genetic engineering Flashcards

1
Q

genetic engineering

A

manip of an org’s DNA

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2
Q

tranformed organisms

A

DNA altered by GE

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3
Q

recombinant DNA

A

mol of DNA consists of DNA from two sources joined togther

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4
Q

final goal of techniques

A

getting a host org to prod proteins encoded by a new gene that has been inserted into the host’s DNA

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5
Q

why are plasmids a perfect vector

A

can be transcribed by having simple bacterial promoter region upstream of the gene

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6
Q

main req of org

A

large quantites of a protien can be prod as cheaply and easily as possible

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7
Q

org needs to be

A

grow faast
easily manip
naturally occing vectors- plasmids

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8
Q

good option for org

A

yeasts or bacteria

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9
Q

b4 insersion of gene

A

same r,endonucleases used to cut plasmid

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10
Q

where do r.endo cut plasmid

A

specific recognion sites

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11
Q

what does r.endo create in plasmid

A

complimentary sticky ends

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12
Q

what forms bw bases

A

h bonds

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13
Q

DNA ligase

A

joins DNA togther by caalysing formation of phosphodiester bonds

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14
Q

waht are ppd bonds formed bw

A

sugar and phosphate groups of the backbone

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15
Q

transformation

A

injecting the vector in2 the chosen bacterium

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16
Q

why are vectors contaning genes moved to living cells

A

replication and/ expression

17
Q

host cell

A

cells recieving the vector

18
Q

vectors

A

lasrge mols which dont readily cross cell membranes

19
Q

how are vectors made permeable

A

electroporation
viruses
microinjection
liposomes

20
Q

electroporation

A

cells subjected to high voltage pulse, temporarily distrupts the mem and allows vectpr to enter cell

21
Q

viruses

A

vector incrorp into a virus

inj host cels by inj gen mat- containing selected gene

22
Q

microinjection

A

gen mat inj using a micro pipette

23
Q

Ti plasmids

A

only plasmids plant cells take up

24
Q

liposomes

A

DNA warpped in a lipid mol allowing it to pass through phospholipid bilayer

25
steps of gene cloning
isolate gene produce recombinant plasmid tranfrom bacteria that will express the gene
26
isolating euk gene to be cloned
extrac mrna reverse transcriptase prod cdna- no introns pcr to amplify cdna
27
identifyin dna transformed w/recomb plasmids
marker genes- abiotic res/flourescent genes
28
Recognition sites of sticky eNTs are
Palindromic- read same way backwards