Enzymatic Cascade Reactions in Biosynthesis

被引:144
|
作者
Walsh, Christopher T. [3 ]
Moore, Bradley S. [1 ,2 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, Ctr Marine Biotechnol & Biomed, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[3] Stanford Univ, Stanford Univ Chem Engn & Med Human Hlth CheM H, Stanford, CA 94305 USA
关键词
electrophilic cascades; natural products; nucleophilic cascades; pericyclic cascades; radical cascades; GENE-CLUSTER; GIBBERELLIN BIOSYNTHESIS; CRYSTAL-STRUCTURE; CATALYTIC MECHANISM; OXIDATIVE CYCLIZATION; REDUCTIVE CYCLIZATION; COPE REARRANGEMENT; COUPLING REACTION; DIELS-ALDERASE; ATOM ECONOMY;
D O I
10.1002/anie.201807844
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enzyme-mediated cascade reactions are widespread in biosynthesis. To facilitate comparison with the mechanistic categorizations of cascade reactions by synthetic chemists and delineate the common underlying chemistry, we discuss four types of enzymatic cascade reactions: those involving nucleophilic, electrophilic, pericyclic, and radical reactions. Two subtypes of enzymes that generate radical cascades exist at opposite ends of the oxygen abundance spectrum. Iron-based enzymes use O-2 to generate high valent iron-oxo species to homolyze unactivated C-H bonds in substrates to initiate skeletal rearrangements. At anaerobic end, enzymes reversibly cleave S-adenosylmethionine (SAM) to generate the 5 '-deoxyadenosyl radical as a powerful oxidant to initiate C-H bond homolysis in bound substrates. The latter enzymes are termed radical SAM enzymes. We categorize the former as thwarted oxygenases.
引用
收藏
页码:6846 / 6879
页数:34
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