CHAPTER 1 (INTRO OF CHP 1) Flashcards

(15 cards)

1
Q

definitions of genetic engineering

A

the overall field of technology that involves the intentional modification of an organism’s DNA to target (introduce, remove, alter) certain traits.

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2
Q

definition of recombinant DNA

A

the technology to cut and paste DNA from different sources

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3
Q

examples of recombinant DNA

A

combining DNA from human and bacteria

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4
Q

whats plasmid

A

small circular piece of dsDNA found in bacteria (and some other organisms)

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5
Q

characteristics of plasmids

A
  1. separate feom the bacterial chromosome
  2. replicates independently
  3. natural plasmids often carry genes for things like antibiotic resistance
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6
Q

whats vector

A
  • essentially a vehicle
  • any vehicle used to carry DNA into a host cell
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7
Q

what are some types of vector

A
  1. plasmid vector
  2. viral vectors
  3. artificial chromosomes
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8
Q

whats plasmid vector

A

a plasmid that have been modified to be a delivery tool for cloning or genetic engineering

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9
Q

what does the plasmid vector usually contains

A
  1. cloning site
  2. selectable marker
  3. an origin of replication (ORI)
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10
Q

where to get DNA to clone

A
  1. genomic DNA
  2. cDNA
  3. Amplified DNA
  4. synthetic DNA
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11
Q

what are the sources of DNA?

A
  1. blood
  2. buccal cells
  3. cultured cells (plant and animals)
  4. bacteria
  5. biopsies
  6. forensic samples (body fluids, teeth roots, etc)
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12
Q

whats the golden rice project?

A

a project where scientists genetically engineered rice to make beta carotene which is a source of vitamin A, inside the rice grain.

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13
Q

the purpose of nucleic acid extraction?

A
  1. release NA from the cell for use in other procedures
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14
Q
  1. NA must be free from____
  2. only use ___NA for testing.
A
  1. NA must be free from contamination with protein, carbohydrates, lipids, or other NA
  2. only use pure NA for testing
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15
Q

what happened if NA is impure?

A
  1. enzymes wont work properly
  2. measurements like conc. will not be accurate
  3. PCR, cloning, sequencing could fail or give wrong results
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