IP Library Patent Application 16746490
Patent Application
App. No. 16/746,490

Methods of Producing and Using Single-Stranded Deoxyribonucleic Acids and Compositions for Use in Practicing the Same

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Patent No.
US None
App. No.
16/746,490
Abstract

Methods of producing single-stranded deoxyribonucleic acids (ssDNAs) are provided. Aspects of the methods include generating a double stranded deoxyribonucleic acid (dsDNA) and then selectively degrading one strand of the dsDNA to produce a ssDNA. ssDNAs produced using methods of the invention find use in a variety of applications, including genomic modification applications. Also provided are compositions, e.g., kits, that find use in practicing various embodiments of the invention.

Claims (26)

1 .- 37 . (canceled)

38 . A kit for generating a ssDNA, the kit comprising:

a nucleic acid comprising a 5′ phosphate or one or more protective base modifications; and

an exonuclease.

39 . The kit according to claim 38 , wherein the nucleic acid is a ssDNA primer or dsDNA segment comprising a 5′ phosphate.

40 . The kit according to claim 39 , wherein the dsDNA segment comprises a 5′ phosphate and one or more protective base modifications.

41 . The kit according to claim 38 , wherein the kit further comprises a ssDNA primer comprising one or more protective base modifications.

42 . The kit according to claim 38 , wherein the exonuclease is an exonuclease having activity that is blocked by the one or more protective base modifications.

43 . The kit according to claim 38 , wherein the exonuclease is a 5′-phosphate-dependent exonuclease.

44 . The kit according to claim 43 , wherein the 5′-phosphate-dependent exonuclease is a lambda exonuclease.

45 . The kit according to claim 38 , where in the exonuclease is a dsDNA-dependent 3′ to 5′ exonuclease.

46 . The kit according to claim 45 , wherein the dsDNA-dependent 3′ to 5′ exonuclease is an exonuclease III.

47 . The kit according to claim 38 , wherein the kit comprises two or more different exonucleases.

48 . The kit according to claim 47 , wherein the two or more different exonucleases comprise a 5′-phosphate-dependent exonuclease and a dsDNA-dependent 3′ to 5′ exonuclease.

49 . The kit according to claim 38 , wherein the kit further comprises a PCR polymerase, a ligase or both.

50 . The kit according to claim 38 , wherein the kit is configured for modifying genomic DNA and further comprises a genome-cleaving nuclease.

51 . The kit according to claim 50 , wherein the genome-cleaving nuclease is selected from the group consisting of: a Cas9 nuclease, a zinc-finger nuclease and a transcription activator-like effector nuclease.

52 . A kit comprising:

(a) a double-stranded vector;

(b) a bacterial host cell; and

(c) a cleaving agent.

53 . The kit according to claim 52 , wherein said double-stranded vector comprises an M13 vector.

54 . The kit according to claim 52 , wherein said cleaving agent is selected from the group consisting of: a restriction endonuclease and a CRISPR/Cas9 ribonucleoprotein complex.

55 . The kit according to claim 52 , further comprising instructions for use.

56 . The kit according to claim 52 , wherein the kit further comprises a PCR polymerase, a ligase or both.

57 . The kit according to claim 52 , wherein said bacterial host cell is a competent cell.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2020
From: MATSUMOTO, HIROYUKI; HAUGWITZ, MICHAEL; FARMER, ANDREW; BOSTICK, MAGNOLIA
To: TAKARA BIO USA, INC.
Reel/Frame 052589/0303 →