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BIOC0001 EXAM QUESTIONS AND ANSWERS WITH COMPLETE SOLUTIONS VERIFIED

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BIOC0001 EXAM QUESTIONS AND ANSWERS WITH COMPLETE SOLUTIONS VERIFIED Phase contrast microscopy Allows to examine transparent/ living specimens without staining them. Light microscopy (bring field) Haemotoxylin (binds yo acidic molecules -DNA) and eosin stain (amino acids). Confocal microscopy Light microscope that uses fluorescent stains and laser to make two- and three-dimensional images through thick cells. Conventional fluorescent microscopy limitations Cutting destroys material, fluorescent emitted light causes blurriness. Electron microscopy Causes breakage of chemical bonds and created free radical but coating specimens with heavy metals can protect against this, but reduce the resolution. Transmission electron microscope (TEM) 2D, image shown on fluorescent screen. Cryo Allows examination of hydrated, unfixed and unstained biological specimens. Samples need to be frozen in liquid nitrogen/ ethene. Very low temperature keeps the =water from evaporating in the vacuum. Pyrimidines TUC Purines (two rings) GA Generation fo new combinations of double sanded DNA sequences during gene cloning The generation of sticky ends following DNA restriction allows complementary DNA sequences to hybridise. As long as the ends pieces of the DNA are complementary at the restriction site, foreign DNA can be introduced. DNA hybridization Separation of the double stranded DNA can be achieved using heat and alkali conditions. Reversing the conditions allows the DNA to re-anneal. Palindromic sequences Can be read both ways Central dogma theory DNA-transcription-RNA-translation-protein (genetic information can only flow this way) Replisome Complex of DNA polymerase and other enzymes that catalyzes the synthesis of DNA. Prokaryotes DNA replication Origin of replication OriC, one replicon. Eukaryotes DNA replication Multiple replicons: origins 3 & 5 initiate, followed by 1, 2 and 4 are passively replicated. Replication initiation

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BIOC0001 EXAM QUESTIONS AND ANSWERS WITH

COMPLETE SOLUTIONS VERIFIED

Phase contrast microscopy

Allows to examine transparent/ living specimens without staining them.

Light microscopy (bring field)

Haemotoxylin (binds yo acidic molecules -DNA) and eosin stain (amino acids).

Confocal microscopy

Light microscope that uses fluorescent stains and laser to make two- and three-

dimensional images through thick cells.

Conventional fluorescent microscopy limitations

Cutting destroys material, fluorescent emitted light causes blurriness.

Electron microscopy

Causes breakage of chemical bonds and created free radical but coating specimens

with heavy metals can protect against this, but reduce the resolution.

Transmission electron microscope (TEM)

2D, image shown on fluorescent screen.

Cryo

Allows examination of hydrated, unfixed and unstained biological specimens. Samples

need to be frozen in liquid nitrogen/ ethene. Very low temperature keeps the =water

from evaporating in the vacuum.

Pyrimidines

TUC

,Purines (two rings)

GA

Generation fo new combinations of double sanded DNA sequences during gene

cloning

The generation of sticky ends following DNA restriction allows complementary DNA

sequences to hybridise. As long as the ends pieces of the DNA are complementary at

the restriction site, foreign DNA can be introduced.

DNA hybridization

Separation of the double stranded DNA can be achieved using heat and alkali

conditions. Reversing the conditions allows the DNA to re-anneal.

Palindromic sequences

Can be read both ways

Central dogma theory

DNA-transcription-RNA-translation-protein (genetic information can only flow this way)

Replisome

Complex of DNA polymerase and other enzymes that catalyzes the synthesis of DNA.

Prokaryotes DNA replication

Origin of replication OriC, one replicon.

Eukaryotes DNA replication

Multiple replicons: origins 3 & 5 initiate, followed by 1, 2 and 4 are passively replicated.

Replication initiation

, DNAa binds at oriC at DnaA boxes. DnaB helices unwinds DNA and SSB's (single

stranded DNA binding protein) keep strands from reannealing. DnaC- helices loader

transfers helices to replication origins.

DNA primase

Forms short RNA primer complementary to the unwound template strands. The primer,

still base-paired to its complementary DNA strands, is then elongated by DNA

polymerase, thereby forming new daughter cell.

Initiator protein

DnaA, recognizes DNA and binds.

Tropoisomerase type 1

Relax DNA by nicking and closing one strand of duplex DNA. (negative supercoils)

Tropoisomerase type 2

Change DNA topology by breaking and rejoining ds DNA. (overwound region, positive

supercoils) Decatenation.

DNA polymerase I

Encodes for polyA gene, fills the gaps, repairs, bidirectional, removes RNA primer form

5 to 3, only acts on lagging strand.

RNA polymerase II

mRNA

RNA polymerase III

tRNA transcription

DNA replication is accurate due to...

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