A novel AA10 from Paenibacillus curdlanolyticus and its synergistic action on crystalline and complex polysaccharides.

Broad substrate specificity Family 10 auxiliary activity of lytic polysaccharide monooxygenase Lignocellulosic biomass Non-catalytic domain Paenibacillus curdlanolyticus β-1,4 Glycosidic linkage substrate

Journal

Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 28 05 2020
accepted: 24 06 2020
revised: 18 06 2020
pubmed: 12 7 2020
medline: 15 5 2021
entrez: 12 7 2020
Statut: ppublish

Résumé

Lytic polysaccharide monooxygenases (LPMOs) play an important role in the degradation of complex polysaccharides in lignocellulosic biomass. In the present study, we characterized a modular LPMO (PcAA10A), consisting of a family 10 auxiliary activity of LPMO (AA10) catalytic domain, and non-catalytic domains including a family 5 carbohydrate-binding module, two fibronectin type-3 domains, and a family 3 carbohydrate-binding module from Paenibacillus curdlanolyticus B-6, which was expressed in a recombinant Escherichia coli. Comparison of activities between full-length PcAA10A and the catalytic domain polypeptide (PcAA10A_CD) indicates that the non-catalytic domains are important for the deconstruction of crystalline cellulose and complex polysaccharides contained in untreated lignocellulosic biomass. Interestingly, PcAA10A_CD acted not only on cellulose and chitin, but also on xylan, mannan, and xylan and cellulose contained in lignocellulosic biomass, which has not been reported for the AA10 family. Mutation of the key residues, Trp51 located at subsite - 2 and Phe171 located at subsite +2, in the substrate-binding site of PcAA10A_CD revealed that these residues are substantially involved in broad substrate specificity toward cellulose, xylan, and mannan, albeit with a low effect toward chitin. Furthermore, PcAA10A had a boosting effect on untreated corn hull degradation by P. curdlanolyticus B-6 endo-xylanase Xyn10D and Clostridium thermocellum endo-glucanase Cel9A. These results suggest that PcAA10A is a unique LPMO capable of cleaving and enhancing lignocellulosic biomass degradation, making it a good candidate for biotechnological applications. KEY POINTS: • PcAA10A is a novel modular LPMO family 10 from Paenibacillus curdlanolyticus. • PcAA10A showed broad substrate specificity on β-1,4 glycosidic linkage substrates. • Non-catalytic domains are important for degrading complex polysaccharides. • PcAA10A is a unique LPMO capable of enhancing lignocellulosic biomass degradation.

Identifiants

pubmed: 32651597
doi: 10.1007/s00253-020-10758-x
pii: 10.1007/s00253-020-10758-x
doi:

Substances chimiques

Polysaccharides 0
Chitin 1398-61-4
Mixed Function Oxygenases EC 1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7533-7550

Subventions

Organisme : Thailand Research Fund
ID : PHD/0106/2553

Auteurs

Puangpen Limsakul (P)

School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Paripok Phitsuwan (P)

School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Rattiya Waeonukul (R)

Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Patthra Pason (P)

Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Chakrit Tachaapaikoon (C)

Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Kanokwan Poomputsa (K)

School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Akihiko Kosugi (A)

Biological Resources and Post-harvest Division, Japan International Research Center for Agricultural Sciences, Tsukuba, Ibaraki, 305-8686, Japan.

Makiko Sakka (M)

Graduated School of Bioresources, Mie University, Tsu, Mie, 514-8507, Japan.

Kazuo Sakka (K)

Graduated School of Bioresources, Mie University, Tsu, Mie, 514-8507, Japan. sakka@bio.mie-u.ac.jp.

Khanok Ratanakhanokchai (K)

School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand. khanok.rat@kmutt.ac.th.

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