Transformation Lab Flashcards

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1
Q

Frederick Griffith

A

studied strains of pneumonia in mice (S) Smooth Strain, (R) Rough Strain

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2
Q

Alfred Hershey, Martha Chase

A

studies showing that DNA is the genetic material of phage known as T2

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3
Q

Edwin Chargaff

A

analyzed base (ATCG) to prove DNA is the genetic material

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4
Q

Rosalind Franklin

A

Took photo 51, showing the double helix, a discovery that was essential in unlocking the mystery of how life is passed down from generation to generation.

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5
Q

Structure of DNA

A

AT CG sugar attached to phosphate group through covalent bonds. Hydrogen bonds (weak) connect the two nitrogenous bases together

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6
Q

Semi-conservative

A

after one round of replication, every new DNA double helix would be a hybrid that consisted of one strand of old DNA bound to one strand of newly synthesized DNA.

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7
Q

Process of DNA replication

A

1) DNA double helix
2) Hydrogen bonds break and the helix opens
3) Each strand of DNA acts as a template for the synthesis of a new, complementary strand
4) Replication produces two identical DNA double helicases, each with one old and one new strand

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8
Q

Leading and Lagging

A

During DNA replication, one new strand (the leading strand) is made as a continuous piece. The other (the lagging strand) is made in small pieces.

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9
Q

5’ and 3’ carbon ends

A

For instance, if you know that the sequence of one strand is 5’-AATTGGCC-3’, the complementary strand must have the sequence 3’-TTAACCGG-5’. This allows each base to match up with its partner:

DNA polymerase only synthesizes DNA in the 5’ to 3’ direction only

5’ ends with the phosphate, and 3’ ends with the deoxyribose sugar.

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10
Q

Helicase

A

untwists and separates strands

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11
Q

single strand binding proteins

A

holds DNA strands apart

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12
Q

primase

A

enzymes whose continual activity is required at the DNA replication fork

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13
Q

DNA polymerase

A

adds DNA nucleotides to new strand

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14
Q

DNA ligase

A

joins DNA fragments together

If two pieces of DNA have matching ends, ligase can link them to form a single, unbroken molecule of DNA

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15
Q

DNA pol 1

A

removes RNA primer and replaces with DNA

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16
Q

Okazaki fragments

A

segments of lagging strand

17
Q

Gel electrophoresis

A

a technique used to separate DNA fragments according to their size

18
Q

DNA primer

A

a short nucleic acid sequence that provides a starting point for DNA synthesis

19
Q

Mismatch repair enzymes

A

detect distortions caused by mismatched bases inserted during DNA synthesis

20
Q

nuclease in DNA proofreading and repair

A

A nuclease enzyme cuts the damaged DNA strand at two points and the damaged section is removed. Repair synthesis by a DNA polymerase fills in the missing nucleotides. DNA ligase seals the Free end of the new DNA To the old DNA, making the strand complete.

21
Q

telomeres

A

A telomere is a region of repetitive DNA sequences at the end of a chromosome. Telomeres protect the ends of chromosomes from becoming frayed or tangled. Each time a cell divides, the telomeres become slightly shorter. Eventually, they become so short that the cell can no longer divide successfully, and the cell dies.

22
Q

significance of telomeres in regular and cancerous cells

A

Dont contain genes; DNA typically consists of multiple repetitions of one short nucleotide sequence

23
Q

Distinguish between heterochromatin and euchromatin.

A

More condensed, non-transcribed = heterochromatin
Less condensed, transcribed = euchromatin

24
Q

Describe how the packing of chromatin changes during the course of the cell cycle

A

In interphase, the chromatin is highly extended. Preparing for mitosis, the chromatin coils or condenses and forms chromosomes in metaphase.

25
Q

Topoisomerase

A

relieves strain caused by unwinding