Responsible Center: TRISH
Grant Monitor:
Center Contact:
Unique ID: 13957
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Solicitation / Funding Source: 2020 TRISH BRASH1901: Translational Research Institute for Space Health (TRISH) Biomedical Research Advances for Space Health
Grant/Contract No.: NNX16AO69A-T0504
Project Type: Ground
Flight Program:
TechPort: No |
No. of Post Docs: 1
No. of PhD Candidates: 0
No. of Master's Candidates: 0
No. of Bachelor's Candidates: 3
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No. of PhD Degrees: 0
No. of Master's Degrees: 0
No. of Bachelor's Degrees: 1
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Research Impact/Earth Benefits: |
During this reporting period we have developed three key technologies with significant impact beyond this project:
Impact 1: Porous membranes for controlled release of bacteria. We developed a technology to tune the release rate of bacteria. This technology may have application generally for the controlled release of bacteria in therapeutics or other applications where controlled release may be required (e.g., plant probiotics). While there has been extensive work in developing technologies for controlling the release profiles of small molecules from different types of matrices, the technology described here fills a growing need to control the release of bacteria that are intended as therapeutics.
Impact 2: Matrices for dosing and manipulating dry bacteria. Bacteria are traditionally handled as liquid suspensions, slurries, or frozen pastes. All these modalities require a dedicated environment (e.g., wet bench laboratory) and expert personnel to handle. In contrast to these, commercially available bacterial pills (i.e., probiotics) present a tantalizing alternative. However, our previously funded Translational Research Institute for Space Health (TRISH) work demonstrated that many of these commercial products do not have the viabilities promised and some have extremely poor recovery of viable bacteria. The technology developed during this reporting period builds on our previously developed bacterial formulations, expanding them to incorporation of bacteria directly into easily handled matrices. Furthermore, we showed that the bacteria not only can be recovered with high viability but also that maximal enzymatic/metabolic activity is recovered in less than 1 hr. Such a simple medium for manipulating, aliquoting, and dosing bacteria may have impacts beyond this project including streamlined manufacturing workflows of components that may use the incorporated bacteria for treating, sensing, or controlling down stream components.
Impact 3: Transfer of biosynthetic pathways to probiotic bacteria. In the proposed project we selected target molecules that are currently part of the NASA med kit and which have biosynthetic pathways previously established to differing degrees in bacteria. This strategic choice enhanced the likelihood of success achieving a traditionally challenging goal (i.e., biosynthesis of any molecule) in the abbreviated duration of the project. During this reporting period, we have established these biosynthetic pathways in a probiotic strain with a proven track record for use in humans. These strains may have impacts beyond this project by demonstrating and defining the challenges of biosynthesizing Food and Drug Administration (FDA) approved molecules in probiotic strains which are being actively used by commercial entities seeking FDA approval for microbial therapeutics. |