• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/20

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

20 Cards in this Set

  • Front
  • Back
properties of hereditary molecule (4)
Diversity of structure-contains stable form of information translated into phenotype
Ability to replicate-accurately transmit information from cell to cell and gen to gen
Mutability-changes to produce variation nec for adaptation and evolution
Expression-ability to turn genetic info into biochemical or physical characters
griffith experiment (1982)

transformation principle
Observed mice die of pneumonia when injected with smooth virulent strain but not rough virulent bacteria

IIIR had been transformed into IIIS; concluded agent was a protein
Avery-MacLeod-McCarty Experiment (1944)
Identify transforming agent
Lysed IIIS cells and plated with living IIR bacteria and they transformed into IIIS
Enzymes degraded macromolecules- transformation when proteins were degraded. no transformation when nucleic acids degraded
Avery-MacLeod-McCarty Experiment
RNA vs DNA
RNA nuclease degraded the RNA and transformation occurred

DNA nuclease degraded DNA and no transformation occurred *TRANSFORMING AGENT*
Hersey-Chase Experiment (1952)
Verified DNA as transforming agent
Difference in atomic composition of DNA- phosphorus atoms in DNA, sulfur atoms in protein
DNA radioactively tagged with 32P (pink)
Protein radioactively tagged with 35S (yellow)
Hersey-Chase Experiment steps (3)
1) tag. T2 bacteriophage infects E.Coli and 32P incorporated into viral DNA 35S incorporated into viral coat
2) Isolate labeled bacteriophage from lysed radioactive E.Coli and reinfect different E.Coli in non-radioactive medium
3) Examine newly infected for radioactive labels
35S label recovered from phage ghosts but not bacterium -not transmitted
32P label recovered from bacterium and phage progeny *DNA INFORMATION MOLECULE* -transmitted
Experimental Evidence summary
molecules from infectious bacteria can transform non infectious bacteria (griffith)

enzymes that degrade DNA prevent bacterial transformation (avery macleod mccarty)

labeled DNA transmitted by bacteriophages (hershey chase)
Primary structure

secondary structure

tertiary structure
nucleotide sequence (DNA and RNA)

double-helix brings together two polynucleotide strands

condensation of chromosomes to fit inside cell
nucleotide
composed of pentose sugar, phosphate groups, and nitrogenous bases

DeoxyNucleotide MonoPhosphate (dNMP)
Pentose Sugar
circular in aqueous solution
RNA=ribose 2' and 3' OH group
DNA=deoxyribose 3' OH group only
Phosphate Group
single phosphate group group attached to 5' carbon=monophosphate
negatively charged
nitrogenous base

purine
pyrimidines
attached to 1' carbon of pentose sugar

two rings- adenine and guanine (wider)
one ring- cytosine and thymine(DNA)/uracil(RNA) (narrower)
nucleotide linkage
phosphodiester bonds
5'-3' polarity = phosphate sugar backbone

5' phosphate group of incoming dNTP (deoxynucleotide triphosphate) and 3' OH group of preceding nucleotide
Chargaff's rules
determined the proportions of nitrogenous bases in DNA molecules
% Adenine = % Thymine
% Guanine = % Cytosine
% Purines (A,G) = % Pyrimidines (T,C)
(A+G)/(C+T)=1
X-ray diffraction crystallography
visualize molecular structure through patterns of x-ray diffraction

Rosalind Franklin concluded DNA had a helical structure
Watson and Crick's Model

anti-parrallel

sugar-phosphate backbone
DNA as a double Helix
DNA composed of two strands in right-handed double helix

one strand runs from 5'-3' and the other runs 3'-5'

face out, bases oriented toward central axis
1 degree

2 degree
single polynucleotide strands with 5'-3' polarity

two polynucleotide strands line up in antiparallel orientation
complementary strands
purine always binds with pyrimidine and contributes to constant width of double helix = 2nm wide
strands are held together by hydrogen bonds

T comp A with 2 H bonds (less energy to denature)
C comp G with 3 H bonds (more energy to denature)
Spacing in DNA
2nm wide

.34nm between nucleotides

one turn of a helix 3.4nm

twisting caused by hydrogen bonds (major groove, minor groove)
special secondary tructure
somplementary regions of DNA and RNA form hairpin loops