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MIMG 101 MIDTERM STUDY GUIDE EXAM AND ACTUAL ANSWERS UPDATED.

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robert hooke - Answer first description of microorganisms leeuwenhoek - Answer first person to see bacteria louis pasteur - Answer did not believe in spontaneous generation, heat experiment and seal experiment, organisms still grow robert koch - Answer linked cause and effect in an infectious disease Koch's Postulates - Answer 1. The suspected pathogen must be present in all cases of the disease and absent from healthy animals. 2. The suspected pathogen must be grown in pure culture. 3. Cells from a pure culture of the suspected pathogen must cause disease in a healthy animal. 4. The suspected pathogen must be reisolated and shown to be the same as the original. common features to ALL cells - Answer dna/rna, plasma membrane, cytoplasm, ribosomes magnification vs resolution - Answer Magnification enlarges, resolution distinguishes objects 5 types of compound light microscopes - Answer bright field, phase contrast, differential interface contrast, dark field, fluorescence bright field - Answer microscope detects light scattered by cells, stained/pigmented scatter light better phase contrast - Answer difference between diffracted and undiffracted light is amplified, difference accentuated, living/unpigmented cells, best for internal structures dark field - Answer light directed toward cell from sides, only scattered reaches lens, best for small organisms & flagella

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MIMG 101
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MIMG 101 Midterm 2 Test Questions
and All Actual Answers 2026 Updated.
how does the Trp repressor work? what is it called when trp is around and not around? -
Answer No trp: it is an aporepressor- it does not bind to operon and transcription occurs

Yes trp: it is a holorepressor- trp binds to repressor and turns it into a holorepressor. the
holorepressor binds to operon and supresses transcription. NOTE! the holorepressor is a leaky
repressor, some transcription continues to occur- this is why there are more means to control
expression



what is transcriptional attenuation? - Answer -uses ribosomes to sensor amino acid level

-ability to translate mRNA determines whether transcription continues: usually it comes from
mRNA folding into alternative secondary structures



transcriptional attenuation in Trp

-leader sequence

-structures formed by what? - Answer trp gene has a leader sequence- no enzymatic
product!! this encodes a trp mRNA has 4 sequences (1,2,3,4). Just before sequence 1, there are
2 codons for trp there is a also a stop codon in between 2 and 3. The mRNA can form

1) anti-attenuator stem loop- btwn 2 and 3

2) attenuator stem loop - btwn 1-2 and 3-4



transcriptional attenuation- high amount of trp in cell - Answer when plenty of trp, ribosome
moves quickly through the mRNA and 1-2 and 3-4 stemloop forms: the attenuator stemloop.

this causes RNA pol to pause. the newly transcribed region is attached to DNA, but it has a lot of
Uracil= weak bonding.

The mRNA easily separates from DNA and RNA Pol falls off before reading trp gene



transcriptional attenuation- low amount of trp in cell - Answer when no trp, ribosome gets
stuck at the codons before sequence 1 that need trp. This allows for the 2-3 stemloop to form:
anti-attenuator stemloop.

RNA pol can continue transcribing the trp gene



types of regulatory RNAs - Answer sRNA

asRNA



sRNA - Answer small RNA

-post transcriptional control

,-bind to complementary sequences on target mRNA

- can stimulate/prevent translation or degradation



asRNA - Answer cis-antisence RNA

-transcribed from the non-template strand of DNA that lays opposite of mRNA encoding
template strand

-base pair with conjugate mRNA and control expression



what do some sRNA's require? - Answer RNA chaperone protein called: Hfq

-stabilizes sRNA

-hexameric ring protein with sRNA and mRNA binding faces



sRNA- inhibit translation - Answer sRNA will base pair with mRNA's ribosome binding site to
prevent ribosome from attaching, therefore inhibiting translation



sRNA- enhance translation - Answer sRNA will bind to part of long 5' cap upstream of RBS-->
prevents mRNA from folding in a way that hides the RBS. The RBS is exposed and ribosome can
bind and begin translation



RBS - Answer ribosome binding site



sRNA- promote degradation - Answer sRNA alters mRNA folding to expose RNase cleavage
sites



sRNA- prevent degradation - Answer sRNA binds to RNaseE-binding site and blocks it form
RNase



sRNA- mRNA processing - Answer sRNA can help separate monocistronic mRNA from
polycistronic mRNA by exposing RNase cleavage sites



what is the benefit of sRNA vs large regulatory protein for controlling gene expression? - Answer
sRNA:

-does not require protein synthesis

-can diffuse rapidly

-can act on preexisting messages

an economical way to inhibit gene expression

, what molecular structures can recognize and bind to low molecular weight structures? - Answer
proteins and ribozymes



what is a ribozyme - Answer ribozyme: catalytic RNA

with a 3D structure that had enzymatic functions



riboswitch- what is it, where is it found, what does it do? - Answer riboswitch:

-mRNA found at the 5' untranslated region upstream of coding sequence.

-it can take on 2 alternative stemloop structures, in response to a metabolite.



resembles activator/repressor protein bc it binds to a cell metabolite to control gene expression



riboswitch- affects translation - Answer excess ligand (amino acid or vitamin):

the ligan will bind to the riboswitch, which stabilizes it into a structure that hids the RBS,
preventing translation of mRNA

no ligand:

alternative riboswitch structure exposes RBS, translation occurs



what will you not have on an sRNA gene? - Answer ATG- methionine codon



riboswitch: affects transcription - Answer ligand binds to riboswitch prevents transcription
termination! coding region is expressed



northern blot - Answer RNA blot- study gene expression thru detection of mRNA



experiment to show that trp gene can be controlled by attenuation - Answer S1 nuclease
mapping:

create probe: radioactive antisense RNA that will base pair with gene of interest.

expose hybrids to S1 nuclease- which digests all

ss mRNA!

-if long mRNA, it has long probe so the non-digested pieces will be large and heavy.

-If short mRNA (product of attenuation- just leader sequence), the non-digested pieces will be
small and short.

Do this to cells with trp and without trp.

Northern blot

Cells with Trp: have small mRNA after s1 nuclease. meaning attenuation happened

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