High-throughput DNA fragment assembly

US9752154B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9752154-B2
Application numberUS-201314416799-A
CountryUS
Kind codeB2
Filing dateJul 23, 2013
Priority dateJul 26, 2012
Publication dateSep 5, 2017
Grant dateSep 5, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

This invention is related to methods and systems for vector assembly for transgenic plants. A uniform modular process is used to reduce cycle time and the methods and systems provided herein can increase cloning throughput using multiple-well plates, for example 96-well plates. In some embodiments, the methods and systems provided herein eliminate or reduce the need for sequencing confirmation because no PCR is involved in the vector assembly process.

First claim

Opening claim text (preview).

We claim: 1. A method for DNA assembly, comprising, (a) providing a first DNA molecule comprising a Kozak sequence, wherein the Kozak sequence is selected from the group consisting of SEQ ID NOs: 1-43 and 64-74; (b) providing a second DNA molecule comprising the same Kozak sequence of step (a) at one end and a six frame stop sequence at the other end, wherein the six frame stop sequence is selected from the group consisting of SEQ ID NOs: 75-80; (c) providing a third DNA molecule comprising the same six frame stop sequence of step (b); (d) providing a fourth DNA molecule comprising a linear vector sequence; and (e) assembling a product vector using the DNA molecules of steps (a), (b), (c), and (d) in the presence of at least one recombinase, where the Kozak sequence and the six frame stop sequence provide junction homologies for DNA recombination and wherein the product vector has sequences in the order of the DNA molecules from steps (a), (b), (c), and (d). 2. The method of claim 1 , wherein the DNA molecules of steps (a), (b), (c), and (d) are obtained using PCR amplification or direct DNA synthesis. 3. The method of claim 1 , wherein no DNA amplification technique is used. 4. The method of claim 1 , wherein polymerase chain reaction is not used. 5. The method of claim 1 , wherein the fourth DNA molecule comprises a lethal gene. 6. The method of claim 5 , wherein the lethal gene is ccdB. 7. The method of claim 1 , wherein the same Kozak sequence of both step (a) and (b) comprises a same three-frame stop sequence at its 5′ end. 8. The method of claim 7 , wherein the three-frame stop sequence is selected from the group consisting of SEQ ID NOS 44-62.

Assignees

Inventors

Classifications

  • C12N15/68Primary

    Stabilisation of the vector · CPC title

  • C12N15/82Primary

    for plant cells {, e.g. plant artificial chromosomes (PACs)} · CPC title

  • Selection, visualisation of transformants, reporter constructs, e.g. antibiotic resistance markers · CPC title

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What does patent US9752154B2 cover?
This invention is related to methods and systems for vector assembly for transgenic plants. A uniform modular process is used to reduce cycle time and the methods and systems provided herein can increase cloning throughput using multiple-well plates, for example 96-well plates. In some embodiments, the methods and systems provided herein eliminate or reduce the need for sequencing confirmation …
Who is the assignee on this patent?
Dow Agrosciences Llc, Kumar Sandeep, Evans Steven L, and 1 more
What technology area does this patent fall under?
Primary CPC classification C12N15/68. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).