» Articles » PMID: 34834021

Towards a Synthetic Biology Toolset for Metallocluster Enzymes in Biosynthetic Pathways: What We Know and What We Need

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2021 Nov 27
PMID 34834021
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Microbes are routinely engineered to synthesize high-value chemicals from renewable materials through synthetic biology and metabolic engineering. Microbial biosynthesis often relies on expression of heterologous biosynthetic pathways, i.e., enzymes transplanted from foreign organisms. Metallocluster enzymes are one of the most ubiquitous family of enzymes involved in natural product biosynthesis and are of great biotechnological importance. However, the functional expression of recombinant metallocluster enzymes in live cells is often challenging and represents a major bottleneck. The activity of metallocluster enzymes requires essential supporting pathways, involved in protein maturation, electron supply, and/or enzyme stability. Proper function of these supporting pathways involves specific protein-protein interactions that remain poorly characterized and are often overlooked by traditional synthetic biology approaches. Consequently, engineering approaches that focus on enzymatic expression and carbon flux alone often overlook the particular needs of metallocluster enzymes. This review highlights the biotechnological relevance of metallocluster enzymes and discusses novel synthetic biology strategies to advance their industrial application, with a particular focus on iron-sulfur cluster enzymes. Strategies to enable functional heterologous expression and enhance recombinant metallocluster enzyme activity in industrial hosts include: (1) optimizing specific maturation pathways; (2) improving catalytic stability; and (3) enhancing electron transfer. In addition, we suggest future directions for developing microbial cell factories that rely on metallocluster enzyme catalysis.

Citing Articles

A metal-trap tests and refines blueprints to engineer cellular protein metalation with different elements.

Clough S, Young T, Tarrant E, Scott A, Chivers P, Glasfeld A Nat Commun. 2025; 16(1):810.

PMID: 39827241 PMC: 11742986. DOI: 10.1038/s41467-025-56199-w.


History of Maturation of Prokaryotic Molybdoenzymes-A Personal View.

Magalon A Molecules. 2023; 28(20).

PMID: 37894674 PMC: 10609526. DOI: 10.3390/molecules28207195.

References
1.
Weyman P, Vargas W, Chuang R, Chang Y, Smith H, Xu Q . Heterologous expression of Alteromonas macleodii and Thiocapsa roseopersicina [NiFe] hydrogenases in Escherichia coli. Microbiology (Reading). 2011; 157(Pt 5):1363-1374. DOI: 10.1099/mic.0.044834-0. View

2.
Kalms J, Schmidt A, Frielingsdorf S, Utesch T, Gotthard G, von Stetten D . Tracking the route of molecular oxygen in O-tolerant membrane-bound [NiFe] hydrogenase. Proc Natl Acad Sci U S A. 2018; 115(10):E2229-E2237. PMC: 5877991. DOI: 10.1073/pnas.1712267115. View

3.
Shen L, Kohlhaas M, Enoki J, Meier R, Schonenberger B, Wohlgemuth R . A combined experimental and modelling approach for the Weimberg pathway optimisation. Nat Commun. 2020; 11(1):1098. PMC: 7046635. DOI: 10.1038/s41467-020-14830-y. View

4.
Senger M, Stripp S, Soboh B . Proteolytic cleavage orchestrates cofactor insertion and protein assembly in [NiFe]-hydrogenase biosynthesis. J Biol Chem. 2017; 292(28):11670-11681. PMC: 5512064. DOI: 10.1074/jbc.M117.788125. View

5.
Atkinson J, Campbell I, Thomas E, Bonitatibus S, Elliott S, Bennett G . Metalloprotein switches that display chemical-dependent electron transfer in cells. Nat Chem Biol. 2018; 15(2):189-195. PMC: 6898983. DOI: 10.1038/s41589-018-0192-3. View