Preview

Dead or Alive Results

Good Essays
Open Document
Open Document
392 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Dead or Alive Results
BIOSC 0050
Oct. 9, 2012
Dead or Alive? (Week 2) Post-Lab Assignment
Results:
The results of the Feulgen’s Schiff’s Stain test are that samples ALV-188-23 and ALV-843-20 turned magenta and samples ALV-882-21 and ALV-694-02 did not turn magenta. The result of the tetrazolium test is that all four of the samples did not turn pink. We were not able to conduct the detailed analysis of cultured plates with growth, so not results are available for this test.
Discussion:
For the Feulgen’s/Schiff’s Stain that tests for DNA, the samples that contain DNA will show up under a compound light microscope as a magenta color while samples that do not contain DNA will not show up as magenta. A sample of bacteria from an agar plate was used as a control for the DNA test, and it showed up as magenta from the Feulgen stain; this confirms that the test accurately indicates the presence of DNA. The results show that samples ALV-188-23 and ALV-843-20 contain DNA, which means that the samples are organisms that are either alive or once living, according to the test. Also, the results show that samples ALV-882-21 and ALV-694-02 do not contain DNA, so these samples were never alive.
The tetrazolium test indicates the presence of redox reaction, which signifies metabolic activity by turning samples that perform metabolism a pink color. Sucrose was used as a control to show that the test is accurate in that it does not turn samples that do not perform metabolism pink. Sucrose was not turned pink, which validates the accuracy of the tetrazolium test. As expected, samples ALV-882-21 and ALV-694-02 did not turn pink; the Feulgen’s/Schiff’s Stain that was done previously showed that samples ALV-882-21 and ALV-694-02 were never living, so it makes sense that they would not have any metabolic activity. Since samples ALV-188-23 and ALV-843-20 did not turn pink, yet contain DNA, we conclude that these two samples are organisms that are now dead.
We were not able to conduct the detailed

You May Also Find These Documents Helpful

  • Good Essays

    Endospore Test Lab Report

    • 691 Words
    • 3 Pages

    The primary dye malachite green is a weakly binding dye to the spore wall and cell wall. The dye will be locked in the spore wall, which has peptidoglycan deeper in the walls. The keratin forming the outer portion of the endospore wall resists dye. The heating of the bacteria will make the spore wall more permeable to the malachite green, and it then attaches to the peptidoglycan. Thus, we can detect the bacteria that have the endospore based on this test. On a clean glass slide a drop of distilled water will be added to the slide. A smear will be prepared on this droplet by using fresh culture of bacteria and then will be air dried and heat fixed. The smear will be flooded with malachite green (0.5% aqueous solution). The slide will be heated so that malachite green will be steamed for 5 min but will not allow evaporating. More malachite will be added by heating the slide over again. Then the slide will be cooled and will be washed under running water. Then, the smear will be flooded with counter stain safranine for 30 second. Then the slide will be washed with distilled water to remove extra stain. The slide will be examined under microscope spores will appear green inside the bacteria while absence of green colour will show non-endospore forming bacteria (Ali et al.,…

    • 691 Words
    • 3 Pages
    Good Essays
  • Good Essays

    This was done by melting a solution composed of 0.7% agarose in 1x TBE and 0.005% ethidium bromide, and pouring the resulting liquid into comb-containing gel tray until the thickness reached about 6 mm. Once the gel had been allowed to cool for about 20 minutes, it was removed from the tray, placed in a horizontal gel apparatus, and immersed in 1x TBE buffer. Next, three different solutions were prepared from an aliquot of HindII digested lambda DNA and 3 microliters of 6x loading dye, an aliquot of EcoRI digested lambda DNA and 3 microliters of 6x loading dye, and 1 kb DNA ladder and 3 microliters of 6x loading dye. The resulting solutions were then transferred into separate wells within the gel, and the apparatus was connected to a constant current source (45mA) for 60 minutes. After producing clearly visible bands, the gel was taken out of the apparatus and photographed with an ultraviolet light box (Displayed in Figure…

    • 1568 Words
    • 7 Pages
    Good Essays
  • Powerful Essays

    Stickleback Lab

    • 3141 Words
    • 13 Pages

    Stallsmith, B. Laboratory Manual for Organismic Biology. 2nd ed. Mason (OH): Cengage; 2006. p. 9-17.…

    • 3141 Words
    • 13 Pages
    Powerful Essays
  • Better Essays

    Unknown Lab Report

    • 2145 Words
    • 9 Pages

    The oxidase test was performed only on gram (-) bacteria and was used to test for the presence of cytochrome oxidase. Living bacteria were placed on a paper towel and saturated with a chromogenic reducing agent. Within seconds the reagent, acting as an artificial electron acceptor, will turn purple if oxidized cytochrome oxidase is present, indicating a positive test. If no color change is observed, no cytochrome oxidase is present and the test is negative.…

    • 2145 Words
    • 9 Pages
    Better Essays
  • Better Essays

    Tortora, G., Funke, B., & Case, C. (2010). Staining Techniques. Retrieved April 25, 2015, from http://www.cliffsnotes.com/sciences/biology/microbiology/microscopy/staining-techniques…

    • 1286 Words
    • 4 Pages
    Better Essays
  • Powerful Essays

    Hola

    • 2255 Words
    • 10 Pages

    Perform the following test and record your observations in Table 1 on page 8 of this packet. Use a hand lens or microscope as needed.…

    • 2255 Words
    • 10 Pages
    Powerful Essays
  • Powerful Essays

    These results were completed through the gel electrophoresis lab that was carried out. Gel electrophoresis is a lab technique used in biochemistry in order to separate out pieces of cut DNA. This process requires that you have an electrical field passing through the gel in a specific direction. To allow for charge to flow across, you must have something that will conduct electricity, a buffer that's usually composed of ions works as a conduit for the electrical charge. An agarose and TBE solution was prepared and used to completely cover the entire gel. The DNA has a negatively charged backbone because of all the phosphate groups so they moved towards the positive end of the gel…

    • 1175 Words
    • 5 Pages
    Powerful Essays
  • Better Essays

    Using the Quadrant Streak technique the unknown and ubiquity were streaked onto a trypticase soy agar (TSA) plate. This method was performed as stated in the Leboffe & Pierce lab manual(1). The TSA plates were incubated at 30 degrees Celsius for 48 hours. This process was repeated until isolated colonies appeared. At this point cell morphology was observed and recorded. At this time the unknowns were renamed as Unknown Red (UK-R) and Unknown White (UK-W) because the pigment production was a deep red for one and a cream colored white for the other. The ubiquity was also renamed at this time as…

    • 862 Words
    • 4 Pages
    Better Essays
  • Powerful Essays

    Slime Mold and pH

    • 2068 Words
    • 9 Pages

    Patterson, B., R. Hallick, W. Grimes, M. Hewiett, J. Aronson, and B. Fishel. Biology 181…

    • 2068 Words
    • 9 Pages
    Powerful Essays
  • Powerful Essays

    Norfolk State University Department of Biology Course Syllabus Biological Science (BIO 100-03) 3 Credit Hours MWF: 11:00 AM- 12:00 PM WSB 118…

    • 2239 Words
    • 9 Pages
    Powerful Essays
  • Powerful Essays

    Isolation of Mitochondria

    • 2221 Words
    • 9 Pages

    Assay of succinate dehydrogenase of after isolation of mitochondria in Cauliflower (Brassica oleracea) using differential centrifugation.…

    • 2221 Words
    • 9 Pages
    Powerful Essays
  • Better Essays

    In 2008, the President’s Council on Bioethics published the ‘Controversies in the Determination of Death’. Within the publication, the Council discusses the various criterions that need to be met in order for death to be declared. The criterions include those of a neurological level, which have been observed for over three decades. Although there have recently been objections to the neurological criterion in regards to death determination, the Council decided to maintain the criterion. In keeping the neurological criterion, the Council was correct, but the justification of the criteria is insufficient.…

    • 1222 Words
    • 5 Pages
    Better Essays
  • Good Essays

    The materials used in the lab were two agar petri plates, a permanent marker, labeling tape, sterile scalpel, compound microscope, toothpick, microscope slide, water, cover slip, and the ascospore Sordaria cultures, which included wildtype (dark), tan, and grey (mutant) fungi.…

    • 1043 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Introduction: In 1866 an Austrian monk, Gregor Mendel, presented the results of painstaking experiments on the inheritance patterns of garden peas. Those results were heard, but probably not understood, by Mendel’s audience. Now, more than a century later, Mendel’s work seems elementary to modern–day geneticists, but its importance cannot be overstated. The principles generated by Mendel’s pioneering experimentation are the foundation for genetic counseling so important today to families with health disorders having a genetic basis. It’s also the framework for the modern research that is making inroads in treating diseases previously believed to be incurable. In this era of genetic engineering the incorporation of foreign DNA into chromosomes of unrelated species—it easy to lose sight of the basics of the process that makes it all possible. These were his conclusions: The hereditary determinants are of a particulate nature. These determinants are called genes. Each parent has a gene pair in each cell for each trait studied. The F1 from a cross of two pure lines contains one allele for the dominant phenotype and one for the recessive phenotype. These two alleles comprise the gene pair. One member of the gene pair segregates into a gamete, thus each gamete only carries one member of the gene pair. Gametes unite at random and irrespective of the other gene pairs involved.(Carlson)…

    • 810 Words
    • 4 Pages
    Good Essays
  • Good Essays

    ♣ Microscopy (staining) ♣ growth on enrichment, selective, differential or characteristic media ♣ specimen biochemical test (rapid test methods) ♣ immunological techniques ♣ molecular (genotypic) methods.…

    • 3783 Words
    • 16 Pages
    Good Essays