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Bio 99 Exam 2 - 2021: SUMMER S2: MOLECULAR BIO

Bio 99 Exam 2 - 2021

Question 1 1 / 1 pts


Figure 1:

The crRNA and target DNA are bound together by what interaction

H-bonding

Covalent bonding

Ionic interaction

Nucleophilic bonding


Question 2 1 / 1 pts


Figure 1:

The domain that cuts the DNA on the crRNA bound strand is



HNH

Ruv C

TxlA

CRH


Question 3 1 / 1 pts

Figure 1:

The domain that cuts the DNA on the PAM strand is

Ruv C

HNH

CRH

Alx A


Question 4 0 / 1 pts

Figure 1:

When we say the DNA was "cleaved", it means that there is a break in bonding induced by a

covalent, nucleophile

H, nucleophile

H, nucleotide


covalent, nucleotide

Question 5 1 / 1 pts

Figure 2:

What is the purpose of the green section of the plasmid? (Amp)

to allow only bacteria containing plasmid to survive

to allow gene editing in that location

to allow for replication by DNA pol

to send a fluorescent "green" signal

Question 6 1 / 1 pts

Figure 2: What is the purpose of the lightblue section of the plasmid? (pMB1 ori)




to allow for DNA replication

to allow only bacteria containing plasmid to survive

to allow cutting sites so genes can be ligated in


to catalyze the reaction of non-fluorescent substrate into fluorescent product

Question 7 1 / 1 pts

Figure 2: What is the purpose of the MCS?

to allow cutting sites so genes can be ligated in

to add reversible nucleotides, DNA gyrase enzyme

to allow only bacteria containing plasmid to survive

0 to allow for DNA replication


Question 8

1 / 1 pts

Figure 3: In the FRET experiment shown here, we would

the molecule to induce the FRET system.

excite, green

excite, red

0 emit, red


emit, green


Question 9 0 / 1 pts

Figure 3:


In a FRET experiment if the donor molecule (HNH in the Doudna talk) has an excitation wavelength of 250 nm, and an emission wavelength of 285 nm; what would be the best "target excitation" for the FRET acceptor (the molecule we are trying to see if HNH is close to).

285 nm

250 nm

340 nm

700 nm



Question 10 1 / 1 pts

Figure 4:

The experimental goal was to get GFP into the bacteria by genetic engineering. We introduce the plasmid by using

.

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transformation, Ca2+ heat shock


transformation, Mg2+ cooling

transformase, enzymes

transluciferase, Ca2+ heat shock