FINAL Flashcards

1
Q

Cellular Respiration

A

Glycolysis
Kreb Cycle
Electron Transport Chain

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2
Q

Yeast

A

able to use sucrose as a substrate

uses glucose as energy source

unable to use lactose as a substrate because yeast doesnt have the enzyme lactase to degrade lactose

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3
Q

What sugars were yeast able to fermentate?

A
sucrose 
glucose 
glucose-Mg
glucose-F
glucose-citrate-F
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4
Q

What sugars were yeast not able to fermentate?

A

lactose

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5
Q

Magnesium

A

serves as a cofactor for glycolytic enzymes because its an activator of glycolysis

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6
Q

Glycolytic enzymes that are cofactors

A
pyruvate kinse 
phosphoglycerokinase 
phosphofuctokinase 
enolase 
hexokinase 
glyceldehyde 
phosphatedehydrogenase
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7
Q

Flouride

A

it is an inhibitor of glycolysis

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8
Q

Azide

A

it is an inhibitor of glycolysis because it interfers with CO2 production in yeast

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9
Q

Enzymes that are inhibitors of glycolysis

A
phosphofuctokinase 
phosphoglycerokinase 
pyruvate kinase
hexokinase 
glyceraldehyde phosphate 
dehydrogenase 
enolase
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10
Q

what is the wavelength of violet

A

400-420

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11
Q

what is the wavelength of blue

A

440-480

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12
Q

what is the wavelength of green

A

500-560

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13
Q

what is the wavelength of yellow

A

580

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14
Q

what is the wavelength of orange

A

600-620

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15
Q

what is the wavelength of red

A

640-700

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16
Q

Prophase

A

nuclear envelope dissipates and mitotic spindle forms

microtubules attach in two locations in the plasma membrane anchored by cell wall

microtubules are anchored to the organelles known as centrosomes

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17
Q

Prometaphase

A

kinetochore microtubules attach to the replicated chromosomes and starts to move to the chromosomes towards the center of cell

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18
Q

Metaphase

A

chromosomes line up along the metaphase plate of cell

each chromosome have two kinetochore microtubules attached to centromeres

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19
Q

Anaphase

A

checkpoint

two sister chromatids of each chromosome must split apart and move toward each spindle formation

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20
Q

Telophase

A

final phase of karyokinesis

chromosomes has moved to either end of the cell

nuclear envelope will form around each set of chromosomes

21
Q

In Meiosis where does DNA Replication take place?

22
Q

In Meiosis where are the centrioles replicated?

A

Prophase 2

23
Q

In Meiosis where does crossing over and synapsis occur?

A

Prophase 1

24
Q

In Meiosis where does the alignment of homologues occur?

A

Metaphase 1 in the metaphase plate

25
In Meiosis where does reduction division occur?
Anaphase 1
26
In Meiosis where does separation of sister chromatids occur?
Anaphase 2
27
Dominant
it is the allele that is fully expressed in a phenotype
28
Recessive
allele that is not expressed in heterozygote and has to be a homozygous recessive to be expressed
29
Codominant
both alleles contribute to the phenotype of the organism | ex: AB blood type and cows lol
30
Incomplete dominance
neither allele given from the parents are dominant and a third phenotype is shown ex: pink flower from red and white flower parents (its a mix)
31
Allele
possible variant for a particular trait
32
Locus
location of a gene on a chromosome
33
P Generations
parent generation
34
F1 Generations
offspring of P generation
35
F2 Generations
offspring of F1 generation
36
Genotype
genetic makeup of chromosomes
37
Phenotype
outward appearance based on the genotype
38
Rule of Multiplication
probability of two independent events both occurring is the multiplication of their individual probabilities
39
Rule of Addition
probability that an event can occur in two or more different ways is the sum of the separate probabilities
40
Law of Independent Assortment
as long as genes are not on the same chromosomes they will assort independently (align randomly on the metaphase plate)
41
Frameshift mutation
an insertion or deletion of a base that changes the entire reading frame for translation
42
Point mutation
results in a change of a single codon-- like base substitution
43
Nonsense mutation
a codon that specifies an amino acid is changed to a stop codon, and translation is prematurely terminated-- significant alteration in protein function
44
Missense mutation
due to a single base change which results in a change in the amino acid coded for the amino acid is in a location on the protein that does not result in altered structure or function also called neutral mutation
45
Forms of Aneuploidy in human population
Downs Syndrome Pataus Syndrome Edwards Syndrome
46
Excision repair mechanism of DNA repair
damaged bases are cut out within a string of nucleotides and replaced with DNA as directed by the undamaged template strands
47
Mismatch repair mechanism of DNA repair
process that corrects mismatched nucleotides in the otherwise complementary paired DNA strands arising from DNA replication errors and recombination
48
Silent mutation
a point mutation due to a base substitution in DNA -- results in no change in the resulting protein