Abstract
Diversity of scaffold structure and function is a hallmark of the >50,000 isoprenoid natural products such as taxol. Whereas most members of this class are assembled by iterative head-to-tail enzymatic joining reactions between Δ2 and Δ 3-isopentenyl diphosphate (IPP) monomers, dimerization of two Δ2-IPP molecules has now been shown to account for three additional modes of "irregular" coupling patterns at the level of C10 monoterpene scaffolds. © 2007 by American Chemical Society.
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CITATION STYLE
Walsh, C. T. (2007). Revealing coupling patterns in isoprenoid alkylation biocatalysis. ACS Chemical Biology, 2(5), 296–298. https://doi.org/10.1021/cb700094s
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