DOE OSTI · 3018369
Harnessing evolution: leveraging bacterial isoprenoid pathway diversity toward improved bioengineering strategies
Abstract
Isoprenoids play vital roles in all domains of life, from beta-carotene in bacteria to heme in humans. Two distinct metabolic pathways have evolved to synthesize the critical precursor of all mature isoprenoids: the mevalonate (MEV) and the methylerythritol phosphate (MEP) pathways. Here, we quantify the extensive inter- and intra-genus heterogeneity in the usage of these two pathways with particular emphasis on rare bacteria that encode both, or neither, pathways. Furthermore, MEP intermediates themselves have non-isoprenogenic roles that may underlie evolutionary pressures driving pathway diversification. Understanding isoprenoid biosynthesis in bacteria offers new avenues toward more sustainable engineering of economically relevant molecules in microbes.
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Qabar, Christine M. [University of California, Berkeley, CA (United States)] (ORCID:0000000283459225), Marshall, Bailey A. [Univ. of Wisconsin, Madison, WI (United States)] (ORCID:0009000392134857), Landick, Robert [Univ. of Wisconsin, Madison, WI (United States)] (ORCID:0000000250420383), Cox, Jeffery S. [University of California, Berkeley, CA (United States)] (ORCID:0000000250616618). 2026-03-17. Harnessing evolution: leveraging bacterial isoprenoid pathway diversity toward improved bioengineering strategies. https://doi.org/10.1128/jb.00441-25
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