Chem Bio

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49 Terms

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Adenine

A

<p>A</p>
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Guanine

G

<p>G</p>
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Thymine

T

<p>T</p>
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Cytosine

C

<p>C</p>
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Uracil

U

<p>U</p>
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Nucleotide

Structure that contains one or more phosphate groups

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Nucleoside

Base + 5 carbon Sugar

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A Nucleoside RNA

Adenosine

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A nucleotide RNA

Adenlyate

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A Nucleotide DNA

Deoxyadenylate

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A Nucleoside DNA

Deoxyadenosine

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C DNA Nucleoside

Deoxycytidine

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C DNA Nucleotide

Deoxycytidylate

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T DNA Nucleoside

Deoxythymidine

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T DNA Nucleotide

Deoxythymidylate

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RNA is Base Sensitive

2’ OH on ribose

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DNA is Acid Sensitive

Hydrolysis of P coordinated with Mg2+ and water

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- DNA Polymerase I (DNA Pol I)

Enzyme responsible for removing RNA primers and replacing them with DNA during replication in E. coli. Has 5′→3′ polymerase, 3′→5′ proofreading exonuclease, and 5′→3′ exonuclease activities.

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DNA Polymerase III (DNA Pol III)

Primary enzyme responsible for chromosomal DNA replication in E. coli. Synthesizes DNA in the 5′→3′ direction and possesses 3′→5′ proofreading exonuclease activity.

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3′→5′ Exonuclease (Proofreading)

Enzymatic activity that removes incorrectly incorporated nucleotides from the 3′ end of a growing DNA strand, increasing replication fidelity.

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5′→3′ Exonuclease

Enzymatic activity associated with DNA Pol I that removes nucleotides ahead of the polymerase, including RNA primers during Okazaki fragment processing.

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DNA Ligase

Enzyme that seals nicks in the DNA sugar-phosphate backbone by forming phosphodiester bonds. Requires an energy source such as ATP or NAD⁺.

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DNA Helicase (DnaB

ATP-dependent enzyme that unwinds double-stranded DNA at the replication fork by disrupting base-pairing interactions.

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Primase

Enzyme that synthesizes short RNA primers, providing a free 3′-OH that DNA polymerase can extend.

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Single-Stranded DNA-Binding Protein (SSB)

Protein that binds exposed single-stranded DNA, preventing it from reannealing or forming secondary structures.

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β Sliding Clamp

Ring-shaped protein that encircles DNA and holds DNA Pol III near its template, increasing polymerase processivity.

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Core (α, ε, θ)

Catalytic assembly containing the polymerization subunit (α), proofreading subunit (ε), and an accessory subunit (θ) that stabilizes ε.

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Processivity

Number of nucleotides added by a polymerase before it dissociates from its DNA template.

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RNA Polymerase (RNAP)

Enzyme that synthesizes RNA complementary to a DNA template in the 5′→3′ direction. Unlike DNA polymerase, it does not require a primer.

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Sigma Factor (σ)

Bacterial transcription initiation factor that recognizes promoter sequences and directs RNA polymerase to appropriate transcription start sites.

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Rho Factor (ρ)

ATP-dependent RNA helicase involved in rho-dependent transcription termination by promoting separation of the RNA transcript from its DNA template.

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TATA-Binding Protein (TBP)

Protein that recognizes the TATA box in promoters containing that element and helps assemble the eukaryotic transcription initiation complex.

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−35 Element

Bacterial promoter sequence located approximately 35 nucleotides upstream of the transcription start site. Consensus sequence: 5′-TTGACA-3′.

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−10 Element (Pribnow Box)

AT-rich bacterial promoter sequence located approximately 10 nucleotides upstream of the transcription start site. Consensus sequence: 5′-TATAAT-3′.

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TATA Box

AT-rich core promoter element found in some eukaryotic genes, commonly near position −30, recognized by TBP.

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RNA Hairpin

RNA secondary structure formed when complementary sequences within the same RNA molecule base-pair, producing a stem and loop.

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Rho Utilization Site (rut Site)

– Region of nascent RNA recognized by rho, allowing rho to bind and participate in transcription termination.

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Aminoacyl-tRNA Synthetase

Enzyme that attaches the correct amino acid to its corresponding tRNA using ATP, forming a charged aminoacyl-tRNA.

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