Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli

Synthetic biology greatly accelerated the building process of potential microbial cell factories for the production of industrially relevant compounds, e.g., chitooligosaccharides (COS) which have an enormous application potential in multiple industries, i.e., pharma, cosmetics and agrifood. COS are...

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Main Authors: Chiara Guidi, Xevi Biarnés, Antoni Planas, Marjan De Mey
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Current Research in Biotechnology
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Online Access:http://www.sciencedirect.com/science/article/pii/S2590262824000819
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author Chiara Guidi
Xevi Biarnés
Antoni Planas
Marjan De Mey
author_facet Chiara Guidi
Xevi Biarnés
Antoni Planas
Marjan De Mey
author_sort Chiara Guidi
collection DOAJ
description Synthetic biology greatly accelerated the building process of potential microbial cell factories for the production of industrially relevant compounds, e.g., chitooligosaccharides (COS) which have an enormous application potential in multiple industries, i.e., pharma, cosmetics and agrifood. COS are produced by the heterologous expression of the chitin oligosaccharide synthase, NodC, in Escherichia coli, mainly yielding mixtures of chitintetraose (A4) and/or chitinpentaose (A5). We rationalised here product formation limitations based on molecular modelling of the structures of several NodC enzymes. We used this information to protein engineer NodC, rendering longer COS. Hence, an in vivo platform of defined COS-producing strains with different degrees of polymerisation was developed and experimentally characterised. Significantly, several strains were producing long COS, such as chitinhexaose (A6) and −heptaose (A7), not identified in any other natural producer. Additionally, other engineered strains efficiently produce almost 100% specific A4 or A5 product. Altogether, our results indicate that electrostatics-driven dynamics effects are to be considered in the molecular ruler hypothesis. Charge density at the transmembrane helices of NodC affects the opening of the integral binding pocket and in this way the length of the produced chitin oligomers can be modulated. As a result, the internal ruler mechanism elaborated and validated in this manuscript can serve as a guideline to perform site-directed mutagenesis at positions in related NodC and chitin synthase enzymes for both industrial applications as for identification of therapeutic targets.
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spelling doaj-art-90df8e98a2054e02b5ce9daa4cf2a8a22025-08-20T02:30:30ZengElsevierCurrent Research in Biotechnology2590-26282024-01-01810025510.1016/j.crbiot.2024.100255Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coliChiara Guidi0Xevi Biarnés1Antoni Planas2Marjan De Mey3Centre for Synthetic Biology, Ghent University, Coupure Links 653 9000, Ghent, BelgiumLaboratory of Biochemistry, Institut Químic de Sarrià, Universitat Ramon Llull, Via Augusta 390 08017, Barcelona, SpainLaboratory of Biochemistry, Institut Químic de Sarrià, Universitat Ramon Llull, Via Augusta 390 08017, Barcelona, SpainCentre for Synthetic Biology, Ghent University, Coupure Links 653 9000, Ghent, Belgium; Corresponding author.Synthetic biology greatly accelerated the building process of potential microbial cell factories for the production of industrially relevant compounds, e.g., chitooligosaccharides (COS) which have an enormous application potential in multiple industries, i.e., pharma, cosmetics and agrifood. COS are produced by the heterologous expression of the chitin oligosaccharide synthase, NodC, in Escherichia coli, mainly yielding mixtures of chitintetraose (A4) and/or chitinpentaose (A5). We rationalised here product formation limitations based on molecular modelling of the structures of several NodC enzymes. We used this information to protein engineer NodC, rendering longer COS. Hence, an in vivo platform of defined COS-producing strains with different degrees of polymerisation was developed and experimentally characterised. Significantly, several strains were producing long COS, such as chitinhexaose (A6) and −heptaose (A7), not identified in any other natural producer. Additionally, other engineered strains efficiently produce almost 100% specific A4 or A5 product. Altogether, our results indicate that electrostatics-driven dynamics effects are to be considered in the molecular ruler hypothesis. Charge density at the transmembrane helices of NodC affects the opening of the integral binding pocket and in this way the length of the produced chitin oligomers can be modulated. As a result, the internal ruler mechanism elaborated and validated in this manuscript can serve as a guideline to perform site-directed mutagenesis at positions in related NodC and chitin synthase enzymes for both industrial applications as for identification of therapeutic targets.http://www.sciencedirect.com/science/article/pii/S2590262824000819Chitin oligosaccharide synthaseMolecular dynamicsNodCProtein engineeringSynthetic biology
spellingShingle Chiara Guidi
Xevi Biarnés
Antoni Planas
Marjan De Mey
Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
Current Research in Biotechnology
Chitin oligosaccharide synthase
Molecular dynamics
NodC
Protein engineering
Synthetic biology
title Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
title_full Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
title_fullStr Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
title_full_unstemmed Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
title_short Expanding the chitin oligosaccharide portfolio by engineering NodC chitin synthases in Escherichia coli
title_sort expanding the chitin oligosaccharide portfolio by engineering nodc chitin synthases in escherichia coli
topic Chitin oligosaccharide synthase
Molecular dynamics
NodC
Protein engineering
Synthetic biology
url http://www.sciencedirect.com/science/article/pii/S2590262824000819
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