Citation
Meyerowitz, Joseph Toshiro (2023) Engineering and Rapid Prototyping for Biology in Extreme Conditions. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/9gbb-n831. https://resolver.caltech.edu/CaltechTHESIS:12022022-073109279
Abstract
In this thesis we show three projects in which biological systems are engineered for increased robustness to environmental stressors such as toxic small molecules. Several lignocellulose-derived growth inhibitors commonly found in industrial feedstocks for fermentation were used to grow a panel of yeast knockouts for several efflux pumps and detoxifying enzymes. Some specific knockout strains showed slowed growth on specific growth inhibitors, while other knockout strains showed the same growth rate as the wild-type. One efflux pump was identified for vanillin, YHK8, and was overexpressed in yeast. The overexpression strain did not show an improved tolerance to vanillin, and grew more slowly than the wild-type. To regulate the expression of the vanillin pump, a sensor for vanillin was created. The starting enzyme was the wild-type qacR transcription factor, and several variants were generated using computational protein design. The designs were synthesized and tested using in vitro transcription-translation (TX-TL) as part of a rapid prototyping process. This rapid prototyping considerably sped up the design-build-test process. Finally, four bacteria, Pseudomonas synxantha 2-79, Pseudomonas chlororaphis PCL1391, Pseudomonas aureofaciens 30-84, and E. coli are tested against the same lignocellulose growth inhibitors. The Pseudomonas spp. show an improved tolerance to the growth inhibitors. We then develop some ability to engineer and prototype in all three species. A panel of promoter parts were integrated into the P. synxantha genome to produce a collection of test strains. These same promoter parts were also used as DNA templates for TX-TL reactions. The in vivo measurements of promoter strength and in vitro measurements show similar relative strengths between the parts, showing the Pseudomonas-based TX-TL systems can be used for design-build-test activities in these non-model organisms. This alternate approach to developing tolerance, starting with a species that already has a working tolerance to the stressor in question, changes the problem to one of building engineering capabilities in the new chassis.
Item Type: | Thesis (Dissertation (Ph.D.)) | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Subject Keywords: | synthetic biology, in vitro transcription-translation, non-model organisms, rapid prototyping | ||||||||||||
Degree Grantor: | California Institute of Technology | ||||||||||||
Division: | Chemistry and Chemical Engineering | ||||||||||||
Major Option: | Biochemistry and Molecular Biophysics | ||||||||||||
Thesis Availability: | Public (worldwide access) | ||||||||||||
Research Advisor(s): |
| ||||||||||||
Thesis Committee: |
| ||||||||||||
Defense Date: | 5 October 2022 | ||||||||||||
Funders: |
| ||||||||||||
Projects: | Development of in vitro transcription-translation systems with three wild-type pseudomonas species, Engineering transcriptional regulator effector specificity using computational design and in vitro rapid prototyping: developing a vanillin sensor, Engineering a synthetic microbial stress response | ||||||||||||
Record Number: | CaltechTHESIS:12022022-073109279 | ||||||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechTHESIS:12022022-073109279 | ||||||||||||
DOI: | 10.7907/9gbb-n831 | ||||||||||||
Related URLs: |
| ||||||||||||
ORCID: |
| ||||||||||||
Default Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | ||||||||||||
ID Code: | 15071 | ||||||||||||
Collection: | CaltechTHESIS | ||||||||||||
Deposited By: | Joseph Meyerowitz | ||||||||||||
Deposited On: | 23 Jan 2023 18:05 | ||||||||||||
Last Modified: | 08 May 2024 18:06 |
Thesis Files
PDF
- Final Version
See Usage Policy. 8MB |
Repository Staff Only: item control page