The Space Station Biological Research Project - Habitat development and capabilities

2001 ◽  
Author(s):  
Beverly Girten ◽  
Orlando Santos ◽  
Esther Hill ◽  
Melissa Kirven-Brooks ◽  
Frances Donovan ◽  
...  
2001 ◽  
Author(s):  
G. J. Nakamura ◽  
M. Kirven-Brooks ◽  
N. M. Scheller

1986 ◽  
Author(s):  
Gary R. Primeaux ◽  
Ladonna J. Miller ◽  
Roger B. Michaud

1990 ◽  
Author(s):  
L. CHAMBERS ◽  
P. STABEKIS ◽  
R. TEETER

2021 ◽  
Vol 7 (24) ◽  
pp. eabg5554
Author(s):  
Sayaka Wakayama ◽  
Daiyu Ito ◽  
Yuko Kamada ◽  
Toru Shimazu ◽  
Tomomi Suzuki ◽  
...  

Space radiation may cause DNA damage to cells and concern for the inheritance of mutations in offspring after deep space exploration. However, there is no way to study the long-term effects of space radiation using biological materials. Here, we developed a method to evaluate the biological effect of space radiation and examined the reproductive potential of mouse freeze-dried spermatozoa stored on the International Space Station (ISS) for the longest period in biological research. The space radiation did not affect sperm DNA or fertility after preservation on ISS, and many genetically normal offspring were obtained without reducing the success rate compared to the ground-preserved control. The results of ground x-ray experiments showed that sperm can be stored for more than 200 years in space. These results suggest that the effect of deep space radiation on mammalian reproduction can be evaluated using spermatozoa, even without being monitored by astronauts in Gateway.


Eos ◽  
1987 ◽  
Vol 68 (45) ◽  
pp. 1579
Author(s):  
Richard S. Young

2020 ◽  
Vol 4 (2) ◽  
pp. 20-27
Author(s):  
Sarahann Hutchinson ◽  
Proma Basu ◽  
Sarah E. Wyatt ◽  
Darron R. Luesse

AbstractLarge-scale omics approaches make excellent choices for research aboard the International Space Station (ISS) because they provide large amounts of data that can be continually mined even after the original research has been completed. A proteomic approach can provide information about which proteins are produced, degraded, or post-translationally modified, potentially shedding light on cellular strategies that cannot be discerned from transcriptomic data. To collect sufficient tissue from a Biological Research In Canisters (BRIC)-grown experiment on the ISS for proteomic analysis, several modifications were made to existing protocols. Approximately 800–1000 seeds were housed in each Petri Dish Fixation Units (PDFU). These were germinated up to 120 h after planting by transferring the BRIC from cold stasis to room temperature. Growth continued for only 72 h after germination to allow sufficient tissue for extraction, and to minimize the impact of ethylene and crowding stress. Seedlings were then exposed to RNAlater®. Results indicate that RNAlater® - treated Arabidopsis seedlings yield an equal amount of protein to those flash-frozen in liquid nitrogen.


1990 ◽  
Author(s):  
A. KRIKORIAN ◽  
CATHERINE JOHNSON

2021 ◽  
Vol 2 ◽  
Author(s):  
Wayne L. Nicholson ◽  
Patricia Fajardo-Cavazos ◽  
Caleb Turner ◽  
Taylor M. Currie ◽  
Geoffrey Gregory ◽  
...  

The major factor influencing the behavior of microbes growing in liquids in space is microgravity. We recently measured the transcriptomic response of the Gram-positive bacterium Bacillus subtilis to the microgravity environment inside the International Space Station (ISS) in spaceflight hardware called Biological Research in Canisters-Petri Dish Fixation Units (BRIC-PDFUs). In two separate experiments in the ISS, dubbed BRIC-21 and BRIC-23, we grew multiple replicates of the same B. subtilis strain in the same hardware, growth medium, and temperature with matching ground control samples (npj Micrograv. 5:1.2019, doi: 10.1038/s41526-018-0061-0). In both experiments we observed similar responses of the transcriptome to spaceflight. However, we also noted that the liquid cultures assumed a different configuration in microgravity (a toroidal shape) compared with the ground control samples (a flat disc shape), leading us to question whether the transcriptome differences we observed were a direct result of microgravity, or a secondary result of the different liquid geometries of the samples affecting, for example, oxygen availability. To mitigate the influence of microgravity on liquid geometry in BRIC canisters, we have designed an insert to replace the standard 60-mm Petri dish in BRIC-PDFU or BRIC-LED sample compartments. In this design, liquid cultures are expected to assume a more disk-like configuration regardless of gravity or its absence. We have: (i) constructed a prototype device by 3D printing; (ii) evaluated different starting materials, treatments, and coatings for their wettability (i.e., hydrophilicity) using contact angle measurements; (iii) confirmed that the device performs as designed by drop-tower testing and; (iv) performed material biocompatibility studies using liquid cultures of Bacillus subtilis and Staphylococcus aureus bacteria. Future microgravity testing of the device in the ISS is planned.


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