# Mechanism of Polyester Hydrolysis by Marine Bacterium PE‑H Enzyme: an Atomistic and Thermodynamic Characterization

## TL;DR

This paper explores how a marine bacterium enzyme breaks down plastic, revealing a two-step process and key structural features that could help improve plastic recycling.

## Contribution

The study provides a detailed atomistic and thermodynamic characterization of the PE-H enzyme's PET hydrolysis mechanism.

## Key findings

- The PE-H enzyme hydrolyzes PET through a two-stage reaction involving acylation and deacylation.
- Deacylation is the rate-limiting step with a free energy barrier of about 10.6 kcal·mol–1.
- Structural features like the S171, H249, D217 triad and F98, M172 aid in catalysis and stabilization of intermediates.

## Abstract

Polyethylene terephthalate (PET) is a widely used plastic
due to
its durability and adaptability; however, its resistance to natural
degradation has led to severe accumulation in the environment. Recently,
a PET-degrading marine bacterium, Pseudomonas aestusnigri, was identified and proposed for possible use in sustainable plastic
recycling, particularly the PE-H enzyme, which hydrolyses PET with
MHET as the main hydrolysis product. In this work, we investigate
the reaction mechanism of PE-H through umbrella sampling hybrid quantum
mechanics/molecular mechanics molecular dynamics simulations at the
PBE/AMBER level. Our results show a two-stage reaction pathway: acylation
and deacylation, both of which proceed stepwise via tetrahedral intermediate
formation. We identified deacylation as the rate-limiting step with
a free energy barrier of approximately 10.6 kcal·mol–1, which is relatively lower than the barrier of other PET hydrolyses.
Our analysis suggests that structural features promoting oxyanion
hole formation or enhancing substrate accommodation contribute to
lower free energy barrier and promote catalysis. We highlight the
role of the S171, H249 and D217 triad responsible for the catalysis
of proton transfer and nucleophilic attack reactions, and of F98 and
M172 responsible for the formation of the oxyanion hole contributing
to the stabilization of tetrahedral intermediates formed along the
path. These findings provide mechanistic insights into PE-H catalysis
and suggest structural factors that could be extended to other enzymes,
providing a basis for future studies to understand enzymatic plastic
degradation.