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Activity-Based Protein Profiling of Chitin Catabolism.
Zegeye, Elias K; Sadler, Natalie C; Lomas, Gerard X; Attah, Isaac K; Jansson, Janet K; Hofmockel, Kirsten S; Anderton, Christopher R; Wright, Aaron T.
Afiliação
  • Zegeye EK; The Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, 1505 NE Stadium Way, Pullman, WA 99164, USA.
  • Sadler NC; Biological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Box 999, Richland, WA 99354, USA.
  • Lomas GX; Biological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Box 999, Richland, WA 99354, USA.
  • Attah IK; Biological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Box 999, Richland, WA 99354, USA.
  • Jansson JK; Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, 3335 Innovation Boulevard, Richland, WA 99354, USA.
  • Hofmockel KS; Biological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Box 999, Richland, WA 99354, USA.
  • Anderton CR; Biological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Box 999, Richland, WA 99354, USA.
  • Wright AT; Department of Ecology, Evolution and Organismal Biology Iowa State University, 251 Bessey Hall, Ames, Iowa (USA) 50011.
Chembiochem ; 22(4): 717-723, 2021 02 15.
Article em En | MEDLINE | ID: mdl-33049124
ABSTRACT
The microbial catabolism of chitin, an abundant and ubiquitous environmental organic polymer, is a fundamental cog in terrestrial and aquatic carbon and nitrogen cycles. Despite the importance of this critical bio-geochemical function, there is a limited understanding of the synergy between the various hydrolytic and accessory enzymes involved in chitin catabolism. To address this deficit, we synthesized activity-based probes (ABPs) designed to target active chitinolytic enzymes by modifying the chitin subunits N-acetyl glucosamine and chitotriose. The ABPs were used to determine the active complement of chitinolytic enzymes produced over time by the soil bacterium Cellvibrio japonicus treated with various C substrates. We demonstrate the utility of these ABPs in determining the synergy between various enzymes involved in chitin catabolism. The strategy can be used to gain molecular-level insights that can be used to better understand microbial roles in soil bio-geochemical cycling in the face of a changing climate.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Quitina / Quitinases / Cellvibrio / Proteoma Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Quitina / Quitinases / Cellvibrio / Proteoma Idioma: En Ano de publicação: 2021 Tipo de documento: Article