Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Volume 565 Issue 7737, 3 January 2019

Unnatural selection

The catalytic replacement of a carbon–hydrogen bond with a carbon–carbon bond is an attractive strategy for building organic molecules. In this week’s issue, Frances Arnold and her colleagues report that a cytochrome P450 enzyme can be evolved to perform this transformation efficiently within bacteria. Their iron-haem enzymes catalyse carbene insertion into sp3 hybridized C–H bonds, and deliver alkylated products with high enantioselectivity. The team’s results highlight that iron can be used to achieve this challenging reaction, indicating that this metal could replace less abundant elements, such as rhodium and iridium, that have previously been used for such functionalization. Although nature’s chemical repertoire does not include carbene C–H insertion, an existing enzyme produced within a microbe can be modified to perform these abiological reactions.

Cover image: Lei Chen/California Institute of Technology

This Week

Top of page ⤴

News in Focus

Top of page ⤴

Comment

Top of page ⤴

Technology

Top of page ⤴

Careers

Top of page ⤴

Futures

  • Time to go home?

    • Laurence Raphael Brothers
    Futures
Top of page ⤴

Research

Top of page ⤴

Amendments & Corrections

Top of page ⤴
Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing

Search

Quick links