Publications

  1. Overproduction of Native and Click-able Colanic Acid Slime from Engineered Escherichia coli. J. C. Sadler, R. C. Brewster, A. F. González, J. S. Nirkko, S. Varzandeh, S. Wallace*, JACS Au 2023, DOI: https://doi.org/10.1021/jacsau.2c00583 - link

  2. Engineering Biology for Sustainable 1,4-Butanediol Synthesis. C. L. Trotter, G. S. Babu, S. Wallace*, Trends Biotechnol. 2023, DOI: https://doi.org/10.1016/j.tibtech.2023.01.006 - link

  3. A New PETase from the Human Saliva Metagenome and Its Functional Modification via Genetic Code Expansion in Bacteria. M. F. M. White, S. Wallace*, Angew. Chem. Int. Ed. 2023, DOI: https://doi.org/10.1102/anie.202216963 - link

  4. Bread Waste - A Potential Feedstock for Sustainable Circular Biorefineries. V. Kumar*, P. Brancoli, V. Narisetty, S. Wallace, D. Charalampopoulos, B. K. Dubey, G. Kumar, A. Bhatnagar, S. K. Bhatia, M. J. Taherzadeh, Bioresour. Technol. 2022, DOI: org/10.1016/j.biortech.2022.128449 - link

  5. Palladium Nanoparticles from Desulfovibrio alaskensis G20 Catalyze Biocompatible Sonogashira and Biohydrogenation Cascades. Y. Era, J. A. Dennis, L. E. Horsfall*, S. Wallace*, JACS Au 2022, 2, 11, 2446–2452 - link

  6. Tyramine Derivatives Catalyze the Aldol Dimerization of Butyraldehyde in the Presence of Escherichia coli. J. A. Dennis, J. C. Sadler, S. Wallace*, ChemBioChem. 2022, e202200238 - link

  7. Micellar Catalysis of the Suzuki Miyaura Reaction using Biogenic Pd Nanoparticles from Desulfovibrio alaskensis. Y. Era, J. A. Dennis, L. E. Horsfall*, S. Wallace*, Green Chem. 2021, 23, 8886–8890 - link

  8. Microbial Synthesis of Vanillin from Waste poly(ethylene terephthalate). J. C. Sadler, S. Wallace*, Green Chem. 2021, 23, 4665–4672 - link - press release

  9. Interfacing Non-Enzymatic Catalysis with Living Microorganisms. J. C. Sadler, J. A. Dennis, N. W. Johnson, S. Wallace*, RSC Chem. Biol. 2021, 2, 1073–1083 - link 

  10. Optimizing the Biosynthesis of Oxygenated and Acylated Taxol Precursors in Saccharomyces cerevisiae using Advanced Bioprocessing Strategies. L. E. Walls, K. Malci, B. Nowrouzi, R. A. Li, L. d'Espaux, J. Wong, J. A. Dennis, A. J. C. Semiao, S. Wallace, J. L. Martinez, J. D. Keasling, L. Rios-Solis, Biotechnol. Bioeng. 2020, 118, 279–293 - link

  11. One-Pot Synthesis of Adipic Acid from Guaiacol in Escherichia coli. J. T. Suitor, S. Varzandeh, S. Wallace*, ACS Synth. Biol. 2020, 9, 2472–2476 - link - press release 

  12. Transition Metal-Free Reduction of Activated Alkenes Using a Living Microorganism. R. C. Brewster, J. T. Suitor, A. W. Bennett, S. Wallace*, Angew. Chem. Int. Ed. 2019, 58, 12409–12414 - link

  13. Synthetic Methodologies in Chemical Biology. In book: Biomolecular and Bioanalytical Techniques: Theory, Methodology and Applications. R. C. Brewster, S. Wallace*. John Wiley & Sons, Inc. Editor: V. Ramesh, 2019, ISBN: 9781119483977

  14. Computationally Guided Discovery of a Reactive, Hydrophilic trans-5-Oxocene Dienophile for Bioorthogonal Labeling. W. D Lambert, S. L. Scinto, O. Dmittrenko, S. J. Boyd, R. A. Mehl, J. W. Chin*, J. M. Fox*, S. Wallace*, Org. Biomol. Chem. 2017, 15, 6640–6644 - link

  15. Protein Modification via Alkyne Hydrosilylation Using a Substoichiometric Amount of Ruthenium(II) Catalyst. T. T. L. Kwan, O. Boutureira, E. C. Frye, S. J. Walsh, M. K. Gupta, S. Wallace, Y. Wu, F. Zhang, H. F. Sore, W. R. J. D. Galloway, J. W. Chin, M. Welch, G. J. L. Bernardes, D. R. Spring, Chem. Sci. 2017, 8, 3871–3878 - link

  16. Interfacing Biocompatible Reactions with Engineered Escherichia coli. S. Wallace, E. P. Balskus, Methods Mol. Biol. 2017, 1586, 409–421 - link

  17. Designer Micelles Accelerate Flux Through Engineered Metabolism and Support Biocompatible Chemistry. S. Wallace, E. P. Balskus, Angew. Chem. Int. Ed. 2016, 55, 6023–6027 - link

  18. Interfacing Microbial Styrene Production with a Biocompatible Cyclopropanation Reaction. S. Wallace, E. P. Balskus, Angew. Chem. Int. Ed. 2015, 54, 7106–7109 - link

  19. Using Non-Enzymatic Chemistry to Influence Microbial Metabolism. S. Wallace, E. E. Shultz, E. P. Balskus, Curr. Opin. Chem. Biol. 2015, 25, 71–79 - link

  20. Opportunities for Merging Chemical and Biological Synthesis. S. Wallace, E. P. Balskus, Curr. Opin. Biotechnol. 2014, 30, 1–8 - link

  21. Strain-Promoted Sydnone Bicyclo-[6.1.0]-nonyne Cycloaddition. S. Wallace, J.  W. Chin, Chem. Sci. 2014, 5, 1742–1744 - link

  22. Conformationally Strained trans-Cyclooctene with Improved Stability and Excellent Reactivity in Tetrazine Ligation. A. Darko, S. Wallace, O. Dmitrenko, M. M. Machovina, R. A. Mehl, J. W. Chin, J. M. Fox, Chem. Sci. 2014, 5, 3770–3776 - link

  23. Optimized Orthogonal Translation of Unnatural Amino Acids Enables Spontaneous Protein Double-Labeling and FRET. K. Wang, A. Sachdeva, D. J. Cox, N. W. Wilf, S. Wallace, R. A. Mehl, J. W. Chin, Nat. Chem. 2014, 6, 393–403 - link

  24. A Cascade Strategy Enables a Total Synthesis of (–)-Gephyrotoxin. S. Chu, S. Wallace, M. D. Smith, Angew. Chem. Int. Ed. 2014, 53, 13826–13829 - link

  25. Genetic Encoding of Bicyclononynes and trans-Cyclooctenes for Site-Specific Protein Labeling in vitro and in Live Mammalian Cells. K. Lang, L. Davis, S. Wallace, M. Mahesh, D. J. Cox, M. L. Blackman, J. M. Fox, J. W. Chin, J. Am. Chem. Soc. 2012, 134, 10317–10320 - link

  26. Rapid Synthesis and Zebrafish Evaluation of a Phenanthridine-Based Small Molecule Library. L. R. Donaldson, S. Wallace, D. Haigh, E. E. Paton, A. N. Hulme, Org. Biomol. Chem. 2011, 9, 2233–2239 - link