IP Library Granted Patent US 11,319,579
Granted Patent B2
US 11,319,579 · App. 16/371,766 · Granted May 3, 2022

Method of amplifying circular DNA

Inventors: Masayuki Su'etsugu (Tokyo, JP); Hiroko Kobayashi (Tokyo, JP)
Assignee: OriCiro Genomics, Inc.
C12Q1/6846C12N9/00C12N9/12C12N9/16C12N9/90C12N15/09C12P19/34C12Q1/686C12Q1/6853C12N15/00
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Quick Facts
Patent No.
US 11,319,579
App. No.
16/371,766
Granted
May 3, 2022
Kind
B2
Abstract

The present invention provides a method for easily and exponentially amplifying circular DNA, particularly long chain circular DNA, in a cell-free system. Specifically, the present invention provides a method for amplifying circular DNA in which circular DNA having a replication origin sequence (origin of chromosome (oriC)) is mixed with a reaction solution containing the following enzyme groups to form a reaction mixture, which is then reacted under an isothermal condition, the enzyme groups being: (1) a first enzyme group that catalyzes replication of circular DNA; (2) a second enzyme group that catalyzes an Okazaki fragment maturation and synthesizes two sister circular DNAs constituting a catenane and (3) a third enzyme group that catalyzes a separation of two sister circular DNAs.

Claims (28)

1. A kit for amplifying circular DNA comprising a mixture of the following three enzyme groups in a single container, wherein each of the enzymes is a recombinant enzyme:

(a) a first enzyme group that catalyzes replication of circular DNA;

(b) a second enzyme group that catalyzes an Okazaki fragment maturation and synthesizes two sister circular DNAs constituting a catenane; and

(c) a third enzyme group that catalyzes a separation of two sister circular DNAs, which is an enzyme group comprising at least two enzymes selected from a group consisting of an enzyme having topoisomerase III activity, an enzyme having topoisomerase IV activity, and an enzyme having RecQ activity.

2. The kit according to claim 1 , wherein

the first enzyme group comprises a combination of an enzyme having DnaA activity, one or more types of nucleoid protein, an enzyme or enzyme group having DNA gyrase activity, single-strand binding protein (SSB), an enzyme having DNA helicase activity, an enzyme having DNA helicase loader activity, an enzyme having DNA primase activity, an enzyme having DNA clamp activity, and an enzyme or enzyme group having DNA polymerase III activity; and wherein

the second enzyme group comprises a combination of an enzyme having DNA polymerase I activity, and an enzyme having DNA ligase activity.

3. The kit according to claim 1 , further comprising tRNA.

4. The kit according to claim 2 , further comprising tRNA.

5. The kit according to claim 1 , further comprising potassium glutamate.

6. The kit according to claim 2 , further comprising potassium glutamate.

7. The kit according to claim 3 , further comprising potassium glutamate.

8. A kit for exponentially amplifying circular DNA by repeating replication cycles, comprising a mixture of the following three enzyme groups in a single container, wherein each of the enzymes is a recombinant enzyme:

(a) a first enzyme group that catalyzes replication of circular DNA;

(b) a second enzyme group that catalyzes an Okazaki fragment maturation and synthesizes two sister circular DNAs constituting a catenane; and

(c) a third enzyme group that catalyzes a separation of two sister circular DNAs.

9. A kit for amplifying circular DNA comprising a mixture of the following three enzyme groups in a single container, wherein each of the enzymes is a recombinant enzyme:

(a) a first enzyme group that catalyzes replication of circular DNA;

(b) a second enzyme group that catalyzes an Okazaki fragment maturation and synthesizes two sister circular DNAs constituting a catenane; and

(c) a third enzyme group that catalyzes a separation of two sister circular DNAs, and

an additional constituent, wherein

said additional constituent is a constituent which describes a method of exponentially amplifying circular DNA by repeating replication cycles in a reaction mixture composed of a reaction solution containing said first, second and third enzyme groups and circular DNA that constitutes a template.

10. The kit of claim 1 , further comprising rNTPs and dNTPs in the same or a separate container.

11. The kit of claim 8 , further comprising rNTPs and dNTPs in the same or a separate container.

12. The kit of claim 9 , further comprising rNTPs and dNTPs in the same or a separate container.

13. The kit of claim 1 , wherein the mixture is in solution.

14. The kit of claim 8 , wherein the mixture is in solution.

15. The kit of claim 9 , wherein the mixture is in solution.

Assignments (5)
CHANGE OF NAME Recorded May 4, 2023
From: ORICIRO GENOMICS K.K.
To: MODERNA ENZYMATICS CO., LTD.
Reel/Frame 063534/0546 →
CHANGE OF NAME Recorded May 4, 2023
From: ORICIRO GENOMICS, INC.
To: ORICIRO GENOMICS K.K.
Reel/Frame 064657/0419 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2020
From: JAPAN SCIENCE AND TECHNOLOGY AGENCY
To: ORICIRO GENOMICS, INC.
Reel/Frame 051996/0219 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2019
From: SU'ETSUGU, MASAYUKI; KOBAYASHI, HIROKO
To: RIKKYO EDUCATIONAL CORPORATION
Reel/Frame 048768/0317 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2019
From: RIKKYO EDUCATIONAL CORPORATION
To: JAPAN SCIENCE AND TECHNOLOGY AGENCY
Reel/Frame 048768/0426 →
Priority Claims (1)
JP 2014-233563 · Nov 18, 2014 · national
Continuity (2)
Division 15527560
Related Publication 20190249236A1 · Aug 15, 2019