Modern Applications of Microbial Genetics Flashcards

1
Q

Define Biotechnology and give examples

A

use of microorganism, cells, or cell components to make a product
ex. foods, antibiotics, vitamins, enzymes

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2
Q

Define recombinent DNA technology

A

insertion or modification of genes to produce desired proteins
ex. insulin, put gene in bacteria and they grow it

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3
Q

Define vector

A

self replicating DNA molecule
transport foreign DNA into a cell
plasmids and viruses

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4
Q

Define clones

A

population of genetically identical cells arising from 1 cell
carries vector

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5
Q

Define restriction enzymes

A

cut specific nucleotide
sequence of DNA
molecular scissors

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6
Q

What are the 6 steps in the genetic modification procedure

A

1) vector, such as a plasmid, is isolated
2) DNA containing the gene of interest from a different species is cleaved by an enzymes into fragments
3) the desired gene is selected and inserted into a plasmid
4) the plasmid istaken up by a cell,such as a bacterium
5) cells with gene of interest are cloned with either of 2 goals in mind
6a) create and harvest copies of a gene
6b) creat and harvest proteins products of a gene

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7
Q

Define polymerase chain reaction

A

process that amplifies DNA for analysis

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8
Q

What is PCR used for (3)

A

identifying microbes that can’t be cultured
detecting pathogens
diagnostic tests for genetic diseases

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9
Q

What are the 5 steps in PCR

A

1) The required components are placed in a test tube and inserted into the thermal cycler
2) heating the DNA separates the double stranded DNA into 2 separate single strands, allowing primers to bind to complementary sequences
3) TAQ polymerases uses the free nucleotides to initiate DNA synthesis, using the primer as a start site
4) 2 double stranded molecules of DNA are produced from the 1 original DNA molecule
5) this process is repeated many times with each cycle doubling the amount of DNA

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10
Q

What is needed in pcr ( material wise)

A

buffer,4 free nucleotides ( dATP,dTTP,dCTP,dGTP)

primer (RNA), TAQ polymerase

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11
Q

Why doesnt TAQ polymerase denature at high temp

A

comes from thermophilic bacteria

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12
Q

What are the respective temperture for the steps in PCR

A

1) DENATURATION: 94 C
2) PRIMING: 60 C
3) EXTENSION: 72 C

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