(Reverse) Evolution of a Promiscuous Isochorismate Pyruvate Lyase into an Efficient Chorismate Mutase


Date

2025-08-05

Publication Type

Journal Article

ETH Bibliography

yes

Citations

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Data

Abstract

PchB is an isochorismate pyruvate lyase (IPL) involved in siderophore biosynthesis in Pseudomonas aeruginosa . Besides catalyzing the [1,5]-sigmatropic rearrangement of isochorismate, PchB also has weak chorismate mutase (CM) activity, promoting the [3,3]-sigmatropic transformation of chorismate. It has been suggested that the secondary metabolism enzyme PchB evolved from a primary metabolism CM precursor. Here, we employed directed evolution to convert PchB (back) into an efficient CM. A total of seven residues around the active site differing between PchB and a prototypical CM from Escherichia coli were randomized, and the resulting gene library was subjected to selection for CM activity. After growth selection in an auxotrophic strain, a catalyst with 10-fold increased CM activity emerged. The improved enzyme was again randomized at three active site positions and subjected to selection, leading to a PchB variant with a k cat/K m of 96,000 M-1 s-1, which is 40 times higher than that of the parent enzyme and well within the range of dedicated natural CMs. The facile conversion of an IPL into a CM by directed evolution coincides with the fact that both reactions proceed through mechanistically interesting pericyclic processes, reaction types otherwise rarely used by enzymes. When probing typical established CMs for catalytic promiscuity, we discovered spurious IPL activity for the secreted CM from Mycobacterium tuberculosis . Our results hint at active site features, particularly a Val at the bottom of the substrate-binding pocket that may have served as a steppingstone for the evolution of IPL activity in a primordial CM.

Publication status

published

Editor

Book title

Journal / series

Volume

64 (15)

Pages / Article No.

3459 - 3473

Publisher

American Chemical Society

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Bacteria; Genetics; Monomers; Peptides And Proteins; Protein Engineering

Organisational unit

Notes

Funding

182648 - Exploring structure, function, and mechanism of atypical bacterial chorismate mutases (SNF)

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