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Frederick Griffith uncovered genetic role of DNA Transformation- change in genotype and phenotype due to assimilation of external DNA by a cell Pathogenicity.

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Presentation on theme: "Frederick Griffith uncovered genetic role of DNA Transformation- change in genotype and phenotype due to assimilation of external DNA by a cell Pathogenicity."— Presentation transcript:

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2 Frederick Griffith uncovered genetic role of DNA Transformation- change in genotype and phenotype due to assimilation of external DNA by a cell Pathogenicity was inherited by all descendants of transformed bacteria Oswald Avery determined DNA was the transforming agent

3 1.Incorporate radioactive sulfur on the protein surface of viruses 3. Mix bacteria and viruses in blender and centrifuge 4. Bacteria forms a pellet on bottom and viruses remain in the liquid 2. Viruses infect bacteria

4 Same process as before except radioactive phosphorus was incorporated into phage DNA Experiment showed DNA is phage’s genetic material

5 A pairs with TG pairs with C Erwin Chargaff found that the four nitrogenous bases were present in specific ratios in all organisms. Could not explain his discovery A= 30.9% G= 19.9% T= 29.4% C=19.8%

6 Watson saw an image of DNA produced by x-ray crystallography and deduced DNA has a helical shape. Watson and Crick built a model of DNA with a double helix

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8 Conservative Semiconservative Dispersive Grow first in heavy isotope culture then light isotope culture

9 Bacterial DNA Origin of Replication Daughter Strand Parent Strand Replication Fork Replication Fork- y shaped region where new strands of DNA elongate

10 DNA Polymerase- an enzyme that catalyzes elongation of new DNA Energy for polymerization of DNA comes from nucleotide triphosphate As each monomer joins the growing strand, the nucleotide triphosphate loses 2 phosphate groups (pyrophosphate)

11 3’ end- hydroxyl group 5’ end- phosphate group

12 DNA elongates in the 5’ to 3’ direction Leading strand Lagging strand Okazaki fragment- 100-200 nucleotides long DNA Polymerase- adds new nucleotides to new DNA strand DNA Ligase- joins the Okazaki fragments

13 DNA polymerase can not initiate synthesis of polynucleotide Primer- existing RNA chain bound to template DNA to which nucleotides are added during DNA synthesis Primase- an enzyme that joins RNA nucleotides to make the primer Only one primer required for leading strand; each Okazaki fragment of lagging strand must be primed

14 Initiation of Replication Helicase- enzyme that untwists the double helix, separating the two strands Single-Strand Binding Protein- holds the two template strands apart while new strands are synthesized Synthesis of Leading StrandSynthesis of Lagging Strand Primase- priming DNA Polymerase- elongation DNA Polymerase- replacement of RNA primer with DNA Primase- priming for Okazaki fragments DNA Polymerase- elongation of fragment DNA Polymerase- replacement of RNA primer with DNA Ligase- joining of fragments

15 Nuclease- DNA cutting enzyme During DNA replication, DNA polymerase itself proofreads each nucleotide Nucleotide Excision repair- replaces damaged DNA using undamaged strand as guide

16 DNA polymerase can only add nucleotides to the 3’ end of a preexisting polynucleotide (elongation occurs from 5’ to 3’)

17 Telomere- multiple repetition of one short nucleotide sequence at the end of eukaryotic DNA; in humans the repeated nucleotide sequence is TTAGGG Telomerase- enzyme that catalyzes the lengthening of telomeres; includes a molecule of RNA that serves as a template for new telomere segments Telomeres are not present in most cells of multicellular organisms


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