Replica Plating Lab Report

Improved Essays
It has been proven that yeast can grow on both YPD and SD plates. In this lab we cross several yeast strains through the process called replica plating. For this identification test only one dominant allele is required. One copy of each gene is essential to produce enough of each enzyme needed in order to make a histidine. Through the study of Saccharomyces cerevisiae we prove that by transferring yeast cells onto YPD and SD plates over a period of 24-72 hours in a thirty degrees Celsius incubator, in return will grow yeast.

Introduction

Yeast can reproduce both asexually and sexually, which makes it very easy to grow in the laboratory, as it is very small in size. Mutant yeast can be easily isolated considering yeast consists of a single cell and can be grown as a haploid or diploid. Diploid cells are formed by the combination of MATa and MAT alpha cells. However, under
…show more content…
Replica plating consists of using sterile velvet placed onto the replica block with the ring holding the velvet in place. Gently place the media and colonies down onto the velvet leaving a copy of the yeast on the velvet in order to transfer to another plate. Only use the velvet once per plate to avoid contamination. You can place either an YPD, SD, SD+His, SD+His+Leu, SD+His+Ura, and SD+His+Leu+Ura plates. An YPD plate contains all amino acids while an SD plate does not contain amino acids and only contains the essential nutrients. The SD+ plates will contain either an amino acid such as histidine or leucine, or a nitrogenous base such as uracil or any combination of the three. In order for yeast to grow on any of these plates, they need to be placed in an incubator at thirty degrees Celsius. If you wish to slow down or stall the growth of the yeast you may place the plates at four degrees Celsius, which is a temperature that can be obtained in a

Related Documents

  • Improved Essays

    Next reflame the loop, then return to the TSA turning it at 90 degree angle while streaking quadrant two dragging some of the substance from quadrant one. Follow the same steps until all three quadrants are completed, but avoid entering quadrant one only take from quadrant two. The purpose of the streak plate method is to produce isolated colonies of an organism. The TSA plate was incubated for approximately 48 hours at 37 degrees simply to grow bacteria. After returning back to the laboratory and noticing growth on the TSA plate the same streak plate method was applied to the MacConkey agar and the Mannitol salt agar.…

    • 416 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Next, using a graduated cylinder, tap water (10 mL) was added to each vial containing the culture medium. Upon addition of water, white culture medium turned blue. Additional amounts of tap water were added to each vial to provide more moisture. Next, three grains of yeast were added to each of the four vials. The vials were capped.…

    • 731 Words
    • 3 Pages
    Improved Essays
  • Great Essays

    Tetrahymena Experiment

    • 1363 Words
    • 6 Pages

    Tetrahymena contractions with different solutions Purpose: How fast will the Tetrahymena contractile vacuole contract in different solutions? Introduction: In this experiment, the organism that is used are the Tetrahymena.…

    • 1363 Words
    • 6 Pages
    Great Essays
  • Superior Essays

    The gram-stain process of colonies then reveal its shape and morphology, using aseptic…

    • 1514 Words
    • 7 Pages
    Superior Essays
  • Decent Essays

    1.1 Analysis Worksheet

    • 515 Words
    • 3 Pages

    spt15-300 mutants had higher growth yields than the control, some as high as 13x spt15-300 had better growth than taf-300 mutants, which did not grow in 6% ethanol media In absence of ethanol and glucose, the growth rate of spt15-300 and taf-300 mutants were near controls. d. What conclusion is drawn from these results? spt15 mutants grew best in elevated concentrations of ethanol and glucose. Mutations present in different transcription-regulating genes will probably exhibit different changes in phenotype.…

    • 515 Words
    • 3 Pages
    Decent Essays
  • Improved Essays

    Bio 13 Lab Report

    • 1034 Words
    • 5 Pages

    In the four-week long experiment conducted in the Bio 13 Lab, we were able to conduct a genetic analysis of the yeast S. cerevisiae, particularly investigating the inheritance and linkage of three genes: HIS4, LEU2, and LYS2. In week one, a suspension of spores was received and aliquots of the suspension were plates onto two YPD plates. After a week of yeast growth, haploid spore clones were carefully picked from the plates by sterile toothpicks and used to make patches on a new YPD plate, the master plate. In week three, the master plate was replicated onto three dropout plates: -His, -Leu, and -Lys. In the final week, the growth of the patches on the dropout plates were analyzed and class data was collected in order to conduct calculations for…

    • 1034 Words
    • 5 Pages
    Improved Essays
  • Superior Essays

    Unknown Lab Report Sample

    • 1696 Words
    • 7 Pages

    I obtained the unknown broth tube #15. I used two Tryptic Soy Agar (TSA) plates in order to make a streak plate. The streak plate is used to separate the two different bacterial organisms that were present in the broth. The plates were placed in the incubator at 37C and in 48 hours there should be isolated colonies on the plates. April 19, 2018.…

    • 1696 Words
    • 7 Pages
    Superior Essays
  • Improved Essays

    E. Coli Lab Report

    • 494 Words
    • 2 Pages

    By using a more diluted sample, the number of colonies may be less plentiful, thus allowing for an easier count of the colonies on each plate or possibly only allowing for growth on the 37°C, as it is suggested to be the most optimal temperature for growth (Piispanen, 2017, Fall Lecture). By decreasing the number of bacterium in the starting dilution, it may allow only the plate incubated at the optimal temperature of 37°C to produce colonies, and restricting the other plates incubated at other…

    • 494 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    In order to do the streaking method, an inoculating loop was sterilized with the Bunsen burner, and put into the unknown specimen then placed onto the TSA. After the plate was streaked it was then incubated at 37 degrees Celsius for 48 hours. The second step was observing the agar after incubation and identifying two different bacteria from the TSA. The third step after observation; was taking out the two bacteria with a sterilized loop and streaking it onto two Mueller Hinton plates. This allowed the separate colonies to grow further for testing.…

    • 1057 Words
    • 5 Pages
    Improved Essays
  • Superior Essays

    Cellular Respiration Lab

    • 1244 Words
    • 5 Pages

    The pyruvate strains only grew when it is added with fatty acids and heated to the restrictive temperature. I conclude that enzymes mutated could possibly stop the process of glycolysis, Krebs cycle, and electron transfer chain and different conditions could improve growth of each…

    • 1244 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Part B Two test tubes were labeled, one with “yeast” and the other with “water”. 1 ml of yeast suspension and 4 ml of distilled water was added to the “yeast’ labeled tube. 5 ml of distilled water was added to the “water” tube. 5 ml of sucrose solution was added to each test tube and stirred.…

    • 1180 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Yeast Fermentation Lab

    • 1039 Words
    • 5 Pages

    According to the graph above, the class results trend supported the hypothesis, as the yeast concentration increases, the rate of fermentation increases as well. The rate of fermentation is measured by the voulume of carbon dioxide gas produced through the chemcial reaction. Enzymes in yeasts catalysed the reaction. The increase in yeast concentration means more…

    • 1039 Words
    • 5 Pages
    Improved Essays
  • Decent Essays

    A colony is a organism living together in the same area. In this experiment, we tested how many colonies we will have in two different types of agar plates. One will be our control and treatment. As a control, we used our unwashed hands and a Q-tip to swab our hand from the bottom of the thumb to the opposite side. Once we swabbed our hand, we spread the bacteria from the Q-tip to the plate agar.…

    • 166 Words
    • 1 Pages
    Decent Essays
  • Superior Essays

    Essay On Biochemical Test

    • 1565 Words
    • 6 Pages

    This procedure is done once a week and stored at a 24°C incubator after 24-48 hours of initial growth. After transfer is completed, student can begin working on their first step of biochemical testing. The first procedure in the biochemical tests of enteric bacteria was to use a bunsen burner to sterilize the inoculation loop then streak unknown bacteria on to the MAC agar plate using streak plate technique referred from the lab manual in exercise 7. The MAC agar plate was then stored in the incubator at 37°C for about 48 hours until the next lab time.…

    • 1565 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    There will be three assays will be made and tested with both known and unknown plasmid. The first assay contains both PGEX-F1 primer and PGEX-R primer. Both primers enable to do replication with PCR in both Watson(top) strand and Crick(bottom). The presence of Saw1 insertion gene will not matter in this assay.…

    • 734 Words
    • 3 Pages
    Improved Essays