Biosynthetic mechanisms of natural products primarily
depend on
systems of protein catalysts. However, within the field of biosynthesis,
there are cases in which the inherent chemical reactivity of metabolic
intermediates and substrates evades the involvement of enzymes. These
reactions are difficult to characterize based on their reactivity
and occlusion within the milieu of the cellular environment. As we
continue to build a strong foundation for how microbes and higher
organisms produce natural products, therein lies a need for understanding
how protein independent or nonenzymatic biosynthetic steps can occur.
We have classified such reactions into four categories: intramolecular,
multicomponent, tailoring, and light-induced reactions. Intramolecular
reactions is one of the most well studied in the context of biomimetic
synthesis, consisting of cyclizations and cycloadditions due to the
innate reactivity of the intermediates. There are two subclasses that
make up multicomponent reactions, one being homologous multicomponent
reactions which results in dimeric and pseudodimeric natural products,
and the other being heterologous multicomponent reactions, where two
or more precursors from independent biosynthetic pathways undergo
a variety of reactions to produce the mature natural product. The
third type of reaction discussed are tailoring reactions, where postmodifications
occur on the natural products after the biosynthetic machinery is
completed. The last category consists of light-induced reactions involving
ecologically relevant UV light rather than high intensity UV irradiation
that is traditionally used in synthetic chemistry. This review will
cover recent nonenzymatic biosynthetic mechanisms and include sources
for those reviewed previously.
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