IP Library Granted Patent US 8,664,378
Granted Patent B2
US 8,664,378 · App. 13/250,040 · Granted Mar 4, 2014

Purification of nucleic acids

Inventors: Chris Suh (San Jose, CA); Lee Hoang (Santa Clara, CA); Douglas T. Gjerde (Saratoga, CA)
Assignee: PhyNexus, Inc.
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Quick Facts
Patent No.
US 8,664,378
App. No.
13/250,040
Granted
Mar 4, 2014
Kind
B2
Abstract

The present invention solves the problem of isolating nucleic acids from cells in the presence of the growth medium. The invention is particularly useful for isolating extrachromosomal replicons such as plasmids. Cells are lysed in the presence of the medium in which they were grown and nucleic acids are isolated using a pipette tip column. A liquid handling robot can be used to isolate nucleic acids from multiple samples simultaneously without the need for human intervention.

Claims (16)

1. A method for isolating plasmid DNA from cells in a liquid culture, comprising:

a. providing a liquid culture comprised of growth medium and cells, wherein the cells contain plasmid DNA;

b. lysing the cells in the liquid culture in the presence of the growth medium to produce a mixture, wherein the cells in the liquid culture are not centrifuged prior to lysis;

c. providing a pipette tip column; and

d. passing at least a portion of the mixture though the pipette tip column, whereby a portion of the plasmid DNA is captured on the pipette tip column.

2. The method of claim 1 , wherein the mixture is passed through the pipette tip column by repeated aspirate and expel steps.

3. The method of claim 2 , wherein between step (b) and step (d), a chaotropic solution is added to the mixture, and wherein the pipette tip column is further comprised of a silica solid phase.

4. An automated method for isolating plasmid DNA from cells in a liquid culture, comprising:

a. providing a liquid culture comprised of growth medium and cells, wherein the cells contain plasmid DNA;

b. lysing the cells in the liquid culture in the presence of the growth medium to produce a mixture, wherein the cells in the liquid culture are not centrifuged prior to lysis;

c. providing a pipette tip column; and

d. passing at least a portion of the mixture though the pipette tip column, whereby a portion of the plasmid DNA is captured on the pipette tip column,

wherein steps (b) and (d) are performed at pre-determined times.

5. The method of claim 4 , wherein the mixture is passed through the pipette tip column by repeated aspirate and expel steps.

6. The method of claim 5 , wherein between step (b) and step (d), a chaotropic solution is added to the mixture, and wherein the pipette tip column is further comprised of a silica solid phase.

7. The method of claim 4 , wherein steps (a) and (b) are performed in a microplate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2014
From: SUH, CHRIS; HOANG, LEE; GJERDE, DOUGLAS T.
To: PHYNEXUS, INC.
Reel/Frame 032111/0470 →
Continuity (4)
Continuation In Part PCTUS2011030232 · Mar 29, 2011
Provisional Application 61388460 · Sep 30, 2010
Provisional Application 61414855 · Nov 17, 2010
Related Publication 20120083598A1 · Apr 5, 2012