TY - JOUR
T1 - Biosensor for branched-chain amino acid metabolism in yeast and applications in isobutanol and isopentanol production
AU - Zhang, Yanfei
AU - Cortez, Jeremy D.
AU - Hammer, Sarah K.
AU - Carrasco-López, César
AU - García Echauri, Sergio
AU - Wiggins, Jessica B.
AU - Wang, Wei
AU - Avalos, José L.
N1 - Funding Information:
The authors thank Christina DeCoste and Katherine Rittenbach, who assisted with all flow cytometry instrumentation. We also thank Wenyun Lu and Joshua D. Rabinowitz, who generously provided equipment and assistance in measuring intracellular α-IPM metabolite concentrations. This work was supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research, Genomic Science Program under award number DE-SC0019363, as well as by the National Science Foundation, and NSF CAREER Award CBET-1751840 (to J.L.A.). This work was also supported by the NSF Graduate Research Fellowship Program grant DGE-1656466, the P.E.O. Scholar Award, and the Harold W. Dodds Fellowship from Princeton University (to S.K.H.), as well as by the NIGMS of the National Institutes of Health under grant number T32GM007388 (to J.D.C.). The content of this article is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. J.L.A. is also supported by The Pew Charitable Trusts, The Camille Dreyfus Teacher-Scholar Award, The Eric and Wendy Schmidt Transformative Technology Fund, and grants from Princeton University and the Andlinger Center for Energy and the Environment.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Branched-chain amino acid (BCAA) metabolism fulfills numerous physiological roles and can be harnessed to produce valuable chemicals. However, the lack of eukaryotic biosensors specific for BCAA-derived products has limited the ability to develop high-throughput screens for strain engineering and metabolic studies. Here, we harness the transcriptional regulator Leu3p from Saccharomyces cerevisiae to develop a genetically encoded biosensor for BCAA metabolism. In one configuration, we use the biosensor to monitor yeast production of isobutanol, an alcohol derived from valine degradation. Small modifications allow us to redeploy Leu3p in another biosensor configuration that monitors production of the leucine-derived alcohol, isopentanol. These biosensor configurations are effective at isolating high-producing strains and identifying enzymes with enhanced activity from screens for branched-chain higher alcohol (BCHA) biosynthesis in mitochondria as well as cytosol. Furthermore, this biosensor has the potential to assist in metabolic studies involving BCAA pathways, and offers a blueprint to develop biosensors for other products derived from BCAA metabolism.
AB - Branched-chain amino acid (BCAA) metabolism fulfills numerous physiological roles and can be harnessed to produce valuable chemicals. However, the lack of eukaryotic biosensors specific for BCAA-derived products has limited the ability to develop high-throughput screens for strain engineering and metabolic studies. Here, we harness the transcriptional regulator Leu3p from Saccharomyces cerevisiae to develop a genetically encoded biosensor for BCAA metabolism. In one configuration, we use the biosensor to monitor yeast production of isobutanol, an alcohol derived from valine degradation. Small modifications allow us to redeploy Leu3p in another biosensor configuration that monitors production of the leucine-derived alcohol, isopentanol. These biosensor configurations are effective at isolating high-producing strains and identifying enzymes with enhanced activity from screens for branched-chain higher alcohol (BCHA) biosynthesis in mitochondria as well as cytosol. Furthermore, this biosensor has the potential to assist in metabolic studies involving BCAA pathways, and offers a blueprint to develop biosensors for other products derived from BCAA metabolism.
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U2 - 10.1038/s41467-021-27852-x
DO - 10.1038/s41467-021-27852-x
M3 - Article
C2 - 35022416
AN - SCOPUS:85122893593
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 270
ER -