Heterologous expression of a new lytic polysaccharide monooxygenase from Hahella ganghwensis and their functional characterization.
The powerful class of oxidative enzymes, lytic polysaccharide monooxygenases (LPMOs) - also named Auxiliary Activity (AA) - are able to oxidize recalcitrant polysaccharides on lignocellulosic biomass. In this work, we successfully expressed three catalytic domains from bacterial LPMOs in the yeast Komagataella phaffii: domain MdAA10.1-SD (from Moritella dasanensis), domain VmAA10.2-SD (from Verrucosispora maris), and domain HgAA10.1-SD (from Hahella ganghwensis). Heterologous expression was analyzed by SDS-PAGE, Western-Blot, and Dot-Blot, while functional activity of these proteins was investigated by a combination of mass spectrometric and chromatographic methods. The recombinant LPMO catalytic domain HgAA10.1-SD from H. ganghwensis, a C1-oxidizer, was able to promote an oxidative cleavage of phosphoric-acid swollen cellulose (PASC) substrate in the presence of ascorbic acid as an electron donor, showing its potential for cellulose depolymerization.
Principais autores: | , , , , , , |
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Outros Autores: | |
Formato: | Separatas biblioteca |
Idioma: | English eng |
Publicado em: |
2019-09-23
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Assuntos: | Spectrometric, Chromatographic, |
Acesso em linha: | http://www.alice.cnptia.embrapa.br/alice/handle/doc/1112393 |
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