; light passes through oil directly into galss objective lens, little light escapes after entering the condenser. Refractive Index of immersion oil is same as glass. |
How do you Adjust light on scope? ; ; Iris deaphragm Condesnser, Voltage regulator |
Rule of Agar ; ; ; Not a good food source, that is why not a good media ; hardens at 100c and resolidifys at 45c |
When did we use Methyl Cellulose? ; ; That is same as Proto-Slo and was used only on Wet Mounts ; ; ; |
What was the result in class on the Environmental Culture? ; ; ; ; NG would be found where metals, credit cards cuz they dont support growth. |
Bacterial Population Counts: ; ; SPC -; counts what?? ; ; only viable organisms are counted ; Direct microscopic Counts - ; ;both dead and alive are counted ; ; ; Turbidometric methods - both dead and alive |
Invisiable Killer Movie ; ; Stachybotrys toxic Mold(Black mold) ; grows due to water damage causes brain damage,seizures, brain fogginess equalibruim off, vomiting diahreea |
Group B Strep ; ; Common Bacteria found in intestines if passed to baby it will dye. ; Causes brain damage. Mental Retardation.1/3 of women carry it. 1-2% will get it. Prevention is simple if antibodics during labor or test whil preganet. |
Transverse Mylitis ; ; ; 34,000 cases in this county couldnt breath, couldnt feel limbs paralze are syndrome that hits the spinal cord and |
Hemolytic Uremic Syndrome ; ; ; E. coli from well water Attacks internal organs attacks liver, kidneys brain, You can find E coli anywhere Little girls that died |
Capsule Stain ; ; It is a combo of NEgative stain and the Simple Stain |
Capsule Stain; ; ; ; ; Org used: Klebsiella Pneumoniae,Bacillus megaterium or Saccharomyces cerevisiae ; |
Capsule Stain ; ; ; Stains used: Primary dye: India ink (used for Push Smear) Decolorizer: 0.1NHC1 Counterstain: Safranin ; Background will be brown Capsule will be clear w/pink in center(that is the vegetative cell) |
What is the Bacterial Capsule called? ; ; ; Termed Glycocalyx |
What is the purpose of the bacterial Capsule? ; ; gives an addl layer of protection to the cell It resists being engulf by white blood cell |
What are capsules;made of? ; ; ; mucoid polysaccharides or gelantinous polypeptides. |
Quanatative means ; ; The actual counted growth |
Why will capsule stain sensitive to heat? ; ; because the normal heat fix step of smear preparation. it would cause some non encapsulated cells to shrink, leaving holes in the stain that appear to be capsules. But if you dont heat the org will wash off the slide during the dying process. |
Capsule stain; 2 genera that produces capsule:: Streptococcus pnemonia Klebsiella pneumonia ; ; How does this stain work? It has 2 different stains, neg and simple ; ; Orgs used:Klebsiella pneumoniae bacillus megatridium saccharomyces cerevisiae Capsule Stain Procedure Make a push smear add a drop of india ink to the slide mix in a small part of a colony or 2 loopfuls from a broth into the India Ink MIX gently push smear allow to dry flood smear for 30 sec. w 0.1.NHC1 Pour off excess acid and air dry again Counterstain w/ safranin for 1min rinse safranin w tap water Air Dry view under OI ; |
What;are the results of a Capsule Stain? ; ; Red colored rods(K.pneumoniae or B megaterium or S.cerevisiae) The Red color is the vegetative cell. ; Clear area around the colored cells indicate the capsule. seen against a red or BLUE background. |
qualitative evaluation - ; ; ; ; You look at it and say NG or Growth ; ; amount of microbial growth in our lab media, estimating turbidity in broths. |
Colony forming units CFU- Why use to know this term? Since it is impossible if a colony formed from a single cell, or from a number of cells clumped together, it is more accurate and generally accepted in industry to use the notation CFU |
Characteristics and requirements of each Gram type ; ; GRAM -;;; wall contains alcohol-soluble lipids producers of endotoxins Sensitive to tetracycling antibiotics aminoglycoside antibiotics Susceptible to chlorine,detergent,iodine, Lipid A: endotoxemia - need; to give a slow dosage,; Endotoxins released into blood, shock ; ;;;;;; GRAM+;;;lacks the lipids and retains crystal violet-iodine complex used. Producers of exotoxins susceptible to certain antibiotics and phenol disinfectants ; ; |
What is a subculture? ; ; making org from original primary plate or broth |
Acid Fast Stain ; Ziehl-Neelson stain Mycobacterium: Thick waxy; coat exterior(lipoidal coat-mycolic acid) extremely resistant to most decolorizing agents; Dual Smear: two bacterial species on one side quality control Result:Acid-Fast-Bacilli: Bright fushsia pink Non Acid - BLue |
Special Stains: ; ; Flagella, endospores,capsules, |
Schaeffer Fulton Endospore Stain ; ; Org used: Bacillus subtilis Purpose:; to differentiate between org that can produce endosportes and those that cant. IT TESTS for tetanus, botulis ; ; Thick:;;outer coat: cell wall material, calcium diplocholinate,Kertain ; ; Stains used. Malachite Green,decol: water and counter:;safranin |
Is Algae motile or non motile? ; ; Non-motile |
Is protozoa motile or non?? ; ; ; Motile |
Tell me all you know about B subtilis |
Requirements for Microbial Growth ; Nutrional reg. ; CAP HC ; ; Carbon - most essential element for life on earth Autotrophs - can fix carbon fromCO2 found in the atmosphere, which is inorganic. Heterotrophs must obtain their carbon from organic and sources such as meat and veggies ; Energy source - to survive, all orgs must be agble to produce energy (ATP) on a daily basis. Some org are phototrophs, meaning they use radiant sunlight for their energy source. These are rare, most org energy is obtained from a chemical source in the media in the form of Carbs or amino acids. These orgs are called Chemotrophs, which are by far and away, the most abudant life forms on earth. |
Nutrional Requirements contd ; Growth factors - these factors are specific ing.that must be included in lab media like amino acids, vit.,blood cell, components; or materials the orgs. are unable to produce on its own ; Minerals - elements like sodium,potassium, calcium,magnesium,iron,zinc,copper, phosphorous and cobalt. they are neccessary for cellular metabolism by aiding in enzyme structure and function. ; Nitrogen - essential in the composition of proteins and nucleic acids. ; Vitamins - water -Since water makes up about 70-85% of a cell, it must be provided in all lab media.Tap water is never used cuz it contains excess calcium/magnesium ions. Distilled water is used |
What is Agar made of?? ; ; Agar;is a polysaccharide derived from marine algae(a seaweed called RHODOPHYTA. This is used to thicken media to the desired consistency. |
Physical Req. ; Ph of the;media; - greatly affects metabolic enzyme activity.Most org like it around neutral or 7. A change in either direction if too drastic, usually harms the org, sometimes fatal. ; Lab media is generally in neutral range which suffices for most microbial growth fungi being a notable exception |
Types of Respiration: ; ; Aerobic Anaerobic Facultative Microaerophilic ; |
What is Saprophytic? ; ; ; Break down dead organic matter vs parisite |
;what do you know about Bacillus subtilus ; ; ; ; Known;;as Hay or grass bacillus Is Gram Positive Found in Soil Rod-shaped Is a Obligate aerobe Is not a human pathogen |
Streptococcus Mutans ; ; ; Gram Positive Facultative anaerobic Found in Human oral cavity Contributor to tooth decay |
Mycobacterium smegmatis ; ; ; Generally considered a non pathogen GPR non motile Used in Acid fast stain ; |
;Staphylococcus Aureus ; ; ; Gram Positive Coccus Facultative anaerobic Appears as grape like clusters Most common cause of staph infections Found in the skin, nose and throat It can cause a wide range of illnesses from pimples, boils to life threating like pneumonia, meningitis ; Growth pattern = look at notes ; |
Micrococcus luteus ; ; ; Gram Positive Found in many places in the environment, water, soil, dust. Most are mesophiles It can be;a Opportunistic pathogen |
Bacillus megaterium ; ; Rod shaped Gram Positive Found in Soil Can survive in extreme conditions such as desert environments. Is used to make Penicillin |
Streptococcus Lactis ; ; Gram Positive Found as a contaminant in milk, dairy products Common cause of Souring and coagulation |
Pseudomonas Fluorescens ; ; ; Gram Negative Rod Shaped Has multiple flagella Found in Soil and water Obligate Aerobe Green You smell it on Patients, smells like Tortilla |
E. Coli ; Gram neg. rod haloduric saccrophilic Find in the bowel |
2 ways to get a Isolated Culture ; QSP Pour plates |
What is an A jar called ; ; ; ;Anaerogen anaerobic Jar ; ; What is the environment in the A jar? ; ; removal of free 02 produces anaerobic conditions w/in the jar |
WHAT IS THE indicator for the A jar? ; methylane blue if it is blue it means that there is oxy if clear no oxy. So if blue data not valid |
3 experiments we used Methylene Blue ; Acid Simple AJar |
What are the char. of S.cervesciae ; dull, creamy,mounted macroscopic;growth Yeast grown on SAB Saccrophilic Acidophilic ; |
How do you inculate a Slant ; Lazy S toward the top ; |
How does a Bacterial cell repair itself? ; ; ; ;endonuclease- snips out the faulty dimers.; DNA polymerase - brings in new pairs DNA ligase - seals it up |
Agar Deep ; ; ; Same as a plate but in a Tube |
What is titer? ; ; ; A measure of antibody level in a patient, determined by agglutination method |
What is Sabourand Dextrose Agar ? What are some of their unique characteristics? ; ; It is a special selective media used w/ fungi Has a PH of 5.6 and increased sugar concentration. It works well since Fungi are both acidophilic and saccharophilic, this medium works weel to encourage growth while inhibiting most bacteria ; ; How does SAB inhibit the growth of unwanted Bacterial species? ; ; It is acidic and has a high sugar concentration |
What are some characteristics of YEAST? ; ; Dull, mounted and creamy |
What are some characteristics of Bacteria? ; ; Flat and shiny |
Disinfectant ; ; you can only use on any surface that is not alive |
Antiseptic ; ; ; Used on live tissues but not meant to be taken in |
Chemotherapy ; ; ; meant to be taken into the body 2 subgroups - antibodic made from nature synthetic - made in Lab |
Broad ; ; ; ; can kill pos. and neg gram |
Narrow ; ; ; can kill all one like all Gram pos or all Gram ng. |
Why would you prescribe a Intermiade antibodic vs. Sensitive?? ; ; ; Pt. too weak to take more cost effective Pt allergic |
Describe;;Confluent Lawn Pattern ; ; down, side, horizontal and around |
In what experiment did we use the Agar Diffusion Method? ; ; Chemical Control Agents |
What organism were used in the Chemical Control agents; ; ; BES ; ; ; Staph. aureus(GPC) E.coli (GNR) Bacillus megaterium(GPR) |
Zone of Inhibition ; ; Clear are of no growth around a specific disc |
What does the Zone of Inhibition tell us about the agent? ; ; ; if it is effective if the org. is sensitive |
How do you determine the kind of Effect? cidal or static? ; ; You subculture from zones to NB ; If org grow right up to the edge of disc then it is? ; Resistant and a subculture would not be neccessary in this case |
In Chemical Control why can you only say R and S? ; ; Because we did not measure, this is not standarized |
Name 10 things on KB? ; ; ; ; Confluent lawn mueller hinton plate spacing, pre-labeling 18-24 0.4mm agar deep incubation 37 + 0.1 oC |
What do you know about Seratia marcescens? It is a luxary enzyme In good condition more pink less will get clear ; In past was not a pathogen and used to test air currents ; But known to be a pathogen in some cases ; ; |
What is the plate called we used in KB? ; ; Mueller Hinton Plate |
Saccharomyces cervisiae |
Alcaligenes Faecalis |
Name 4 ways that KB is standardized? ; ; |
Trichothecium ; ; It will be blue and cigars will have;a split or divide |
What is a reason why we would Subculture? ; because you want a pure culture You want more because you need more |
How does the env. created in the Ajar differ from that of a candle jar? ; ; CJar has small amount of o2, increased CO2 and CO Ajar removal of free O2 produces anerobic conditions w/in the jar |
Define Capneic? ; ; grows better in CO2 under conditions of increased Carbon dioxide in the atmosphere because as humnas we carry CO2, we convert OXy into CO2 |
What is Resazurin? ; ; It is a oxy. indicator for Thios broth |
What color is Resazurin when oxygenated? ; ; Red/Pink |
Resazurin when anaerobic? ; ; CLEAR |
What is the oxy indicator for Cjar and Ajar ; ; Methylene Blue |
What are the two components that make up the endospores thick outer coat? ; ; Keratin ; Calcium diplocolinate |
What are the orgs we used in the smear prep ; SA B.cereus E. coli |
What is most common media for Fungi? ; ; Sabouraud Dextroseagar ; ; Why ; Since fungi are both acidophilic and saccharophic, this medium works well to encourage their growth while inhibiting bacterial species |
;How does heat control microbial growth ; ; ; ; ; By denaturing proteins and damaging cell membranes and other internal components |
;What is the difference in the procedure between making a smear of an org from a broth versus Solid media? ; ; Procedures are the same except you add a drop of water to the slide before putting on the org ; Reason is it helps emulsify the org that is most likey chunky or sticky |
What kind; dye is best for staining a bacterial slide? ; ; Basic dye - because bacteria contain a neg charge, so you need a dye that has the opposite charge |
Name 3 types of special Methods we will use to mimic the different atmospheric conditions. ; ; Thioglycollate broths candle jars Anaerogen anaerobic jar |
Why is it important not to shake the Thio? ; ; ; ; It may disrupt the oxygen gradient |
In the Osmotic Pressure exp. we used a GRADIENT PLATE. What is that? ; ; ; Is a double layered agar plate w/ concentration gradient of a particular solute in the bottom layer of the agar. ; Why? to give the effect of a hypertonic environment |
How does PH affect an org? ; ; it has one of the greatest influences.All orgs have a prefered ph, where they grow best. But if you go out of the range it is equally as damaging |
What is the environment of a C jar? ; has a small amount of O2, increased CO2 and CO |
What is purpose of an Agar Slant? ; ; are very helpful for observation of surface growth ; and can be saved for a long time |
Define Serial Dilution ; ; ; a way to arrive at a desired concentration. It is a stepwise dilution of a substance in a solution. |
List the steps of KB procedure that are standardized mueller hinton agar spacing of disc time 16-18hr age of culture 18-24 ph 7.2-7.4 |
Thio indicator ; ; resazurin ; Red - if oxy present |
Staphylococcus Aureus How does org grow in NB?? What is the Growth pattern? ; like a tornado |
UV - What repairs dna in bacteria ; ; Enzymes ; ; Endonucleases- snip out faulty dimers DNA; polymeracse brings in new pairs Dna ligase - seals it up |
what is the differene between bacteria and yeast? ; Eukarotic, |
;What are the difference between KB;and Chemical control ; ; ; subculture KB is standardized |
Dirt or soil is gram liquid is ml ; CFU per gram CFU per ml |
Sample of an Antibodic and synthetic ; ; Pencillin sulfa |
;Growth pattern for Semi Solid ; motile will look like xmas tree or just a few dots ; non motile - just see growth down the middle of the TB. not on the sides |
;Tell me about Klebsiella pneumoniae ; ;Gram-negative, non-motile, ;encapsulated, lactose fermenting, ;facultative anaerobic, rod shaped bacterium ;found in the normal flora of the mouth, skin, and intestines. |
Serratia marcescens; ;Gram-negative, rod-shaped bacterium . A human pathogen,; ; , urinary tract infections; ;wound infections,[1][2] and is responsible for 1.4% of nosocomial bacteremia cases in the United States.[3] It is commonly found in the respiratory and urinary tracts of hospitalized adults and in the gastrointestinal system of childrenS |
What are some Environmental factors that influence the growth of microorganism? ; ; Temp osmotic presure ph UV |
Bacterial Population Count was org was used?? ; ; ; ; E. coli |
Anaerobic Cultures What org were used ; MESC ; ; ; ; ; Micrococcus luteus staphylococcus aureus escherichia coli clostridium sporogenes |
Chemical Control what orgs were used: ; ; ; BES ; ; Bacillius megaterium Escherichia coli staphylococcus aureus |
KB what orgs are used? ; ; ; ESSP ; ecoli stahphylococcus aureus s.marcescen Pseudomonas aeruginosa ; Pseudomonas aeruginosa ; ; ; |
What orgs do we use in Moist heat ; ; ; BBEM ; ; Bacillus subtilis Bacillus endospore e. coli mycobacterium smegmatis |
What orgs in Temp. ; ; ; ; ; PSB ; ; ; pseudomonas aeruginosa streptocoocus lactis bacillus stearothermophilus |
What orgs in PH ; ; ; EASS ; ; ; ; ecoli alcaligenes faecalis saccharomyces cerevisiae staphylococcus aureus |
What orgs in Semi Solid media? ; ; ; ; PS ; ; ; proteus mirabilis staphylococcus epiderimidis |
What org in Hanging Drop? ; ; ; MP ; ; ; ; Micrococcus luteus pseudomonas aeroginosa |
;What is another name for Acid fast stain? ; ; ; It is a dual stain |