
Concept explainers
RECALL What is the difference in the requirement for a primer in RNA transcription compared to

Interpretation:
The difference between the requirement of primer in RNA transcription and DNA replication is to be explained.
Concept introduction:
Primer is a short stretch of oligonucleotide needed for the initiation of DNA replication.
Primer is synthesized by the enzyme primase at the beginning of DNA replication.
Primase copies a small stretch of template DNA strand to produce an RNA primer.
The process of producing two identical copies of DNA molecule from original DNA molecule is called DNA replication.
The process of copying of DNA into a new molecule of mRNA is called transcription.
Answer to Problem 1RE
Solution: Primer is not required for the activity of RNA polymerase, the enzyme that carries out RNA transcription. However, DNA polymerases need an RNA primer during initiation step of DNA replication to be able to start the polymerization reaction.
Explanation of Solution
Given information: Primer, RNA transcription, and DNA replication
RNA transcription is carried out by an enzyme called RNA polymerase, which is a DNA-dependent polymerase that needs DNA as a template in order to synthesize RNA. Only one strand of DNA is used for transcription. The strand of DNA, which is read in the 3’ to 5’ direction by the RNA polymerase, is known as the template strand or antisense strand. The template DNA sequence, which signals the start of RNA transcription, is known as a promoter. RNA polymerase binds to the promoter sequence and synthesizes RNA using all four ribonucleoside triphosphates (ATP, GTP, UTP, and CTP). In the process of RNA synthesis, RNA polymerase does not require primer due to its ability to de novo synthesize RNA by positioning a ribonucleoside triphosphates (usually a purine) complementary to the template strand.
During replication, both the strands of DNA are required as template by DNA polymerase to synthesize the leading and lagging strand. DNA polymerase needs a free 3’- hydroxyl group already in place in order to synthesize the DNA chain. The RNA primer synthesized by the enzyme primase at the beginning of replication helps provide a free 3’- hydroxyl group for the initiation of DNA replication. In the absence of a primer, DNA polymerase cannot catalyze the DNA polymerization reaction. Once the DNA strands have been completely synthesized, primer is removed and replaced with deoxynucleotides by DNA polymerase I using the exonuclease and polymerase activity, respectively. DNA polymerases possess proof reading activity to check for any errors in the newly synthesized DNA strands. The presence of proofreading activity in DNA polymerase is compensated by the absence of primer synthesis ability, thereby making sure that DNA replication is an error proof process.
RNA polymerase can initiate a primer free transcription, whereas DNA polymerase needs primer to initiate the replication of DNA.
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Chapter 11 Solutions
Biochemistry
- To map the active site of -lactamase, the enzyme was hydrolyzed with trypsin to yield a hexapeptide (P1) with the following amino acids. Glu, Lys, Leu, Phe, Met, and Ser. Treatment of P1 with phenyl isothiocyanate yielded a PTH derivative of phenylalanine and a peptide (P2). Treatment of P1 with cyanogenbromide gave an acidic tetrapeptide (P3) and a dipeptide (P4).Treatment of P2 with 1-fluoro-2,4-dinitrobenzene, followed by complete hydrolysis, yields N-2,4-dinitrophenyl-Glu. P1, P2, and P3 contain the active site serine. question: the b-lactamase hydrolyzes the lactam-ring in antibiotics like penicillin. Describe the mechanism, of hydrolysis, insuring to include the involvement of S, D, and K in the reaction sequence. Please help!arrow_forwardThree of these amino acids participate in the proteolytic hydrolysis of polypeptides. Show the charge-relay network generated by the serine proteases and identify the nucleophilic species that initiates the hydrolysis. please help!arrow_forwardYou have isolated a protein and determined that the native molecular weight of the holoenzyme is 160 kD using size exclusion chromatography. Analysis of this protein using SDS-PAGE revealed 2 bands, one at 100 kD and one at 30 kD. 1. Describe the architecture of the polypeptide component of this enzyme. 2. The enzyme was found to be 0.829% NAD (by weight). What further can be said regarding the architecture? can you please help me with question number 2arrow_forward
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- +NH+ CO₂ +P H₂N + ATP H₂N NH₂ +ADParrow_forwardWhich type of enzyme catalyses the following reaction? oxidoreductase, transferase, hydrolase, lyase, isomerase, or ligase.arrow_forwardWhich features of the curves in Figure 30-2 indicates that the enzyme is not consumed in the overall reaction? ES is lower in energy that E + S and EP is lower in energy than E + P. What does this tell you about the stability of ES versus E + S and EP versus E + P.arrow_forward
- BiochemistryBiochemistryISBN:9781305961135Author:Mary K. Campbell, Shawn O. Farrell, Owen M. McDougalPublisher:Cengage Learning
