bio 3/4

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1
What is the monomer of a protein?
Amino acid
2
What is a polypeptide?
A chain of amino acids linked by peptide bonds
3
What happens during condensation polymerization?
A covalent bond is formed between monomers and a water molecule is eliminated
4
What is a hydrolysis reaction?
Breaking a bond by adding -H and -OH to separate molecules
5
What is the primary structure of a protein?
The sequence of amino acids
6
What defines the secondary structure of a protein?
The 3D form of local segments, such as alpha helices and beta-pleated sheets
7
What is the tertiary structure of a protein?
The overall 3D shape of a protein that determines its function
8
What is the quaternary structure of a protein?
More than one polypeptide chain in a single protein
9
What is a protein prosthetic group?
A non-amino acid component bound to a protein to form a conjugated protein
10
What is the function of proteins?
To play specific roles in biological systems, influenced by their structure
11
What is the proteome?
All the proteins found in a cell
12
What is a nucleotide?
A chain of nucleic acids
13
What is a nucleic acid?
Made of pentose sugar, nitrogen-containing base, and a phosphate group
14
What is the sugar phosphate backbone in nucleic acids?
Phosphate and pentose sugar bonded, with nucleotides adding to the 3' end
15
What is a phosphodiester bond?
A bond between the pentose sugar of one nucleotide and the phosphate group of another
16
What is a hydrogen bond in nucleic acids?
A bond between complementary base pairs
17
What is DNA?
Double-stranded, carries genetic information across generations
18
What is RNA?
Single-stranded, present in most living organisms and viruses
19
What does rRNA do?
Makes up 60% of the ribosome
20
What is the role of mRNA?
Carries an expendable copy of a gene to the ribosome
21
What is the role of tRNA?
Links mRNA with the correct amino acids
22
What is a gene?
A section of DNA that carries the code to make a protein
23
What is gene expression?
The production of a gene product encoded by a gene
24
What is a triplet?
A sequence of 3 DNA nucleotides
25
What is a codon?
A sequence of 3 mRNA nucleotides
26
What is degeneracy in genetics?
More than one triplet can code for the same amino acid
27
What is the universality of DNA?
All living organisms use the same codons to code for the same amino acids
28
What is an exon?
coding region of a gene that is retained in the final, mature mRNA (messenger RNA) transcript after introns are removed during RNA splicinh
29
What is an intron?
A non-coding region of DNA (in eukaryotes)
30
What is a promoter region?
A binding site for DNA that indicates the direction of transcription
31
What is an operator in prokaryotes?
A binding site for repressor proteins
32
What is transcription?
The process of synthesizing RNA from a DNA template
33
What is translation?
The process of synthesizing proteins using mRNA as a template
34
What is the template strand of DNA?
The strand that guides RNA synthesis during transcription
35
What is the coding strand of DNA?
The strand that has the same sequence as mRNA, except with thymine instead of uracil
36
What is RNA polymerase?
An enzyme responsible for synthesizing RNA from a DNA template
37
What is mRNA?
A type of RNA that carries genetic instructions from DNA to the ribosome. expendable
38
What is RNA processing?
Modifications that pre-mRNA undergoes to become mature mRNA
39
What is splicing in RNA processing?
The removal of introns and joining of exons
40
What is alternate splicing?
The process of combining different exons to produce multiple proteins from one gene
41
What is gene regulation?
Processes that control when and how much a gene is expressed
42
Why downregulate gene expression?
To conserve energy and prevent accumulation of unnecessary proteins
43
Why upregulate gene expression?
To ensure sufficient protein production for homeostasis and reproduction
44
What are structural genes and regulatory genes?
Structural genes code for proteins; regulatory genes code for transcription factors
45
What is an operon?
A cluster of linked genes transcribed together under a common promoter
46
What is the TRP operon?
A regulatory system that controls tryptophan production in bacteria
47
What is tryptophan?
An essential amino acid required for protein synthesis
48
What is attenuation?
A mechanism that reduces operon expression when tryptophan levels are high -terminating hair pin loop
49
What is repression in gene regulation of trp?
A repressor protein prevents transcription when tryptophan levels are high
50
What happens when tryptophan is low?
Regulatory genes do not undergo conformational change, or an anti-terminator hairpin loop forms
51
What are structural genes?
Genes that code for proteins or non-coding RNA involved in the cell's function
52
What are transcription factors?
Proteins that bind to genes or RNA polymerase to activate or repress transcription
53
What is the function of the nucleus in protein secretion?
mRNA is transcribed and sent to the rough ER
54
What role do ribosomes play in protein secretion?
Ribosomes, made of rRNA and proteins, are attached to the rough ER to synthesize proteins
55
What does the rough ER do in protein secretion?
It synthesizes, modifies, and packages proteins into vesicles for transport
56
What is the Golgi apparatus's role in protein secretion?
It further modifies proteins and packages them into secretory vesicles
57
What is exocytosis?
The process by which vesicles fuse with the plasma membrane to release contents
58
What is a catalyst?
A substance that speeds up a chemical reaction without being consumed
59
What is an enzyme?
A biological catalyst that speeds up biochemical reactions
60
What is a substrate in enzyme activity?
The molecule that an enzyme acts upon during a biochemical reaction
61
What is a product in enzyme activity?
The substance formed from an enzyme-catalyzed reaction
62
What are active sites?
The specific region on an enzyme where the substrate binds and the reaction occurs
63
What is enzyme specificity?
The ability of an enzyme to recognize and bind to a specific substrate
64
What is substrate concentration?
The amount of substrate available, which affects the rate of enzyme-catalyzed reactions
65
What is optimal pH for enzymes?
The pH at which an enzyme functions most efficiently
66
What is the optimal temperature for enzymes?
The temperature at which an enzyme works most efficiently without denaturing
67
What is saturation in enzyme activity?
A state where all active sites of an enzyme are occupied by substrates
68
What is enzyme concentration?
The amount of enzyme available for catalysis, which affects reaction rate
69
What are biochemical pathways?
Interconnected chemical reactions within a cell, where one product becomes the substrate for the next
70
What are limiting factors in enzyme reactions?
Factors such as enzyme concentration, substrate concentration, temperature, or pH that restrict the rate of reaction
71
What is denaturing?
When an enzyme's structure is disrupted, impairing its function
72
What is an allosteric site?
A site on an enzyme where coenzymes or inhibitors bind to regulate activity
73
What is induced fit in enzymes?
When a substrate binds and induces a temporary conformational change in the enzyme's active site
74
What are the models of active site interactions?
Lock and key model and induced fit model
75
What are reversible reactions in enzyme catalysis?
Reactions that can be catalyzed in both directions by the same or different enzymes
76
What is activation energy?
The energy required to start a chemical reaction
77
What are coenzymes?
Non-protein organic molecules that assist enzymes in catalysis
78
What is the difference between anabolic and catabolic reactions?
Anabolic reactions require energy; catabolic reactions release energy
79
What is the loaded form of a coenzyme?
A coenzyme carrying energy for biochemical reactions
80
Why manipulate DNA?
To genetically engineer organisms, perform DNA profiling, or study genes
81
What is an endonuclease?
An enzyme that cuts DNA or RNA at specific internal sites
82
What is a palindromic sequence in DNA?
A sequence that reads the same forwards and backwards
83
What are sticky ends in DNA?
The ends of DNA fragments that can temporarily bind with complementary DNA
84
What is ligase?
An enzyme that joins DNA or RNA strands by forming covalent bonds
85
What is polymerase?
An enzyme that synthesizes DNA or RNA strands by adding nucleotides
86
What is a restriction enzyme?
A type of endonuclease that cuts DNA at specific sequences
87
What is a genome?
The complete set of genes in an organism
88
What is CRISPR?
A natural defense mechanism in bacteria used to store information about viral DNA
89
What is Cas9?
An endonuclease used in CRISPR to cut DNA
90
What is a PAM?
A short DNA sequence used to mark target sites in CRISPR systems
91
What are spacers in CRISPR?
Segments of viral DNA inserted between repeats in the CRISPR system
92
What is gRNA?
Guide RNA produced by spacers to direct Cas9 to the target DNA
93
What is sgRNA in CRISPR?
Synthetic
94
PCR amplification
amplifies small samples of DNA to make a sample large enough to be analyzed, in vitro
95
Denaturation - PCR
PCR reagents are mixed and heated to approx 95 degrees to break hydrogen bonds into separate DNA strands
96
Annealing - PCR
mixture is called to 50-60 degrees for primers to bind to complementary single-strand templates
97
Elongation - PCR
temperature increased to optimal 72 degrees. Polymerase extends primers by adding complementary nucleotides in a (5’-3’ direction)
98
Reagents in PCR
Sample DNA, DNA primers, DNA polymerase, nucleotides, and buffer
99
DNA primers
short synthetic DNA pieces complementary to DNA template, 18-30 nucleotides, and there is a forward and reverse primer
100
Buffer
ensures DNA polymerase can operate at optimal pH and Mg2+ (co-factor)
101
Wells
Small indentations in the agarose gel where DNA samples are loaded before electrophoresis. The DNA moves from the wells toward the positive electrode during the process
102
Standard ladder
DNA fragments of known sizes used as a reference to estimate the size of unknown DNA fragments in a gel
103
DNA profiling
A technique that uses gel electrophoresis to analyze an individual's DNA, commonly used in forensic investigations and paternity testing. It relies on comparing band patterns of STRs (short tandem repeats)
104
STR
Repeating sequences of DNA that vary between individuals. STR analysis, often used in forensic DNA profiling, involves amplifying and separating these sequences via gel electrophoresis
105
Running a gel
Restriction enzymes cut DNA into different sized fragments, which are loaded into wells in the porous gel. A positive electrode is placed at the other end to the well and the electric current moves through the gel. Negatively charged DNA moves towards the positive electrode
106
Effecting factors for gel electrophoresis
Size and length (small = fast), Concentration/viscosity of gel (would make it overall slower/harder to pass), Voltage and power used (would make it overall faster if more voltage is used)
107
Uncut gene
A gene or DNA fragment that has not been digested by restriction enzymes. It appears as a single, larger band on a gel
108
Digested gene
A gene that has been cut into smaller fragments by restriction enzymes. These fragments will appear as multiple bands on a gel during electrophoresis
109
Recombination
Combines DNA from 2 different sources
110
Transformation
Process by which foreign DNA is introduced into a cell
111
Recombinant plasmid
Plasmid with foreign DNA
112
Transformed bacteria
DNA that has taken on the recombinant plasmid
113
Vector
A type of plasmid that carries DNA fragments to one organism from another without needing to reproduce. They self-replicate and are easily modified
114
Genomic DNA
Contains bacterial genome, 1 circular chromosome with the essential genes for survival and metabolism, passed to daughter cells
115
Plasmid DNA
Small additional chromosomes that carry beneficial genes to break down chemicals or fight viruses
116
Multiple cloning sites
A short segment of DNA within a cloning vector that contains multiple unique restriction enzyme recognition sites
117
Bacterial host
Simple organism that reproduces quickly, ethical
118
Gene of interest
What is wanted to be inserted
119
Heat shock
Bacterial cells are exposed to cold + CaCl, then heated in a water bath (42 degrees). The increase in heat creates pores in the membrane for DNA to enter the cell
120
Process of recombination
Isolate gene of interest and plasmid, recombination, transform, growth, and purification
121
antibiotic selection
Bacteria are grown on an antibacterial plate to kill off all the bacteria without the antibiotic-resistant plasmid
122
Alteration of genome
Results in genes being silenced, insertedemoved, or altered by replacing nucleotides (GMO)
123
Transgenic organism
Has genes from a different organism from a different species
124
Cisgenic organism
Has genes from a different organism from the same species
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