SBIR-STTR Award

SARD: a Novel Surveying Method to Develop Genomic Reagents
Award last edited on: 1/25/2006

Sponsored Program
SBIR
Awarding Agency
DOE
Total Award Amount
$849,568
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Matthew Ashby

Company Information

Taxon Biosciences Inc

3152 Paradise Drive
Tiburon, CA 94920
   (415) 435-5116
   contact@taxon.com
   www.taxon.com
Location: Single
Congr. District: 02
County: Marin

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2004
Phase I Amount
$99,757
Microbes play a vital role in all aspects of our lives, yet our ability to understand these processes is limited by the availability of the appropriate tools. Current microbial survey methods capture only the most abundant organisms in complex populations, organisms that may represent less than 1% of the species present. This project involves the further development of a new genomics tool, known as SARD (Serial Analysis of Ribosomal DNA), which enables deep surveys of complex microbial populations by creating an inventory of short DNA sequence tags representing members of the population. A particular application of the technology is the identification of bacterial species that can be used to locate hydrocarbon plumes that originate from sub-surface petroleum reservoirs. In Phase I, the SARD diversity profiling technology will undergo further development and a set of SARD tag sequence inventories will be created from a transect of samples collected from a producing oilfield in Texas. These profiles will be compared to concurrent geophysical data in order to determine whether specific sequence tags can be identified that show strong correlation to the producing areas of the oilfield.

Commercial Applications and Other Benefits as described by the awardee:
By creating inventories of any microbial population, the SARD profiling technology should have commercial application to petroleum and mineral exploration, pollutant detection, and clinical diagnostics. In addition, the SARD DNA sequence tags themselves represent a genomic resource that should find use as: (1) a PCR (polymerase chain reaction) primer to recover the corresponding full-length 16S rRNA gene; (2) a primer in a quantitative PCR assay to query the presence of the tag sequence in a large sample collection; (3) a fluorescently labeled probe in fluorescent in situ hybridization (FISH) experiments; and 4) a probe on a DNA microarray for hybridization-based surveys

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
2005
Phase II Amount
$749,811
Microbes play a vital role in all aspects of our lives, yet our ability to understand these processes is limited by the availability of appropriate tools. Current microbial survey methods capture only the most abundant organisms in complex communities, organisms that may represent less than 1% of the species present. This project involves the development of a new genomics tool, known as SARD (Serial Analysis of Ribosomal DNA), which enables deep surveys of complex microbial communities by creating an inventory of short DNA sequence tages representing members of the community. A particular application of the technology is the identification of bacterial species that can be used to locate hydrocarbon plumes that originate from sub-surface petroleum reservoirs. Phase I isolated a greater number of unique sequence tages than currently reside in any public database, identified clusters of sequences that correlate with propane/butane abundance, developed quantitative assays, and conducted surveys to show the geographical distributions of these sequences. In Phase II, the technology will be further developed by profiling on-shore exploratory well sites and marine samples from known reservoirs. These profiles will be further analyzed to determine the ability of this technology to accurately predict a commercially viable well.

Commercial Applications and Other Benefits as described by the awardee:
By creating inventories of any microbial community, the SARD profiling technology should have commercial application to petroleum and mineral exploration, pollutant detection, and clinical diagnostics. In addition, the SARD DNA sequence tages themselves represent a genomic resource that should find use as: (1) a PCR (polymerase chain reaction) primer to recover the corresponding full-length 16S rRNA gene; (2) a primer in a quantitative PCR assay to query the presence of the tage sequence in a large sample collection; (3) a fluorescently-labeled probe in fluorscent in situ hybridization (FISH) experiments; and 4) a probe on a DNA microarray for hybridization-based surveys.