• About

    I am a postdoc in the Lidstrom and Baker labs at the University of Washington. I am interested in using enzyme and metabolic engineering to improve one-carbon metabolism in bioproduction and agriculture.

     

    Previously, I was a scientist at Ginkgo Bioworks, where I did bioinformatic enzyme discovery. Before that I did my PhD in the Springer Lab at Harvard Medical School, where my thesis was on natural genetic variation in yeast sugar signaling.

     

    See my CV for more details on my research and publications.

  • Research

    Metagenomic enzyme discovery and screening

    Synthetically designed metabolic pathways use parts from across the tree of life, but the existing "codebase" of enzymes is often limited to a few model examples. Using modern sequence databases and DNA synthesis technology, it is now possible to systematically evaluate many members of an enzyme family for fine-tuned functional diversity. At Ginkgo, I developed computational tools to identify enzymes in metagenomic data and support functional screens. We aimed not only to establish a useful codebase for synthetic biology, but also to better understand how sequences encode the biochemical properties of enzymes.

    Natural variation and tradeoffs in nutrient decisions

    Microbes growing in mixtures of nutrients have to decide which nutrient(s) to consume first. In a paper from my PhD, we studied yeast strains from different geographic and ecological niches and found that the strains make different nutrient decisions, corresponding to whether they "prepare" for impending depletion of a preferred nutrient. Because this preparation requires costly gene expression, it leads to a fitness tradeoff, perhaps explaining the diversity of decision-making phenotypes across extant yeast strains. In a followup, we mapped genomic regions causing the differences across strains. In another related work, we analyzed the genetics of variation in bimodal activation of sugar-responsive genes.

  • Publications

    Natural Genetic Variation Can Independently Tune the Induced Fraction and Induction Level of a Bimodal Signaling Response

    Wang J., Palme J., Lee K. B., Springer, M. (2017) bioRxiv:10.1101/131938

    Polymorphisms in the Yeast Galactose Sensor Underlie a Natural Continuum of Nutrient-Decision Phenotypes

    Lee K. B.*, Wang J.*, Palme J., Escalante-Chong R., Hua B., Springer, M. (2017) PLoS Genetics. 10.1371/journal.pgen.1006766

    *Equal contribution

    Natural Variation in Preparation for Nutrient Depletion Reveals a Cost-Benefit Tradeoff

    Wang J., Atolia E., Hua B., Savir Y., Escalante-Chong R., Springer M. (2015) PLoS Biology. 10.1371/journal.pbio.1002041.

    Large-effect beneficial synonymous mutations mediate rapid and parallel adaptation in a bacterium

    Agashe, D., Sane, M., Phalnikar, K., Diwan, G. D., Habibullah, A., Cecilia Martinez-Gomez, N., Sahasrabuddhe V., Polachek W., Wang J., Chubiz L. M., Marx C. J. (2016) Molecular Biology and Evolution, 33(6), 1542–1553. 10.1093/molbev/msw035

    Galactose metabolic genes in yeast respond to a ratio of galactose and glucose

    Escalante-Chong R., Savir Y., Carroll S. M., Ingraham J. B., Wang J., Marx C. J., Springer M. (2015) PNAS 112(5): 1636-1641.

    A chromatin-based mechanism for limiting divergent noncoding transcription

    Marquardt S., Escalante-Chong R., Pho N., Wang J., Churchman L. S., Springer M., Buratowski S. (2014) Cell 157: 1712–23.

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