Artificial Recombinants (Bacteria) Flashcards

To learn the different methods and proceeders that Biotechnologist use to structural change gene expression in bacterial (prokaryotic unicellular) (37 cards)

1
Q

RNase

A

Ribonuclease (Full name), Is an enzyme that is used to break down the exciting structures of RNA (RiboNucleic Acid). This is widely used in operation of plasmid mini-prep.

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2
Q

DNase

A

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3
Q

Transformation (Bacterial Recombination)

A

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4
Q

Competent Cells

A

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5
Q

Electroporation

A

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6
Q

Replica Plating

A

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7
Q

Insertional Inactivation

A

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8
Q

Direct Selection

A

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9
Q

Vector (Bacterial Recombination)

A

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10
Q

‘Unique’ Restriction Site

A

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11
Q

Library Screening

A

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12
Q

The Griffiths & Avery experiment

A

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13
Q

Selectable Marker Genes

A

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14
Q

Origin of Replication

A

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15
Q

What are the three important characteristics of pUC plasmids?

A

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16
Q

Direct selection

17
Q

Genomic Library

18
Q

pUC Plasmid

19
Q

LacZ

20
Q

What are the befits of library screening?

21
Q

Plasmid Purification (What is it and why do we do it?)

22
Q

What are the different steps of ‘plasmid mini preps’?

23
Q

CaCl2+HeatShock Therapy

24
Q

Restriction Enzymes

25
Palindrome
q
26
Antiparallel cleavage
q (Sticky end)
27
Parallel cleavage
q (Blunt end)
28
Dimeric Enzymes
q
29
Genetic palindromes can very in length, what is the standard length of bases in a palindrome and what are the common extents of them?
q (C6-base palin, can range from 4-8 base palin though)
30
What befits are there to cleaving a restriction site in an asymmetrical faction?
q (The base sequence can be exposed and we can get allot of stick end reassosiactions based on the natural hydrogen bonds that can accrue between complementary base pairs.
31
DNA Ligase
q (Is unspecific to what it joins up so can fix foreign DNA or even connect different fragments that the original cleave site. This can result in gene linkage, and can be a process where my we can control where genes are located on a chromosome.) Can join any DNA with compatible sticky end.
32
Recombinant DNA
q
33
What are the benefits of recombinant DNA?
(New bacteria with new useful properties, and can allow a natural protein synthesis factory.)
34
Genome
q
35
PCR
q
36
Plasmids (What are they, where do they come from, and what are their function?)
(accessory Chromosomes)
37
How can we clone the gene of interest in organic systems?
q