
NSF Org: |
DBI Division of Biological Infrastructure |
Recipient: |
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Initial Amendment Date: | September 22, 1998 |
Latest Amendment Date: | July 22, 1999 |
Award Number: | 9808891 |
Award Instrument: | Continuing Grant |
Program Manager: |
Gerald Selzer
DBI Division of Biological Infrastructure BIO Directorate for Biological Sciences |
Start Date: | October 1, 1998 |
End Date: | September 30, 2001 (Estimated) |
Total Intended Award Amount: | $147,252.00 |
Total Awarded Amount to Date: | $147,252.00 |
Funds Obligated to Date: |
FY 1999 = $69,946.00 |
History of Investigator: |
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Recipient Sponsored Research Office: |
110 INNER CAMPUS DR AUSTIN TX US 78712-1139 (512)471-6424 |
Sponsor Congressional District: |
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Primary Place of Performance: |
110 INNER CAMPUS DR AUSTIN TX US 78712-1139 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): | LIVING STOCK COLLECTIONS |
Primary Program Source: |
app-0199 |
Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.074 |
ABSTRACT
9808891
Brand
This award renews support of efforts to define effective methods for cryopreservation of a large variety of single-celled algae (microalgae) including over 2000 strains found in the UTEX collection of freshwater algae directed by the principal investigator of this award. Such microalgae are used for basic research in genetics, ecology and physiology, and for varied commercial purposes. Development of reliable methods for their cryopreservation will eliminate the need for maintenance of strains through serial culture techniques. Serial culture techniques are costly and, as importantly, permit the genetic makeup of the strains to change over time, thereby limiting their usefulness for some types of research. Thus the development of reliable cryopreservation methods is of scientific as well as economic importance to the researchers and others who use microalgae. Progress to date suggests that well over 50% of the strains in the UTEX collection can be cryopreserved. Work supported through this work will allow completion of the testing of the collection and additional efforts aimed at development of new methods for dealing with those strains so far refractory to existing cryopreservation methodology.
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