SBIR/STTR Research Award

Method for High Throughput Assembly of Long DNA Fragments in vitro

Award identifier 615e77c9303453a960033885a3c3a15a675d955004fc2e5d402a1c4989d23987Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$301,203

Program and phase

SBIR · Phase I

Award year

2017

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Pharmaseq, Inc
Proposal award date
2017-09-14
Contract end date
2019-08-31
UEI
VFRLNECLH8F4
Solicitation number
PA16-302
Topic code
200

Research abstract

SUMMARY The main project goal is to develop principles and demonstrate the feasibility of a fast in vitro method that will increase the length of synthetic double stranded DNA from its current limit of about kb to kb This in turn will facilitate the ability to more rapidly create artificial genes and chromosomes and thus become an important tool in synthetic biology The proposed approach involves ligations of kb DNA fragments Building Blocks into larger approximately kb DNAs which are then transferred into larger structures by transformation into yeast cells The key element facilitating ligations relies on stretching the DNA Building Blocks by first immobilizing the DNA on micro or nanoparticles and then subjecting the particles and DNA to either magnetic or electric field during the ligation reaction Major tasks include Development of hardware suitable for a feasibility study The system will include a custom instrument which generates and control the electric and magnetic fields We will also build a special test tube andquot L tubeandquot for conducting ligations during which an electric and magnetic field are applied to the ligation reaction components in the new instrument Assembly a kb DNA construct Toward this goal we will study the ligation efficiency in a special assay in which DNA fragments are fluorescently labeled the ligation efficiency is monitored by observing fluorescence The DNA Building Blocks will be combined in vitro in a stepwise fashion to yield the final product Transfer of the kb ligated DNA fragment into yeast by electroporation to confirm the integrity of the assembled DNA which will be established by biological selection and screening for proper biomarkers as well as by q PCR and DNA sequencing The large assembled DNA fragments can be used in gene expression experiments to create novel biological products in different organisms NARRATIVE The purpose of this project is to design a new generation of scientific instruments and related methods that will enable the realization of synthetic biology This will be done by developing and characterizing novel methods that allow scientists to quickly and easily assemble many synthetic permutations of genetic material found in many organisms for testing genetic constructs Such major advancements in synthetic genomics will have wide applicability in improved crop production alternative energy animal husbandry drug discovery and other areas such as deciphering human noncoding DNA variants It is anticipated that the methods being created will be adopted worldwide by a wide range of scientists in academia government and private industries

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

27 SBIR/STTR records share this UEI (1998–2020). Reported award amounts total $13,992,574. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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