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A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor.
Jabbour, Dina; Sorger, Anneke; Sahm, Kerstin; Antranikian, Garabed.
Afiliação
  • Jabbour D; Institute of Technical Microbiology, Hamburg University of Technology, Kasernenstr. 12, Hamburg, 21073, Germany. jabbour@msu.edu
Appl Microbiol Biotechnol ; 97(7): 2971-8, 2013 Apr.
Article em En | MEDLINE | ID: mdl-22743714
ABSTRACT
Aiming at the isolation of novel enzymes from previously uncultured thermophilic microorganisms, a metagenome library was constructed from DNA isolated from a pilot-plant biogas reactor operating at 55 °C. The library was screened for starch-degrading enzymes, and one active clone was found. An open reading frame of 1,461 bp encoding an α-amylase from an uncultured organism was identified. The amy13A gene was cloned in Escherichia coli, resulting in high-level expression of the recombinant amylase. The novel enzyme Amy13A showed the highest sequence identity (75%) to α-amylases from Petrotoga mobilis and Halothermothrix orenii. Amy13A is highly thermoactive, exhibiting optimal activity at 80 °C, and it is also highly salt-tolerant, being active in 25% (w/v) NaCl. Amy13A is one of the few enzymes that tolerate high concentrations of salt and elevated temperatures, making it a potential candidate for starch processing under extreme conditions.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Reatores Biológicos / Alfa-Amilases / Metagenoma Idioma: En Revista: Appl Microbiol Biotechnol Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Reatores Biológicos / Alfa-Amilases / Metagenoma Idioma: En Revista: Appl Microbiol Biotechnol Ano de publicação: 2013 Tipo de documento: Article