Lab 7 Biotech Flashcards

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1
Q

Biotechnology

A

The use of organisms or their components to make or modify products

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2
Q

Traditional Biotechnology

A

Selective plant and animal breeding and the use of yeast in fermentation to produce cheese bread beer and wine

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3
Q

Modern biotechnology

A

Manipulation of DNA sequences in genes and the transfer of genes between organisms

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4
Q

Advances in biotechnology in the fields of

A

Forensics, medicine, agriculture, pollution control, evolutionary biotech

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5
Q

DNA is …

A
  • A double stranded molecule
  • Composed of NITROGENOUS BASE, DEOXYRIBOSE, and PHOSPHATE BACKBONE (negative charge)
  • nucleotides are held together by covalent bonds
  • hydrogen bonds between nitrogenous bases
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6
Q

DNA Extraction

A

Accomplished by lysing

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7
Q

Saline Solution

A

Isotonic to the solution inside the cheek cell so the cell doesn’t burst and release the cell prior to collection
The Solution carry a positive charge that neutralizes the negotiate charge on the DNA

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8
Q

Lyses Solution

A

Destroys the plasma membrane and nuclear membrane by disrupting the bonds of the lipids and protines

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9
Q

Alcohol Solution

A

DNA is insoluble in alcohol so it precipitates out of Solution into alcohol

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10
Q

Polymerase Chain Reaction PCR

A

Process that rapidly makes identical copies of DNA sequences

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11
Q

4 ingredients required in PCR

A
  • DNA extract
  • Deoxyribonucleotide triphosphates dNTP
  • Primers initiation
  • DNA polymerase (taq) elongates
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12
Q

3 steps in PCR

A

Denaturation
Anneal primers
Extended primers

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13
Q

Denaturation

A

Heat is added to separate strands

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14
Q

Anneal Primers

A

Cool so that primers can bond to a single strands of DNA

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15
Q

Extended Primers

A

Heat to allow DNA polymerase to add dNDPs to the end of the primers

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16
Q

At what rate is the DNA being made

A

Exponentially billions within hours

17
Q

Restriction fragment analysis

A

Enables an indirect comparison of nucleotide sequences in different amplified DNA samples through the use of restriction enzymes which cut DNA within specific recognition sequences/ restriction sites

18
Q

Restriction fragments

A

Resulting lengths of DNA

19
Q

Steps in restriction fragmentation analysis

A

Restriction Digest

Gel electrophoresis

20
Q

Restriction digest

A

A restriction enzyme is added to the PCR product and the Solution is put in an incubator.
The enzyme cuts DNA Into specific fragment sizes and numbers

21
Q

Gel Electrophoresis

A

Separate restriction fragments into ordered groups based on size differences

22
Q

What charge does DNA have

A

Negative

23
Q

What stain did we use in the lab

A

Fast blast

24
Q

What allowed the DNA to move

A

Porous

25
Q

Principles of obtaining DNA

A

Biological samples are collected
DNA is extracted
Differences in nucleotide sequences between the samples are determined

26
Q

Recombinant DNA

A

DNA from two different sources is combined into one molecule

27
Q

Why is Recombinant DNA engendered

A

Engineered to facilitate the manufacture of numerous medically and agriculturally important proteins

28
Q

GMO or Transgenic organizm

A

An organism that acquired genes through an artificial process

29
Q

Name a type of enzyme

A

EcoR1

30
Q

The principe of gel electrophoresis is based on the negative charge of the —– and the differences in —– of the DNA fragments.

A

DNA , sizes

31
Q

—– fragments travel further in the gel

A

Smaller

32
Q

—— fragments don’t travel far in the gel

A

Larger

33
Q

Why do they submerged the gel in a salt bath

A

Conducts electricity

34
Q

Restriction enzymes are used in

A

Paternity testing, recombinant DNA production