Pglo Plasmid By E. Coli

Improved Essays
Escherichia coli (E. coli) is one of the most widely studied and understood living organisms. It has been used for decades in furthering understanding of gene functionality and gene-protein mechanisms for prokaryotes and eukaryotes alike (Riley et al. 2006).
Prokaryotes, like E. coli, have their DNA in the form of a plasmid. A plasmid is a circular ring of DNA. The plasmid intended to transform the E. coli colonies for the purposes of this study was the pGLO plasmid. The pGLO plasmid contains three main genes: one for GFP (green fluorescent protein), one for ampicillin (an antibiotic) resistance, and one that codes for the sugar arabinose (Bassiri 2011). The process used to transform the E. coli bacteria with the pGLO plasmid was by means
…show more content…
coli is a competent bacteria cell able to take up a pGLO plasmid by means of heat shock genetic transformation. To test this, colonies of E. coli mixed either with a pGLO plasmid or without a pGLO plasmid were placed on four Luria-Bertani (LB) agar nutrient plates. One plate had only LB, two had both LB and ampicillin, and one had LB, ampicillin and arabinose sugar. We hypothesized for this study that the E. coli mixed with the pGLO plasmid would take up the plasmid and would then thrive on the agar plates with ampicillin because the pGLO plasmid contains a gene for ampicillin resistance. It also follows then that the E. coli colonies without the pGLO plasmid (i.e. also without the ampicillin resistance gene) would die off due to the presence of ampicillin in the agar. Furthermore, we hypothesized that E. coli would grow on all of the plates except for the plate with no pGLO plasmid containing LB and ampicillin. Finally, we hypothesized that the E. coli with the added pGLO plasmid would glow on the plate with LB, ampicillin, and arabinose sugar because the arabinose would activate the GFP gene also found in the pGLO plasmid causing the E. coli to produce the protein. The results of this experiment are significant because the way that many genetic processes occur in E. coli parallel the genetic processes in most other organisms (Riley et al. 2006). As such, understanding how genetic transformation works in E. coli can aid in understanding the process for all living

Related Documents

  • Superior Essays

    Bsrg1 Week 1 Lab Report

    • 1912 Words
    • 8 Pages

    The effect of the BsrG1 restriction enzyme on Wild Type and Mutation 1 of E. coli DNA Introduction: What a lac operon is involved in the lactose metabolism of E. coli and it can only work when there is no glucose present to interfere with the lactose metabolism. (Khan Academy) E. coli chooses prefers glucose and other "better" sugars, so if any are present other than lactose the lac operon will not be expressed in the plasmid. (Khan Academy) A plasmid is an "independent, circular, self-replication DNA molecule" that contrasts with the more complex helical shaped DNA of Eukaryotes.…

    • 1912 Words
    • 8 Pages
    Superior Essays
  • Improved Essays

    E. Coli Lab Report

    • 494 Words
    • 2 Pages

    coli is considered a mesophile, meaning it grows at moderate temperatures, between 20°C and 40°C, with its optimal growth temperature being 37°C (Piispanen, 2017, Fall Lecture). The results demonstrates that 37°C is the most optimal temperature for growth, as this plate had the highest number of colonies present. However, to support this statement of E. coli being a mesophile, there would had to have been growth on the plate incubated at 23°C. To clarify these findings further and investigate why there was no growth on the 23°C, the experiment could be performed an additional time. However, the sample could be diluted more, using a dilution other than 10-6, such as 10-8.…

    • 494 Words
    • 2 Pages
    Improved Essays
  • Decent Essays

    Pglo And Pglo Tubes

    • 225 Words
    • 1 Pages

    With two tubes labeled -pGLO and +pGLO to indicate which tube was the test and which was the control. To begin pipette 250 microliters of transformation fluid into each tube and then add e.coli plates. Once done close the lids of the tubes and place them on ice. Using a sterile loop remove a single colony of bacteria from a starter plate. In the +pGLO tube submerge the single colony into the transformation fluid, then return the tube to the ice bath.…

    • 225 Words
    • 1 Pages
    Decent Essays
  • Superior Essays

    E. Coli Lab Report

    • 2621 Words
    • 11 Pages

    In this experiment, E. coli was introduced to two plasmids: pUC18 and lux. Plasmid pUC18 contains a gene that codes for the enzyme beta-lactamase which renders ampicillin and some other antibiotics inactive. Plasmid lux found in V. fischeri contains an operon that codes for luciferase, an enzyme that is involved in a light creating reaction. Within this experiment CaCl2 was used to increase E. coli’s ability to take up plasmids. Once E. coli was able to take up pUC18 and become resistant to ampicillin lux was used to identify E. coli through its light-emitting reaction.…

    • 2621 Words
    • 11 Pages
    Superior Essays
  • Improved Essays

    Both cut and uncut plasmid DNA were transformed into E. coli DH5α. Finally, the transformed DNA was plated on LB and LB with ampicillin agar plates. The procedure for this experiment was followed on pg. 16-23 of the MB 311 laboratory manual. One exception to the protocol was step D-12 on pg.…

    • 1074 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    Egfp Lab Report

    • 3655 Words
    • 15 Pages

    The first two plates should have had green colony growth and possibly also white colony growth, plate #3 should have had green colonies, plate #4 should have no growth as results showed, plate #5 should have white colonies, and plate #6 should have bacterial lawn as results showed. With better and more accurate results, the transformation efficiencies would have changed as well with higher numbers in ug units. Miniprep To Purify And Isolate plasmid DNA-  Figure 3: Miniprep Gel Electrophoresis.…

    • 3655 Words
    • 15 Pages
    Great Essays
  • Improved Essays

    The purpose of this experiment was to determine the working concentration of Tetracycline (TNC) on Escherichia coli (EC). We used EC because of its characteristics of fast growth in different environments, complete gene sequence, and availability. Our antibiotic, TNC, is a broad spectrum antibiotic which is effective to many types of bacteria. This is because it obstructs tRNA anticodon from reading the mRNA codons in the 30S ribosomal subunit which halts the lengthening of the protein chain. My team determined that we would use a wide range concentration between 0 and 100 µg/ml of TNC.…

    • 583 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    E. Colo Cell Lab Report

    • 755 Words
    • 4 Pages

    Colonial growth is the key to discovering whether there was a successful transformation in the bacterium 's cells. If there is colonial growth of E. coli in an ampicillin environment then the plasmids triumphantly transformed the cell and as a result were able to create either the enzyme beta-lactamase, for the pUC18 transformed cells, or the enzyme luciferase, for the lux transformed cells, which would counteract the effect of ampicillin on the cell wall of the bacteria. There were many errors in this experiment. Only two of the agar plates actually developed properly, one of them was the ampicillin agar plate with no plasmid (Fig 1: top left) because there was no growth seen. This was the expected result because since ampicillin kills the bacteria, the E. coli cells should not have been able to survive in the environment…

    • 755 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    This plasmid is a circular DNA molecule that is commonly used as a cloning vector with E.coli (Ke et al., 2008). This plasmid has been engineered to include a unique feature of a gene that codes for antibiotic resistance to ampicillin, an antibiotic that inhibits the synthesis of the cell wall which in result, destroys the cell. This is prevented with the resistance coded gene called β-lactamase, which breaks down the ampicillin prior to it preventing cell wall synthesis. The vector length is 2686 bp with a copy number range of 500-700 per bacterium. To selectively grow bacteria that have been successfully injected with the pUC18 plasmid DNA, it would have to be done in a media containing ampicillin so that the bacteria that do not contain the gene will not be able to survive thus leaving only the ones containing the gene.…

    • 1260 Words
    • 6 Pages
    Improved Essays
  • Great Essays

    1. Non-pathogen name: Bacillus subtilis 2. Description of non-pathogen: B. subtilis is a mesophilic, gram-positive bacillus that is commonly found in soil, although it can also survive in plants (1). B. subtilis are facultative aerobes, using butanediol fermentation or nitrated ammonification when oxygen is unavailable (1). The bacillus is motile by using a single flagellum and commonly forms biofilms which contain several B. subtilis all traveling in the same direction (1).…

    • 1330 Words
    • 6 Pages
    Great Essays
  • Improved Essays

    A second method a bacterium can use to become genetically diverse is transformation. Transformation begins when a bacterium…

    • 363 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Bacteria naturally contain one or more small circular pieces of DNA called plasmids. Plasmid DNA usually contains genes for one or more traits that may be beneficial to bacterial survival. In nature, bacteria can transfer plasmids back and forth, allowing them to share…

    • 321 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    It is beyond a doubt that the founding fathers could ever conceive an American society like the one we are living in today. The discovery of the structure of DNA marks a significant landmark in medical history. This has open the doors to a new realm that deepen our understanding of biological systems and promises a future that once was an abstract idea in science fiction novels. A challenge that my generation is facing is answering whether genetic modifications are ethical. Despite the ongoing debates, it is remarkable that this type of science is even possible, partially because of the universality of DNA.…

    • 537 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    In order to survive in and withstand many environmental pressures, one aspect that is both critical and necessary is the ability for organisms to be able to regulate gene expression. Amongst bacterial species, one gene that has been identified as a main factor is the cell-cycle transcriptional regulator, known as ctrA. It controls at least 25% of the genes involved in the cell cycle process (Mercer et al., 2010). ctrA has been highly studied in the model organism, Caulobacter crescentus, in which it is responsible for controlling various functions during the cell cycle by activating or repressing gene expression of approximately 25% of the 553 cell cycle-regulated genes in the genome (Reisenaur et al., 1999). This protein also blocks initiation of DNA replication by binding to five sites within the chromosomal origin (Brilli et al.,2010). During the G1 phase when C. crescentus transitions from swarmer cells to stalked cells, ctrA suppresses replication in the swarmer…

    • 660 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Pglo Transformation

    • 823 Words
    • 4 Pages

    coli was able to take up DNA (pGLO plasmid) via transformation. It can also be concluded that the ampicillin resistance gene was transferred (form of growth) and the gfp gene was phenotypically expressed (fluorescence from UV light) in the LB/amp/ara medium containing the pGLO+ culture. Overall, the results from the pGLO- and pGLO+ transformations seem to be accurate. However, the results are subject to imperfections due to evenly spreading the transfer DNA to the Luria broth plates. In regards to theory, genetic transformation is an important process in biotechnology.…

    • 823 Words
    • 4 Pages
    Improved Essays