API 20E test API 20 E or analytical profile index 20 E is a standard bio chemical test used to identify the presence of bacteria using 21 miniaturized bio chemical chambers in a slide card. All the reagents in the cupule are found in the dehydrated form. Upon incubation followed by inoculation with bacterial sample, there will be spontaneous color changes with or without addition of extra reagent. Material and equipment I. Agar plates of bacterial species II. Sterile Pasteur pipette III. API 20 E test strips IV. API 20 E test strips incubation tray V. Inoculation loop VI. Bunsen burner VII. API 20 E analytical profile index VIII. McCartney bottle Chemical and reagents 1. 0.85 % Sodium Chloride solution 2. Sterile mineral oil – paraffin …show more content…
Cover the test strips using the lid provided and label the setup with name (unknown sample), date, time, temperature and name of the assessor. IV. The oxidase can be performed on the available kit or separately. The excess bacterial suspension is inoculated into a an agar plate and check for oxidase test (BioMérieux, 2017) • Incubation of strips in the chamber I. Pour 5 ml water to the bottom of the incubation tray and place the strips on the incubation tray II. Incubate the strips for 370c for 18-24 hours • Reading the strips I. After the incubation add proper reagents in the cupules IND – 1 drop of Kovac’s reagent – the result read within few minutes VP - I drop of Barrett’s reagent (A & B) - the result within 10 minutes TDA – I drop of FeCl3 – result within few minutes II. The result is read depending on the color change according to the chart below. If the color change is positive write it as +. Count the numbers within 3 set cupule. III. Check for the seven digit number in the code book. IV. If cupule of GLU tube is negative re-incubation is required further for 18-24 hours before addition of the reagent. (or less than 3 steps showing positive
Last test, inoculation of phenylalanine agar is used to determine if phenylalanine deaminase oxidizes phenylalanine into phenylpyruvic acid and ammonia. Sixth test, is a Multiple Test Media used to determine the physiological characteristics of unknown #398. First test, Inoculation of Kligler 's Iron agar was used to determine the production of hydrogen sulfide from cysteine and fermentation of glucose and lactose. Last test, inoculation of litmus milk is used to determine the fermentation of lactose, casein, lactalbumin, and
Catalase Activity on Substrate Based On Gas Pressure Production Rate Name of the Class Author’s Name Date Enzymes are organic compounds which act as catalysts and speed up biological reactions in biological organisms. They are not destroyed or changed during the reaction but rather they are used over and over again to catalyze many more reactions. Their activity may be affected and altered by factors such as temperature, substrate concentration, enzyme concentration and Ph.
Unknown 6- Isopropyl Alcohol We found that unknown 6 was Isopropyl alcohol. Its chemical name is isopropanol and the chemical formula C₃H₈O but is typically called isopropyl alcohol. Isopropyl alcohol is today used as a primary ingredient in rubbing alcohol. Is smells very unpleasant and is used for disinfecting pads used by medical professionals for tasks such as sanitizing small instruments, wiping down surfaces, and cleaning a patient’s skin before an injection.
Procedure and Observations To begin the lab, first all the correct equipment and materials had to be collected
To do the temperature and dissolved oxygen tests, stick the probe in the water, and it will show numbers. One will be the dissolved oxygen in ppm (parts per million) and the other will be the temperature of the water. To do the pH test, stick the pH paper in the water and compare the color it turns to the scale. To test nitrates, put clear water in a container and dirty water in another, and put powder in them. Shake them and then compare the color they turn to the scale.
Staphylococcus epidermidis is the organism that was identified based on the tests that I had conducted. The tests that I used to identify this organism were the coagulase test and the catalase test. My bacterium was beta hemolytic as well. First, a gram stain had to be done to determine whether the organism was a gram positive organism or a gram negative organism. This determined which set of tests that had to be done.
Each plate serves as a first step to identify the unknowns. The TSA (tryptic soy agar) can be used to do a gram stain, which differentiates gram-negatives from gram-positives, based on the structural make up of the cell wall (Carson, 2015). The blood agar plate is used to test for hemolytic activity, which is useful for distinguishing gram-positives. A MacConkey plate is selective by inhibiting the growth of gram-positives and differential due to the fermentation of lactose by certain gram-negative species. In the
Being able to identify unknown microbes from systematic testing is what makes the field of microbiology so important, especially in infectious disease control. Using the testing procedure laid out by the microbiology field we are able to identify unknown bacteria present in our everyday lives, and along the way learn a lot about their characteristics that separate them from other types of bacteria. Being able to do this is vital in order for us to understand why microbes are present in certain places, how they are able to grow and what restricts their growth, that way they can be combatted if necessary. These techniques for determining unknowns are also important for isolating and testing infectious disease microbes in order to prevent spreading. Another important aspect of being able to identify unknown microbes is the
Starch solution is then placed into the test tube at a quantity of 5 mL. 5 drops of Lugol’s Iodine solution is added to the test tube. If the color changes, then it is known that starches are present in the solution. Proteins are next tested. In order to do this, 5 mL of gelatin solution is added to the test tube. 10 drops of Biuret’s reagent are added to test for protein.
Pat McGurrin October 24, 2015 Period #1 Honors Biology Mr. Dinunzio Murder and Meal Lab Analysis Procedure: 1.) Gather all materials: Safety goggles, 250ml beaker, water, hot-plate, test-tubes, paper bag tear, stomach contents, pipette, Biruet solution, Benedict’s solution, and Iodine solution. 2.) Put on safety glasses.
Exercise 14: Unknown Identification Lab Report The purpose of the study was to identify the unknown bacterium using various biochemical tests in addition to using scientific methods in determining the outcome of the hypothesis. Each biochemical test will help determine the bacteria based on specific characteristics of each organism. I was giving unknown number 232. The first procedure that needed to be done after obtaining unknown bacterial mixture was to isolate the two bacteria in a pure culture using the streak plate method described in Microbiology Laboratory Manual Eight Edition. The material used was trypticase soy agar (TSA) plate, nutrient plate, starch agar, hydrogen peroxide, iodine reagent and microscope.
Do the same for the other test tubes. Let the test tubes not be disturbed for about 3- 4 mins. Then add the Amylase solution to the Starch solution and start the stopwatch (immediately). After every 1 min take one drop from the test tubes and place then in the test plate that were
From the Unknown tube professor Cooper gave me, I scratched a little on the slant surface with the sterilized inoculating loop. Then I place it on a clean prepared slide which already had a slight drop of water. The two substances are mixed together in the middle of the slide and let dry completely. One extra step of “heat fix” is necessary to adhere everything to the surface of the slide. To start gram staining, I slightly pour crystal-violet all over the slide and let it sit for 30 seconds before wash it off with water.
This can be tested by simply mixing the serum of suspected individual which contain the antibodies with the antigens of specific bacteria the accumulation of clumps confirms the presence of particular bacterial infection.[2] This test can be performed in various ways including slide agglutination reaction, tube agglutination reaction, indirect agglutination inhibition reactions etc. Another important practical application involves blood group test of
It also better to ensure that the materials like hemocytometer and pipettes are sterilized and clean so that there would be lesser or no artifacts would be seen under the microscope. The researcher was to use trypan blue exclusion method to test for cell viability, observe the non-viable and viable cells, and was able to have a cell count using the