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Application of Thermomyces lanuginosus polygalacturonase produced in Komagataella phaffii in biomass hydrolysis and textile bioscouring.
Serra, Luana Assis; Mendes, Thais Demarchi; Marco, Janice Lisboa De; de Almeida, João Ricardo Moreira.
Affiliation
  • Serra LA; Laboratory of Genetics and Biotechnology, EMBRAPA Agroenergy, Brasília, Brazil; Graduate Program of Microbial Biology, Institute of Biology, University of Brasília, Brazil.
  • Mendes TD; Laboratory of Genetics and Biotechnology, EMBRAPA Agroenergy, Brasília, Brazil.
  • Marco JL; Department of Cellular Biology, University of Brasília, Brasília, Brazil.
  • de Almeida JRM; Laboratory of Genetics and Biotechnology, EMBRAPA Agroenergy, Brasília, Brazil; Graduate Program of Microbial Biology, Institute of Biology, University of Brasília, Brazil. Electronic address: joao.almeida@embrapa.br.
Enzyme Microb Technol ; 177: 110424, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38479075
ABSTRACT
In this work, the polygalacturonase (TL-PG1) from the thermophilic fungus Thermomyces lanuginosus was heterologously produced for the first time in the yeast Komagataella phaffii. The TL-PG1 was successfully expressed under the control of the AOX1 promoter and sequentially purified by His-tag affinity. The purified recombinant pectinase exhibited an activity of 462.6 U/mL toward polygalacturonic acid under optimal conditions (pH 6 and 55 ˚C) with a 2.83 mg/mL and 0.063 µmol/minute for Km and Vmax, respectively. When used as supplementation for biomass hydrolysis, TL-PG1 demonstrated synergy with the enzymatic cocktail Ctec3 to depolymerize orange citrus pulp, releasing 1.43 mg/mL of reducing sugar. In addition, TL-PG1 exhibited efficiency in fabric bioscouring, showing potential usage in the textile industry. Applying a protein dosage of 7 mg/mL, the time for the fabric to absorb water was 19.77 seconds (ten times faster than the control). Adding the surfactant Triton to the treatment allowed the reduction of the enzyme dosage by 50% and the water absorption time to 6.38 seconds. Altogether, this work describes a new versatile polygalacturonase from T. lanuginosus with the potential to be employed in the hydrolysis of lignocellulosic biomass and bioscouring.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polygalacturonase / Fungal Proteins / Saccharomycetales Language: En Journal: Enzyme Microb Technol Year: 2024 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polygalacturonase / Fungal Proteins / Saccharomycetales Language: En Journal: Enzyme Microb Technol Year: 2024 Document type: Article Affiliation country: Brazil