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1.
J Biotechnol ; 224: 68-9, 2016 Apr 20.
Artigo em Inglês | MEDLINE | ID: mdl-26988396

RESUMO

A newly isolated strain P121 was identified as Pseudomonas fragi. The complete genome sequence of P.fragi P121 was carried out using the PacBio RSⅡ platform. The genome contains a circular chromosome with 5,101,809bp. The genome sequence suggests that the P121 exhibited the ability of degradation of toxic compounds. Genome sequencing information provides the genetic basis for the analysis of toxic compounds and the mechanism of extreme environmental adaptation of the strain.


Assuntos
Genoma Bacteriano , Pseudomonas fragi/genética , Análise de Sequência de DNA/métodos , Adaptação Fisiológica , Composição de Bases , Tamanho do Genoma
2.
Chinese Journal of Biotechnology ; (12): 545-553, 2014.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-279484

RESUMO

The gene encoding thermostable lactate dehydrogenase (Tm-LDH) was cloned into the plasmid pHsh from Thermotoga maritima, and expressed in Escherichia coli JM 109. The recombinant protein was purified to homogeneity by a simple step, heat treatment. The recombinant enzyme had a molecular mass of 33 kDa. The optimal temperature and pH of Tm-LDH were observed 95 degrees C and 7.0. The purified enzyme had a half-life of 2 h at 90 degrees C, and exhibited better stability over a pH range from 5.5 to 8.0. The K(m) and V(max) values were 1.7 mmol/L, 3.8 x 10(4) U/mg of protein for pyruvate, and 7.2 mmol/L and 1.1 x 10(5) U/mg for NADH, respectively. The expression of Tm-LDH in T7 system could not obtain high efficiency, but it has been soluble over-expression in pHsh system and reached 340 mg/L. The superior stability and productivity of Tm-LDH will lay the foundation of its industrial-scale fermentation and application in the NAD regeneration.


Assuntos
Clonagem Molecular , Estabilidade Enzimática , Escherichia coli , Metabolismo , L-Lactato Desidrogenase , Peso Molecular , Proteínas Recombinantes , Temperatura , Thermotoga maritima
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