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Directed Evolution of Cytochrome c for Carbon–Silicon Bond Formation: Bringing Silicon to Life

机译:指导细胞色素c进化为碳-硅键的形成:将硅赋予生命

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摘要

Enzymes that catalyze carbon–silicon bond formation are unknown in nature, despite the natural abundance of both elements. Such enzymes would expand the catalytic repertoire of biology, enabling living systems to access chemical space previously only open to synthetic chemistry. We have discovered that heme proteins catalyze the formation of organosilicon compounds under physiological conditions via carbene insertion into silicon–hydrogen bonds. The reaction proceeds both in vitro and in vivo, accommodating a broad range of substrates with high chemo- and enantioselectivity. Using directed evolution, we enhanced the catalytic function of cytochrome c from Rhodothermus marinus to achieve more than 15-fold higher turnover than state-of-the-art synthetic catalysts. This carbon–silicon bond-forming biocatalyst offers an environmentally friendly and highly efficient route to producing enantiopure organosilicon molecules.
机译:尽管两种元素天然丰富,但催化碳-硅键形成的酶在自然界尚不为人所知。这种酶将扩大生物学的催化范围,使生命系统能够进入以前仅对合成化学开放的化学空间。我们发现,在生理条件下,血红素蛋白通过卡宾插入硅氢键来催化有机硅化合物的形成。该反应可在体外和体内进行,可容纳多种具有高化学和对映选择性的底物。使用定向进化,我们增强了来自海藻的细胞色素c的催化功能,以实现比最先进的合成催化剂高15倍以上的营业额。这种形成碳硅键的生物催化剂为生产对映纯有机硅分子提供了一条环境友好且高效的途径。

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