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​Which one of the following statements made about the bacterial replisome is INCORRECT?​
Question

Which one of the following statements made about the bacterial replisome is INCORRECT?

A.

The rate of forward movement of DnaB helicase on the DNA increases ~10-fold when DnaB and DNA Pol III interact, thus ensuring that the helicase does not move ahead rapidly without the polymerase.

B.

The transient interaction of the primase with the helicase allows activation of primase activity by ~1000-fold, promoting RNA primer synthesis.

C.

The length of the Okazaki fragments is typically 1000-2000 nucleotides.

D.

The E. coli oriC carries repeats of two sequence motifs: repeats of a 9-mer that collectively form the site at which the origin first becomes single-stranded, and repeats of a 13-mer to which the DnaA initiator protein binds.

Correct option is D

Explanation-

Option a: The rate of forward movement of DnaB helicase along the template DNA increases ~10-fold when DnaB and DNA Pol III interact, thus ensuring that the helicase does not move ahead rapidly without the polymerase.
 Correct.
This is a known coordination mechanism in the replisome — the helicase (DnaB) and DNA polymerase III interact to synchronize their movement. When DnaB is not coupled with DNA Pol III, its activity is slower; the interaction accelerates helicase movement appropriately.

Option b: The transient interaction of the primase with the helicase allows activation of primase activity by ~1000-fold, promoting RNA primer synthesis.
Correct.
The interaction between primase and helicase is essential for primer synthesis, and this interaction indeed activates primase activity substantially (often cited as ~1000-fold). This allows timely RNA primer production.

Option c: The length of the Okazaki fragments is typically restricted to 1000-2000 nucleotides.
Correct.
In prokaryotes, Okazaki fragments typically range from 1000 to 2000 nucleotides. This is a well-established fact.

Option d: The E. coli oriC carries repeats of two sequence motifs: repeats of a 9-mer that collectively form the site at which the origin first becomes single-stranded, and repeats of a 13-mer to which the DnaA initiator protein binds.
Incorrect.
This statement mixes up the function of the 9-mer and 13-mer motifs. The 9-mer sequences are binding sites for DnaA, the initiator protein. The 13-mer sequences are AT-rich regions that become single-stranded (melted) first during initiation.
So, the roles of 9-mer and 13-mer are reversed in the statement.

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