초록
<▼1><P>New types of asymmetric functionalizations of alkenes are highly desirable for chemical synthesis. Here, we develop three novel types of regio- and enantioselective multiple oxy- and amino-functionalizations of terminal alkenes via cascade biocatalysis to produce chiral α-hydroxy acids, 1,2-amino alcohols and α-amino acids, respectively. Basic enzyme modules 1–4 are developed to convert alkenes to (<I>S</I>)-1,2-diols, (<I>S</I>)-1,2-diols to (<I>S</I>)-α-hydroxyacids, (<I>S</I>)-1,2-diols to (<I>S</I>)-aminoalcohols and (<I>S</I>)-α-hydroxyacids to (<I>S</I>)-α-aminoacids, respectively. Engineering of enzyme modules 1 & 2, 1 & 3 and 1, 2 & 4 in <I>Escherichia coli</I> affords three biocatalysts over-expressing 4–8 enzymes for one-pot conversion of styrenes to the corresponding (<I>S</I>)-α-hydroxyacids, (<I>S</I>)-aminoalcohols and (<I>S</I>)-α-aminoacids in high e.e. and high yields, respectively. The new types of asymmetric alkene functionalizations provide green, safe and useful alternatives to the chemical syntheses of these compounds. The modular approach for engineering multi-step cascade biocatalysis is useful for developing other new types of one-pot biotransformations for chemical synthesis.</P></▼1><▼2><P>[GRAPHIC OMISSION]Biocatalysis can perform highly selective multi-step synthesis in one pot, but with a limited range of non-natural reactions and products. Here, the authors report regio- and enantioselective bio-cascades, able to convert styrenes into a number of nitrogen and oxygen containing chiral molecules.</P></▼2>