Professional Education

  • Doctor of Philosophy, Baylor College Of Medicine (2012)
  • Bachelor of Science, University of Texas Austin (2006)

Stanford Advisors

All Publications

  • GTP dysregulation in Bacillus subtilis cells lacking (p)ppGpp results in phenotypic amino acid auxotrophy and failure to adapt to nutrient downshift and regulate biosynthesis genes Journal of Bacteriology Kriel, A., et al 2013
  • Direct Regulation of GTP Homeostasis by (p)ppGpp: A Critical Component of Viability and Stress Resistance MOLECULAR CELL Kriel, A., Bittner, A. N., Kim, S. H., Liu, K., Tehranchi, A. K., Zou, W. Y., Rendon, S., Chen, R., Tu, B. P., Wang, J. D. 2012; 48 (2): 231-241


    Cells constantly adjust their metabolism in response to environmental conditions, yet major mechanisms underlying survival remain poorly understood. We discover a posttranscriptional mechanism that integrates starvation response with GTP homeostasis to allow survival, enacted by the nucleotide (p)ppGpp, a key player in bacterial stress response and persistence. We reveal that (p)ppGpp activates global metabolic changes upon starvation, allowing survival by regulating GTP. Combining metabolomics with biochemical demonstrations, we find that (p)ppGpp directly inhibits the activities of multiple GTP biosynthesis enzymes. This inhibition results in robust and rapid GTP regulation in Bacillus subtilis, which we demonstrate is essential to maintaining GTP levels within a range that supports viability even in the absence of starvation. Correspondingly, without (p)ppGpp, gross GTP dysregulation occurs, revealing a vital housekeeping function of (p)ppGpp; in fact, loss of (p)ppGpp results in death from rising GTP, a severe and previously unknown consequence of GTP dysfunction.

    View details for DOI 10.1016/j.molcel.2012.08.009

    View details for Web of Science ID 000310423800009

    View details for PubMedID 22981860