U3 AOS1 Flashcards

(45 cards)

1
Q

Amino Acid

A

Monomers that make up proteins. Connected by peptide bonds.
Consist of
- carboxyl group
- amino group
- variable R group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Translation

A

make proteins at ribosomes using instructions on mRNA
Steps:
- mRNA to the ribosome
- tRNA brings amino acid, and attaches to mRNA with anti-codon
- each new amino acid bonds to each other (peptide bond)
- mRNA goes all the way through, stop codon, new polypeptide disconnects and starts folding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Protein

A

organic compound consisting of amino acid chains connected by peptide bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

polymerase

A

an enzyme that catalyses the formation of nucleic acids
- DNA polymerase
- RNA polymerase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Vector

A

a tool to put something into something else, e.g. a plasmid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Transformed bacteria

A

bacteria that have a plasmid inserted into it, the plasmid can be used to insert genes into bacteria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Plasmid

A

circular piece of DNA found in a prokaryote and can contain genes.
- Bacteria exchange them through horizontal gene transfer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Endonucleases

A

Restriction enzymes— cut DNA at very specific points (restriction sites)
- sticky end, have an overhanging sequence
- blunt end

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

DNA Ladder

A

predetermined DNA sample to use as a reference to compare the samples in gel electrophoresis against

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Gel Electrophoresis

A

A method for separating molecules based on size/charge/weight
mostly but not solely used on DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Steps of PCR

A
  1. Denaturation (95º) hydrogen bonds are broked due to heat. DNA is now single stranded
  2. Annealing (50-60º) primers bind to single stranded DNA (polymerase won’t bind to only 1 strand)
  3. Extention (72º, optimal taq polymerase temperature) maks a copy of the DNA starting from the primers. 5’ to 3’ direction.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is PCR

A

Polymerase Chain Reaction. A process for replicating a section of DNA many times (DNA amplification)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Recombinant plasmid

A

a plasmid with DNA artificially inserted into it. put into bacteria either by heat shocking or electrocuting the bacteria.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Cas9

A

the endonuclease. Part of RNA from CRISPR ‘guide RNA’, in nature there are two parts to the guide RNA, artificially a single unit sgRNA is used.
- protospacer is the part that will match to the target, approx. 20bp.
- matches to sequence next to PAM (protospacer adjascent motif)
- cuts DNA blunt end

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

CRISPR

A

Cluster of Reglularly Interspaced Short Palindromic Repeats.
- a part off the circular chromosome in prokaryotes that has collected pieces of viral DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

CRISPR- Cas9

A

An endonuclease where the restriction site can be modified, and is escpecially long, approx. 20bp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

DNA profiling

A

examins short tandem repeats (STR), regions of nosn- coding DNA between genes, they are highly variable so if many are analysed it is unlikely they will be the same between people.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

GMO vs. Transgenic

A

GMO— organism with modified DNA
Transgenic— organism with DNA from a different species in it.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Reporter Genes

A

Artificially inserted into plasmids to easily see if they have been uptaken by bacteria.
at least 2 are necessary
1. to see if plasmid has been uptaken by bacteria
2. to break with new DNA inserted into plasmid

20
Q

Ligase

A

catalyses phosphodiester bonds, sticks them back together.

21
Q

non- malegicence

A

avoid causation of harm

22
Q

beneficence

A

commitment to maximising benifits and minimising risks and harms

23
Q

justice

A

moral obligation towards fairness for all groups. A fair distribution of benefits and lack of unfair burden

24
Q

Integrity

A

honesty in reporting and communication of results in ways that permit scrutiny

25
virtues based approach
person rather than action-based. morality of character. What would a good person do?
26
Duty-/rules-based approach
concerned with the means, how people act, regardless of consequence. - certain ethical rules must be followed. e.g. law, religious teachings
27
consequence-based approach
central importance on minimisation of harm and maximising positive outcomes. - if consequences of an action: good>bad then it is ethical
28
respect
value living things, respect; liberty, welfare, beliefs/heritige. of both the individual and the collective
28
secondary structure
folding of amino acid chain, held together with hydrogen bonds. Types: - Alpha helix - beta pleated sheet - random coil
29
tRNA
transport RNA. Transfers amino acids to ribosomes for making proteins. has 3 bases (anti-codon) that is complementary to mRNA codons.
30
denaturing
break hydrogen bonds, etc. Breaks protein shape and therefore its function. Because: - temperature - pH - cofactors
31
Triplets/codons
3 bases code for 1 amino acid. it is degenerate because multiple codons code for the same amino acid sequence, this leads to redundancy.
32
Primary structure
linear sequence of amino acids joined by peptide bonds (with the carboxyl and amino groups) Codon: bits of DNA that code for an amino acid.
33
peptide bond
made by condensation polymerisation reactions. carboxyl and amino groups leading to a peptide bond and water
34
gene expression
start with a gene, end with a protein. The formation of proteins using the instructions from a gene 1. transcription—nucleus 2. RNA processing— nucleus 3. translation —cytosol
35
rRNA
ribosomal RNA. makes up the structure of ribosomes
36
RNA processing
mRNA altered by the spliceosome which cuts out introns and then reconnects exons in various orders (alternative splicing) and adds a metholated cap (5') and poly-a tail (3'). This makes the mRNA stable and mature.
37
Transcription
production of mRNA - RNA polymerase binds to the DNA at the promoter region - the polymerase then moves along the template strand in the 5' to 3' direction - this process creates a complementary strand of mRNA
38
mRNA
messanger RNA, takes the information from the DNA to the ribosomes, it is made by RNA polymerase
39
nitrogenous bases
Pyrimidines (single ringed) - cytosine - thymine/uracil Purines (oule ringed) - Guanine -Adenine. C,G has 3 hydrogen bonds A, T/U has 2 hydrogen bonds
40
secretory pathway
-proteins synthesised by ribosomes on r.e.r. - moves through r.e.r. -mdified often by addition of carbohydrates - goes into a vesicle, moves to cis face of the golgi - in golgi further modified - exocytosis
41
nucleic acids
monomers that make up RNA/DNA joined by phosphodiester bonds. Components - Phosphate group - nitrogenous base - and deoxy/ribose sugar
42
proteome
complete set of proteins in an organism
43
quaternary structure
multiple polypeptides ( and or prosthetic groups) that form 1 protein. This is not present in all proteins
44
tertiary structure
3D structure formed by R group interactions. The function is formed by structure