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PACER: a novel 3D plant cell wall model for the analysis of non-catalytic and enzymatic responses.
Monschein, Mareike; Jurak, Edita; Paasela, Tanja; Koitto, Taru; Lambauer, Vera; Pavicic, Mirko; Enjalbert, Thomas; Dumon, Claire; Master, Emma R.
Affiliation
  • Monschein M; Department of Bioproducts and Biosystems, Aalto University, Kemistintie 1, 02150, Espoo, Finland.
  • Jurak E; Department of Bioproducts and Biosystems, Aalto University, Kemistintie 1, 02150, Espoo, Finland.
  • Paasela T; Department of Bioproduct Engineering, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands.
  • Koitto T; Department of Agricultural Sciences, Viikki Plant Science Centre, University of Helsinki, P.O. Box 27, 00014, Helsinki, Finland.
  • Lambauer V; Department of Bioproducts and Biosystems, Aalto University, Kemistintie 1, 02150, Espoo, Finland.
  • Pavicic M; Department of Bioproducts and Biosystems, Aalto University, Kemistintie 1, 02150, Espoo, Finland.
  • Enjalbert T; Department of Agricultural Sciences, Viikki Plant Science Centre, University of Helsinki, P.O. Box 27, 00014, Helsinki, Finland.
  • Dumon C; Toulouse Biotechnology Institute (TBI), Université de Toulouse, CNRS, INRAE, INSA, 31077, Toulouse, France.
  • Master ER; Toulouse Biotechnology Institute (TBI), Université de Toulouse, CNRS, INRAE, INSA, 31077, Toulouse, France.
Biotechnol Biofuels Bioprod ; 15(1): 30, 2022 Mar 16.
Article in En | MEDLINE | ID: mdl-35296345
BACKGROUND: Substrate accessibility remains a key limitation to the efficient enzymatic deconstruction of lignocellulosic biomass. Limited substrate accessibility is often addressed by increasing enzyme loading, which increases process and product costs. Alternatively, considerable efforts are underway world-wide to identify amorphogenesis-inducing proteins and protein domains that increase the accessibility of carbohydrate-active enzymes to targeted lignocellulose components. RESULTS: We established a three-dimensional assay, PACER (plant cell wall model for the analysis of non-catalytic and enzymatic responses), that enables analysis of enzyme migration through defined lignocellulose composites. A cellulose/azo-xylan composite was made to demonstrate the PACER concept and then used to test the migration and activity of multiple xylanolytic enzymes. In addition to non-catalytic domains of xylanases, the potential of loosenin-like proteins to boost xylanase migration through cellulose/azo-xylan composites was observed. CONCLUSIONS: The PACER assay is inexpensive and parallelizable, suitable for screening proteins for ability to increase enzyme accessibility to lignocellulose substrates. Using the PACER assay, we visualized the impact of xylan-binding modules and loosenin-like proteins on xylanase mobility and access to targeted substrates. Given the flexibility to use different composite materials, the PACER assay presents a versatile platform to study impacts of lignocellulose components on enzyme access to targeted substrates.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biotechnol Biofuels Bioprod Year: 2022 Document type: Article Affiliation country: Finland Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biotechnol Biofuels Bioprod Year: 2022 Document type: Article Affiliation country: Finland Country of publication: United kingdom